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Machine learning approaches to explore digenic inheritance

Trends in genetics, 2022-10, Vol.38 (10), p.1013-1018

2022

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Genetic linkage analysis in the age of whole-genome sequencing

Nature reviews. Genetics, 2015-05, Vol.16 (5), p.275

2015

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To aggregate or not, that is the question. A commentary on single-nucleotide variant proportion in genes: a new concept to explore major depression based on DNA sequencing data

Journal of human genetics, 2017-05, Vol.62 (5), p.523-523

Ott, Jurg

2017

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Population genetics: past, present, and future

Human genetics, 2021-02, Vol.140 (2), p.231-240

2021

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A multi-threaded approach to genotype pattern mining for detecting digenic disease genes

Frontiers in genetics, 2023-08, Vol.14, p.1222517-1222517

2023

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Analyses of polymorphisms of intron 2 of OPRK1 (kappa-opioid receptor gene) in association with opioid and cocaine dependence diagnoses in an African-American population

Neuroscience letters, 2022-01, Vol.768, p.136364-136364, Article 136364

2022

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Implication of Melanocortin Receptor Genes in the Familial Comorbidity of Type 2 Diabetes and Depression

International journal of molecular sciences, 2022-08, Vol.23 (15), p.8350

2022

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A 3' UTR SNP rs885863, a cis-eQTL for the circadian gene VIPR2 and lincRNA 689, is associated with opioid addiction

PloS one, 2019-11, Vol.14 (11), p.e0224399

2019

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Mathematical multi-locus approaches to localizing complex human trait genes

Nature reviews. Genetics, 2003-09, Vol.4 (9), p.701-709

2003

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AprioriGWAS, a new pattern mining strategy for detecting genetic variants associated with disease through interaction effects

PLoS computational biology, 2014-06, Vol.10 (6), p.e1003627-e1003627

2014

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Distribution and characterization of regulatory elements in the human genome

Genome research, 2002-12, Vol.12 (12), p.1827

2002

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Comorbidity of Novel CRHR2 Gene Variants in Type 2 Diabetes and Depression

International journal of molecular sciences, 2022-09, Vol.23 (17), p.9819

2022

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Complement Factor H Polymorphism in Age-Related Macular Degeneration

Science (American Association for the Advancement of Science), 2005-04, Vol.308 (5720), p.385-389

2005

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A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjögren's syndrome at 7q11.23

Nature genetics, 2013-11, Vol.45 (11), p.1361-1365

2013

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Genotype Pattern Mining for Pairs of Interacting Variants Underlying Digenic Traits

Genes, 2021-07, Vol.12 (8), p.1160

2021

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Editorial: Multi-Omics Study in Revealing Underlying Pathogenesis of Complex Diseases: A Translational Perspective

Frontiers in genetics, 2021-10, Vol.12, p.789294-789294

2021

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Genome-wide association scan in north Indians reveals three novel HLA-independent risk loci for ulcerative colitis

Gut, 2015-04, Vol.64 (4), p.571-579

2015

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Common Regulatory Variants of CYFIP1 Contribute to Susceptibility for Autism Spectrum Disorder (ASD) and Classical Autism

Annals of human genetics, 2015-09, Vol.79 (5), p.329-340

2015

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Drug Addiction and Stress‐Response Genetic Variability: Association Study in African Americans

Annals of human genetics, 2014-07, Vol.78 (4), p.290-298

2014

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Trimming, weighting, and grouping SNPs in human case-control association studies

Genome research, 2001-12, Vol.11 (12), p.2115

2001

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Multilocus association mapping using generalized ridge logistic regression

BMC bioinformatics, 2011-09, Vol.12 (1), p.384-384, Article 384

2011

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The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia

Nature genetics, 2005-09, Vol.37 (9), p.931-933

2005

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Re-evaluation of the KMSK scales, rapid dimensional measures of self-exposure to specific drugs: Gender-specific features

Drug and alcohol dependence, 2018-09, Vol.190, p.179-187

2018

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CFH and LOC387715/ARMS2 Genotypes and Treatment with Antioxidants and Zinc for Age-Related Macular Degeneration

Ophthalmology (Rochester, Minn.), 2008-06, Vol.115 (6), p.1019-1025

2008

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HDR: a statistical two-step approach successfully identifies disease genes in autosomal recessive families

Journal of human genetics, 2016-11, Vol.61 (11), p.959-963

2016

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Machine learning approaches to explore digenic inheritance

Genetic linkage analysis in the age of whole-genome sequencing

To aggregate or not, that is the question. A commentary on single-nucleotide variant proportion in genes: a new concept to explore major depression based on DNA sequencing data

Population genetics: past, present, and future

A multi-threaded approach to genotype pattern mining for detecting digenic disease genes

Analyses of polymorphisms of intron 2 of OPRK1 (kappa-opioid receptor gene) in association with opioid and cocaine dependence diagnoses in an African-American population

Implication of Melanocortin Receptor Genes in the Familial Comorbidity of Type 2 Diabetes and Depression

A 3' UTR SNP rs885863, a cis-eQTL for the circadian gene VIPR2 and lincRNA 689, is associated with opioid addiction

Mathematical multi-locus approaches to localizing complex human trait genes

AprioriGWAS, a new pattern mining strategy for detecting genetic variants associated with disease through interaction effects

Distribution and characterization of regulatory elements in the human genome

Comorbidity of Novel CRHR2 Gene Variants in Type 2 Diabetes and Depression

Complement Factor H Polymorphism in Age-Related Macular Degeneration

A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjögren's syndrome at 7q11.23

Genotype Pattern Mining for Pairs of Interacting Variants Underlying Digenic Traits

Editorial: Multi-Omics Study in Revealing Underlying Pathogenesis of Complex Diseases: A Translational Perspective

Genome-wide association scan in north Indians reveals three novel HLA-independent risk loci for ulcerative colitis

Common Regulatory Variants of CYFIP1 Contribute to Susceptibility for Autism Spectrum Disorder (ASD) and Classical Autism

Drug Addiction and Stress‐Response Genetic Variability: Association Study in African Americans

Trimming, weighting, and grouping SNPs in human case-control association studies

Multilocus association mapping using generalized ridge logistic regression

The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia

Re-evaluation of the KMSK scales, rapid dimensional measures of self-exposure to specific drugs: Gender-specific features

CFH and LOC387715/ARMS2 Genotypes and Treatment with Antioxidants and Zinc for Age-Related Macular Degeneration

HDR: a statistical two-step approach successfully identifies disease genes in autosomal recessive families

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