Jinchuan Xing

Rutgers, The State University of New Jersey

Also affiliated with Rutgers Sexual and Reproductive Health and Rights

Agricultural and Biological SciencesBiochemistry, 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

36.3Author DataRank

Indexed papers

7in 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 7 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 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

Papers

Driven by 27 papers — median percentile 97. Top paper: “A global reference for human genetic variation”.

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

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

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

Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects

Nature Communications(2018)10.1038/s41467-018-06159-4

Top 3%

6.6DataRank

Top 3%260 citations

Yossi Farjoun, Ilya Shlyakhter, Olga Krasheninina, Hyun Min Kang, Daniel P. Howrigan +16 more

Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects

bioRxiv (Cold Spring Harbor Laboratory)(2018)10.1101/269316

Top 16%

1.3DataRank

Top 16%34 citations

Yossi Farjoun, David Larson, Olga Krasheninina, Hyun Min Kang, Daniel P. Howrigan +19 more

Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD

Nature Communications(2023)10.1038/s41467-023-43776-0

N/A

0.657DataRank · unranked

24 citations

Belinda Wang, Vanessa Drury, Sam Drake, Nawei Sun, Hasan Alkhairo +63 more

Dysregulation of mTOR signaling mediates common neurite and migration defects in both idiopathic and 16p11.2 deletion autism neural precursor cells

eLife(2024)10.7554/elife.82809

N/A

0.597DataRank · unranked

19 citations

Bharati Dev, Cynthia Peng, Monal Mehta, Rohan Alibutud, Robert Connacher +7 more

Predicting embryonic aneuploidy rate in IVF patients using whole-exome sequencing

Human Genetics(2022)10.1007/s00439-022-02450-z

N/A

0.500DataRank · unranked

16 citations

Maximilian Miller, Yanran Wang, Katarzyna M. Tyc, Xiaolong Cao, Richard T. Scott +5 more

Polymorphic mobile element insertions contribute to gene expression and alternative splicing in human tissues

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.05.23.111310

Top 44%

0.427DataRank

Top 44%5 citations

Yeting Zhang, Lindsay M. Payer, Hannah Lords, Jared P. Steranka, Kathleen H. Burns +2 more

Identifying risk variants for embryo aneuploidy using ultra-low coverage whole-genome sequencing from preimplantation genetic testing

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.11.002

N/A

0DataRank · unranked

17 citations

Mansour Aboelenain, Daniel Ariad, Mary E. Haywood, Charles R. Wageman, M. Duke +7 more

Assessing the Expression of Long INterspersed Elements (LINEs) via Long-Read Sequencing in Diverse Human Tissues and Cell Lines

Genes(2023)10.3390/genes14101893

N/A

0DataRank · unranked

11 citations

Mingyi Xia, Mian Umair Ahsan, Jinchuan Xing, Kai Wang, Karleena Rybacki

Whole Transcriptome and Functional Analyses Identify Novel Genes Involved in Meiosis and Fertility in Drosophila melanogaster

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.05.12.540472

N/A

0DataRank · unranked

0 citations

Tyler Defosse, A E Boyd, Joel Sop, Faith Verderose, Diya Surray +9 more

Identifying risk genes for embryo aneuploidy using ultra-low coverage whole-genome sequencing

medRxiv(2023)10.1101/2023.07.22.23292618

N/A

0DataRank · unranked

0 citations

Mansour Aboelenain, Daniel Ariad, Mary E. Haywood, Charles R. Wageman, M. Duke +7 more

Maternal genetic variants in kinesin motor domains prematurely increase egg aneuploidy

Proceedings of the National Academy of Sciences(2024)10.1073/pnas.2414963121

N/A

0DataRank · unranked

9 citations

Katarzyna M. Tyc, Mansour Aboelenain, Siqi Sun, Iva Dundović, Kruno Vukušić +9 more

Whole transcriptome screening for novel genes involved in meiosis and fertility in Drosophila melanogaster

