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

Ravikumar Balasubramanian

Massachusetts General Hospital

ORCID: 0000-0001-6008-5585
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 100%percentile
0Author DataRank

Indexed papers

0in pilot corpus
datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 16 papers. Top paper: “Genome-wide analyses identify 25 infertility loci and relationships with reproductive traits across the allele frequency spectrum”.

Genome-wide analyses identify 25 infertility loci and relationships with reproductive traits across the allele frequency spectrum

Nature Genetics(2025)10.1038/s41588-025-02156-8
N/A
0.464DataRank · unranked
21 citations

Laura B. L. Wittemans, Duncan S. Palmer, Nikolas Baya, Teresa Ferreira, Barney Hill +57 more

The p190 RhoGAPs, ARHGAP35, and ARHGAP5 are implicated in GnRH neuronal development: Evidence from patients with idiopathic hypogonadotropic hypogonadism, zebrafish, and in vitro GAP activity assay

Genetics in Medicine(2022)10.1016/j.gim.2022.08.025
N/A
0.330DataRank · unranked
8 citations

Wanxue Xu, Abigail A Smith, Xinyu Miao, Agathe Lafont, Omar Shennib +23 more

SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome

UNC Libraries(2020)10.17615/tdb3-bx52
N/A
0DataRank · unranked
0 citations

Hemant Bengani, Joseph A. Marsh, Angela M. Kaindl, Koh-ichiro Yoshiura, Katharina Steindl +73 more

Reproductive Phenotypes and Genotypes in Men With IHH

The Journal of Clinical Endocrinology & Metabolism(2022)10.1210/clinem/dgac615
N/A
0DataRank · unranked
14 citations

Maria Stamou, Ella Anghel, Shira Hornstein, Danna Chen, Kathryn Salnikov +5 more

Reversible hypogonadotropic hypogonadism in men with the fertile eunuch/Pasqualini syndrome: A single-center natural history study

Frontiers in Endocrinology(2022)10.3389/fendo.2022.1054447
N/A
0DataRank · unranked
5 citations

Maria Stamou, Isabella R. McDonald, Ella Anghel, Kimberly H. Cox, Kathryn Salnikov +4 more

POU6F2 mutation identified in humans with pubertal failure shifts isoform formation and alters GnRH transcript expression

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.10.12.511883
N/A
0DataRank · unranked
0 citations

Fatih Gürbüz, Maria Stamou, Leman Damla Kotan, Stephen M. Farmer, Şule Can +14 more

POU6F2 mutation in humans with pubertal failure alters GnRH transcript expression

Frontiers in Endocrinology(2023)10.3389/fendo.2023.1203542
N/A
0DataRank · unranked
11 citations

Fatih Gürbüz, Maria Stamou, Leman Damla Kotan, Stephen M. Farmer, Şule Can +14 more

Heterozygous mutations in SOX2 may cause idiopathic hypogonadotropic hypogonadism via dominant-negative mechanisms

JCI Insight(2023)10.1172/jci.insight.164324
N/A
0DataRank · unranked
8 citations

Maria Stamou, Kimberly W. Keefe, Kaitlin E. Sung, Celine Bojo, Karen J. Tonsfeldt +14 more

How human genetic context can inform pathogenicity classification: FGFR1 variation in idiopathic hypogonadotropic hypogonadism

Human Genetics(2023)10.1007/s00439-023-02601-w
N/A
0DataRank · unranked
3 citations

Lacey Plummer, Stephanie B. Seminara, Ravikumar Balasubramanian, Margaret Lippincott, Wanxue Xu

A functional spectrum of PROKR2 mutations identified in isolated hypogonadotropic hypogonadism

Human Molecular Genetics(2023)10.1093/hmg/ddad014
N/A
0DataRank · unranked
3 citations

Danna Chen, Yaguang Zhao, Meichao Men, Zhiheng Chen, Fang Jiang +6 more

Lack of a genetic risk continuum between pubertal timing in the general population and idiopathic hypogonadotropic hypogonadism

Journal of Neuroendocrinology(2024)10.1111/jne.13445
N/A
0DataRank · unranked
1 citations

Ravikumar Balasubramanian, Maria Stamou, Mark Campbell, Pranav Dewan, Nora Bryant +4 more

Expanding the Spectrum of Endocrine Abnormalities Associated With SOX11-related Disorders

The Journal of Clinical Endocrinology & Metabolism(2024)10.1210/clinem/dgae620
N/A
0DataRank · unranked
1 citations

Maria Stamou, Sara L Stockman, Mark Campbell, Lacey Plummer, Kathryn Salnikov +7 more

Genome-wide analyses identify 21 infertility loci and over 400 reproductive hormone loci across the allele frequency spectrum

medRxiv(2024)10.1101/2024.03.19.24304530
N/A
0DataRank · unranked
15 citations

Laura B. L. Wittemans, Duncan S. Palmer, Nikolas Baya, Teresa Ferreira, Barney Hill +46 more

TCF12 haploinsufficiency causes autosomal dominant Kallmann syndrome and reveals network-level interactions between causal loci

Human Molecular Genetics(2020)10.1093/hmg/ddaa120
N/A
0DataRank · unranked
22 citations

Ravikumar Balasubramanian, Zachary A Kupchinsky, David L. Keefe, Lacey Plummer, Kamal Khan +19 more

De novo rare EMX2 variants lead to idiopathic hypogonadotropic hypogonadism

Genetics in Medicine(2025)10.1016/j.gim.2025.101623
N/A
0DataRank · unranked
0 citations

Miranda Tompkins, Hannah Bow, Jessica Kearney, Maleeha Akram, Harrison Brand +15 more

Hypothalamic Ceramides and the Ovarian Sympathetic System: At the Crossroads of Obesity and Puberty

Cell Metabolism(2020)10.1016/j.cmet.2020.11.012
N/A
0DataRank · unranked
6 citations

Ravikumar Balasubramanian, Maria Stamou