Gil Atzmon

Also affiliated with Haifa Medical Center, University of Haifa

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

8.5Author DataRank

Indexed papers

5in 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 5 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 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

Papers

Driven by 47 papers — median percentile 56. 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 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

Large-scale sequencing identifies multiple genes and rare variants associated with Crohn’s disease susceptibility

Nature Genetics(2022)10.1038/s41588-022-01156-2

N/A

3.7DataRank · unranked

195 citations

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

Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes

Nature Communications(2021)10.1038/s41467-021-23556-4

N/A

2.7DataRank · unranked

110 citations

Moriel Singer‐Berk, Rachel G. Son, Abigail Sveden, Jordan C. Wood, Eleina England +95 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

Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.11.021

N/A

1.3DataRank · unranked

70 citations

Peter Dornbos, Mark Chaffin, Dajiang J. Liu, Minxian Wang, Margaret Sunitha Selvaraj +95 more

Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees

Proceedings of the National Academy of Sciences(2017)10.1073/pnas.1705859115

N/A

1.2DataRank · unranked

36 citations

Alisa Manning, Marcio Almeida, Matthew Zawistowski, Katharina Domschke, Tanya M. Teslovich +82 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

Similar burden of pathogenic coding variants in exceptionally long‐lived individuals and individuals without exceptional longevity

Aging Cell(2020)10.1111/acel.13216

Top 25%

0.806DataRank

Top 25%13 citations

Gabriel Lidzbarsky, Sofiya Milman, Tina Gao, Patrick Sin‐Chan, Claudia Gonzaga‐Jauregui +5 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

Genome-wide data from medieval German Jews show that the Ashkenazi founder event pre-dated the 14th century

Cell(2022)10.1016/j.cell.2022.11.002

N/A

0.624DataRank · unranked

63 citations

Daniel Backenroth, Éadaoin Harney, Stefan Flohr, Nadia C. Neff, Gina Buckley +27 more

Rare coding variants in 35 genes associate with circulating lipid levels – a multi-ancestry analysis of 170,000 exomes

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.12.22.423783

N/A

0.534DataRank · unranked

11 citations

Peter Dornbos, Mark Chaffin, Dajiang J. Liu, Minxian X. Wang, Margaret Sunitha Selvaraj +95 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

Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome

Translational Psychiatry(2023)10.1038/s41398-023-02341-5

N/A

0.494DataRank · unranked

26 citations

Tyne W. Miller‐Fleming, Apostolia Topaloudi, Dongmei Yu, Petros Drineas, Marianthi Georgitsi +89 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

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

Genome-wide data from medieval German Jews show that the Ashkenazi founder event pre-dated the 14 th century

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.05.13.491805

Top 65%

0.208DataRank

Top 65%3 citations

Daniel Backenroth, Éadaoin Harney, Stefan Flohr, Nadia C. Neff, Gina Buckley +22 more

Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms

UNC Libraries(2020)10.17615/0ngn-wz27

N/A

0.114DataRank · unranked

1 citations

Juliana C.N. Chan, Karen L. Mohlke, Graeme I. Bell, Robin Young, Steven Wiltshire +53 more

Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls

RePEc: Research Papers in Economics(2021)10.17615/ctnf-k559

N/A

0.104DataRank · unranked

1 citations

Nancy J. Cox, T D-GENES, M. Laakso, C. Pihoker, L. Groop +95 more

Novel ultra-rare exonic variants identified in a founder population implicate cadherins in schizophrenia

Neuron(2021)10.1016/j.neuron.2021.03.004

N/A

0DataRank · unranked

29 citations

Jin Yu, Raiyan R. Khan, Erin Flaherty, Shai Carmi, Max Lam +19 more

Genetic signature of human longevity in PKC and NF‐κB signaling

Aging Cell(2021)10.1111/acel.13362

N/A

0DataRank · unranked

24 citations

Jeehae Han, Trina M. Norden‐Krichmar, Quanwei Zhang, Seunggeun Lee, Zhengdong Zhang +7 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

0DataRank · unranked

10 citations

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

Greater Effect of Polygenic Risk Score for Alzheimer’s Disease Among Younger Cases who are Apolipoprotein E-ε4 Carriers

medRxiv(2020)10.1101/2020.04.06.20052332

N/A

0DataRank · unranked

1 citations

Alison Goate, Robert P. Adelson, Jeremy Koppel, Marc L. Gordon, Nir Barzilai +4 more

Genetic analysis of mitochondrial DNA copy number and associated traits identifies loci implicated in nucleotide metabolism, platelet activation, and megakaryocyte proliferation, and reveals a causal association of mitochondrial function with mortality

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.01.25.428086

N/A

0DataRank · unranked

8 citations

Stephanie Yang, Christina A. Castellani, Wen Shi, John Lane, ML Grove +47 more

Novel Ultra-Rare Exonic Variants Identified in a Founder Population Implicate Cadherins in Schizophrenia

medRxiv(2020)10.1101/2020.05.29.20115352

N/A

0DataRank · unranked

5 citations

Jin Yu, Raiyan R. Khan, Shai Carmi, Max Lam, Danny Ben‐Avraham +17 more

A rare human centenarian variant of SIRT6 enhances genome stability and interaction with Lamin A

The EMBO Journal(2022)10.15252/embj.2021110393

N/A

0DataRank · unranked

66 citations

Jiping Yang, Jonathan Gigas, Eric J. Earley, Eric Hillpot, Lei Zhang +27 more

Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes

medRxiv(2020)10.1101/2020.09.22.20195529

N/A

0DataRank · unranked

11 citations

Moriel Singer‐Berk, Rachel G. Son, Abigail Sveden, Jordan C. Wood, Eleina England +95 more