Scientific Reports(2024)10.1038/s41598-024-53346-z

N/A

0DataRank · unranked

6 citations

Tyler Defosse, A E Boyd, Joel Sop, Faith Verderose, Diya Surray +9 more

Identifying a Genetic Link Between Lung Function and Psoriasis

Annals of Human Genetics(2024)10.1111/ahg.12587

N/A

0DataRank · unranked

2 citations

Melinda C. Aldrich, James Jaworski, Jinchuan Xing, Satoshi Okawa, Divay Chandra +3 more

Genomic Evidence for the Complex Evolutionary History of Macaques (Genus Macaca)

Journal of Molecular Evolution(2024)10.1007/s00239-024-10166-z

N/A

0DataRank · unranked

0 citations

Rusong Zhang, Anbo Zhou, Jody Hey, Yang Song, Naoki Osada +5 more

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

UNC Libraries(2024)10.17615/bjv3-ys88

Top 100%

0DataRank

Top 100%0 citations

S.S. Rich, Elizabeth L. Appelbaum, Ryan M. Layer, Subra Kugathasan, Scott M. Damrauer +95 more

Identifying Distinct Tourette Disorder Subtypes using Clinical Data

medRxiv(2025)10.1101/2025.11.09.25339700

N/A

0DataRank · unranked

0 citations

Tourette International Collaborative Genetics (TIC Genetics), Robert A. King, Jay A. Tischfield, Gary A. Heiman, Jinchuan Xing +1 more

Meiosis interrupted: the genetics of female infertility via meiotic failure

Reproduction(2020)10.1530/rep-20-0422

N/A

0DataRank · unranked

80 citations

Katarzyna M. Tyc, Warif El Yakoubi, Katie Morgan, Jinchuan Xing, Karen Schindler +1 more

Exome sequencing links CEP120 mutation to maternally derived aneuploid conception risk

Human Reproduction(2020)10.1093/humrep/deaa148

N/A

0DataRank · unranked

25 citations

Warif El Yakoubi, Aishee Bag, J. Landis, Yiping Zhan, Nathan R. Treff +5 more

Integrated Mobile Element Scanning (ME-Scan) method for identifying multiple types of polymorphic mobile element insertions

Mobile DNA(2020)10.1186/s13100-020-00207-x

N/A

0DataRank · unranked

6 citations

Hongseok Ha, Timothy Lin, Nawei Sun, Kathleen H. Burns, Jinchuan Xing +1 more

Polymorphic mobile element insertions contribute to gene expression and alternative splicing in human tissues

Genome biology(2020)10.1186/s13059-020-02101-4

N/A

0DataRank · unranked

40 citations

Yeting Zhang, Lindsay M. Payer, Hannah Lords, Jared P. Steranka, Kathleen H. Burns +2 more

Origins and mechanisms leading to aneuploidy in human eggs

Prenatal Diagnosis(2021)10.1002/pd.5927

N/A

0DataRank · unranked

79 citations

Karen Schindler, Melina Schuh, Jennifer R. Gruhn, Eva R. Hoffmann, Rajiv C. McCoy +2 more

Genomics and epigenetics guided identification of tissue-specific genomic safe harbors

Genome biology(2022)10.1186/s13059-022-02770-3

N/A

0DataRank · unranked

28 citations

Aishee Bag, Ruiqiong Wu, Yeting Zhang, Xing Tang, Qian Qi +3 more

Rare Maternally Inherited Coding Variants on Chromosome X Carry Predominantly Male Risk in Autism, Tourette Syndrome, and Attention-deficit/Hyperactivity Disorder

medRxiv(2022)10.1101/2022.09.22.22280248

N/A

0DataRank · unranked

1 citations

Belinda Wang, Vanessa Drury, Sam Drake, Nawei Sun, Hasan Alkhairo +16 more

Dysregulation of mTOR Signaling Mediates Common Neurite and Migration Defects in Both Idiopathic and 16p11.2 Deletion Autism Neural Precursor Cells

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.09.17.508382

N/A

0DataRank · unranked

0 citations

Bharati Dev, Cynthia Peng, Monal Mehta, Rohan Alibutud, Robert Connacher +7 more

Jinchuan Xing

Indexed papers

Top data-sharing exemplar

Papers