Benjamin M. Neale

Also affiliated with Massachusetts General Hospital

Arts and HumanitiesPsychology

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 1%percentile

19.4Author DataRank

Indexed papers

14in 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 14 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.

A cross-disorder dosage sensitivity map of the human genome

Cell(2022)10.1016/j.cell.2022.06.036

Top 5%

4.7DataRank

Top 5%367 citations

Joseph Glessner, Eleonora Porcu, Maarja Lepamets, Rhonda Brandon, Christopher Lauricella +46 more

Papers

Driven by 93 papers — median percentile 80. Top paper: “Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism”.

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

Cell(2020)10.1016/j.cell.2019.12.036

N/A

9.5DataRank · unranked

2470 citations

Jack A. Kosmicki, Jiebiao Wang, Michael S. Breen, Silvia De Rubeis, Joon‐Yong An +95 more

Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains

Nature Genetics(2023)10.1038/s41588-022-01285-8

N/A

6.1DataRank · unranked

775 citations

G. Bragi Walters, Georgios Athanasiadis, Raymond K. Walters, Karen Therrien, Trine Tollerup Nielsen +81 more

A cross-disorder dosage sensitivity map of the human genome

Cell(2022)10.1016/j.cell.2022.06.036

Top 5%

4.7DataRank

Top 5%367 citations

Joseph Glessner, Eleonora Porcu, Maarja Lepamets, Rhonda Brandon, Christopher Lauricella +46 more

Hematopoietic mosaic chromosomal alterations increase the risk for diverse types of infection

Nature Medicine(2021)10.1038/s41591-021-01371-0

N/A

4.7DataRank · unranked

194 citations

Shu‐Hong Lin, Alexander G. Bick, Aoxing Liu, Kaavya Paruchuri, Chen Wang +95 more

Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia

Nature Genetics(2022)10.1038/s41588-022-01034-x

N/A

3.5DataRank · unranked

214 citations

Daniel P. Howrigan, Sinéad B. Chapman, Rolf Adolfsson, Nick Bass, Douglas Blackwood +42 more

A first update on mapping the human genetic architecture of COVID-19

Nature(2022)10.1038/s41586-022-04826-7

Top 6%

3.5DataRank

Top 6%176 citations

Leadership, Gita A. Pathak, Juha Karjalainen, Christine Stevens, Benjamin M. Neale +86 more

FAVOR: functional annotation of variants online resource and annotator for variation across the human genome

Nucleic Acids Research(2022)10.1093/nar/gkac966

Top 8%

2.7DataRank

Top 8%143 citations

Theodore Arapoglou, Xihao Li, Zilin Li, Xiuwen Zheng, Jill E. Moore +20 more

A harmonized public resource of deeply sequenced diverse human genomes

Genome Research(2024)10.1101/gr.278378.123

Top 8%

2.6DataRank

Top 8%130 citations

Mary T. Yohannes, Lethukuthula L. Nkambule, Xuefang Zhao, Julia K. Goodrich, Heesu Ally Kim +16 more

The genetic architecture of sporadic and multiple consecutive miscarriage

Nature Communications(2020)10.1038/s41467-020-19742-5

N/A

2.6DataRank · unranked

122 citations

Ana Gonçalves Soares, Teresa Ferreira, Jodie N. Painter, Jenny C. Censin, Samantha Laber +50 more

Multi-ancestry meta-analysis of asthma identifies novel associations and highlights the value of increased power and diversity

Cell Genomics(2022)10.1016/j.xgen.2022.100212

N/A

2.4DataRank · unranked

118 citations

Wei Zhou, Ying Wang, Masahiro Kanai, Shinichi Namba, Rahul Gupta +8 more

Genome-wide risk prediction of common diseases across ancestries in one million people

Cell Genomics(2022)10.1016/j.xgen.2022.100118

N/A

2.3DataRank · unranked

93 citations

Sini Kerminen, Yen‐Chen Anne Feng, Masahiro Kanai, Kristi Läll, Laurent F. Thomas +15 more

A cross-disorder dosage sensitivity map of the human genome

medRxiv(2021)10.1101/2021.01.26.21250098

N/A

2.0DataRank · unranked

54 citations

Joseph Glessner, Eleonora Porcu, Lisa‐Marie Niestroj, Jacob C. Ulirsch, Georgios Kellaris +28 more

