Michael P. Epstein

Biochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

1in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome

Scientific Reports(2021)10.1038/s41598-021-94021-x

Top 100%

0DataRank

Top 100%0 citations

Aaron M. Holleman, Holly Corbitt, Cheryl L. Maslen, Tracie C. Rosser, David J. Cutler +21 more

Papers

Driven by 75 papers — median percentile 0. Top paper: “Integrating human brain proteomes with genome-wide association data implicates new proteins in Alzheimer’s disease pathogenesis”.

Integrating human brain proteomes with genome-wide association data implicates new proteins in Alzheimer’s disease pathogenesis

Nature Genetics(2021)10.1038/s41588-020-00773-z

N/A

7.6DataRank · unranked

409 citations

Yue Liu, Ekaterina S. Gerasimov, Jake Gockley, Benjamin A. Logsdon, Duc M. Duong +12 more

SNP Set Association Analysis for Familial Data

Genetic Epidemiology(2012)10.1002/gepi.21676

N/A

5.6DataRank · unranked

110 citations

Michael P. Epstein, Lawrence F. Bielak, Min A. Jhun, Sharon L. R. Kardia, Patricia A. Peyser +2 more

OTTERS: a powerful TWAS framework leveraging summary-level reference data

Nature Communications(2023)10.1038/s41467-023-36862-w

N/A

1.1DataRank · unranked

56 citations

Geyu Zhou, Luca Pinello, Urmo Võsa, Lude Franke, Alexis Battle +81 more

Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome

Scientific Reports(2020)10.1038/s41598-020-74650-4

N/A

0.955DataRank · unranked

26 citations

Aaron M. Holleman, Holly Corbitt, Cheryl L. Maslen, Tracie C. Rosser, David J. Cutler +21 more

Cerebrospinal fluid proteomics define the natural history of autosomal dominant Alzheimer’s disease

Nature Medicine(2023)10.1038/s41591-023-02476-4

N/A

0.781DataRank · unranked

181 citations

Shijia Bian, Rafi U. Haque, Kathleen Carter, Caroline M Watson, Brian A. Gordon +93 more

Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discovery

EBioMedicine(2022)10.1016/j.ebiom.2022.104079

N/A

0.561DataRank · unranked

41 citations

Colin A. Ellis, Ingrid E Scheffer, Shiva Ganesan, Costin Leu, Lynette G. Sadleir +12 more

Association of inflammation-related exposures and ovarian cancer survival in a multi-site cohort study of Black women

British Journal of Cancer(2023)10.1038/s41416-023-02385-w

N/A

0.500DataRank · unranked

9 citations

Anthony J. Alberg, Elisa V. Bandera, Lauren C. Peres, Maxwell Akonde, Lindsay J. Collin +14 more

Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting

Genetics in Medicine(2023)10.1016/j.gim.2023.100918

N/A

0.477DataRank · unranked

23 citations

Sarah W. Curtis, Alba Sanchis-Juan, Xuefang Zhao, S. Taylor Head, Samantha Ho +18 more

Association between maternal depression during pregnancy and newborn DNA methylation

Translational Psychiatry(2021)10.1038/s41398-021-01697-w

N/A

0.477DataRank · unranked

23 citations

Nicole Gladish, Nastassja Koen, Michael P. Epstein, Michael S. Kobor, Heather J. Zar +3 more

Pruning and thresholding approach for methylation risk scores in multi-ancestry populations

Epigenetics(2023)10.1080/15592294.2023.2187172

N/A

0.442DataRank · unranked

18 citations

Evan Gatev, Todd M. Everson, Karen N. Conneely, Nastassja Koen, Michael P. Epstein +5 more

Trio-based GWAS identifies novel associations and subtype-specific risk factors for cleft palate

Human Genetics and Genomics Advances(2023)10.1016/j.xhgg.2023.100234

N/A

0.406DataRank · unranked

14 citations

Trenell J. Mosley, Kenneth S. Rivera-González, Christopher R. Jabbarpour, Sarah W. Curtis, Wasiu Lanre Adeyemo +16 more

