Coleen Damcott

University of Maryland, Baltimore

Biochemistry, Genetics and Molecular BiologyMedicine

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

51.1Author DataRank

Indexed papers

8in 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 8 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.

Analysis of protein-coding genetic variation in 60,706 humans

Nature(2016)10.1038/nature19057

Top 1%

13.0DataRank

Top 1%10410 citations

Monkol Lek, Konrad J. Karczewski, Eric V. Minikel, Kaitlin E. Samocha, Iain Mathieson +76 more

Papers

Driven by 58 papers — median percentile 98. Top paper: “Analysis of protein-coding genetic variation in 60,706 humans”.

Analysis of protein-coding genetic variation in 60,706 humans

Nature(2016)10.1038/nature19057

Top 1%

13.0DataRank

Top 1%10410 citations

Monkol Lek, Konrad J. Karczewski, Eric V. Minikel, Kaitlin E. Samocha, Iain Mathieson +76 more

A global reference for human genetic variation

Nature(2015)10.1038/nature15393

Top 1%

10.6DataRank

Top 1%20166 citations

Gonçalo R. Abecasis, Richard M. Durbin, Panagiotis Deloukas, Aravinda Chakravarti, Peter Donnelly +516 more

Genome sequence, comparative analysis and haplotype structure of the domestic dog

Nature(2005)10.1038/nature04338

Top 2%

9.2DataRank

Top 2%2636 citations

Claire M. Wade, Tarjei S. Mikkelsen, Elinor K. Karlsson, David B. Jaffe, Michael Kamal +46 more

Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel

Nature Communications(2014)10.1038/ncomms4934

Top 2%

8.3DataRank

Top 2%460 citations

Jonathan Marchini, Peter Donnelly, Gerton Lunter, Jonathan L. Marchini, Simon Myers +364 more

A structural variation reference for medical and population genetics

Nature(2020)10.1038/s41586-020-2287-8

Top 3%

6.7DataRank

Top 3%1180 citations

Harrison Brand, Konrad J. Karczewski, Xuefang Zhao, Jessica Alföldi, Laurent C. Francioli +201 more

Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes

Nature Communications(2020)10.1038/s41467-019-12438-5

N/A

5.6DataRank · unranked

143 citations

James Zou, Beryl B. Cummings, Jessica Alföldi, Laurent C. Francioli, Laura D. Gauthier +174 more

Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals

Nature Communications(2020)10.1038/s41467-019-10717-9

N/A

5.2DataRank · unranked

191 citations

Konrad J. Karczewski, Xiaolei Zhang, Sonia Chothani, Miriam J. Smith, D. Gareth Evans +181 more

The effect of LRRK2 loss-of-function variants in humans

Nature Medicine(2020)10.1038/s41591-020-0893-5

N/A

4.9DataRank · unranked

114 citations

Irina M. Armean, Aaron Kleinman, Jamie L. Marshall, Eric V. Minikel, Julia K. Goodrich +214 more

Survey of variation in human transcription factors reveals prevalent DNA binding changes

Science(2016)10.1126/science.aad2257

N/A

4.7DataRank · unranked

153 citations

Anastasia Vedenko, Jesse V. Kurland, Julia M. Rogers, Stephen S. Gisselbrecht, Elizabeth J. Rossin +19 more

Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

Nature Communications(2018)10.1038/s41467-018-04668-w

N/A

3.7DataRank · unranked

109 citations

Sanni Ruotsalainen, Robert E. Handsaker, Maris Alver, Jonathan M. Bloom, Timothy Poterba +442 more

Ultra-rare disruptive and damaging mutations influence educational attainment in the general population

Nature Neuroscience(2016)10.1038/nn.4404

N/A

3.3DataRank · unranked

113 citations

Giulio Genovese, Daniel P. Howrigan, Andrea Byrnes, Mitja I Kurki, Seyedeh M. Zekavat +31 more

An open resource of structural variation for medical and population genetics

bioRxiv (Cold Spring Harbor Laboratory)(2019)10.1101/578674

Top 9%

2.2DataRank

Top 9%44 citations

Harrison Brand, Konrad J. Karczewski, Xuefang Zhao, Jessica Alföldi, Laurent C. Francioli +37 more

PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses

The American Journal of Human Genetics(2007)10.1086/519795

N/A

1.6DataRank · unranked

35753 citations

Preben Bo Mortensen, Kathe Todd-Brown, Lori Thomas, Manuel A.R. Ferreira, David Bender +12 more