Analysis of genetic dominance in the UK Biobank

Science(2023)10.1126/science.abn8455

Top 12%

1.7DataRank

Top 12%72 citations

Wei Zhou, Liam Abbott, Emilie M. Wigdor, Nikolas Baya, Claire Churchhouse +7 more

Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups

Nature Genetics(2022)10.1038/s41588-022-01171-3

N/A

1.7DataRank · unranked

76 citations

Jakob Grove, Thomas D. Als, Joanna Martin, Georgios Voloudakis, Sandra Meier +29 more

A harmonized public resource of deeply sequenced diverse human genomes

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.01.23.525248

Top 13%

1.6DataRank

Top 13%48 citations

Mary T. Yohannes, Lethukuthula L. Nkambule, Xuefang Zhao, Julia K. Goodrich, Heesu Ally Kim +16 more

Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains

medRxiv(2022)10.1101/2022.02.14.22270780

N/A

1.5DataRank · unranked

63 citations

G. Bragi Walters, Georgios Athanasiadis, Raymond K. Walters, Karen Therrien, Leila Farajzadeh +42 more

Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals

Nature Communications(2023)10.1038/s41467-023-39539-6

N/A

1.2DataRank · unranked

56 citations

David Lewis‐Smith, Ryan L. Collins, Lisa‐Marie Niestroj, Shridhar Parthasarathy, Julie Xian +94 more

Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions

Cell Genomics(2023)10.1016/j.xgen.2023.100356

N/A

1.0DataRank · unranked

43 citations

Maxwell A. Sherman, Giulio Genovese, Thomas G. Gilgenast, Tushar Kamath, S.J. Burris +95 more

Genome-wide association study of school grades identifies genetic overlap between language ability, psychopathology and creativity

Scientific Reports(2023)10.1038/s41598-022-26845-0

N/A

0.970DataRank · unranked

30 citations

Andrea Ganna, Jonathan R. I. Coleman, Andrea G. Allegrini, Georgios Voloudakis, Jakob Grove +48 more

Mapping and characterization of structural variation in 17,795 human genomes

Nature(2020)10.1038/s41586-020-2371-0

N/A

0.885DataRank · unranked

365 citations

David E. Larson, Allison A. Regier, Colby Chiang, Indraniel Das, Krishna Kanchi +13 more

Phenome-wide heritability analysis of the UK Biobank

PLOS Genetics(2017)10.1371/journal.pgen.1006711

N/A

0.813DataRank · unranked

225 citations

Chia‐Yen Chen, Benjamin M. Neale, Mert R. Sabuncu, Jordan W. Smoller, Tian Ge

Human genetic analyses of organelles highlight the nucleus in age-related trait heritability

eLife(2021)10.7554/elife.68610

N/A

0.809DataRank · unranked

26 citations

Konrad J. Karczewski, Daniel P. Howrigan, Benjamin M. Neale, Vamsi K. Mootha, Rahul Gupta

A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts

Biological Psychiatry(2021)10.1016/j.biopsych.2021.04.018

N/A

0.801DataRank · unranked

207 citations

Jian Zeng, Joana Revez, Ying Wang, Zhili Zheng, Tian Ge +95 more

Nuclear genetic control of mtDNA copy number and heteroplasmy in humans

Nature(2023)10.1038/s41586-023-06426-5

N/A

0.785DataRank · unranked

187 citations

Masahiro Kanai, Timothy Durham, Kristin Tsuo, Jason G. McCoy, Anna V. Kotrys +7 more

Pan-UK Biobank GWAS improves discovery, analysis of genetic architecture, and resolution into ancestry-enriched effects

medRxiv(2024)10.1101/2024.03.13.24303864

N/A

0.774DataRank · unranked

173 citations

Rahul Gupta, Masahiro Kanai, Wenhan Lu, Kristin Tsuo, Ying Wang +24 more

Mapping the genetic landscape across 14 psychiatric disorders

Nature(2025)10.1038/s41586-025-09820-3

N/A

0.750DataRank · unranked

75 citations

Josefin Werme, Wouter J. Peyrot, Oleksandr Frei, Christiaan de Leeuw, Lucy Bicks +95 more

SAIGE-GENE+ improves the efficiency and accuracy of set-based rare variant association tests