Omnibus proteome-wide association study identifies 43 risk genes for Alzheimer disease dementia

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.07.001

N/A

0.396DataRank · unranked

13 citations

Randy L. Parrish, Qile Dai, Aron S. Buchman, Shinya Tasaki, Rajesh K. Soni +4 more

Testing in Microbiome-Profiling Studies with MiRKAT, the Microbiome Regression-Based Kernel Association Test

UNC Libraries(2020)10.17615/xwgx-9y24

N/A

0.345DataRank · unranked

9 citations

Tamar Ringel‐Kulka, Michael P. Epstein, Hua Zhou, Michael C. Wu, Jun Chen +5 more

Metabolic effects of the schizophrenia-associated 3q29 deletion

Translational Psychiatry(2022)10.1038/s41398-022-01824-1

N/A

0.330DataRank · unranked

8 citations

Ryan H. Purcell, Timothy P. Rutkowski, Tamika Malone, Kimberly Pachura, Gary J. Bassell +10 more

Bridging cell morphological behaviors and molecular dynamics in multi-modal spatial omics with MorphLink

Nature Communications(2025)10.1038/s41467-025-61142-0

N/A

0.330DataRank · unranked

8 citations

Chenyang Yuan, Jiahui Jiang, Jianfeng Chen, Sunil Badve, Yesim Gökmen‐Polar +9 more

Proteome-wide association studies using summary pQTL data of brain, CSF, and plasma identify 30 risk genes of Alzheimer’s disease dementia

Alzheimer s Research & Therapy(2025)10.1186/s13195-025-01774-y

N/A

0.312DataRank · unranked

7 citations

Qiang Liu, Qile Dai, Aron S. Buchman, David A. Bennett, Shinya Tasaki +6 more

Generalized, focal, and combined epilepsies in families: New evidence for distinct genetic factors

Epilepsia(2020)10.1111/epi.16732

N/A

0.312DataRank · unranked

7 citations

Ruth Ottman, Michael P. Epstein, Samuel F. Berkovic, Colin A. Ellis

Newborn Differential DNA Methylation and Subcortical Brain Volumes as Early Signs of Severe Neurodevelopmental Delay in a South African Birth Cohort Study

medRxiv(2020)10.1101/2020.03.13.20035501

N/A

0.269DataRank · unranked

5 citations

Catherine J. Wedderburn, Nynke A. Groenewold, Nicole Gladish, Meaghan J. Jones, Nastassja Koen +9 more

The Quantitative Genetics of Human Disease: 2 Polygenic Risk Scores

Human Population Genetics and Genomics(2024)10.47248/hpgg2404030008

N/A

0.269DataRank · unranked

5 citations

Kiana Jodeiry, Andrew J. Bass, Michael P. Epstein, David J. Cutler

Genome-wide study of gene-by-sex interactions identifies risks for cleft palate

Human Genetics(2024)10.1007/s00439-024-02704-y

N/A

0.241DataRank · unranked

4 citations

Randy L. Parrish, Wasiu Lanre Adeyemo, Terri H. Beaty, Azeez Butali, Carmen J. Buxó +13 more

Pruning and thresholding approach for methylation risk scores in multi-ancestry populations

medRxiv(2022)10.1101/2022.06.09.22276204

N/A

0.208DataRank · unranked

3 citations

Evan Gatev, Todd M. Everson, Karen N. Conneely, Nastassja Koen, Michael P. Epstein +5 more

Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 818 trios

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.09.009

N/A

0.208DataRank · unranked

3 citations

Sarah W. Curtis, Justin Paschall, Wasiu Lanre Adeyemo, Terri H. Beaty, Azeez Butali +14 more

Rare variants in PRKCI cause Van der Woude syndrome and other features of peridermopathy

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.08.008

N/A

0.208DataRank · unranked

3 citations

Sunil Kumar Singh, Rachel B Walkup, Dorelle V. Fawwal, Kendra Vilfort, Amanda Koloskee +25 more

Novel Variance-Component TWAS method for studying complex human diseases with applications to Alzheimer’s dementia

