🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Yunping Lei

ORCID: 0000-0003-1504-0884

MedicineBiochemistry, 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 6%percentile

0.224Author DataRank

Indexed papers

1in 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 1 indexed paper 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.

Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child–parent trios and a case–control design to identify novel rare variants

UNC Libraries(2024)10.17615/2btg-0082

Top 62%

0.224DataRank

Top 62%2 citations

Jessica X. Chong, NISC Comparative Sequencing Program University of Washington Center for Mendelian Genomics, Jennifer E. Posey, Cynthia A. Moore, Sanjiv Harpavat +29 more

Papers

Driven by 19 papers — median percentile 38. Top paper: “Excess folic acid intake increases DNA de novo point mutations”.

Excess folic acid intake increases DNA de novo point mutations

Cell Discovery(2023)10.1038/s41421-022-00512-0

N/A

1.6DataRank · unranked

40 citations

Jianfeng Xu, Ying Lin, Robert M. Cabrera, Qiuying Chen, Chaofan Zhang +10 more

Exome‐wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child–parent trios and a case–control design to identify novel rare variants

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63185

N/A

0.292DataRank · unranked

6 citations

Aniko Sabo, Lynn M. Almli, Mary M. Jenkins, Wendy N. Nembhard, A. J. Agopian +28 more

CIC missense variants contribute to susceptibility for spina bifida

Human Mutation(2022)10.1002/humu.24460

N/A

0.292DataRank · unranked

6 citations

Xuanye Cao, Vanessa Aguiar‐Pulido, Wei Yang, Menuka Karki, Paula Andrea Pimienta Ramírez +9 more

Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child–parent trios and a case–control design to identify novel rare variants

UNC Libraries(2024)10.17615/2btg-0082

Top 62%

0.224DataRank

Top 62%2 citations

Jessica X. Chong, NISC Comparative Sequencing Program University of Washington Center for Mendelian Genomics, Jennifer E. Posey, Cynthia A. Moore, Sanjiv Harpavat +29 more

Actuation Enhances Patterning in Human Neural Tube Organoids

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.09.22.308411

N/A

0DataRank · unranked

9 citations

Brian Daza, Gregorius Rustandi, Miguel Ángel Berrocal-Rubio, Benjamin Gorissen, Suresh Poovathingal +12 more

Gene Environment Interactions in the Etiology of Neural Tube Defects

Frontiers in Genetics(2021)10.3389/fgene.2021.659612

N/A

0DataRank · unranked

108 citations

Carlo Donato Caiaffa, Sung‐Eun Kim, Yunping Lei, John Steele, Xuanye Cao +5 more

Actuation enhances patterning in human neural tube organoids

Nature Communications(2021)10.1038/s41467-021-22952-0

N/A

0DataRank · unranked

92 citations

Brian Daza, Gregorius Rustandi, Miguel Ángel Berrocal-Rubio, Benjamin Gorissen, Suresh Poovathingal +14 more

Hypermethylation of PI3K-AKT signalling pathway genes is associated with human neural tube defects

Epigenetics(2021)10.1080/15592294.2021.1878725

N/A

0DataRank · unranked

19 citations

Xinyuan Lai, Kuanhui Xiang, Xiao Han, Shengju Yin, Robert M. Cabrera +7 more

Somatic and de novo Germline Variants of MEDs in Human Neural Tube Defects

Frontiers in Cell and Developmental Biology(2021)10.3389/fcell.2021.641831

N/A

0DataRank · unranked

19 citations

Xuanye Cao, Yongyan Chen, Lei Jin, Zhiwen Li, Xiao Han +8 more

KDM6B Variants May Contribute to the Pathophysiology of Human Cerebral Folate Deficiency

Biology(2022)10.3390/biology12010074

N/A

0DataRank · unranked

6 citations

Xuanye Cao, Robert M. Cabrera, Paula Andrea Pimienta Ramírez, Cuilian Zhang, V. Ramaekers +3 more

Functional characterization of age-dependent p16 epimutation reveals biological drivers and therapeutic targets for colorectal cancer

Journal of Experimental & Clinical Cancer Research(2023)10.1186/s13046-023-02689-y

N/A

0DataRank · unranked

22 citations

Xiaomin Chen, Christy Lee, Jiejun Shi, Emily B. Lawrence, Lanjing Zhang +11 more

A mutation in TBXT causes congenital vertebral malformations in humans and mice

Journal of genetics and genomics/Journal of Genetics and Genomics(2023)10.1016/j.jgg.2023.09.009

N/A

0DataRank · unranked

10 citations

Yunping Lei, Yajun Yang, Chennan Liu, Lele Kuang, Jin Li +4 more

Folate regulation of planar cell polarity pathway and F‐actin through folate receptor alpha

The FASEB Journal(2023)10.1096/fj.202300202r

N/A

0DataRank · unranked

7 citations

Xuanye Cao, Robert M. Cabrera, Paula Andrea Pimienta Ramírez, Ying Lin, Bogdan J. Wlodarczyk +4 more

MSL2 variants lead to a neurodevelopmental syndrome with lack of coordination, epilepsy, specific dysmorphisms, and a distinct episignature

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.05.001

N/A

0DataRank · unranked

13 citations

Maria Carla Borroto, Sadegheh Haghshenas, A Namasivayam, Jack Reilly, Michael A. Levy +61 more

Loss ofRAD9Bimpairs early neural development and contributes to the risk for human spina bifida

Human Mutation(2020)10.1002/humu.23969

N/A

0DataRank · unranked

19 citations

Tian Tian, John Steele, Robert M. Cabrera, Vanessa Aguiar‐Pulido, Shruti Wadhwa +12 more

Epigenetic regulation by TET1 in gene-environmental interactions influencing susceptibility to congenital malformations

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.02.21.581196

N/A

0DataRank · unranked

2 citations

Lehua Chen, Spyridon Champeris Tsaniras, Wannes Brangers, Qiuying Chen, Mariana Schroiff +9 more

FKBP8 variants are risk factors for spina bifida

Human Molecular Genetics(2020)10.1093/hmg/ddaa211

N/A

0DataRank · unranked

8 citations

Xuanye Cao, Sung‐Eun Kim, Ying Lin, John Steele, Robert M. Cabrera +13 more

CIC de novo loss of function variants contribute to cerebral folate deficiency by downregulating FOLR1 expression

Journal of Medical Genetics(2020)10.1136/jmedgenet-2020-106987

N/A

0DataRank · unranked

25 citations

Annika Wolf, Sung‐Eun Kim, Robert M. Cabrera, Bogdan Włodarczyk, Huiping Zhu +9 more

Approaches to studying the genomic architecture of complex birth defects

Prenatal Diagnosis(2020)10.1002/pd.5760

N/A

0DataRank · unranked

8 citations

Xuanye Cao, Robert M. Cabrera, Yunping Lei, Richard H. Finnell, Toluwani Taiwo