Nature Genetics(2022)10.1038/s41588-022-01178-w

N/A

0.749DataRank · unranked

146 citations

Wenjian Bi, Zhangchen Zhao, Kushal K. Dey, Karthik A. Jagadeesh, Konrad J. Karczewski +4 more

Findings and insights from the genetic investigation of age of first reported occurrence for complex disorders in the UK Biobank and FinnGen

medRxiv(2020)10.1101/2020.11.20.20234302

Top 27%

0.736DataRank

Top 27%18 citations

Tian Ge, Mattia Cordioli, FinnGen, Andrea Ganna, Jordan W. Smoller +2 more

Low-coverage sequencing cost-effectively detects known and novel variation in underrepresented populations

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.03.012

N/A

0.728DataRank · unranked

127 citations

Elizabeth G. Atkinson, Sinéad B. Chapman, Anne Stevenson, Rocky E. Stroud, Tamrat Abebe +34 more

Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics

Science Translational Medicine(2020)10.1126/scitranslmed.aay6570

N/A

0.718DataRank · unranked

119 citations

Kristi Krebs, Chia‐Yen Chen, Ruth Boxall, Jenny C. Censin, Teresa Ferreira +15 more

Functional Architectures of Local and Distal Regulation of Gene Expression in Multiple Human Tissues

The American Journal of Human Genetics(2017)10.1016/j.ajhg.2017.03.002

N/A

0.712DataRank · unranked

114 citations

Hilary K. Finucane, Alexander Gusev, Gaurav Bhatia, Steven Gazal, Luke O’Connor +6 more

Investigating Shared Genetic Basis Across Tourette Syndrome and Comorbid Neurodevelopmental Disorders Along the Impulsivity-Compulsivity Spectrum

Biological Psychiatry(2021)10.1016/j.biopsych.2020.12.028

N/A

0.700DataRank · unranked

105 citations

Hanrui Wu, Phil H. Lee, Fotis Tsetsos, Lea K. Davis, Dongmei Yu +20 more

Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder

Molecular Psychiatry(2021)10.1038/s41380-020-01006-9

N/A

0.686DataRank · unranked

22 citations

Fernando S. Goes, Adam E. Locke, Duncan S. Palmer, Weiqing Wang, Sarah Cohen‐Woods +71 more

Examining Sex-Differentiated Genetic Effects Across Neuropsychiatric and Behavioral Traits

Biological Psychiatry(2021)10.1016/j.biopsych.2020.12.024

N/A

0.673DataRank · unranked

88 citations

Ekaterina Khramtsova, Slavina B. Goleva, Gabriëlla A.M. Blokland, Michela Traglia, Raymond K. Walters +37 more

Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects

Brain(2020)10.1093/brain/awaa171

N/A

0.661DataRank · unranked

81 citations

Eduardo Pérez‐Palma, Daniel P. Howrigan, Yadi Zhou, Feixiong Cheng, Elmo Saarentaus +86 more

Exome-wide evidence of compound heterozygous effects across common phenotypes in the UK Biobank

Cell Genomics(2024)10.1016/j.xgen.2024.100602

Top 31%

0.652DataRank

Top 31%12 citations

Samvida S. Venkatesh, Nikolas Baya, Barney Hill, Wei Zhou, Alex Bloemendal +6 more

Wrestling with Social and Behavioral Genomics: Risks, Potential Benefits, and Ethical Responsibility

The Hastings Center Report(2023)10.1002/hast.1477

N/A

0.639DataRank · unranked

70 citations

Paul S. Appelbaum, Daniel J. Benjamin, Shawneequa Callier, Nathaniel Comfort, Dalton Conley +14 more

Improving fine-mapping by modeling infinitesimal effects

Nature Genetics(2023)10.1038/s41588-023-01597-3

N/A

0.635DataRank · unranked

68 citations

Roy Elzur, Masahiro Kanai, Jacob C. Ulirsch, Omer Weissbrod, Mark J. Daly +4 more

The impact of rare protein coding genetic variation on adult cognitive function

Nature Genetics(2023)10.1038/s41588-023-01398-8

N/A

0.628DataRank · unranked

65 citations

Ruoyu Tian, Tian Ge, Max Lam, Gabriela Sánchez-Andrade, Tarjinder Singh +76 more

A Polygenic and Phenotypic Risk Prediction for Polycystic Ovary Syndrome Evaluated by Phenome-Wide Association Studies