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.05.26.117515

N/A

0.208DataRank · unranked

3 citations

Aron S. Buchman, Philip L. De Jager, David A. Bennett, Michael P. Epstein, Jingjing Yang +1 more

Association between Maternal Depression during Pregnancy and Newborn DNA Methylation

medRxiv(2021)10.1101/2021.06.02.21258194

N/A

0.165DataRank · unranked

2 citations

Nicole Gladish, Nastassja Koen, Michael P. Epstein, Michael S. Kobor, Heather J. Zar +3 more

Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting

medRxiv(2022)10.1101/2022.08.15.22278795

N/A

0.165DataRank · unranked

2 citations

Sarah W. Curtis, Alba Sanchis-Juan, Xuefang Zhao, S. Taylor Head, Samantha Ho +18 more

Cis - and trans -eQTL TWAS of breast and ovarian cancer identify more than 100 risk associated genes in the BCAC and OCAC consortia

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.11.09.566218

N/A

0.165DataRank · unranked

2 citations

Felipe Segato Dezem, Andrei Todor, Jingjing Yang, Jasmine Plummer, Simon A. Gayther +4 more

The Quantitative Genetics of Human Disease: 3A Interactions—Correlation in State

Human Population Genetics and Genomics(2025)10.47248/hpgg2505040008

N/A

0.104DataRank · unranked

1 citations

Andrew J. Bass, Michael P. Epstein, David J. Cutler, Kiana Jodeiry

Rare variants in PRKCI cause Van der Woude syndrome and other features of peridermopathy

medRxiv(2025)10.1101/2025.01.17.25320742

N/A

0.104DataRank · unranked

1 citations

Sunil Kumar Singh, Rachel B Walkup, Dorelle V. Fawwal, Wasiu Lanre Adeyemo, Terri H. Beaty +21 more

The PAX1 locus at 20p11 is a modifier for bilateral cleft lip only

medRxiv(2020)10.1101/2020.11.30.20241141

N/A

0.104DataRank · unranked

1 citations

Daniel Chang, Myoung Keun Lee, John R. Shaffer, Karlijne Indencleef, Michael P. Epstein +10 more

Identifying condition-related cell-cell communication events using supervised tensor analysis

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.12.15.571918

N/A

0DataRank · unranked

0 citations

Jingjing Yang, Michael P. Epstein, Qile Dai

Investigating the effect of polygenic background on epilepsy phenotype in ‘monogenic’ families

EBioMedicine(2024)10.1016/j.ebiom.2024.105404

N/A

0DataRank · unranked

30 citations

Ingrid E Scheffer, Colin A. Ellis, Bronwyn E. Grinton, Zaid Afawi, Dina Amrom +43 more

SR-TWAS: leveraging multiple reference panels to improve transcriptome-wide association study power by ensemble machine learning

Nature Communications(2024)10.1038/s41467-024-50983-w

N/A

0DataRank · unranked

13 citations

Aron S. Buchman, Shinya Tasaki, Yanling Wang, Denis Avey, Jishu Xu +5 more

Inflation of polygenic risk scores caused by sample overlap and relatedness: Examples of a major risk of bias

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.07.014

N/A

0DataRank · unranked

13 citations

Karen Oliver, Rebekah V. Harris, Ruth Ottman, Ingrid E Scheffer, Heather C Mefford +4 more

Cis- and trans-eQTL TWASs of breast and ovarian cancer identify more than 100 susceptibility genes in the BCAC and OCAC consortia

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.04.012

N/A

0DataRank · unranked

9 citations

Felipe Segato Dezem, Andrei Todor, Jingjing Yang, Jasmine Plummer, Simon A. Gayther +4 more

Identifying latent genetic interactions in genome-wide association studies using multiple traits

Genome Medicine(2024)10.1186/s13073-024-01329-0

N/A

0DataRank · unranked

8 citations

Shijia Bian, Aliza P. Wingo, Thomas S. Wingo, David J. Cutler, Michael P. Epstein +1 more