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

Genome Research(2010)10.1101/gr.107524.110

N/A

1.5DataRank · unranked

29661 citations

Matthew Hanna, Iain Mathieson, Sachet A. Shukla, Kristian Cibulskis, Andrew Kernytsky +8 more

Genome sequencing unveils a regulatory landscape of platelet reactivity

Nature Communications(2021)10.1038/s41467-021-23470-9

N/A

1.5DataRank · unranked

54 citations

Ming‐Huei Chen, Benjamin A.T. Rodriguez, Lisa R. Yanek, Arunoday Bhan, Brady Gaynor +94 more

PGC-1α-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes

Nature Genetics(2003)10.1038/ng1180

N/A

1.4DataRank · unranked

10534 citations

Cecilia M. Lindgren, Karl-Fredrik Eriksson, Aravind Subramanian, Smita Sihag, Joseph Lehar +19 more

The mutational constraint spectrum quantified from variation in 141,456 humans

Nature(2020)10.1038/s41586-020-2308-7

N/A

1.4DataRank · unranked

9958 citations

Laurent C. Francioli, Grace Tiao, Beryl B. Cummings, Jessica Alföldi, Qingbo S. Wang +187 more

Biological insights from 108 schizophrenia-associated genetic loci

Nature(2014)10.1038/nature13595

N/A

1.3DataRank · unranked

8042 citations

Stephan Ripke, Aiden Corvin, Jesse R. Dixon, Kai-How Farh, Peter Holmans +284 more

MAPMAKER: An interactive computer package for constructing primary genetic linkage maps of experimental and natural populations

Genomics(1987)10.1016/0888-7543(87)90010-3

N/A

1.3DataRank · unranked

6696 citations

Philip Green, Jeff Abrahamson, Aaron Barlow, Coleen Damcott, Stephen E. Lincoln +2 more

The landscape of somatic copy-number alteration across human cancers

Nature(2010)10.1038/nature08822

N/A

1.2DataRank · unranked

4101 citations

Craig H. Mermel, Dale A. Porter, Guo Wei, Soumya Raychaudhuri, Jerry Donovan +61 more

Partitioning heritability by functional annotation using genome-wide association summary statistics

Nature Genetics(2015)10.1038/ng.3404

N/A

1.2DataRank · unranked

3020 citations

Hilary K. Finucane, Anders D. Børglum, The RACI Consortium, Brendan K Bulik-Sullivan, Alexander Gusev +22 more

Clinical use of current polygenic risk scores may exacerbate health disparities

Nature Genetics(2019)10.1038/s41588-019-0379-x

N/A

1.2DataRank · unranked

2850 citations

Masahiro Kanai, Yoichiro Kamatani, Karen L. Mohlke, Michael C O'Donovan, Coleen Damcott +1 more

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

Nature(2011)10.1038/nature10251

N/A

1.2DataRank · unranked

2729 citations

Stephen Sawcer, Garrett Hellenthal, Matti Pirinen, Chris C. A. Spencer, Nikolaos A. Patsopoulos +241 more

Schizophrenia risk from complex variation of complement component 4

Nature(2016)10.1038/nature16549

N/A

1.2DataRank · unranked

2481 citations

Nick Patterson, Heather de Rivera, Avery Davis, Timothy R. Hammond, Nolan Kamitaki +15 more

Patterns and rates of exonic de novo mutations in autism spectrum disorders

Nature(2012)10.1038/nature11011

N/A

1.1DataRank · unranked

1794 citations

Yan Kou, Li Liu, Avi Ma’ayan, Kaitlin E. Samocha, Aniko Sabo +60 more

Rewiring of the cellular and inter-cellular landscape of the human colon during ulcerative colitis

bioRxiv (Cold Spring Harbor Laboratory)(2019)10.1101/455451

N/A

1.1DataRank · unranked

19 citations

Moshe Biton, Keri M. Sullivan, Grace Burgin, Daniel B. Graham, Rebecca H. Herbst +24 more

Intra- and Inter-cellular Rewiring of the Human Colon during Ulcerative Colitis

Cell(2019)10.1016/j.cell.2019.06.029

N/A

1.1DataRank · unranked

1412 citations

Moshe Biton, Keri M. Sullivan, Grace Burgin, Daniel B. Graham, Rebecca H. Herbst +28 more

A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipids

Nature Communications(2021)10.1038/s41467-021-23899-y

N/A

1.1DataRank · unranked

45 citations

Michael Mendelson, Rory Wilson, Rahul Gondalia, Roby Joehanes, Elias Salfati +59 more

