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

Hyung‐Goo Kim

Rutgers, The State University of New Jersey

ORCID: 0000-0003-4497-4686

Also affiliated with Johnson University, Environmental and Occupational Health Sciences Institute

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 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 14 papers. Top paper: “Balanced chromosomal rearrangements offer insights into coding and noncoding genomic features associated with developmental disorders”.

Balanced chromosomal rearrangements offer insights into coding and noncoding genomic features associated with developmental disorders

medRxiv(2022)10.1101/2022.02.15.22270795

N/A

0.373DataRank · unranked

11 citations

Mana M. Mehrjouy, Ryan L. Collins, Mads Bak, Olga Dudchenko, Harrison Brand +95 more

Long-Term Follow-Up and Treatment of a Female With Complete Estrogen Insensitivity

The Journal of Clinical Endocrinology & Metabolism(2020)10.1210/clinem/dgaa106

N/A

0DataRank · unranked

6 citations

Lynn P. Chorich, Hyung‐Goo Kim, Laurel A. Coons, John A. Katzenellenbogen, Janet E. Hall +3 more

Genetics of hypogonadotropic Hypogonadism—Human and mouse genes, inheritance, oligogenicity, and genetic counseling

Molecular and Cellular Endocrinology(2021)10.1016/j.mce.2021.111334

N/A

0DataRank · unranked

34 citations

Alexandra Poch, Hyung‐Goo Kim, Afif Ben‐Mahmoud, Soo‐Hyun Kim, Lawrence C. Layman +1 more

Biallelic variants in WARS1 cause a highly variable neurodevelopmental syndrome and implicate a critical exon for normal auditory function

Human Mutation(2022)10.1002/humu.24435

N/A

0DataRank · unranked

29 citations

Barbara Vona, Hillary M. Porter, Mahmoud Izadi, Kevin Huang, Yves Lacassie +20 more

Unexplained Female Infertility Associated with Genetic Disease Variants

New England Journal of Medicine(2023)10.1056/nejmc2211539

N/A

0DataRank · unranked

24 citations

Alexandra M. Poch, Lynn P. Chorich, Zoe Hawkins, Xu Hongyan, Robert A. Roman +8 more

A cryptic microdeletion del(12)(p11.21p11.23) within an unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome

Scientific Reports(2023)10.1038/s41598-023-40037-4

N/A

0DataRank · unranked

5 citations

Shotaro Kishikawa, Vijay Gupta, Natalia T. Leach, Yiping Shen, Oana Moldovan +14 more

A microdeletion del(12)(p11.21p11.23) with a cryptic unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome

Research Square(2023)10.21203/rs.3.rs-2572736/v1

N/A

0DataRank · unranked

1 citations

Shotaro Kishikawa, Vijay Gupta, Natalia T. Leach, Yiping Shen, Oana Moldovan +14 more

Prevalence of pathogenic variants and digenic disease in patients diagnosed with normosmic hypogonadotropic hypogonadism/Kallmann Syndrome

Molecular and Cellular Endocrinology(2024)10.1016/j.mce.2024.112224

N/A

0DataRank · unranked

9 citations

Michael P. Dougherty, Robert A. Roman, Lynn P. Chorich, Zoe Hawkins, Soo‐Hyun Kim +3 more

Exome sequencing reveals neurodevelopmental genes in simplex consanguineous Iranian families with syndromic autism

BMC Medical Genomics(2024)10.1186/s12920-024-01969-6

N/A

0DataRank · unranked

7 citations

Hossein Sadeghi, Feyzollah Hashemi‐Gorji, Reza Mirfakhraie, Vijay Gupta, Afif Ben‐Mahmoud +11 more

An inappropriate decline in ribosome levels drives a diverse set of neurodevelopmental disorders

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.01.09.574708

N/A

0DataRank · unranked

3 citations

Leqian Yu, Barbara Vona, Dayea Park, Yulei Wei, Daniel A. Schmitz +30 more

Cognitive dysfunction in chemobrain: Molecular mechanisms and therapeutic implications

Biomedicine & Pharmacotherapy(2025)10.1016/j.biopha.2025.118581

N/A

0DataRank · unranked

12 citations

Mohammad Abdur Rashid, Michael Poleschuk, Faheem Ullah, Sanghoon Lee, Sang‐Hoon Kim +4 more

De novo variants in KDM2A cause a syndromic neurodevelopmental disorder

medRxiv(2025)10.1101/2025.03.31.25324695

N/A

0DataRank · unranked

2 citations

Stephan Drukewitz, Sukhleen Kour, Anuradha Venkatakrishnan Chimata, Deepa Rajan, Senta Schönnagel +54 more

Deficiency in the endocytic adaptor proteins PHETA1/2 impair renal and craniofacial development

Disease Models & Mechanisms(2020)10.1242/dmm.041913

N/A

0DataRank · unranked

10 citations

Tong Wang, Trevor Moreland, Rajalakshmi Veeranan‐Karmegam, Manxiu Ma, Chelsi Jeter +15 more

Molecular Consequences of a Missense PHF21A Variant, c.1285G > A, Associated With Syndromic Neurodevelopmental Disorder

Cellular and Molecular Neurobiology(2025)10.1007/s10571-025-01584-8

N/A

0DataRank · unranked

0 citations

Yumie Murata-Nakamura, Robert S. Porter, Bradley Cutler, Sehj Rai, Hyung‐Goo Kim +2 more