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A HapMap harvest of insights into the genetics of common disease
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1001/archopht.125.1.55openalex-snapshot
A Prospective Study of 2 Major Age-Related Macular Degeneration Susceptibility Alleles and Interactions With Modifiable Risk Factors
inferredcites →https://doi.org/10.1002/biot.200600213openalex-snapshot
Whole genome genotyping technologies on the BeadArray™ platform
inferredcites →https://doi.org/10.1007/s00125-007-0825-7openalex-snapshot
Genetic studies of diabetes following the advent of the genome-wide association study: where do we go from here?
inferredcites →https://doi.org/10.1016/j.ajhg.2007.11.001openalex-snapshot
Genome-wide Association Study Identifies Genes for Biomarkers of Cardiovascular Disease: Serum Urate and Dyslipidemia
inferredcites →https://doi.org/10.1016/j.cell.2006.10.003openalex-snapshot
The Regulation of INK4/ARF in Cancer and Aging
inferredcites →https://doi.org/10.1016/j.contraception.2004.02.010openalex-snapshot
Venous thromboembolic disease in users of low-estrogen combined estrogen-progestin oral contraceptives
inferredcites →https://doi.org/10.1016/j.mad.2007.03.005openalex-snapshot
A common variant of the p16INK4a genetic region is associated with physical function in older people
inferredcites →https://doi.org/10.1016/j.neuron.2007.05.022openalex-snapshot
GAB2 Alleles Modify Alzheimer's Risk in APOE ɛ4 Carriers
inferredcites →https://doi.org/10.1016/j.survophthal.2006.08.003openalex-snapshot
Unraveling A Complex Genetic Disease: Age-related Macular Degeneration
inferredcites →https://doi.org/10.1016/s0022-3476(88)80289-0openalex-snapshot
Lovastatin therapy in receptor-negative homozygous familial hypercholesterolemia: Lack of effect on low-density lipoprotein concentrations or turnover
inferredcites →https://doi.org/10.1016/s0084-392x(08)79151-2openalex-snapshot
Common Sequence Variants in the LOXL1 Gene Confer Susceptibility to Exfoliation Glaucoma
inferredcites →https://doi.org/10.1016/s0168-9525(01)02410-6openalex-snapshot
On the allelic spectrum of human disease
inferredcites →https://doi.org/10.1016/s1474-4422(07)70037-6openalex-snapshot
Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data
inferredcites →https://doi.org/10.1038/35057062openalex-snapshot
Initial sequencing and analysis of the human genome
inferredcites →https://doi.org/10.1038/35057149openalex-snapshot
A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms
inferredcites →https://doi.org/10.1038/447655aopenalex-snapshot
Replicating genotype–phenotype associations
inferredcites →https://doi.org/10.1038/nature01140openalex-snapshot
Detecting recent positive selection in the human genome from haplotype structure
inferredcites →https://doi.org/10.1038/nature01401openalex-snapshot
Nature, nurture and human disease
inferredcites →https://doi.org/10.1038/nature03001openalex-snapshot
Finishing the euchromatic sequence of the human genome
inferredcites →https://doi.org/10.1038/nature04226openalex-snapshot
A haplotype map of the human genome
inferredcites →https://doi.org/10.1038/nature04244openalex-snapshot
Mapping determinants of human gene expression by regional and genome-wide association
inferredcites →https://doi.org/10.1038/nature05329openalex-snapshot
Global variation in copy number in the human genome
inferredcites →https://doi.org/10.1038/nature05616openalex-snapshot
A genome-wide association study identifies novel risk loci for type 2 diabetes
inferredcites →https://doi.org/10.1038/nature05887openalex-snapshot
Genome-wide association study identifies novel breast cancer susceptibility loci
inferredcites →https://doi.org/10.1038/nature05911openalex-snapshot
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
inferredcites →https://doi.org/10.1038/nature06007openalex-snapshot
Variants conferring risk of atrial fibrillation on chromosome 4q25
inferredcites →https://doi.org/10.1038/nature06010openalex-snapshot
A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene
inferredcites →https://doi.org/10.1038/nature06014openalex-snapshot
Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma
inferredcites →https://doi.org/10.1038/nature06250openalex-snapshot
Genome-wide detection and characterization of positive selection in human populations
inferredcites →https://doi.org/10.1038/nature06258openalex-snapshot
A second generation human haplotype map of over 3.1 million SNPs
inferredcites →https://doi.org/10.1038/ng.2007.13openalex-snapshot
Genetic determinants of hair, eye and skin pigmentation in Europeans
inferredcites →https://doi.org/10.1038/ng.2007.18openalex-snapshot
A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk
inferredcites →https://doi.org/10.1038/ng.2007.27openalex-snapshot
Two independent alleles at 6q23 associated with risk of rheumatoid arthritis
inferredcites →https://doi.org/10.1038/ng.2007.52openalex-snapshot
Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis
inferredcites →https://doi.org/10.1038/ng.2007.61openalex-snapshot
Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides
inferredcites →https://doi.org/10.1038/ng.74openalex-snapshot
Common variants in the GDF5-UQCC region are associated with variation in human height
inferredcites →https://doi.org/10.1038/ng.75openalex-snapshot
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans
inferredcites →https://doi.org/10.1038/ng.76openalex-snapshot
Newly identified loci that influence lipid concentrations and risk of coronary artery disease
inferredcites →https://doi.org/10.1038/ng.79openalex-snapshot
Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus
inferredcites →https://doi.org/10.1038/ng.81openalex-snapshot
Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci
inferredcites →https://doi.org/10.1038/ng1007-1181openalex-snapshot
The NCBI dbGaP database of genotypes and phenotypes
inferredcites →https://doi.org/10.1038/ng1090openalex-snapshot
Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease
inferredcites →https://doi.org/10.1038/ng1562openalex-snapshot
Fine-scale structural variation of the human genome