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

Nature Genetics(2016)10.1038/ng.3725

N/A

1.1DataRank · unranked

1129 citations

Daniel P. Howrigan, Daniele Merico, Bhooma Thiruvahindrapuram, Wenting Wu, Douglas S. Greer +267 more

A framework for the interpretation of de novo mutation in human disease

Nature Genetics(2014)10.1038/ng.3050

N/A

1.1DataRank · unranked

1119 citations

Elise B Robinson, Stephan J. Sanders, Christine Stevens, Aniko Sabo, Lauren M. McGrath +25 more

The genetic architecture of type 2 diabetes

Nature(2016)10.1038/nature18642

N/A

1.1DataRank · unranked

1106 citations

Menachem Fromer, Tanya M. Teslovich, Anubha Mahajan, Vineeta Agarwala, Kyle J. Gaulton +334 more

Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

Nature Genetics(2008)10.1038/ng.237

N/A

1.0DataRank · unranked

809 citations

Finny G. Kuruvilla, Steven A. McCarroll, Alec Wysoker, Taras K. Oleksyk, Simon Cawley +12 more

Seven new loci associated with age-related macular degeneration

Nature Genetics(2013)10.1038/ng.2578

N/A

1.0DataRank · unranked

798 citations

Lars G. Fritsche, Wei Chen, Brian L. Yaspan, Yi Yu, Guðmar Þorleifsson +141 more

Human loss-of-function variants suggest that partial LRRK2 inhibition is a safe therapeutic strategy for Parkinson’s disease

bioRxiv (Cold Spring Harbor Laboratory)(2019)10.1101/561472

N/A

0.977DataRank · unranked

17 citations

Irina M. Armean, Aaron Kleinman, Jamie L. Marshall, Eric Vallabh Minikel, Konrad J. Karczewski +35 more

Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program

Genome Medicine(2021)10.1186/s13073-021-00917-8

Top 21%

0.976DataRank

Top 21%35 citations

Jiwon Lee, Tamar Sofer, Heming Wang, Man Zhang, Han Chen +94 more

Abundant contribution of short tandem repeats to gene expression variation in humans

Nature Genetics(2015)10.1038/ng.3461

N/A

0.928DataRank · unranked

485 citations

Thomas Willems, Audrey Guilmatre, Haoyang Zeng, Barak Markus, Stoyan Georgiev +6 more

Validating, augmenting and refining genome-wide association signals

Nature Reviews Genetics(2009)10.1038/nrg2544

N/A

0.888DataRank · unranked

372 citations

Gilles Thomas, Coleen Damcott, John P. A. Ioannidis

Effect of predicted protein-truncating genetic variants on the human transcriptome

Science(2015)10.1126/science.1261877

N/A

0.877DataRank · unranked

345 citations

Matti Pirinen, Donald F. Conrad, Monkol Lek, Emily K. Tsang, Konrad J. Karczewski +206 more

Extremely low-coverage sequencing and imputation increases power for genome-wide association studies

Nature Genetics(2012)10.1038/ng.2283

N/A

0.868DataRank · unranked

326 citations

Nicholas Mancuso, Paul J. McLaren, Kiran Garimella, Noah Zaitlen, Alexandra P. Lewis +23 more

Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing

Nature Genetics(2013)10.1038/ng.2543

N/A

0.862DataRank · unranked

313 citations

Andreas Gnirke, David B. Jaffe, Veronika Barešová, Nathalie Pochet, Brendan Blumenstiel +43 more

Variant-specific inflation factors for assessing population stratification at the phenotypic variance level

Nature Communications(2021)10.1038/s41467-021-23655-2

N/A

0.840DataRank · unranked

21 citations

Xiuwen Zheng, Cecelia Laurie, Stephanie M. Gogarten, Jennifer A. Brody, Matthew P. Conomos +91 more

Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration

Human Molecular Genetics(2011)10.1093/hmg/ddr270

N/A

0.832DataRank · unranked

256 citations

Jesen Fagerness, Stephan Ripke, Gudmar Thorleifsson, Perciliz L. Tan, Eric H. Souied +50 more

Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants

Nature Neuroscience(2019)10.1038/s41593-019-0527-8

N/A

0.815DataRank · unranked

228 citations

F. Kyle Satterstrom, Tarjinder Singh, Emilie M. Wigdor, Jurgen Del‐Favero, Ditte Demontis +17 more

Transcript expression-aware annotation improves rare variant interpretation

Nature(2020)10.1038/s41586-020-2329-2

N/A

0.796DataRank · unranked

201 citations

Konrad J. Karczewski, Ditte Demontis, Eleanor G. Seaby, Nicholas A. Watts, Moriel Singer-Berk +177 more