Familial aggregation of seizure outcomes in four familial epilepsy cohorts

Epilepsia(2024)10.1111/epi.18004

N/A

0DataRank · unranked

1 citations

Danni Tu, Karen Oliver, Heather C. Mefford, W. Allen Hauser, Jeffrey Buchhalter +5 more

Proteome-wide association studies using summary pQTL data of three tissues identified 30 risk genes of Alzheimer’s disease dementia

medRxiv(2024)10.1101/2024.03.28.24305044

N/A

0DataRank · unranked

4 citations

Qiang Liu, Qile Dai, Randy L. Parrish, Aron S. Buchman, Shinya Tasaki +7 more

A powerful framework for differential co-expression analysis of general risk factors

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.11.29.626006

N/A

0DataRank · unranked

0 citations

David J. Cutler, Michael P. Epstein, Andrew J. Bass

Mapping Inherited Genetic Variation with Opposite Effects on Autoimmune Disease and Four Cancer Types Identifies Candidate Drug Targets Associated with the Anti-Tumor Immune Response

Genes(2025)10.3390/genes16050575

N/A

0DataRank · unranked

3 citations

Michael P. Epstein, Joellen M. Schildkraut, Siddhartha Kar, Junyu Chen

CADET: Enhanced transcriptome-wide association analyses in admixed samples using eQTL summary data

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.05.010

N/A

0DataRank · unranked

1 citations

Qile Dai, Joellen Schildkraut, David J. Cutler, Jingjing Yang, Michael P. Epstein +1 more

Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 816 trios

medRxiv(2025)10.1101/2025.03.03.25323233

N/A

0DataRank · unranked

0 citations

Sarah W. Curtis, Justin Paschall, Terri H. Beaty, Azeez Butali, Carmen J. Buxó +12 more

A powerful framework for differential co-expression analysis of general risk factors

Bioinformatics(2025)10.1093/bioinformatics/btaf565

N/A

0DataRank · unranked

0 citations

David J. Cutler, Michael P. Epstein, Andrew J. Bass

Haploinsufficiency of GRHL2 is associated with orofacial clefting in humans

Human Molecular Genetics(2025)10.1093/hmg/ddaf163

N/A

0DataRank · unranked

0 citations

Cinderella Yang, Alba Sanchis-Juan, Katherine Singleton, Terri H. Beaty, Florian Erger +16 more

Supplementary Table S2 from An Analytic Pipeline to Obtain Reliable Genetic Ancestry Estimates from Tumor-Derived RNA Sequencing Data

Figshare(2025)10.1158/1055-9965.30029666

N/A

0DataRank · unranked

0 citations

Ximing Ran, Julia Wrobel, Natalie R. Davidson, Casey S. Greene, Michael P. Epstein +5 more

The Quantitative Genetics of Human Disease: 3B Interactions—Non-Additivity and Missing Heritability

Human Population Genetics and Genomics(2025)10.47248/hpgg2505040009

N/A

0DataRank · unranked

0 citations

Andrew J. Bass, Michael P. Epstein, David J. Cutler, Kiana Jodeiry

An Analytic Pipeline to Obtain Reliable Genetic Ancestry Estimates from Tumor-Derived RNA Sequencing Data

Cancer Epidemiology, Biomarkers & Prevention(2025)10.1158/1055-9965.epi-25-0371

N/A

0DataRank · unranked

0 citations

Ximing Ran, Julia Wrobel, Natalie R. Davidson, Casey S. Greene, Michael P. Epstein +5 more

Supplementary Table S1 from An Analytic Pipeline to Obtain Reliable Genetic Ancestry Estimates from Tumor-Derived RNA Sequencing Data

Figshare(2025)10.1158/1055-9965.30029669

N/A

0DataRank · unranked

0 citations

Ximing Ran, Julia Wrobel, Natalie R. Davidson, Casey S. Greene, Michael P. Epstein +5 more

Supplementary Figure S1 from An Analytic Pipeline to Obtain Reliable Genetic Ancestry Estimates from Tumor-Derived RNA Sequencing Data