inferredcites →https://doi.org/10.1038/ng1582openalex-snapshot
Genomic screening and replication using the same data set in family-based association testing
inferredcites →https://doi.org/10.1038/ng1695openalex-snapshot
Common deletions and SNPs are in linkage disequilibrium in the human genome
inferredcites →https://doi.org/10.1038/ng1790openalex-snapshot
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization
inferredcites →https://doi.org/10.1038/ng1899openalex-snapshot
Transferability of tag SNPs in genetic association studies in multiple populations
inferredcites →https://doi.org/10.1038/ng1999openalex-snapshot
Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24
inferredcites →https://doi.org/10.1038/ng2015openalex-snapshot
Multiple regions within 8q24 independently affect risk for prostate cancer
inferredcites →https://doi.org/10.1038/ng2022openalex-snapshot
Genome-wide association study of prostate cancer identifies a second risk locus at 8q24
inferredcites →https://doi.org/10.1038/ng2032openalex-snapshot
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis
inferredcites →https://doi.org/10.1038/ng2043openalex-snapshot
A variant in CDKAL1 influences insulin response and risk of type 2 diabetes
inferredcites →https://doi.org/10.1038/ng2058openalex-snapshot
A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21
inferredcites →https://doi.org/10.1038/ng2061openalex-snapshot
Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility
inferredcites →https://doi.org/10.1038/ng2062openalex-snapshot
Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes
inferredcites →https://doi.org/10.1038/ng2064openalex-snapshot
Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor–positive breast cancer
inferredcites →https://doi.org/10.1038/ng2068openalex-snapshot
Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes
inferredcites →https://doi.org/10.1038/ng2075openalex-snapshot
A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer
inferredcites →https://doi.org/10.1038/ng2080openalex-snapshot
Copy-number variation and association studies of human disease
inferredcites →https://doi.org/10.1038/ng2085openalex-snapshot
A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21
inferredcites →https://doi.org/10.1038/ng2089openalex-snapshot
Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24
inferredcites →https://doi.org/10.1038/ng2099openalex-snapshot
Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions
inferredcites →https://doi.org/10.1038/ng2101openalex-snapshot
A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease
inferredcites →https://doi.org/10.1038/ng2108openalex-snapshot
A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15
inferredcites →https://doi.org/10.1038/ng2121openalex-snapshot
A common variant of HMGA2 is associated with adult and childhood height in the general population
inferredcites →https://doi.org/10.1038/ng2127openalex-snapshot
New models of collaboration in genome-wide association studies: the Genetic Association Information Network
inferredcites →https://doi.org/10.1038/nmeth718openalex-snapshot
Genotyping over 100,000 SNPs on a pair of oligonucleotide arrays
inferredcites →https://doi.org/10.1038/nmeth842openalex-snapshot
Whole-genome genotyping with the single-base extension assay
inferredcites →https://doi.org/10.1038/nrg1351openalex-snapshot
Integrating ethics and science in the International HapMap Project
inferredcites →https://doi.org/10.1038/nrg1521openalex-snapshot
Genome-wide association studies for common diseases and complex traits
inferredcites →https://doi.org/10.1038/nrg1522openalex-snapshot
Genome-wide association studies: theoretical and practical concerns
inferredcites →https://doi.org/10.1038/nrg2187openalex-snapshot
Recent and ongoing selection in the human genome
inferredcites →https://doi.org/10.1038/sj.ejhg.5201583openalex-snapshot
An utter refutation of the ‘Fundamental Theorem of the HapMap’
inferredcites →https://doi.org/10.1038/sj.mp.4001449openalex-snapshot
Will haplotype maps be useful for finding genes?
inferredcites →https://doi.org/10.1038/sj.mp.4001983openalex-snapshot
Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia
inferredcites →https://doi.org/10.1038/sj.mp.4002012openalex-snapshot
A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder
inferredcites →https://doi.org/10.1056/nejmoa072366openalex-snapshot
Genomewide Association Analysis of Coronary Artery Disease
inferredcites →https://doi.org/10.1056/nejmoa072743openalex-snapshot
A Genetic Risk Factor for Periodic Limb Movements in Sleep
inferredcites →https://doi.org/10.1056/nejmoa073491openalex-snapshot
TRAF1–C5 as a Risk Locus for Rheumatoid Arthritis — A Genomewide Study
inferredcites →https://doi.org/10.1056/nejmoa073493openalex-snapshot
Risk Alleles for Multiple Sclerosis Identified by a Genomewide Study
inferredcites →https://doi.org/10.1056/nejmp068126openalex-snapshot
What Genome-wide Association Studies Can Do for Medicine
inferredcites →https://doi.org/10.1056/nejmp078120openalex-snapshot
Drinking from the Fire Hose — Statistical Issues in Genomewide Association Studies
inferredcites →https://doi.org/10.1056/nejmsb042979openalex-snapshot
The Family History — More Important Than Ever
inferredcites →https://doi.org/10.1073/pnas.0706645104openalex-snapshot
Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci
inferredcites →https://doi.org/10.1086/368203openalex-snapshot
Undetected Genotyping Errors Cause Apparent Overtransmission of Common Alleles in the Transmission/Disequilibrium Test
inferredcites →https://doi.org/10.1086/508942openalex-snapshot
Analysis of High-Resolution HapMap of DTNBP1 (Dysbindin) Suggests No Consistency between Reported Common Variant Associations and Schizophrenia
inferredcites →https://doi.org/10.1086/522235openalex-snapshot
A Genomewide Association Study of Skin Pigmentation in a South Asian Population
inferredcites →https://doi.org/10.1093/genetics/155.2.945openalex-snapshot
Inference of Population Structure Using Multilocus Genotype Data
inferredcites →https://doi.org/10.1093/hmg/11.20.2417openalex-snapshot
The allelic architecture of human disease genes: common disease-common variant... or not?