The Journal of Clinical Endocrinology & Metabolism(2020)10.1210/clinem/dgz326

N/A

0.626DataRank · unranked

64 citations

Ky’Era V. Actkins, Jennifer A. Pacheco, Anna O. Basile, Robert J. Carroll, David R. Crosslin +66 more

Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.04.009

N/A

0.617DataRank · unranked

60 citations

Gundula Povysil, Ryan S. Dhindsa, Kate E. Stanley, Andrew S. Allen, Yen‐Chen Anne Feng +95 more

Synaptic processes and immune-related pathways implicated in Tourette syndrome

Translational Psychiatry(2021)10.1038/s41398-020-01082-z

N/A

0.612DataRank · unranked

58 citations

Dongmei Yu, Jae Hoon Sul, Alden Y. Huang, Cornelia Illmann, Lisa Osiecki +66 more

Non-parametric Polygenic Risk Prediction via Partitioned GWAS Summary Statistics

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.05.004

N/A

0.584DataRank · unranked

48 citations

Maxim Imakaev, Daniel Hui, Nikolaos A. Patsopoulos, Benjamin M. Neale, Sekar Kathiresan +3 more

SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues

Cell Reports(2021)10.1016/j.celrep.2021.110020

N/A

0.581DataRank · unranked

47 citations

Jennifer Nguyen, Timothy D. Arthur, Hiroko Matsui, Agnieszka D’Antonio‐Chronowska, Kelly A. Frazer +85 more

Efficient and accurate frailty model approach for genome-wide survival association analysis in large-scale biobanks

Nature Communications(2022)10.1038/s41467-022-32885-x

N/A

0.578DataRank · unranked

46 citations

Wei Zhou, Tuomo Kiiskinen, Aki S. Havulinna, Amanda Elliott, Juha Karjalainen +9 more

Examining sex-differentiated genetic effects across neuropsychiatric and behavioral traits

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.05.04.076042

N/A

0.567DataRank · unranked

13 citations

Ekaterina Khramtsova, Slavina B. Goleva, Gabriëlla A.M. Blokland, Michela Traglia, Raymond K. Walters +27 more

Principled distillation of UK Biobank phenotype data reveals underlying structure in human variation

Nature Human Behaviour(2024)10.1038/s41562-024-01909-5

N/A

0.564DataRank · unranked

18 citations

Rebecca Shafee, Robbee Wedow, Amanda Elliott, Duncan S. Palmer, John Compitello +14 more

Genome-Wide Association Study Points to Novel Locus for Gilles de la Tourette Syndrome

Biological Psychiatry(2023)10.1016/j.biopsych.2023.01.023

N/A

0.520DataRank · unranked

31 citations

Apostolia Topaloudi, Pritesh Jain, Zhiyu Yang, Dongmei Yu, Petros Kolovos +94 more

Genetic structure correlates with ethnolinguistic diversity in eastern and southern Africa

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.07.013

N/A

0.505DataRank · unranked

28 citations

Shareefa Dalvie, Yakov Pichkar, Allan Kalungi, Lerato Majara, Anne Stevenson +37 more

Multi-ancestry meta-analysis identifies 2 novel loci associated with ischemic stroke and reveals heterogeneity of effects between sexes and ancestries

medRxiv(2022)10.1101/2022.02.28.22271647

N/A

0.503DataRank · unranked

18 citations

Kuan-Han H. Wu, Whitney Hornsby, Brooke N. Wolford, Fred Shen, Wei Zhou +17 more

Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestries

Cell Genomics(2023)10.1016/j.xgen.2023.100345

N/A

0.483DataRank · unranked

24 citations

Kuan-Han Wu, Whitney Hornsby, Brooke N. Wolford, Fred Shen, Wei Zhou +16 more

Decoding Genetics, Ancestry, and Geospatial Context for Precision Health

medRxiv(2023)10.1101/2023.10.24.23297096

N/A

0.483DataRank · unranked

24 citations

Ying Wang, Kaavya Paruchuri, Md Mesbah Uddin, So Mi Jemma Cho, Sarah Urbut +12 more

Incorporating family history of disease improves polygenic risk scores in diverse populations

