Andrew J. Sharp

Also affiliated with Icahn School of Medicine at Mount Sinai

Biochemistry, Genetics and Molecular BiologyAgricultural and Biological Sciences

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 3%percentile

1.2Author 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.

Limitations of lymphoblastoid cell lines for establishing genetic reference datasets in the immunoglobulin loci

PLoS ONE(2021)10.1371/journal.pone.0261374

Top 32%

0.610DataRank

Top 32%14 citations

Andrew J. Sharp, Corey T. Watson, Oscar L. Rodriguez

Papers

Driven by 31 papers — median percentile 67. Top paper: “Abundant contribution of short tandem repeats to gene expression variation in humans”.

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

Structural Variation of the Human Genome

Annual Review of Genomics and Human Genetics(2006)10.1146/annurev.genom.7.080505.115618

N/A

0.859DataRank · unranked

306 citations

Ze Cheng, Evan E. Eichler, Andrew J. Sharp

A meta-analysis of epigenome-wide association studies in Alzheimer’s disease highlights novel differentially methylated loci across cortex

Nature Communications(2021)10.1038/s41467-021-23243-4

N/A

0.773DataRank · unranked

172 citations

Ehsan Pishva, Gemma Shireby, Adam R. Smith, Janou A. Y. Roubroeks, Eilís Hannon +23 more

Limitations of lymphoblastoid cell lines for establishing genetic reference datasets in the immunoglobulin loci

PLoS ONE(2021)10.1371/journal.pone.0261374

Top 32%

0.610DataRank

Top 32%14 citations

Andrew J. Sharp, Corey T. Watson, Oscar L. Rodriguez

A phenome-wide association study of tandem repeat variation in 168,554 individuals from the UK Biobank

Nature Communications(2024)10.1038/s41467-024-54678-0

Top 34%

0.578DataRank

Top 34%15 citations

Bharati Jadhav, Paras Garg, Mariya Shadrina, William Lee, Gabrielle Altman +3 more

Rare genetic variation at transcription factor binding sites modulates local DNA methylation profiles

PLoS Genetics(2020)10.1371/journal.pgen.1009189

N/A

0.571DataRank · unranked

44 citations

Nihir Patel, Felix Richter, Bharati Jadhav, Paras Garg, Sarah U. Morton +16 more

Increased frequency of repeat expansion mutations across different populations

medRxiv(2023)10.1101/2023.07.03.23292162

N/A

0.406DataRank · unranked

14 citations

Bharati Jadhav, Matteo Zanovello, Delia Gagliardi, Christopher Clarkson, Stefano Facchini +26 more

Notch Signaling Commits Mesoderm to the Cardiac Lineage

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.02.20.958348

N/A

0.385DataRank · unranked

12 citations

Bharati Jadhav, Nadeera M. Wickramasinghe, Amélie Rezza, Michael Rendl, Andrew J. Sharp +2 more

A phenome-wide association study of methylated GC-rich repeats identifies a GCC repeat expansion in AFF3 associated with intellectual disability

Nature Genetics(2024)10.1038/s41588-024-01917-1

N/A

0.373DataRank · unranked

11 citations

Paras Garg, Joke J.F.A. van Vugt, Kristina Ibáñez, Delia Gagliardi, William Lee +19 more

Pervasive cis effects of variation in copy number of large tandem repeats on local epigenetics and gene expression

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.12.16.423078

N/A

0DataRank · unranked

0 citations

Alejandro Martin-Trujillo, Oscar L. Rodriguez, Scott J Gies, Bharati Jadhav, Andrew J. Sharp +1 more

Pervasive cis effects of variation in copy number of large tandem repeats on local DNA methylation and gene expression

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.03.016

N/A

0DataRank · unranked

47 citations

Alejandro Martin-Trujillo, Oscar L. Rodriguez, Scott J Gies, Elina Hadelia, Bharati Jadhav +4 more

Limitations of lymphoblastoid cell lines for establishing genetic reference datasets in the immunoglobulin loci

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.07.15.452448

N/A

0DataRank · unranked

2 citations

Andrew J. Sharp, Corey T. Watson, Oscar L. Rodriguez

Clinical Characterization of Copy Number Variants Associated With Neurodevelopmental Disorders in a Large-scale Multiancestry Biobank

JAMA Psychiatry(2022)10.1001/jamapsychiatry.2021.4080

N/A

0DataRank · unranked

44 citations

Behrang Mahjani, Ruth J. F. Loos, Andrew J. Sharp, Rebecca Birnbaum

A phenome-wide association study identifies effects of copy-number variation of VNTRs and multicopy genes on multiple human traits

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.04.016

N/A

0DataRank · unranked

25 citations

Bharati Jadhav, William Lee, Oscar L. Rodriguez, Alejandro Martin-Trujillo, Andrew J. Sharp +1 more

Genome-wide evaluation of the effect of short tandem repeat variation on local DNA methylation

Genome Research(2022)10.1101/gr.277057.122

N/A

0DataRank · unranked

30 citations

Paras Garg, Nihir Patel, Bharati Jadhav, Andrew J. Sharp, Alejandro Martin-Trujillo