inferredcites →https://doi.org/10.1093/hmg/ddh057openalex-snapshot
Progress in defining the molecular basis of type 2 diabetes mellitus through susceptibility-gene identification
inferredcites →https://doi.org/10.1093/hmg/ddl057openalex-snapshot
Structural variants: changing the landscape of chromosomes and design of disease studies
inferredcites →https://doi.org/10.1093/jnci/djh075openalex-snapshot
Assessing the Probability That a Positive Report is False: An Approach for Molecular Epidemiology Studies
inferredcites →https://doi.org/10.1097/01.ogx.0000279314.45442.bbopenalex-snapshot
A Common Allele on Chromosome 9 Associated With Coronary Heart Disease
inferredcites →https://doi.org/10.1101/gr.2014904openalex-snapshot
Parallel Genotyping of Over 10,000 SNPs Using a One-Primer Assay on a High-Density Oligonucleotide Array
inferredcites →https://doi.org/10.1101/gr.5629106openalex-snapshot
Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays
inferredcites →https://doi.org/10.1126/science.1069424openalex-snapshot
The Structure of Haplotype Blocks in the Human Genome
inferredcites →https://doi.org/10.1126/science.1092500openalex-snapshot
The Fine-Scale Structure of Recombination Rate Variation in the Human Genome
inferredcites →https://doi.org/10.1126/science.1105436openalex-snapshot
Whole-Genome Patterns of Common DNA Variation in Three Human Populations
inferredcites →https://doi.org/10.1126/science.1109557openalex-snapshot
Complement Factor H Polymorphism in Age-Related Macular Degeneration
inferredcites →https://doi.org/10.1126/science.1133807openalex-snapshot
HTRA1 Promoter Polymorphism in Wet Age-Related Macular Degeneration
inferredcites →https://doi.org/10.1126/science.1135245openalex-snapshot
A Genome-Wide Association Study Identifies IL23R as an Inflammatory Bowel Disease Gene
inferredcites →https://doi.org/10.1126/science.1136678openalex-snapshot
Relative Impact of Nucleotide and Copy Number Variation on Gene Expression Phenotypes
inferredcites →https://doi.org/10.1126/science.1141634openalex-snapshot
A Common Variant in the FTO Gene Is Associated with Body Mass Index and Predisposes to Childhood and Adult Obesity
inferredcites →https://doi.org/10.1126/science.1142358openalex-snapshot
Genome-Wide Association Analysis Identifies Loci for Type 2 Diabetes and Triglyceride Levels
inferredcites →https://doi.org/10.1126/science.1142364openalex-snapshot
Replication of Genome-Wide Association Signals in UK Samples Reveals Risk Loci for Type 2 Diabetes
inferredcites →https://doi.org/10.1126/science.1142382openalex-snapshot
A Genome-Wide Association Study of Type 2 Diabetes in Finns Detects Multiple Susceptibility Variants
inferredcites →https://doi.org/10.1126/science.1142447openalex-snapshot
A Common Allele on Chromosome 9 Associated with Coronary Heart Disease
inferredcites →https://doi.org/10.1126/science.1142842openalex-snapshot
A Common Variant on Chromosome 9p21 Affects the Risk of Myocardial Infarction
inferredcites →https://doi.org/10.1126/science.1143767openalex-snapshot
A Whole-Genome Association Study of Major Determinants for Host Control of HIV-1
inferredcites →https://doi.org/10.1126/science.1146554openalex-snapshot
Common Sequence Variants in the LOXL1 Gene Confer Susceptibility to Exfoliation Glaucoma
inferredcites →https://doi.org/10.1126/science.1152422openalex-snapshot
Sequence Variants in the RNF212 Gene Associate with Genome-Wide Recombination Rate
inferredcites →https://doi.org/10.1126/science.274.5287.536openalex-snapshot
The New Genomics: Global Views of Biology
inferredcites →https://doi.org/10.1126/science.278.5343.1580openalex-snapshot
Variations on a Theme: Cataloging Human DNA Sequence Variation
inferredcites →https://doi.org/10.1159/000017120openalex-snapshot
Apolipoprotein E Genetic Variation and Alzheimer’s Disease
inferredcites →https://doi.org/10.1159/000092553openalex-snapshot
Effects of Differential Genotyping Error Rate on the Type I Error Probability of Case-Control Studies
inferredcites →https://doi.org/10.1159/000099178openalex-snapshot
Genes, Environment, Health, and Disease: Facing up to Complexity
inferredcites →https://doi.org/10.1159/000101761openalex-snapshot
Community Engagement and Informed Consent in the International HapMap Project
inferredcites →https://doi.org/10.1186/1471-2156-6-s1-s134openalex-snapshot
Power and type I error rate of false discovery rate approaches in genome-wide association studies
inferredcites →https://doi.org/10.1210/jc.2006-2275openalex-snapshot
Effects of the Type 2 Diabetes-AssociatedPPARGP12A Polymorphism on Progression to Diabetes and Response to Troglitazone
inferredcites →https://doi.org/10.1371/journal.pbio.0040072openalex-snapshot
A Map of Recent Positive Selection in the Human Genome
inferredcites →https://doi.org/10.1371/journal.pgen.0020190openalex-snapshot
Population Structure and Eigenanalysis
inferredcites →https://doi.org/10.1371/journal.pgen.0030058openalex-snapshot
Novel Crohn Disease Locus Identified by Genome-Wide Association Maps to a Gene Desert on 5p13.1 and Modulates Expression of PTGER4
inferredcites →https://doi.org/10.1371/journal.pgen.0030115openalex-snapshot
Genome-Wide Association Scan Shows Genetic Variants in the FTO Gene Are Associated with Obesity-Related Traits
inferredcites →https://doi.org/10.1371/journal.pgen.0030170openalex-snapshot
Power to Detect Risk Alleles Using Genome-Wide Tag SNP Panels
inferredcites →https://doi.org/10.1371/journal.pgen.0030190openalex-snapshot
Copy Number Variants and Common Disorders: Filling the Gaps and Exploring Complexity in Genome-Wide Association Studies
inferredcites →https://doi.org/10.1371/journal.pgen.0030194openalex-snapshot
The GLUT9 Gene Is Associated with Serum Uric Acid Levels in Sardinia and Chianti Cohorts
inferredcites →https://doi.org/10.1586/14737159.7.4.371openalex-snapshot
Recent development in pharmacogenomics: from candidate genes to genome-wide association studies
