Kiran Garimella

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 1%percentile

15.8Author DataRank

Indexed papers

6in 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 6 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 map of human genome variation from population-scale sequencing

Nature(2010)10.1038/nature09534

Top 2%

9.1DataRank

Top 2%8109 citations

Min Hu, Yuan Chen, Matthew N. Bainbridge, Richard M. Durbin, Si Quang Le +319 more

Papers

Driven by 34 papers — median percentile 79. Top paper: “A genomic mutational constraint map using variation in 76,156 human genomes”.

A genomic mutational constraint map using variation in 76,156 human genomes

Nature(2023)10.1038/s41586-023-06045-0

N/A

9.6DataRank · unranked

1369 citations

Laurent C. Francioli, Julia K. Goodrich, Ryan L. Collins, Masahiro Kanai, Qingbo S. Wang +95 more

A map of human genome variation from population-scale sequencing

Nature(2010)10.1038/nature09534

Top 2%

9.1DataRank

Top 2%8109 citations

Min Hu, Yuan Chen, Matthew N. Bainbridge, Richard M. Durbin, Si Quang Le +319 more

Transcriptome variation in human tissues revealed by long-read sequencing

Nature(2022)10.1038/s41586-022-05035-y

N/A

6.6DataRank · unranked

320 citations

Garrett Garborcauskas, Paul Hoffman, Nava Ehsan, Lihua Jiang, Alper Gokden +19 more

High-throughput RNA isoform sequencing using programmed cDNA concatenation

Nature Biotechnology(2023)10.1038/s41587-023-01815-7

N/A

3.9DataRank · unranked

181 citations

Jonathan T. Smith, Kiran Garimella, Mehrtash Babadi, Victoria Popic, Moshe Sade-Feldman +14 more

Mitochondrial DNA variation across 56,434 individuals in gnomAD

Genome Research(2022)10.1101/gr.276013.121

Top 6%

3.6DataRank

Top 6%156 citations

Nicole J. Lake, Nicholas A. Watts, Megan Shand, Andrea Haessly, Laura D. Gauthier +12 more

Beyond the exome: What’s next in diagnostic testing for Mendelian conditions

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.06.009

N/A

2.2DataRank · unranked

123 citations

Chloe Reuter, Shruti Marwaha, Medhat Mahmoud, Michael Duyzend, Hayk Barseghyan +91 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

Transcriptome variation in human tissues revealed by long-read sequencing

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.01.22.427687

Top 15%

1.4DataRank

Top 15%34 citations

Garrett Garborcauskas, Paul Hoffman, Nava Ehsan, Lihua Jiang, Alper Gokden +19 more

From FastQ Data to High‐Confidence Variant Calls: The Genome Analysis Toolkit Best Practices Pipeline

Current Protocols in Bioinformatics(2013)10.1002/0471250953.bi1110s43

N/A

1.3DataRank · unranked

7169 citations

Mauricio O. Carneiro, Christopher Hartl, Ryan Poplin, Guillermo del Angel, Ami Levy‐Moonshine +11 more

Familial thrombocytopenia due to a complex structural variant resulting in a WAC-ANKRD26 fusion transcript

The Journal of Experimental Medicine(2021)10.1084/jem.20210444

N/A

1.1DataRank · unranked

32 citations

Jeffrey M. Verboon, Leif S. Ludwig, Susan Black, Wendy Luo, Kopal Garg +13 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

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

Mitochondrial DNA variation across 56,434 individuals in gnomAD

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.07.23.453510

Top 27%

0.757DataRank

Top 27%20 citations

Nicole J. Lake, Nicholas A. Watts, Megan Shand, Andrea Haessly, Laura D. Gauthier +12 more

The Somatic Mosaicism across Human Tissues Network

Nature(2025)10.1038/s41586-025-09096-7

N/A

0.672DataRank · unranked

43 citations

Ji Won Oh, Yujin Angelina Choi, Nam Seop Lim, Boxun Zhao, Adam Voshall +365 more

Integrative genotyping of cancer and immune phenotypes by long-read sequencing

Nature Communications(2024)10.1038/s41467-023-44137-7

N/A

0.546DataRank · unranked

37 citations

Mehdi Borji, Adi Nagler, Haoxiang Lyu, Wesley S. Lu, Nicoletta Cieri +12 more

Whole-genome long-read sequencing downsampling and its effect on variant-calling precision and recall

Genome Research(2023)10.1101/gr.278070.123

N/A

0.542DataRank · unranked

36 citations

Peter Ebert, Jana Ebler, Peter A. Audano, Katherine M. Munson, Kendra Hoekzema +6 more

A common flanking variant is associated with enhanced stability of the FGF14-SCA27B repeat locus

Nature Genetics(2024)10.1038/s41588-024-01808-5

N/A

0.533DataRank · unranked

34 citations

Giulia Gobbo, Madeline Couse, Egor Dolzhenko, Sathiji Nageshwaran, Warren Cheung +95 more

