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

Andrés Hernández

Palo Alto University

ORCID: 0000-0002-5343-5513

Also affiliated with Baylor College of Medicine, University of Carabobo

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 5%percentile
0.461Author 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 →

Top data-sharing exemplar

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Identifying phenotypic expansions for congenital diaphragmatic hernia plus (CDH+) using DECIPHER data

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62919
Top 41%
0.461DataRank
Top 41%9 citations

Aliska M. Berry, Ian M. Campbell, Xiaonan Zhao, Pengfei Liu, Amanda Gerard +41 more

Papers

Driven by 14 papers — median percentile 59. Top paper: “Identifying phenotypic expansions for congenital diaphragmatic hernia plus (CDH+) using DECIPHER data”.

Identifying phenotypic expansions for congenital diaphragmatic hernia plus (CDH+) using DECIPHER data

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62919
Top 41%
0.461DataRank
Top 41%9 citations

Aliska M. Berry, Ian M. Campbell, Xiaonan Zhao, Pengfei Liu, Amanda Gerard +41 more

Sox7‐positive endothelial progenitors establish coronary arteries and govern ventricular compaction

EMBO Reports(2023)10.15252/embr.202255043
N/A
0.385DataRank · unranked
8 citations

David Humphrey, Richard J. Mills, Peter Kaltzis, Shikha Pachauri, Matthew S. Graus +16 more

FOXP1 Haploinsufficiency Contributes to the Development of Congenital Diaphragmatic Hernia

Journal of Pediatric Genetics(2023)10.1055/s-0043-1767731
N/A
0.269DataRank · unranked
5 citations

Andrés Hernández, Jennifer M. Lyu, Ian M. Campbell, Chad A. Shaw, Julie Vogt +5 more

SOX7 deficiency causes ventricular septal defects through its effects on endocardial-to-mesenchymal transition and the expression of Wnt4 and Bmp2

Human Molecular Genetics(2023)10.1093/hmg/ddad050
N/A
0.208DataRank · unranked
3 citations

Katherine E. Pendleton, Sangbae Kim, Yumei Li, Bum Joon Kim, Hitisha P. Zaveri +7 more

Evidence that FGFRL1 contributes to congenital diaphragmatic hernia development in humans

Molecular Genetics and Metabolism(2021)10.1016/s1096-7192(21)00212-2
N/A
0DataRank · unranked
0 citations

Laura Mackay, Keren Machol, Sundeep G. Keswani, Lorraine Potocki, Eleonora Di Gregorio +5 more

Enzymatically dissociated muscle fibers display rapid dedifferentiation and impaired mitochondrial calcium control

iScience(2022)10.1016/j.isci.2022.105654
N/A
0DataRank · unranked
16 citations

Sonia Youhanna, Sabine U. Vorrink, Sara Henriksson, Andrés Hernández, Arthur J. Cheng +11 more

Early initiation of B‐vitamin supplementation may reduce symptoms and explain intrafamilial variability: Insights from two sibling pairs from the TANGO2 natural history study

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63331
N/A
0DataRank · unranked
17 citations

Saad A. Ehsan, Lilei Zhang, Samuel Mackenzie, Mahshid S. Azamian, Daryl A. Scott +3 more

PLS3 missense variants affecting the actin-binding domains cause X-linked congenital diaphragmatic hernia and body-wall defects

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.09.002
N/A
0DataRank · unranked
8 citations

Mauro Longoni, Julie Wells, Richard S. Maser, Eric L. Bogenschutz, Matthew J. Dysart +34 more

Associations between resting state functional connectivity of large-scale brain networks and parent-reported symptoms of social anxiety in early adolescence

Journal of Affective Disorders(2025)10.1016/j.jad.2025.120238
N/A
0DataRank · unranked
0 citations

Andrés Hernández, Emily R. Barbera, Johanna Pozo-Neira, Natalie Totah, Naomi Edwards +3 more

SOX7 deficiency causes ventricular septal defects through its effects on endocardial-to-mesenchymal transition and the expression of Wnt4 and Bmp2

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.12.04.412288
N/A
0DataRank · unranked
0 citations

Sangbae Kim, Yumei Li, Bum‐Joon Kim, Hitisha P. Zaveri, Valerie K. Jordan +5 more

WNT4 deficiency impacts heart, diaphragm, and palate development: Insights from human genetics, machine learning, and mouse models

Developmental Biology(2025)10.1016/j.ydbio.2025.09.016
N/A
0DataRank · unranked
0 citations

Bum‐Joon Kim, David Chitayat, Patrick Shannon, Stephanie Hedges, Maria Al Bandari +10 more

SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.01.015
N/A
0DataRank · unranked
93 citations

Kaifang Pang, Andrea Ciolfi, Michael A. Levy, Andrés Hernández, Lucia Pedace +95 more

OTUD5 Variants Associated With X-Linked Intellectual Disability and Congenital Malformation

Frontiers in Cell and Developmental Biology(2021)10.3389/fcell.2021.631428
N/A
0DataRank · unranked
10 citations

Tokiko Fukuda, Daryl A. Scott, Toru Sengoku, Kazuhiro Ogata, Annarita Nicosia +13 more

Missense variants affecting the actin-binding domains of PLS3 cause X-linked congenital diaphragmatic hernia and body wall defects

medRxiv(2021)10.1101/2021.07.07.21259278
N/A
0DataRank · unranked
2 citations

Mauro Longoni, Julie Wells, Richard S. Maser, Matthew J. Dysart, Hannah T. M. Contreras +33 more