inferredcites →https://doi.org/10.32388/mrapt2openalex-snapshot
National Human Genome Research Institute
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.5243602openalex-extracted
Community and Bioethical Perspectives on Ipsc Research Using Biobanked Samples
inferred← citeshttps://doi.org/10.1001/archgenpsychiatry.2009.48openalex-snapshot
Role of GABRA2 in Trajectories of Externalizing Behavior Across Development and Evidence of Moderation by Parental Monitoring
inferred← citeshttps://doi.org/10.1001/archgenpsychiatry.2010.69openalex-snapshot
Suggestion of Roles for Both Common and Rare Risk Variants in Genome-wide Studies of Schizophrenia
inferred← citeshttps://doi.org/10.1001/jama.2009.978-aopenalex-snapshot
Genetic Variants Associated With Cardiac Structure and Function
inferred← citeshttps://doi.org/10.1002/2211-5463.12722openalex-snapshot
Development of a general logistic model for disease risk prediction using multiple SNPs
inferred← citeshttps://doi.org/10.1002/9780470015902.a0005945.pub2openalex-snapshot
Public Health Genomics
inferred← citeshttps://doi.org/10.1002/9780470015902.a0021458openalex-snapshot
Genome‐wide Association Studies
inferred← citeshttps://doi.org/10.1002/9780470015902.a0022428openalex-snapshot
Micro RNA Polymorphisms
inferred← citeshttps://doi.org/10.1002/9780470027318.a0534.pub2openalex-snapshot
Molecular Biological Analyses and Molecular Pathology in Clinical Chemistry
inferred← citeshttps://doi.org/10.1002/9780470567647.ch12openalex-snapshot
Trends and Statistical Challenges in Genomewide Association Studies
inferred← citeshttps://doi.org/10.1002/9780470960844.ch3openalex-snapshot
Nutritional Genomics: Fundamental Role of Diet in Chronic Disease Prevention and Control
inferred← citeshttps://doi.org/10.1002/9781118116494.ch14openalex-snapshot
High‐Throughput Genotyping Technologies for Pharmacogenetics
inferred← citeshttps://doi.org/10.1002/9781118444122.ch30openalex-snapshot
Neuropsychiatric Disease‐Associated Genetic Variation in the Wnt Pathway
inferred← citeshttps://doi.org/10.1002/9781118453926.ch13openalex-snapshot
Human Genome‐Wide Association (GWA) Studies
inferred← citeshttps://doi.org/10.1002/9781119104100.ch11openalex-snapshot
Complex Genetic Interactions/Data Mining/Dimensionality Reduction
inferred← citeshttps://doi.org/10.1002/9781119125556.devpsy208openalex-snapshot
The Trilogy of GxE : Conceptualization, Operationalization, and Application
inferred← citeshttps://doi.org/10.1002/9781119266594.ch47openalex-snapshot
Human Genome‐Wide Association Studies
inferred← citeshttps://doi.org/10.1002/9781444309768.ch21openalex-snapshot
Genetics of Coronary Heart Disease
inferred← citeshttps://doi.org/10.1002/9781444324808.ch12openalex-snapshot
The Genetics of Type 2 Diabetes: From Candidate Gene Biology to Genome‐Wide Studies
inferred← citeshttps://doi.org/10.1002/9781444398595.ch15openalex-snapshot
Single Nucleotide Polymorphisms in Molecular Diagnostics
inferred← citeshttps://doi.org/10.1002/ajhb.20984openalex-snapshot
Human population genetic diversity as a function of SNP type from HapMap data
inferred← citeshttps://doi.org/10.1002/ajmg.b.32166openalex-snapshot
Taiwan schizophrenia linkage study: Lessons learned from endophenotype‐based genome‐wide linkage scans and perspective
inferred← citeshttps://doi.org/10.1002/ana.21911openalex-snapshot
What role for genetics in the prediction of multiple sclerosis?
inferred← citeshttps://doi.org/10.1002/ana.22403openalex-snapshot
Genome‐wide association studies of cerebral white matter lesion burden
inferred← citeshttps://doi.org/10.1002/art.24524openalex-snapshot
Large‐scale analysis of association between GDF5 and FRZB variants and osteoarthritis of the hip, knee, and hand
inferred← citeshttps://doi.org/10.1002/art.30126openalex-snapshot
Personalized medicine in rheumatoid arthritis: Miles to go before we sleep
inferred← citeshttps://doi.org/10.1002/bdra.20566openalex-snapshot
The search for genetic polymorphisms in the homocysteine/folate pathway that contribute to the etiology of human neural tube defects
inferred← citeshttps://doi.org/10.1002/bdra.23066openalex-snapshot
Age of onset and effect size in genome‐wide association studies
inferred← citeshttps://doi.org/10.1002/bimj.200900044openalex-snapshot
Efficient Evaluation of Ranking Procedures when the Number of Units is Large, with Application to SNP Identification
inferred← citeshttps://doi.org/10.1002/cncr.25930openalex-snapshot
A functional single nucleotide polymorphism at the promoter region of cyclin A2 is associated with increased risk of colon, liver, and lung cancers
inferred← citeshttps://doi.org/10.1002/cpns.23openalex-snapshot
Systems Genetic Analysis in GeneNetwork.org
inferred← citeshttps://doi.org/10.1002/dmrr.1221openalex-snapshot
Genome‐wide association studies (GWAS): impact on elucidating the aetiology of diabetes
inferred← citeshttps://doi.org/10.1002/gepi.20396openalex-snapshot
Genetic background comparison using distance‐based regression, with applications in population stratification evaluation and adjustment
inferred← citeshttps://doi.org/10.1002/gepi.20438openalex-snapshot
Were genome‐wide linkage studies a waste of time? Exploiting candidate regions within genome‐wide association studies
inferred← citeshttps://doi.org/10.1002/gepi.20483openalex-snapshot
A statistical method for scanning the genome for regions with rare disease alleles
inferred← citeshttps://doi.org/10.1002/gepi.20497openalex-snapshot
Analyze multivariate phenotypes in genetic association studies by combining univariate association tests
inferred← citeshttps://doi.org/10.1002/gepi.20516openalex-snapshot
Quality control and quality assurance in genotypic data for genome‐wide association studies
inferred← citeshttps://doi.org/10.1002/gepi.20579openalex-snapshot
Evaluating the heritability explained by known susceptibility variants: a survey of ten complex diseases
inferred← citeshttps://doi.org/10.1002/gepi.20593openalex-snapshot