A Genome-Wide Association Study of 2304 Extreme Longevity Cases Identifies Novel Longevity Variants

International Journal of Molecular Sciences(2022)10.3390/ijms24010116

N/A

0DataRank · unranked

25 citations

Anastasia Gurinovich, Tanya T. Karagiannis, Zeyuan Song, Anastasia Leshchyk, Mengze Li +17 more

High-throughput sequencing analysis of nuclear-encoded mitochondrial genes reveals a genetic signature of human longevity

GeroScience(2022)10.1007/s11357-022-00634-z

N/A

0DataRank · unranked

12 citations

Archana Tare, Seungjin Ryu, Simon C. Johnson, Gil Atzmon, Nir Barzilai +3 more

Integrity of hypothalamic–pituitary‐testicular axis in exceptional longevity

Aging Cell(2022)10.1111/acel.13656

N/A

0DataRank · unranked

10 citations

Dimpi Desai, Kenny Ye, Sally Duran, Tina Gao, Jill P. Crandall +4 more

Redox-mediated regulation of aging and healthspan by an evolutionarily conserved transcription factor HLH-2/Tcf3/E2A

Redox Biology(2020)10.1016/j.redox.2020.101448

N/A

0DataRank · unranked

23 citations

Meenakshi Ravichandran, Giovanna Grigolon, Maria Clara Zanellati, Johannes Mansfeld, Kim Zarse +5 more

Dietary Walnuts Preserve Aspects of Health Span and Alter the Hippocampal Lipidome in Aged High-Fat Diet-Fed Mice

International Journal of Molecular Sciences(2023)10.3390/ijms24032314

N/A

0DataRank · unranked

2 citations

Matthew G. Engel, Ruixuan Wang, Kai Mao, Xiaonan Xue, Yam Amir +3 more

Targeted sequencing of the 9p21.3 region reveals association with reduced disease risks in Ashkenazi Jewish centenarians

Aging Cell(2023)10.1111/acel.13962

N/A

0DataRank · unranked

2 citations

Seungjin Ryu, Archana Tare, Nir Barzilai, Gil Atzmon, Yousin Suh +1 more

The regulation of Insulin/IGF-1 signaling by miR-142-3p associated with human longevity

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.05.19.541542

N/A

0DataRank · unranked

3 citations

Hwa Jin Jung, Brandon Milholland, Jinhua Cui, Cagdas Tazearslan, Gil Atzmon +7 more

Targeted Sequencing of the 9p21.3 Region Reveals Association with Reduced Disease risks in Ashkenazi Jewish Centenarians

medRxiv(2023)10.1101/2023.05.19.23290237

N/A

0DataRank · unranked

0 citations

Seungjin Ryu, Archana Tare, Nir Barzilai, Gil Atzmon, Yousin Suh +1 more

Polygenic prediction of human longevity on the supposition of pervasive pleiotropy

medRxiv(2023)10.1101/2023.12.10.23299795

N/A

0DataRank · unranked

0 citations

Jhih-Rong Lin, Quanwei Zhang, Zhen Wang, Joydeep Mitra, Nha Nguyen +8 more

Humanin variant P3S is associated with longevity in APOE4 carriers and resists APOE4‐induced brain pathology

Aging Cell(2024)10.1111/acel.14153

N/A

0DataRank · unranked

16 citations

Su‐Jeong Kim, Kevin Cao, Hemal H. Mehta, Neehar Thumaty, Hiroshi Kumagai +12 more

Greater effect of polygenic risk score for Alzheimer's disease among younger cases who are apolipoprotein E-ε4 carriers

Neurobiology of Aging(2020)10.1016/j.neurobiolaging.2020.09.014

N/A

0DataRank · unranked

27 citations

Alison Goate, Robert P. Adelson, Jeremy Koppel, Marc L. Gordon, Nir Barzilai +4 more

Polygenic prediction of human longevity on the supposition of pervasive pleiotropy

Scientific Reports(2024)10.1038/s41598-024-69069-0

N/A

0DataRank · unranked

3 citations

Jhih-Rong Lin, Quanwei Zhang, Zhen Wang, Joydeep Mitra, Nha Nguyen +9 more

Inflammation and stress-related candidate genes, plasma interleukin-6 levels, and longevity in older adults

UNC Libraries(2020)10.17615/aycf-t384

N/A

0DataRank · unranked

0 citations

Andrea Z. LaCroix, Pui–Yan Kwok, Amy M. Matteini, Nir Barzilai, Gil Atzmon +11 more

The mitochondrial derived peptide humanin is a regulator of lifespan and healthspan

Aging(2020)10.18632/aging.103534

N/A

0DataRank · unranked

105 citations

Hemal H. Mehta, Su‐Jeong Kim, Yanhe Lue, James Hoang, Noel Guerrero +17 more

Genome-wide analysis of mitochondrial DNA copy number reveals loci implicated in nucleotide metabolism, platelet activation, and megakaryocyte proliferation

Human Genetics(2021)10.1007/s00439-021-02394-w

N/A

0DataRank · unranked

73 citations

Stephanie Yang, Christina A. Castellani, Wen Shi, Jon D. Lane, Megan L. Grove +47 more

A genome-wide association study of aging

UNC Libraries(2020)10.17615/raja-vf75

N/A

0DataRank · unranked

0 citations

Johan P. Mackenbach, Pamela L. Lutsey, Gregory J. Tranah, Albert Hofman, Philip L. De Jager +27 more

Gil Atzmon

Indexed papers

Top data-sharing exemplar

Papers