Lacey Plummer

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 13 papers. Top paper: “Increased Burden of Rare Sequence Variants in GnRH-Associated Genes in Women With Hypothalamic Amenorrhea”.

Increased Burden of Rare Sequence Variants in GnRH-Associated Genes in Women With Hypothalamic Amenorrhea

The Journal of Clinical Endocrinology & Metabolism(2020)10.1210/clinem/dgaa609

N/A

1.0DataRank · unranked

24 citations

Adam Burkholder, Christopher A. Lavender, Lacey Plummer, Verónica Mericq, Paulina M. Merino +12 more

Sex-dependent increases in oxytocin levels in response to intravenous kisspeptin in humans

European Journal of Endocrinology(2025)10.1093/ejendo/lvaf001

N/A

0.337DataRank · unranked

8 citations

Franziska Plessow, Lacey Plummer, Mark B Campbell, Shawn Nazarloo, C. Sue Carter +11 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

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

0DataRank · unranked

8 citations

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

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

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

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