Uncovering the total heritability explained by all true susceptibility variants in a genome-wide association study
inferred← citeshttps://doi.org/10.1002/gepi.21786openalex-snapshot
Testing Gene–Gene Interactions in Genome Wide Association Studies
inferred← citeshttps://doi.org/10.1002/gepi.21813openalex-snapshot
Kernel-Machine Testing Coupled with a Rank-Truncation Method for Genetic Pathway Analysis
inferred← citeshttps://doi.org/10.1002/gepi.21833openalex-snapshot
A Custom Correlation Coefficient (CCC) Approach for Fast Identification of Multi‐SNP Association Patterns in Genome‐Wide SNPs Data
inferred← citeshttps://doi.org/10.1002/gepi.21851openalex-snapshot
A Novel Method for Detecting Association Between DNA Methylation and Diseases Using Spatial Information
inferred← citeshttps://doi.org/10.1002/gps.2628openalex-snapshot
Alzheimer's disease genetics: current knowledge and future challenges
inferred← citeshttps://doi.org/10.1002/rrq.439openalex-snapshot
The Role of Neural and Genetic Processes in Learning to Read and Specific Reading Disabilities: Implications for Instruction
inferred← citeshttps://doi.org/10.1002/sim.4057openalex-snapshot
Using ancestry matching to combine family‐based and unrelated samples for genome‐wide association studies
inferred← citeshttps://doi.org/10.1002/sim.4259openalex-snapshot
Perspectives on genome‐wide multi‐stage family‐based association studies
inferred← citeshttps://doi.org/10.1002/sim.5428openalex-snapshot
Rare genetic variants and treatment response: sample size and analysis issues
inferred← citeshttps://doi.org/10.1007/7854_2009_25openalex-snapshot
Neural Markers of Genetic Vulnerability to Drug Addiction
inferred← citeshttps://doi.org/10.1007/7854_2011_184openalex-snapshot
Gene × Environment Interaction Models in Psychiatric Genetics
inferred← citeshttps://doi.org/10.1007/7854_2019_110openalex-snapshot
Genetic Variation in Long-Range Enhancers
inferred← citeshttps://doi.org/10.1007/978-0-387-09488-5_29openalex-snapshot
Candidate Gene and Genome-Wide Association Studies in Behavioral Medicine
inferred← citeshttps://doi.org/10.1007/978-0-387-09488-5_33openalex-snapshot
Genetics of Obesity and Diabetes
inferred← citeshttps://doi.org/10.1007/978-0-387-09841-8_10openalex-snapshot
Genetics of Type 2 Diabetes: From Candidate Genes to Genome-Wide Association Analysis
inferred← citeshttps://doi.org/10.1007/978-0-387-85960-6_31openalex-snapshot
Genetics in Cardiovascular Behavioral Medicine
inferred← citeshttps://doi.org/10.1007/978-0-387-87429-6_39openalex-snapshot
Bioinformatics, Genomics, and Functional Genomics: Overview
inferred← citeshttps://doi.org/10.1007/978-0-387-89443-0_3openalex-snapshot
Genes, Environment, and Cancer Disparities
inferred← citeshttps://doi.org/10.1007/978-0-85729-452-4_11openalex-snapshot
Genomes for Individual Ability (Features)
inferred← citeshttps://doi.org/10.1007/978-1-4020-9464-4openalex-snapshot
The Handbook of Neuropsychiatric Biomarkers, Endophenotypes and Genes
inferred← citeshttps://doi.org/10.1007/978-1-4020-9464-4_5openalex-snapshot
Leveraging High-Dimensional Neuroimaging Data in Genetic Studies of Neuropsychiatric Disease
inferred← citeshttps://doi.org/10.1007/978-1-4419-0769-1_2openalex-snapshot
Molecular Diagnostics as Basis of Personalized Medicine
inferred← citeshttps://doi.org/10.1007/978-1-4419-6752-7_8openalex-snapshot
Approaches to Identify Environmental and Epigenomic Components or Covariates of Cancer and Disease Susceptibility
inferred← citeshttps://doi.org/10.1007/978-1-4419-7338-2_11openalex-snapshot
Genome Wide Association Studies
inferred← citeshttps://doi.org/10.1007/978-1-4471-6542-2_28openalex-snapshot
Concern for Pharmacogenomics and Autologous Cell Therapy: Can This Be a Direction Toward Medicine for the Future?
inferred← citeshttps://doi.org/10.1007/978-1-4614-3961-5_8openalex-snapshot
The Global Burden of Severe Falciparum Malaria: An Immunological and Genetic Perspective on Pathogenesis
inferred← citeshttps://doi.org/10.1007/978-1-4939-0956-8_2openalex-snapshot
Translational Bioinformatics Approaches for Systems and Dynamical Medicine
inferred← citeshttps://doi.org/10.1007/978-1-4939-7868-7_9openalex-snapshot
Novel Methods for Family-Based Genetic Studies
inferred← citeshttps://doi.org/10.1007/978-1-60327-369-5_6openalex-snapshot
Sequencing PCR-Amplified DNA in Lipoprotein and Cardiovascular Disease Research
inferred← citeshttps://doi.org/10.1007/978-1-60327-389-3_2openalex-snapshot
Genetic Mapping and Positional Cloning
inferred← citeshttps://doi.org/10.1007/978-1-61737-954-3_1openalex-snapshot
Technological Issues and Experimental Design of Gene Association Studies
inferred← citeshttps://doi.org/10.1007/978-1-61779-163-5_2openalex-snapshot
Laser Microdissection for Gene Expression Profiling
inferred← citeshttps://doi.org/10.1007/978-1-61779-785-9_15openalex-snapshot
Genetic Mapping of Quantitative Trait Loci for Disease-Related Phenotypes
inferred← citeshttps://doi.org/10.1007/978-1-62703-071-7_20openalex-snapshot
Translational Bioinformatics in Psychoneuroimmunology: Methods and Applications
inferred← citeshttps://doi.org/10.1007/978-1-84882-448-5_7openalex-snapshot
Clinical Research in the Postgenomic Era
inferred← citeshttps://doi.org/10.1007/978-3-030-03934-9_1openalex-snapshot
Systemic Lupus Erythematosus
inferred← citeshttps://doi.org/10.1007/978-3-030-14485-2_1openalex-snapshot
Inheritance in Oral Health Conditions
inferred← citeshttps://doi.org/10.1007/978-3-030-24432-3_19openalex-snapshot
The Microbiome in Liver Diseases
inferred← citeshttps://doi.org/10.1007/978-3-030-36335-2_2openalex-snapshot
Genetics and Individual Predispositions in Contact Dermatitis
inferred← citeshttps://doi.org/10.1007/978-3-030-61646-5_5openalex-snapshot
Methods for Association Studies
inferred← citeshttps://doi.org/10.1007/978-3-030-95350-8_6openalex-snapshot
Gene Mapping and Human Disease
inferred← citeshttps://doi.org/10.1007/978-3-031-05616-1_4openalex-snapshot