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.04.15.439975

N/A

0.470DataRank · unranked

22 citations

Po‐Ru Loh, Benjamin M. Neale, Alkes L. Price, Margaux L. A. Hujoel

Discordant calls across genotype discovery approaches elucidate variants with systematic errors

Genome Research(2023)10.1101/gr.277908.123

N/A

0.464DataRank · unranked

21 citations

Mykyta Artomov, Alexander A. Loboda, Heidi L. Rehm, Daniel G. MacArthur, Konrad J. Karczewski +3 more

Hematopoietic mosaic chromosomal alterations and risk for infection among 767,891 individuals without blood cancer

Research Square(2020)10.21203/rs.3.rs-100817/v1

N/A

0.436DataRank · unranked

6 citations

Seyedeh M. Zekavat, Shu‐Hong Lin, Alexander G. Bick, Aoxing Liu, Kaavya Paruchuri +26 more

Author Correction: A global overview of pleiotropy and genetic architecture in complex traits

Nature Genetics(2020)10.1038/s41588-019-0571-z

N/A

0.434DataRank · unranked

17 citations

Sven Stringer, Oleksandr Frei, Maša Umićević Mirkov, Christiaan de Leeuw, Tinca J. C. Polderman +5 more

Blended Genome Exome (BGE) as a Cost Efficient Alternative to Deep Whole Genomes or Arrays

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.04.03.587209

N/A

0.434DataRank · unranked

17 citations

Jonna Grimsby, Daniel P. Howrigan, Kai Yuan, Sinéad B. Chapman, Christine Stevens +12 more

Genome-Wide Association Study Meta-Analysis of 9619 Cases With Tic Disorders

Biological Psychiatry(2024)10.1016/j.biopsych.2024.07.025

Top 44%

0.421DataRank

Top 44%13 citations

Matthew Halvorsen, Jakob Grove, Bergrún Ásbjörnsdóttir, Pétur Lúðvígsson, Ólafur Thorarensen +93 more

An efficient and accurate frailty model approach for genome-wide survival association analysis controlling for population structure and relatedness in large-scale biobanks

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.10.31.358234

N/A

0.385DataRank · unranked

12 citations

Wei Zhou, Tuomo Kiiskinen, Aki S. Havulinna, Amanda Elliott, Juha Karjalainen +9 more

Genome-wide association meta-analyses of drug-resistant epilepsy

EBioMedicine(2025)10.1016/j.ebiom.2025.105675

N/A

0.385DataRank · unranked

12 citations

Andreja Avberšek, Remi Stevelink, Helena Martins Custodio, Siwei Chen, Doug Speed +88 more

Rare genetic variants confer a high risk of ADHD and implicate neuronal biology

Nature(2025)10.1038/s41586-025-09702-8

N/A

0.377DataRank · unranked

11 citations

Jinjie Duan, Yu-Han H. Hsu, Greta Pintacuda, Jakob Grove, Trine Tollerup Nielsen +29 more

Low-coverage sequencing cost-effectively detects known and novel variation in underrepresented populations

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.04.27.064832

N/A

0.373DataRank · unranked

11 citations

Elizabeth G. Atkinson, Sinéad B. Chapman, Anne Stevenson, Rocky E. Stroud, Tamrat Abebe +34 more

CHARR efficiently estimates contamination from DNA sequencing data

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.10.011

N/A

0.373DataRank · unranked

11 citations

Laura D. Gauthier, Timothy Poterba, Edoardo Giacopuzzi, Julia K. Goodrich, Christine Stevens +5 more

Exome sequencing in bipolar disorder reveals shared risk gene AKAP11 with schizophrenia

medRxiv(2021)10.1101/2021.03.09.21252930

N/A

0.366DataRank · unranked

7 citations

Daniel P. Howrigan, Sinéad B. Chapman, Rolf Adolfsson, Nick Bass, Douglas Blackwood +41 more

Elevated common variant genetic risk for tourette syndrome in a densely-affected pedigree

Molecular Psychiatry(2021)10.1038/s41380-021-01277-w

N/A

0.360DataRank · unranked

10 citations

Jin Szatkiewicz, Poorva Mudgal, Dongmei Yu, H.N. Aschauer, Gil Atzmon +94 more

Genetic contribution to disease-course severity and progression in the SUPER-Finland study, a cohort of 10,403 individuals with psychotic disorders