A phenome-wide association study identifies effects of copy number variation of VNTRs and multicopy genes on multiple human traits

medRxiv(2022)10.1101/2022.01.26.22269891

N/A

0DataRank · unranked

2 citations

Bharati Jadhav, William Lee, Oscar L. Rodriguez, Alejandro Martin-Trujillo, Andrew J. Sharp +1 more

Feeder-free generation and characterization of endocardial and cardiac valve cells from human pluripotent stem cells

iScience(2023)10.1016/j.isci.2023.108599

N/A

0DataRank · unranked

14 citations

Aditi Krishna Prasad, Bharati Jadhav, Yu Liu, Mingxia Gu, Andrew J. Sharp +2 more

Small open reading frames: a comparative genetics approach to validation

BMC Genomics(2023)10.1186/s12864-023-09311-7

N/A

0DataRank · unranked

9 citations

Felix Richter, Ivan Adzhubei, Andrew J. Sharp, Bruce D. Gelb, Niyati Jain

A phenome-wide association study of methylated GC-rich repeats identifies a GCC repeat expansion in AFF3 as a significant cause of intellectual disability

medRxiv(2023)10.1101/2023.05.03.23289461

N/A

0DataRank · unranked

7 citations

Paras Garg, Joke J.F.A. van Vugt, Kristina Ibáñez, Delia Gagliardi, William Lee +16 more

Feeder-Free Generation of Endocardial and Cardiac Valve Cells from Human Pluripotent Stem Cells

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.03.03.530824

N/A

0DataRank · unranked

0 citations

Aditi Krishna Prasad, Bharati Jadhav, Andrew J. Sharp, Bruce D. Gelb, Clifford Z. Liu

Increased frequency of repeat expansion mutations across different populations

Nature Medicine(2024)10.1038/s41591-024-03190-5

N/A

0DataRank · unranked

74 citations

Bharati Jadhav, Matteo Zanovello, Delia Gagliardi, Christopher Clarkson, Stefano Facchini +25 more

A Population‐Wide Exploration of the THAP11 CAG Repeat Size and Structure in the 100,000 Genomes Project and UK Biobank

Movement Disorders(2024)10.1002/mds.30073

N/A

0DataRank · unranked

3 citations

Zhongbo Chen, Clarissa Rocca, Bharati Jadhav, Kristina Ibáñez, Mina Ryten +4 more

A phenome-wide association study of tandem repeat variation in 168,554 individuals from the UK Biobank

medRxiv(2024)10.1101/2024.01.22.24301630

N/A

0DataRank · unranked

6 citations

Bharati Jadhav, Paras Garg, Mariya Shadrina, William Lee, Alejandro Martin-Trujillo +2 more

A Survey of Rare Epigenetic Variation in 23,116 Human Genomes Identifies Disease-Relevant Epivariations and CGG Expansions

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.08.019

N/A

0DataRank · unranked

68 citations

Bharati Jadhav, Oscar L. Rodriguez, Nihir Patel, Alejandro Martin-Trujillo, Miten Jain +8 more

A Novel Framework for Characterizing Genomic Haplotype Diversity in the Human Immunoglobulin Heavy Chain Locus

Frontiers in Immunology(2020)10.3389/fimmu.2020.02136

N/A

0DataRank · unranked

125 citations

William S. Gibson, Tom Parks, Matthew Emery, James Powell, Maya Strahl +10 more

Episignatures Stratifying Helsmoortel-Van Der Aa Syndrome Show Modest Correlation with Phenotype

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.07.003

N/A

0DataRank · unranked

54 citations

Paras Garg, Lara Tang, Danielle Mendonca, Tess Levy, Mafalda Barbosa +24 more

Elucidation of de novo small insertion/deletion biology with parent‐of‐origin phasing

Human Mutation(2020)10.1002/humu.23971

N/A

0DataRank · unranked

4 citations

Felix Richter, Nihir Patel, Oscar L. Rodriguez, Gintaras Deikus, Hardik Shah +7 more

A meta-analysis of epigenome-wide association studies in Alzheimer’s disease highlights novel differentially methylated loci across cortex

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.02.28.957894

N/A

0DataRank · unranked

32 citations

Ehsan Pishva, Gemma Shireby, Adam R. Smith, Janou A. Y. Roubroeks, Eilís Hannon +23 more

A novel framework for characterizing genomic haplotype diversity in the human immunoglobulin heavy chain locus

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.04.19.049270

N/A

0DataRank · unranked

16 citations

William S. Gibson, Tom Parks, Matthew Emery, Jonathan D. Powell, M. Strahl +10 more

Episignatures stratifying ADNP syndrome show modest correlation with phenotype

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.04.01.014902

N/A

0DataRank · unranked

7 citations

Paras Garg, Lara Tang, Danielle Mendonca, Tess Levy, Mafalda Barbosa +23 more

A survey of rare epigenetic variation in 23,116 human genomes identifies disease-relevant epivariations and novel CGG expansions

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.03.25.007864

N/A

0DataRank · unranked

0 citations

Bharati Jadhav, Oscar L. Rodriguez, Nihir Patel, Alejandro Martin-Trujillo, Miten Jain +8 more

Andrew J. Sharp

Indexed papers

Top data-sharing exemplar

Papers