GWAS to Identify SNPs Associated with Common Diseases and Individual Risk: Genome Wide Association Studies (GWAS) to Identify SNPs Associated with Common Diseases and Individual Risk
inferred← citeshttps://doi.org/10.1007/978-3-032-06948-1_13openalex-snapshot
Bioinformatics Approaches in Noncoding RNAs Research
inferred← citeshttps://doi.org/10.1007/978-3-032-25925-7_12openalex-snapshot
The “Geneticists’ Nightmare”: The Promises and Pitfalls of the Common Disease, Common Variant (CDCV) Hypothesis and Common Disease Genetic Epidemiology
inferred← citeshttps://doi.org/10.1007/978-3-319-01574-3_14openalex-snapshot
Transcription Factor 7-Like 2 (TCF7L2)
inferred← citeshttps://doi.org/10.1007/978-3-319-18741-9_10openalex-snapshot
Genetics of Type 2 Diabetes: From Candidate Genes to Genome-Wide Association Analysis
inferred← citeshttps://doi.org/10.1007/978-3-319-20797-1_10-1openalex-snapshot
Genetics of Type 2 Diabetes: From Candidate Genes to Genome-Wide Association Analysis
inferred← citeshttps://doi.org/10.1007/978-3-319-20797-1_10-2openalex-snapshot
Genetics of Type 2 Diabetes: From Candidate Genes to Genome-Wide Association Analysis
inferred← citeshttps://doi.org/10.1007/978-3-319-31689-5_5openalex-snapshot
The Genetic Basis of Bipolar Disorder
inferred← citeshttps://doi.org/10.1007/978-3-319-56234-6_5openalex-snapshot
Introduction to Environment and Exposome-Wide Association Studies: A Data-Driven Method to Identify Multiple Environmental Factors Associated with Phenotypes in Human Populations
inferred← citeshttps://doi.org/10.1007/978-3-319-56970-3_15openalex-snapshot
Using Stochastic Approximation Techniques to Efficiently Construct Confidence Intervals for Heritability
inferred← citeshttps://doi.org/10.1007/978-3-319-72451-5_2-1openalex-snapshot
Genetics and Individual Predispositions in Contact Dermatitis
inferred← citeshttps://doi.org/10.1007/978-3-319-72938-1_9openalex-snapshot
Genetic Risk Factors for Sporadic Frontotemporal Dementia
inferred← citeshttps://doi.org/10.1007/978-3-319-89321-1_12openalex-snapshot
Exposome-Wide Association Studies: A Data-Driven Approach for Searching for Exposures Associated with Phenotype
inferred← citeshttps://doi.org/10.1007/978-3-319-98298-4_6openalex-snapshot
Interdisciplinary Care Model: Cardiovascular Diseases and Oral Health
inferred← citeshttps://doi.org/10.1007/978-3-540-37654-5_2openalex-snapshot
History of Human Genetics*
inferred← citeshttps://doi.org/10.1007/978-3-540-72314-1_12openalex-snapshot
BioGenetic and Host Implications
inferred← citeshttps://doi.org/10.1007/978-3-642-00727-9_7openalex-snapshot
Genotype and Haplotype Reconstruction from Low-Coverage Short Sequencing Reads
inferred← citeshttps://doi.org/10.1007/978-3-642-03827-3_2openalex-snapshot
Genetics and Individual Predispositions in Contact Dermatitis
inferred← citeshttps://doi.org/10.1007/978-3-642-37078-6_7openalex-snapshot
Arteriogenesis and Collateral Formation
inferred← citeshttps://doi.org/10.1007/978-3-642-37195-0_4openalex-snapshot
eALPS: Estimating Abundance Levels in Pooled Sequencing Using Available Genotyping Data
inferred← citeshttps://doi.org/10.1007/978-3-642-37393-0_7-1openalex-snapshot
Arteriogenesis and Collateral Formation
inferred← citeshttps://doi.org/10.1007/978-3-7643-8567-5_5openalex-snapshot
The genetic basis of bipolar disorder
inferred← citeshttps://doi.org/10.1007/978-981-10-0724-8_9openalex-snapshot
Single-Molecule Sequencing
inferred← citeshttps://doi.org/10.1007/978-981-16-6542-4_20openalex-snapshot
Cancer Patient Healthcare Analysis by Genomic Prediction
inferred← citeshttps://doi.org/10.1007/978-981-97-4974-4_2openalex-snapshot
Human Genomics Technology
inferred← citeshttps://doi.org/10.1007/s00103-014-2091-4openalex-snapshot
Methodisch-statistische Herausforderungen an die genombasierte Vorhersage von Erkrankungen
inferred← citeshttps://doi.org/10.1007/s00105-012-2409-9openalex-snapshot
Genodermatosen, die der Praktiker kennen muss
inferred← citeshttps://doi.org/10.1007/s00125-012-2756-1openalex-snapshot
Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes
inferred← citeshttps://doi.org/10.1007/s00221-014-3987-9openalex-snapshot
Association of μ-opioid receptor gene (OPRM1) haplotypes with postoperative nausea and vomiting
inferred← citeshttps://doi.org/10.1007/s00268-011-1056-0openalex-snapshot
Overview of the Development of Personalized Genomic Medicine and Surgery
inferred← citeshttps://doi.org/10.1007/s00335-010-9267-5openalex-snapshot
Analyzing complex traits with congenic strains
inferred← citeshttps://doi.org/10.1007/s00335-011-9346-2openalex-snapshot
The emerging role for rat models in gene discovery
inferred← citeshttps://doi.org/10.1007/s00335-012-9409-zopenalex-snapshot
Association studies in outbred mice in a new era of full-genome sequencing
inferred← citeshttps://doi.org/10.1007/s00423-012-0929-5openalex-snapshot
The molecular basis of chemoradiosensitivity in rectal cancer:implications for personalized therapies
inferred← citeshttps://doi.org/10.1007/s00428-009-0847-2openalex-snapshot
Genome-scale approaches to the epigenetics of common human disease
inferred← citeshttps://doi.org/10.1007/s00432-012-1314-zopenalex-snapshot
A two-SNP IL-6 promoter haplotype is associated with increased lung cancer risk
inferred← citeshttps://doi.org/10.1007/s00439-008-0535-3openalex-snapshot
Comprehensive resequence analysis of a 136 kb region of human chromosome 8q24 associated with prostate and colon cancers
inferred← citeshttps://doi.org/10.1007/s00439-009-0663-4openalex-snapshot
Genome-wide association studies in ADHD
inferred← citeshttps://doi.org/10.1007/s00439-009-0723-9openalex-snapshot
Comprehensive resequence analysis of a 97 kb region of chromosome 10q11.2 containing the MSMB gene associated with prostate cancer
inferred← citeshttps://doi.org/10.1007/s00439-009-0767-xopenalex-snapshot
Evaluation of genetic tests for susceptibility to common complex diseases: why, when and how?