Evaluating drug targets through human loss-of-function genetic variation

Nature(2020)10.1038/s41586-020-2267-z

N/A

0.779DataRank · unranked

179 citations

Konrad J. Karczewski, Hilary C. Martin, Beryl B. Cummings, Nicola Whiffin, Daniel R. Rhodes +150 more

Transcript expression-aware annotation improves rare variant discovery and interpretation

bioRxiv (Cold Spring Harbor Laboratory)(2019)10.1101/554444

N/A

0.746DataRank · unranked

20 citations

Konrad J. Karczewski, Ditte Demontis, Eleanor G. Seaby, Nicholas A. Watts, Moriel Singer-Berk +14 more

Analysis of High-Resolution HapMap of DTNBP1 (Dysbindin) Suggests No Consistency between Reported Common Variant Associations and Schizophrenia

The American Journal of Human Genetics(2006)10.1086/508942

N/A

0.719DataRank · unranked

120 citations

Derek W. Morris, Skye G. Waggoner, Coleen Damcott, Edward M. Scolnick, Jeremiah M. Scharf +1 more

Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum

The American Journal of Human Genetics(2018)10.1016/j.ajhg.2018.05.002

N/A

0.713DataRank · unranked

115 citations

F. Kyle Satterstrom, Seyedeh M. Zekavat, Indraniel Das, Mitja I Kurki, Claire Churchhouse +45 more

Current clinical use of polygenic scores will risk exacerbating health disparities

bioRxiv (Cold Spring Harbor Laboratory)(2018)10.1101/441261

N/A

0.568DataRank · unranked

43 citations

Masahiro Kanai, Yoichiro Kamatani, Karen L. Mohlke, Michael C O'Donovan, Coleen Damcott +1 more

ASD and ADHD have a similar burden of rare protein-truncating variants

bioRxiv (Cold Spring Harbor Laboratory)(2018)10.1101/277707

N/A

0.434DataRank · unranked

17 citations

Tarjinder Singh, Emilie M. Wigdor, Jurgen Del‐Favero, Ditte Demontis, Christine Stevens +18 more

Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

Nature Communications(2020)10.1038/s41467-020-15236-6

Top 57%

0.275DataRank

Top 57%2 citations

Sanni Ruotsalainen, Robert E. Handsaker, Maris Alver, Jonathan M. Bloom, Timothy Poterba +442 more

Genetic predisposition to myeloproliferative neoplasms implicates hematopoietic stem cell biology

bioRxiv (Cold Spring Harbor Laboratory)(2019)10.1101/790626

N/A

0.188DataRank · unranked

2 citations

Satish K. Nandakumar, Xiaotian Liao, Alexander G. Bick, Christel M. Middeldorp, Marcin Tabaka +30 more

Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma

EBioMedicine(2023)10.1016/j.ebiom.2023.104758

N/A

0DataRank · unranked

19 citations

Priyadarshini Kachroo, Tianxiao Huan, David Van Den Berg, Gha Young Lee, Helena Bui +95 more

Extremely low-coverage sequencing and imputation increases power for genome-wide association studies

UNC Libraries(2020)10.17615/haws-ma91

N/A

0DataRank · unranked

0 citations

Nicholas Mancuso, Paul J. McLaren, Kiran Garimella, Noah Zaitlen, Alexandra P. Lewis +19 more

A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipids

UNC Libraries(2024)10.17615/6p9v-ms63

N/A

0DataRank · unranked

0 citations

Themistocles L. Assimes, Alan R. Shuldiner, Min-A Jhun, W. Chen, D. Absher +59 more

Author Index Vol. 64, 2007

Human Heredity(2007)10.1159/000105464

N/A

0DataRank · unranked

0 citations

John P. A. Ioannidis, Wendy S. Post, Haiqing Shen, Coleen Damcott, Dan E. Arking +20 more

cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regions

Nature Methods(2025)10.1038/s41592-025-02919-5

N/A

0DataRank · unranked

0 citations

Yi Zhang, Xihao Li, Margaret Sunitha Selvaraj, Zilin Li, Hufeng Zhou +544 more

Contents Vol. 64, 2007

Human Heredity(2007)10.1159/000105467

N/A

0DataRank · unranked

0 citations

John P. A. Ioannidis, Wendy S. Post, Haiqing Shen, Coleen Damcott, Dan E. Arking +20 more

Coleen Damcott

Indexed papers

Top data-sharing exemplar

Papers