David J. Cutler

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

3in 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 3 indexed papers 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 39 papers — median percentile 0. Top paper: “Rare coding variation provides insight into the genetic architecture and phenotypic context of autism”.

Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

Nature Genetics(2022)10.1038/s41588-022-01104-0

N/A

0.969DataRank · unranked

638 citations

F. Kyle Satterstrom, Minshi Peng, Harrison Brand, Ryan L. Collins, Shan Dong +112 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

Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion

Molecular Psychiatry(2020)10.1038/s41380-020-0654-3

N/A

0.738DataRank · unranked

136 citations

Worrawat Engchuan, Matthew S. Hestand, Tracy Heung, Aaron M. Holleman, H. Richard Johnston +95 more

Genetic control of the human brain proteome

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.01.012

N/A

0.717DataRank · unranked

118 citations

Yue Liu, Wen Fan, Duc M. Duong, Jacob Meigs, Nadia V. Harerimana +13 more

Novel Missense CNTNAP2 Variant Identified in Two Consanguineous Pakistani Families With Developmental Delay, Epilepsy, Intellectual Disability, and Aggressive Behavior

Frontiers in Neurology(2022)10.3389/fneur.2022.918022

N/A

0.669DataRank · unranked

16 citations

Kari A. Mattison, Sohail Ahmad, Pankaj Chopra, H. Richard Johnston, Shakoor Ahmad +8 more

LDL cholesterol is associated with higher AD neuropathology burden independent of APOE

Journal of Neurology Neurosurgery & Psychiatry(2022)10.1136/jnnp-2021-328164

N/A

0.598DataRank · unranked

53 citations

Selina Vattathil, Jiaqi Liu, Wen Fan, David J. Cutler, Allan I. Levey +4 more

Longitudinal DNA methylation profiling of the rectal mucosa identifies cell-specific signatures of disease status, severity and clinical outcomes in ulcerative colitis cell-specific DNA methylation signatures of UC

Clinical Epigenetics(2023)10.1186/s13148-023-01462-4

N/A

0.596DataRank · unranked

15 citations

Hari K. Somineni, Jason D. Matthews, Varun Kilaru, Jeffrey S. Hyams, Lee A. Denson +7 more

Whole-genome sequencing of African Americans implicates differential genetic architecture in inflammatory bowel disease

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.02.001

N/A

0.571DataRank · unranked

44 citations

Sini Nagpal, Suresh Venkateswaran, David J. Cutler, David T. Okou, Talin Haritunians +53 more

Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism

10.1101/2021.12.20.21267194

N/A

0.538DataRank · unranked

35 citations

F. Kyle Satterstrom, Minshi Peng, Harrison Brand, Ryan L. Collins, Shan Dong +60 more

Sequencing of over 100,000 individuals identifies multiple genes and rare variants associated with Crohns disease susceptibility

medRxiv(2021)10.1101/2021.06.15.21258641

N/A

0.500DataRank · unranked

11 citations

Christine Stevens, Guhan Venkataraman, Kai Yuan, Brandon E. Avila, María T. Abreu +95 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

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

The role of admixture in the rare variant contribution to inflammatory bowel disease

Genome Medicine(2023)10.1186/s13073-023-01244-w

N/A

0.345DataRank · unranked

9 citations

Shivam Sharma, Sini Nagpal, David J. Cutler, John D. Rioux, Judy H. Cho +6 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

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

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

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

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

Racial and ethnic diversity of classic and clinical variant galactosemia in the United States

Molecular Genetics and Metabolism(2023)10.1016/j.ymgme.2023.107542

N/A

0DataRank · unranked

4 citations

David J. Cutler, Judith L. Fridovich‐Keil, Nichole M. Stettner

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

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

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

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

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

A Satellite Account for Health in the United States

National Bureau of Economic Research(2020)10.3386/w27848

N/A

0DataRank · unranked

2 citations

Kaushik Ghosh, Kassandra L. Messer, Trivellore E. Raghunathan, Allison B. Rosen, Susan L. Stewart +1 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

Profiling Non-Coding RNA Levels With Clinical Classifiers in Pediatric Crohn’s Disease

Research Square(2020)10.21203/rs.3.rs-88594/v1

N/A

0DataRank · unranked

1 citations

Suresh Venkateswaran, Jason D. Matthews, Yael Haberman, David J. Cutler, Jeffrey S. Hyams +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

Methylation Quantitative Trait Loci are Largely Consistent across Disease States in Crohn’s disease

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.11.16.385534

N/A

0DataRank · unranked

0 citations

Hari K. Somineni, Varun Kilaru, Şeyma Katrinli, Jarod Prince, David T. Okou +9 more

Reciprocal Duplication of the Williams-Beuren Syndrome Deletion on Chromosome 7q11.23 Is Associated with Schizophrenia

UNC Libraries(2020)10.17615/8m0s-na92

N/A

0DataRank · unranked

0 citations

John A. McGrath, Pamela Sklar, Gerald Nestadt, David J. Cutler, Paula Wolyniec +25 more

Ileal Derived Organoids From Crohn’s Disease Patients Show Unique Transcriptomic and Secretomic Signatures

Cellular and Molecular Gastroenterology and Hepatology(2021)10.1016/j.jcmgh.2021.06.018

N/A

0DataRank · unranked

43 citations

Suresh Venkateswaran, Murugadas Anbazhagan, Vasantha L. Kolachala, Jarod Prince, Anne Dodd +8 more

Site- and Taxa-Specific Disease-Associated Oral Microbial Structures Distinguish Inflammatory Bowel Diseases

Inflammatory Bowel Diseases(2021)10.1093/ibd/izab082

N/A

0DataRank · unranked

28 citations

Jordan Weitzner, Suresh Venkateswaran, Anne Dodd, Jarod Prince, Arjuna Karikaran +8 more

Profiling non-coding RNA levels with clinical classifiers in pediatric Crohn’s disease

BMC Medical Genomics(2021)10.1186/s12920-021-01041-7

N/A

0DataRank · unranked

25 citations

Suresh Venkateswaran, Jason D. Matthews, Yael Haberman, David J. Cutler, Jeffrey S. Hyams +3 more

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

Convergent and distributed effects of the 3q29 deletion on the human neural transcriptome

Translational Psychiatry(2021)10.1038/s41398-021-01435-2

N/A

0DataRank · unranked

18 citations

Ryan H. Purcell, the Emory 3q29 Project, Katrina Aberizk, Hallie Averbach, Emily Black +37 more

Sex-specific recombination patterns predict parent of origin for recurrent genomic disorders

BMC Medical Genomics(2021)10.1186/s12920-021-00999-8

N/A

0DataRank · unranked

5 citations

H. Richard Johnston, David J. Cutler, Michael E. Zwick, Jennifer G. Mullé, Trenell J. Mosley

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

Eicosatetraynoic Acid and Butyrate Regulate Human Intestinal Organoid Mitochondrial and Extracellular Matrix Pathways Implicated in Crohn’s Disease Strictures

Inflammatory Bowel Diseases(2022)10.1093/ibd/izac037

N/A

0DataRank · unranked

23 citations

Erin Bonkowski, Elizabeth Angerman, Elizabeth Novak, Alex Huron, Grayce Akers +15 more

David J. Cutler

Indexed papers

Top data-sharing exemplar

Papers