inferred← citeshttps://doi.org/10.1007/s00439-010-0811-xopenalex-snapshot
Two-stage case–control designs for rare genetic variants
inferred← citeshttps://doi.org/10.1007/s00439-010-0824-5openalex-snapshot
Power analysis for case–control association studies of samples with known family histories
inferred← citeshttps://doi.org/10.1007/s00439-011-0956-2openalex-snapshot
Genetic analysis of biological pathway data through genomic randomization
inferred← citeshttps://doi.org/10.1007/s00439-011-1036-3openalex-snapshot
Realizing the promise of population biobanks: a new model for translation
inferred← citeshttps://doi.org/10.1007/s00439-012-1190-2openalex-snapshot
The role of large pedigrees in an era of high-throughput sequencing
inferred← citeshttps://doi.org/10.1007/s00439-012-1237-4openalex-snapshot
Assessment of systematic effects of methodological characteristics on candidate genetic associations
inferred← citeshttps://doi.org/10.1007/s00439-014-1468-7openalex-snapshot
Hypothesis-independent pathway analysis implicates GABA and Acetyl-CoA metabolism in primary open-angle glaucoma and normal-pressure glaucoma
inferred← citeshttps://doi.org/10.1007/s00464-009-0427-1openalex-snapshot
Advanced gastric cancer: is laparoscopic gastrectomy safe?
inferred← citeshttps://doi.org/10.1007/s00500-017-2641-4openalex-snapshot
Fuzzy heaping mechanism for heaped count data with imprecision
inferred← citeshttps://doi.org/10.1007/s00787-010-0091-yopenalex-snapshot
Child and adolescent psychiatric genetics
inferred← citeshttps://doi.org/10.1007/s10115-010-0354-4openalex-snapshot
COAT: COnstraint-based anonymization of transactions
inferred← citeshttps://doi.org/10.1007/s10620-022-07728-wopenalex-snapshot
Missing Causality and Heritability of Autoimmune Hepatitis
inferred← citeshttps://doi.org/10.1007/s10654-008-9293-8openalex-snapshot
Is the time right for translation research in genomics?
inferred← citeshttps://doi.org/10.1007/s10654-009-9387-yopenalex-snapshot
Genetic Scoring Analysis: a way forward in Genome Wide Association Studies?
inferred← citeshttps://doi.org/10.1007/s10815-016-0822-1openalex-snapshot
Copy number variation analysis reveals additional variants contributing to endometriosis development
inferred← citeshttps://doi.org/10.1007/s10897-011-9424-3openalex-snapshot
Giving and Withholding of Information following Genomic Screening: Challenges Identified in a Study of Primary Care Physicians in Estonia
inferred← citeshttps://doi.org/10.1007/s11011-023-01271-xopenalex-snapshot
Schizophrenia in the genetic era: a review from development history, clinical features and genomic research approaches to insights of susceptibility genes
inferred← citeshttps://doi.org/10.1007/s11250-022-03102-0openalex-snapshot
Assessing accuracy of genotype imputation in the Afrikaner and Brahman cattle breeds of South Africa
inferred← citeshttps://doi.org/10.1007/s11357-011-9340-3openalex-snapshot
Gene set analysis of GWAS data for human longevity highlights the relevance of the insulin/IGF-1 signaling and telomere maintenance pathways
inferred← citeshttps://doi.org/10.1007/s11357-011-9362-xopenalex-snapshot
Genomics of human health and aging
inferred← citeshttps://doi.org/10.1007/s11357-011-9374-6openalex-snapshot
Inter-chromosomal level of genome organization and longevity-related phenotypes in humans
inferred← citeshttps://doi.org/10.1007/s11377-010-0489-6openalex-snapshot
Individualisierte Medizin 2011
inferred← citeshttps://doi.org/10.1007/s11892-012-0279-2openalex-snapshot
Insights into the Genetic Architecture of Diabetic Nephropathy
inferred← citeshttps://doi.org/10.1007/s11920-009-0023-zopenalex-snapshot
The genetics of reading disability
inferred← citeshttps://doi.org/10.1007/s11920-013-0349-4openalex-snapshot
Evaluating Rare Variants in Complex Disorders Using Next-Generation Sequencing
inferred← citeshttps://doi.org/10.1007/s12033-014-9734-4openalex-snapshot
Guidelines for the Tetra-Primer ARMS–PCR Technique Development
inferred← citeshttps://doi.org/10.1007/s12041-017-0855-yopenalex-snapshot
Analysis of two susceptibility SNPs in HLA region and evidence of interaction between rs6457617 in HLA-DQB1 and HLA-DRB1*04 locus on Tunisian rheumatoid arthritis
inferred← citeshttps://doi.org/10.1007/s12064-012-0168-xopenalex-snapshot
Systems genetics in “-omics” era: current and future development
inferred← citeshttps://doi.org/10.1007/s12072-013-9512-6openalex-snapshot
Cell therapies and regenerative medicine
inferred← citeshttps://doi.org/10.1007/s12170-009-0003-1openalex-snapshot
Genomewide association studies and lipid risk factors
inferred← citeshttps://doi.org/10.1007/s12291-010-0008-zopenalex-snapshot
MicroRNAs: Potential biomarkers in cancer
inferred← citeshttps://doi.org/10.1007/s12672-024-01446-7openalex-snapshot