Molecular Psychiatry(2024)10.1038/s41380-024-02516-6

N/A

0.360DataRank · unranked

10 citations

Jaana Suvisaari, Markku Lähteenvuo, Tarjinder Singh, Ari Ahola‐Olli, Lea Urpa +33 more

FAVOR-GPT: a generative natural language interface to whole genome variant functional annotations

Bioinformatics Advances(2024)10.1093/bioadv/vbae143

N/A

0.345DataRank · unranked

9 citations

Hufeng Zhou, Vineet Verma, Xiangru Tang, Yanjun Shao, Eric Van Buren +6 more

Genetics and context for precision health in Greater Boston

Nature Communications(2025)10.1038/s41467-025-66598-8

Top 51%

0.345DataRank

Top 51%9 citations

Ying Wang, Kaavya Paruchuri, Md Mesbah Uddin, So Mi Jemma Cho, Sarah Urbut +16 more

Set-based rare variant association tests for biobank scale sequencing data sets

medRxiv(2021)10.1101/2021.07.12.21260400

N/A

0.312DataRank · unranked

7 citations

Wenjian Bi, Zhangchen Zhao, Kushal K. Dey, Karthik A. Jagadeesh, Konrad J. Karczewski +4 more

Principled distillation of multidimensional UK Biobank data reveals insights into the correlated human phenome

medRxiv(2022)10.1101/2022.09.02.22279546

N/A

0.294DataRank · unranked

4 citations

Rebecca Shafee, Amanda Elliott, Duncan S. Palmer, John Compitello, Masahiro Kanai +14 more

Genetic structure correlates with ethnolinguistic diversity in eastern and southern Africa

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.05.19.444732

N/A

0.269DataRank · unranked

5 citations

Shareefa Dalvie, Yakov Pichkar, Allan Kalungi, Lerato Majara, Anne Stevenson +38 more

Human-specific enrichment of schizophrenia risk-genes in callosal neurons of the developing neocortex

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.09.10.459747

N/A

0.269DataRank · unranked

5 citations

Vanessa Murek, Kwanho Kim, Hsu-Hsin Chen, Sara Mancinelli, Paul Oyler +10 more

Ancestry May Confound Genetic Machine Learning: Candidate-Gene Prediction of Opioid Use Disorder as an Example

medRxiv(2020)10.1101/2020.09.12.20193342

N/A

0.269DataRank · unranked

5 citations

Frank R. Wendt, Marco Galimberti, Renato Polimanti, Benjamin M. Neale, Henry R. Kranzler +4 more

CHARR efficiently estimates contamination from DNA sequencing data

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.06.28.545801

N/A

0.208DataRank · unranked

3 citations

Laura D. Gauthier, Timothy Poterba, Edoardo Giacopuzzi, Julia K. Goodrich, Christine Stevens +5 more

Exome-wide evidence of compound heterozygous effects across common phenotypes in the UK Biobank

medRxiv(2023)10.1101/2023.06.29.23291992

N/A

0.208DataRank · unranked

3 citations

Samvida S. Venkatesh, Nikolas Baya, Wei Zhou, Alex Bloemendal, Benjamin M. Neale +5 more

Global multi-ancestry genetic study elucidates genes and biological pathways associated with thyroid cancer and benign thyroid diseases

medRxiv(2025)10.1101/2025.05.15.25327513

Top 70%

0.165DataRank

Top 70%2 citations

Maizy S. Brasher, Jack Pattee, Wei Zhou, Sinéad B. Chapman, Yon Ho Jee +79 more

Multipopulation GWAS for venous thromboembolism identifies novel loci followed by experimental validation in zebrafish

Blood Advances(2025)10.1182/bloodadvances.2024015790

N/A

0.165DataRank · unranked

2 citations

Yakun Zhao, Kuan-Han H. Wu, Xinge Yu, Catherine E. Richter, Laxmi Bhatta +17 more

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

WOS(2020)10.17615/dkeh-7r02

N/A

0.164DataRank · unranked

1 citations

Jian Yang, Guðmar Þorleifsson, Josine L. Min, Andrew R. Wood, Keri L. Monda +27 more

FAVOR 2.0: A reengineered functional annotation of variants online resource for interpreting genomic variation