Figshare(2025)10.1158/1055-9965.30029672

N/A

0DataRank · unranked

0 citations

Ximing Ran, Julia Wrobel, Natalie R. Davidson, Casey S. Greene, Michael P. Epstein +5 more

Data from An Analytic Pipeline to Obtain Reliable Genetic Ancestry Estimates from Tumor-Derived RNA Sequencing Data

(2025)10.1158/1055-9965.c.8012108

N/A

0DataRank · unranked

0 citations

Ximing Ran, Julia Wrobel, Natalie R. Davidson, Casey S. Greene, Michael P. Epstein +5 more

Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.05.018

N/A

0DataRank · unranked

97 citations

Kimberly K. Diaz Perez, Miranda Sun, Samantha Ho, Pankaj Chopra, Nandita Mukhopadhyay +22 more

Association between DNA methylation levels in brain tissue and late-life depression in community-based participants

Translational Psychiatry(2020)10.1038/s41398-020-00948-6

N/A

0DataRank · unranked

41 citations

Chloe Robins, Karen N. Conneely, Philip L. De Jager, David A. Bennett, Michael P. Epstein +3 more

Coding de novo mutations identified by WGS reveal novel orofacial cleft genes

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.04.01.019927

N/A

0DataRank · unranked

0 citations

Kimberly Diaz Perez, Miranda Sun, Samantha Ho, Pankaj Chopra, Nandita Mukhopadhyay +22 more

Metabolic effects of the schizophrenia-associated 3q29 deletion are sex-specific and uncoupled from behavioral phenotypes

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.09.18.303412

N/A

0DataRank · unranked

0 citations

Ryan H. Purcell, Timothy P. Rutkowski, Tamika Malone, Kimberly Pachura, Gary J. Bassell +11 more

Powerful SNP-Set Analysis for Case-Control Genome-wide Association Studies

UNC Libraries(2020)10.17615/g0gb-1k93

N/A

0DataRank · unranked

0 citations

Xihong Lin, Deanne Taylor, Michael C. Wu, Peter Kraft, Michael P. Epstein +2 more

Novel Variance-Component TWAS method for studying complex human diseases with applications to Alzheimer’s dementia

PLoS Genetics(2021)10.1371/journal.pgen.1009482

N/A

0DataRank · unranked

82 citations

Aron S. Buchman, Philip L. De Jager, David A. Bennett, Michael P. Epstein, Jingjing Yang +1 more

Brain DNA Methylation Patterns in CLDN5 Associated With Cognitive Decline

Biological Psychiatry(2021)10.1016/j.biopsych.2021.01.015

N/A

0DataRank · unranked

74 citations

Chloe Robins, Karen N. Conneely, Rachel D. Edgar, Philip L. De Jager, David A. Bennett +4 more

TIGAR-V2: Efficient TWAS tool with nonparametric Bayesian eQTL weights of 49 tissue types from GTEx V8

Human Genetics and Genomics Advances(2021)10.1016/j.xhgg.2021.100068

N/A

0DataRank · unranked

36 citations

Greg Gibson, Michael P. Epstein, Jingjing Yang, Randy L. Parrish

The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip

Human Genetics and Genomics Advances(2021)10.1016/j.xhgg.2021.100025

N/A

0DataRank · unranked

24 citations

Daniel Chang, Myoung Keun Lee, John R. Shaffer, Karlijne Indencleef, Michael P. Epstein +10 more

Identifying susceptibility genes for primary ovarian insufficiency on the high-risk genetic background of a fragile X premutation

Fertility and Sterility(2021)10.1016/j.fertnstert.2021.04.021

N/A

0DataRank · unranked

6 citations

J. Christopher Rounds, Krista Charen, Lisa Shubeck, Heather S. Hipp, Jessica B. Spencer +18 more

TIGAR-V2: Efficient TWAS Tool with Nonparametric Bayesian eQTL Weights of 49 Tissue Types from GTEx V8

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.07.16.452700

N/A

0DataRank · unranked

4 citations

Greg Gibson, Michael P. Epstein, Jingjing Yang, Randy L. Parrish

Efficient Estimation of Indirect Effects in Case-Control Studies Using a Unified Likelihood Framework