Venous thromboembolism and ovarian cancer risk: a Mendelian randomized study
inferred← citeshttps://doi.org/10.1007/s12687-013-0139-zopenalex-snapshot
Anticipating the arrival of low-penetrance genetic testing to primary care medicine
inferred← citeshttps://doi.org/10.1007/s13277-015-3324-3openalex-snapshot
Association of TP53 gene polymorphisms with susceptibility of bladder cancer in Bangladeshi population
inferred← citeshttps://doi.org/10.1007/s13353-012-0096-yopenalex-snapshot
New routes for transgenesis of the mouse
inferred← citeshttps://doi.org/10.1007/s13577-011-0019-yopenalex-snapshot
Construction of Japanese BAC library Yamato-2 (JY2): a set of 330K clone resources of damage-minimized DNA taken from a genetically established Japanese individual
inferred← citeshttps://doi.org/10.1007/s40572-016-0080-5openalex-snapshot
Analytical Complexity in Detection of Gene Variant-by-Environment Exposure Interactions in High-Throughput Genomic and Exposomic Research
inferred← citeshttps://doi.org/10.1016/b978-0-12-369420-1.00040-8openalex-snapshot
Principles of Human Genome Epidemiology
inferred← citeshttps://doi.org/10.1016/b978-0-12-374934-5.00001-5openalex-snapshot
The Foundations of Genomic and Personalized Medicine
inferred← citeshttps://doi.org/10.1016/b978-0-12-374934-5.00021-0openalex-snapshot
Public Health Genomics
inferred← citeshttps://doi.org/10.1016/b978-0-12-375142-3.10001-xopenalex-snapshot
Genetic Architecture of Complex Diseases
inferred← citeshttps://doi.org/10.1016/b978-0-12-380862-2.00007-2openalex-snapshot
Statistical Methods for Pathway Analysis of Genome-Wide Data for Association with Complex Genetic Traits
inferred← citeshttps://doi.org/10.1016/b978-0-12-382026-6.00001-4openalex-snapshot
Transcription and Epigenetic Regulation
inferred← citeshttps://doi.org/10.1016/b978-0-12-382227-7.00018-5openalex-snapshot
Genomic, Personalized Medicine and Public Health
inferred← citeshttps://doi.org/10.1016/b978-0-12-383834-6.00015-xopenalex-snapshot
Population Genetics
inferred← citeshttps://doi.org/10.1016/b978-0-12-387817-5.00013-3openalex-snapshot
Genetic Factors in the Pathogenesis of Drug-Induced Liver Injury
inferred← citeshttps://doi.org/10.1016/b978-0-12-391884-0.00028-7openalex-snapshot
Genetic Influences on Blood Lipids and Cardiovascular Disease Risk
inferred← citeshttps://doi.org/10.1016/b978-0-12-398339-8.00004-5openalex-snapshot
Genetic Polymorphisms Affecting Drug Metabolism
inferred← citeshttps://doi.org/10.1016/b978-0-12-416002-6.00031-6openalex-snapshot
Perspectives on the Human Genome
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.05486-6openalex-snapshot
Population Genetics
inferred← citeshttps://doi.org/10.1016/b978-0-12-802928-2.00026-6openalex-snapshot
Genetic Influences on Blood Lipids and Cardiovascular Disease Risk
inferred← citeshttps://doi.org/10.1016/b978-0-12-809633-8.20232-xopenalex-snapshot
Genome-Wide Association Studies
inferred← citeshttps://doi.org/10.1016/b978-0-12-809954-4.00001-3openalex-snapshot
Transcription and Epigenetic Regulation
inferred← citeshttps://doi.org/10.1016/b978-0-12-811710-1.00029-xopenalex-snapshot
Perspectives on the human genome
inferred← citeshttps://doi.org/10.1016/b978-0-12-812537-3.00012-3openalex-snapshot
Population Genetics
inferred← citeshttps://doi.org/10.1016/b978-0-323-05373-0.00012-9openalex-snapshot
Multifactorial Inheritance and Common Diseases
inferred← citeshttps://doi.org/10.1016/b978-0-323-18907-1.00040-8openalex-snapshot
Type 2 Diabetes Mellitus
inferred← citeshttps://doi.org/10.1016/b978-0-323-95120-3.00004-xopenalex-snapshot
Role of pharmacogenomics for prediction of personalized medicines
inferred← citeshttps://doi.org/10.1016/b978-1-4160-5583-9.00041-1openalex-snapshot
Type 2 Diabetes Mellitus
inferred← citeshttps://doi.org/10.1016/b978-1-4377-0398-6.00007-xopenalex-snapshot
Principles of Cardiovascular Molecular Biology and Genetics
inferred← citeshttps://doi.org/10.1016/b978-1-4377-0398-6.00010-xopenalex-snapshot
Principles of Drug Therapy
inferred← citeshttps://doi.org/10.1016/b978-1-4377-1160-8.10044-2openalex-snapshot
Clinical Genetics (Genomics)
inferred← citeshttps://doi.org/10.1016/b978-1-4557-2758-2.00029-9openalex-snapshot
Hormone Responsive Cancers
inferred← citeshttps://doi.org/10.1016/b978-84-8086-956-0.00007-1openalex-snapshot
10.1016/b978-84-8086-956-0.00007-1
inferred← citeshttps://doi.org/10.1016/b978-84-8086-956-0.00010-1openalex-snapshot
10.1016/b978-84-8086-956-0.00010-1
inferred← citeshttps://doi.org/10.1016/b978-84-9113-949-2.00086-xopenalex-snapshot
10.1016/b978-84-9113-949-2.00086-x
inferred← citeshttps://doi.org/10.1016/j.advms.2013.12.001openalex-snapshot
Advances in individualized and regenerative medicine
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