Nucleic Acids Research(2025)10.1093/nar/gkaf1217

Top 72%

0.115DataRank

Top 72%1 citations

Vineet Verma, Xihao Li, Zilin Li, Nicole Shedd, Thomas Cheng Li +12 more

Bayesian multivariate genetic analysis improves translational insights

iScience(2023)10.1016/j.isci.2023.107854

N/A

0.104DataRank · unranked

1 citations

Satoshi Koyama, Whitney Hornsby, Rohan Bhukar, Sumeet Kheterpal, Buu Truong +6 more

Significance testing for small annotations in stratified LD-Score regression

medRxiv(2021)10.1101/2021.03.13.21249938

N/A

0DataRank · unranked

36 citations

Ran Cui, Luke J. O’Connor, Benjamin M. Neale, Hilary K. Finucane, Katherine Tashman

Association of Exome Sequences With Cardiovascular Traits among Blacks in the Jackson Heart Study

UNC Libraries(2020)10.17615/a9gj-5z87

N/A

0DataRank · unranked

0 citations

Alex P. Reiner, Mark J. Daly, James G. Wilson, Hao Mei, Joshua D. Smith +14 more

Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion

UNC Libraries(2020)10.17615/63sx-0c91

N/A

0DataRank · unranked

0 citations

Mark J. Daly, Johanna Kuusisto, Francis S. Collins, Markku Laakso, Kimberly F. Doheny +24 more

No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study

UCL Discovery (University College London)(2020)10.17615/snbr-qh40

N/A

0DataRank · unranked

0 citations

Kung‐Yee Liang, Per Hoffman, Stefan Herms, Gary Donohoe, Luba Kalaydjieva +94 more

Exome sequencing and the genetic basis of complex traits

UNC Libraries(2020)10.17615/2gxf-xr79

N/A

0DataRank · unranked

0 citations

Kiran Garimella, Benjamin M. Neale, Adam Kieżun, Shaun Purcell, Nathan O. Stitziel +14 more

Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases

UNC Libraries(2020)10.17615/vqrj-3e30

N/A

0DataRank · unranked

0 citations

Patrick F. Sullivan, Chongzhi Zang, David Collier, Hailiang Huang, Eli A. Stahl +24 more

Synaptic processes and immune-related pathways implicated in Tourette Syndrome

medRxiv(2020)10.1101/2020.04.24.20047845

N/A

0DataRank · unranked

7 citations

Dongmei Yu, Jae Hoon Sul, Alden Y. Huang, Cornelia Illmann, Lisa Osiecki +59 more

Human genetic analyses of organelles highlight the nucleus in age-related trait heritability

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.01.22.427431

N/A

0DataRank · unranked

1 citations

Konrad J. Karczewski, Daniel Howrigan, Benjamin M. Neale, Vamsi K. Mootha, Rahul Gupta

zCall: a rare variant caller for array-based genotyping

UNC Libraries(2020)10.17615/2r6r-p404

N/A

0DataRank · unranked

0 citations

George Grant, Jared Maguire, Shaun Purcell, Jennifer L. Moran, Christine Stevens +12 more

Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder

UNC Libraries(2024)10.17615/gad3-dw62

N/A

0DataRank · unranked

0 citations

R.S. Kahn, Gonçalo R. Abecasis, Neil Risch, Andrew McQuillin, Aiden Corvin +71 more

Whole Genome Sequencing of Pedigrees With High Density of Substance Use and Psychiatric Disorders: A Meeting Report

Genes Brain & Behavior(2025)10.1111/gbb.70017

N/A

0DataRank · unranked

0 citations

Howard J. Edenberg, Aiden Corvin, Thorgeir E. Thorgeirsson, Jennifer E. Below, David Goldman +8 more

Genome-wide association study of proteomic aging reveals shared genetic architectures with longevity, early life development, and age-related diseases

medRxiv(2025)10.64898/2025.12.03.25341518

N/A

0DataRank · unranked

0 citations

Robert Loughnan, Ying Wang, Calwing Liao, Baihan Wang, William Cheng +16 more

Functional Architectures of Local and Distal Regulation of Gene Expression in Multiple Human Tissues

UNC Libraries(2020)10.17615/0fks-zm73

N/A

0DataRank · unranked

4 citations

Patrick F. Sullivan, Alkes L. Price, Alexander Gusev, Luke O'Connor, Benjamin M. Neale +6 more

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