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.07.16.452552

N/A

0DataRank · unranked

1 citations

Sarah W. Curtis, Claudia Solís‐Lemus, Elizabeth J. Leslie, Michael P. Epstein, Glen A. Satten

FAT4 Identified as a Potential Modifier of Orofacial Cleft Laterality

medRxiv(2021)10.1101/2021.03.16.21253740

N/A

0DataRank · unranked

0 citations

Daniel Chang, Miranda Sun, Michael P. Epstein, Jeffrey C. Murray, Eleanor Feingold +7 more

Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome

Scientific Reports(2021)10.1038/s41598-021-94021-x

Top 100%

0DataRank

Top 100%0 citations

Aaron M. Holleman, Holly Corbitt, Cheryl L. Maslen, Tracie C. Rosser, David J. Cutler +21 more

A Kernel Method for Dissecting Genetic Signals in Tests of High-Dimensional Phenotypes

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.07.29.454336

N/A

0DataRank · unranked

0 citations

Aaron M. Holleman, Andrei Todor, Bekh Bradley, Kerry J. Ressler, Debashis Ghosh +2 more

OTTERS: A powerful TWAS framework leveraging summary-level reference data

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.03.30.486451

N/A

0DataRank · unranked

3 citations

Geyu Zhou, Luca Pinello, Urmo Võsa, Lude Franke, Alexis Battle +7 more

POIROT: A powerful test for parent-of-origin effects in unrelated samples leveraging multiple phenotypes

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.11.28.517712

N/A

0DataRank · unranked

0 citations

Elizabeth J. Leslie, David J. Cutler, Michael P. Epstein, S. Taylor Head

Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63336

N/A

0DataRank · unranked

7 citations

S. C. S. Chung, S. Taylor Head, Michael P. Epstein, Jacqueline T. Hecht, George L. Wehby +5 more

POIROT: a powerful test for parent-of-origin effects in unrelated samples leveraging multiple phenotypes

Bioinformatics(2023)10.1093/bioinformatics/btad199

N/A

0DataRank · unranked

5 citations

Elizabeth J. Leslie, David J. Cutler, Michael P. Epstein, S. Taylor Head

The quantitative genetics of human disease: 1. Foundations

Human Population Genetics and Genomics(2023)10.47248/hpgg2303040007

N/A

0DataRank · unranked

4 citations

Kiana Jodiery, Andrew J. Bass, Michael P. Epstein, David J. Cutler

Rare genetic variants in SEC24D modify orofacial cleft phenotypes

medRxiv(2023)10.1101/2023.03.24.23287714

N/A

0DataRank · unranked

4 citations

Jenna C. Carlson, Terri H. Beaty, Jeffrey C. Murray, Seth M. Weinberg, Mary L. Marazita +5 more

Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?

medRxiv(2023)10.1101/2023.02.01.23285340

N/A

0DataRank · unranked

1 citations

S. C. S. Chung, S. Taylor Head, Michael P. Epstein, Jacqueline T. Hecht, George L. Wehby +5 more

Identifying latent genetic interactions in genome-wide association studies using multiple traits

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.09.11.557155

N/A

0DataRank · unranked

1 citations

Shijia Bian, Aliza P. Wingo, Thomas S. Wingo, David J. Cutler, Michael P. Epstein +1 more

Mapping inherited genetic variation with opposite effects on autoimmune disease and cancer identifies candidate drug targets associated with the anti-tumor immune response

medRxiv(2023)10.1101/2023.12.23.23300491

N/A

0DataRank · unranked

1 citations

Michael P. Epstein, Joellen M. Schildkraut, Siddhartha Kar, Junyu Chen

SR-TWAS: Leveraging Multiple Reference Panels to Improve TWAS Power by Ensemble Machine Learning

medRxiv(2023)10.1101/2023.06.20.23291605

N/A

0DataRank · unranked

0 citations

Aron S. Buchman, Shinya Tasaki, Yanling Wang, Denis Avey, Jishu Xu +5 more

Michael P. Epstein

Indexed papers

Top data-sharing exemplar

Papers