A Beary Good Genome: Haplotype-Resolved, Chromosome-Level Assembly of the Brown Bear ( Ursus arctos )

Genome Biology and Evolution(2022)10.1093/gbe/evac125

Top 37%

0.530DataRank

Top 37%16 citations

Blair W. Perry, Yongqing Huang, Kiran Garimella, Heiko T. Jansen, Charles T. Robbins +3 more

Exome copy number variant detection, analysis, and classification in a large cohort of families with undiagnosed rare genetic disease

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.03.008

N/A

0.489DataRank · unranked

25 citations

Alba Sanchis‐Juan, Kathryn Russell, Samantha Baxter, Katherine R. Chao, Moriel Singer‐Berk +59 more

Exploring penetrance of clinically relevant variants in over 800,000 humans from the Genome Aggregation Database

Nature Communications(2025)10.1038/s41467-025-61698-x

Top 44%

0.417DataRank

Top 44%14 citations

Moriel Singer‐Berk, Sarah L. Stenton, Julia K. Goodrich, Michael W. Wilson, Jonah Einson +95 more

Whole-genome long-read sequencing downsampling and its effect on variant calling precision and recall

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.05.04.539448

N/A

0.373DataRank · unranked

11 citations

Peter Ebert, Jana Ebler, Peter A. Audano, Katherine M. Munson, Kendra Hoekzema +6 more

Fast and exact gap-affine partial order alignment with POASTA

Bioinformatics(2024)10.1093/bioinformatics/btae757

N/A

0.259DataRank · unranked

4 citations

Abigail L. Manson, Ashlee M. Earl, Kiran Garimella, Thomas Abeel, Lucas R. van Dijk

Exome copy number variant detection, analysis and classification in a large cohort of families with undiagnosed rare genetic disease

medRxiv(2023)10.1101/2023.10.05.23296595

N/A

0.104DataRank · unranked

1 citations

Alba Sanchis‐Juan, Kathryn Russell, Samantha Baxter, Katherine R. Chao, Moriel Singer‐Berk +59 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

Resolution of ring chromosomes, Robertsonian translocations, and complex structural variants from long-read sequencing and telomere-to-telomere assembly

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.09.07.555775

N/A

0DataRank · unranked

0 citations

Philip M. Boone, Yongqing Huang, Kiran Garimella, Kar‐Tong Tan, Bianca Russell +13 more

Utility of long-read sequencing for All of Us

Nature Communications(2024)10.1038/s41467-024-44804-3

N/A

0DataRank · unranked

106 citations

Yongqing Huang, Kiran Garimella, Peter A. Audano, W. Wan, Nripesh Prasad +9 more

Repeat expansions confer WRN dependence in microsatellite-unstable cancers

Nature(2020)10.1038/s41586-020-2769-8

N/A

0DataRank · unranked

200 citations

Sriram Sridharan, William J. Nathan, Anthony Tubbs, Edmond M. Chan, Elsa Callén +28 more

Detection of simple and complex de novo mutations with multiple reference sequences

Genome Research(2020)10.1101/gr.255505.119

N/A

0DataRank · unranked

16 citations

Zamin Iqbal, Michael Krause, Susana Campino, Mihir Kekre, Eleanor Drury +5 more

A polygenic burden of rare disruptive mutations in schizophrenia

UNC Libraries(2020)10.17615/carr-e613

N/A

0DataRank · unranked

0 citations

Sarah E. Bergen, Steven A. McCarroll, Eric S. Lander, Stacey B. Gabriel, Giulio Genovese +27 more

Resolution of ring chromosomes, Robertsonian translocations, and complex structural variants from long-read sequencing and telomere-to-telomere assembly

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.10.006

N/A

0DataRank · unranked

23 citations

Philip M. Boone, Yongqing Huang, Kiran Garimella, Kar‐Tong Tan, Bianca Russell +17 more

Considerations for reporting variants in novel candidate genes identified during clinical genomic testing

Genetics in Medicine(2024)10.1016/j.gim.2024.101199

N/A

0DataRank · unranked

14 citations

Seth Berger, Samantha Baxter, Erica D. Smith, Changrui Xiao, Daniel G. Calame +89 more

Cue: a deep-learning framework for structural variant discovery and genotyping

Nature Methods(2023)10.1038/s41592-023-01799-x

N/A

0DataRank · unranked

61 citations

Chris Rohlicek, Fabio Cunial, Iman Hajirasouliha, Dmitry Meleshko, Kiran Garimella +2 more

High-throughput RNA isoform sequencing using programmable cDNA concatenation

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.10.01.462818

N/A

0DataRank · unranked

26 citations

Jonathan T. Smith, Kiran Garimella, Mehrtash Babadi, Moshe Sade-Feldman, Michael Gatzen +14 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

Kiran Garimella

Indexed papers

Top data-sharing exemplar

Papers