Youn Hee Jee

Also affiliated with Children's National, George Washington University

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 8 papers. Top paper: “DLG2 variants in patients with pubertal disorders”.

DLG2 variants in patients with pubertal disorders

Genetics in Medicine(2020)10.1038/s41436-020-0803-8

N/A

0DataRank · unranked

12 citations

Sehoon Won, Julian C. Lui, Melissa Jennings, Philip Whalen, Shanna Yue +15 more

Genetic evaluation in children with short stature

Current Opinion in Pediatrics(2021)10.1097/mop.0000000000001033

N/A

0DataRank · unranked

33 citations

Benjamin R. Hauser, Youn Hee Jee, Elaine Zhou

A neomorphic variant in SP7 alters sequence specificity and causes a high-turnover bone disorder

Nature Communications(2022)10.1038/s41467-022-28318-4

N/A

0DataRank · unranked

39 citations

Adalbert Raimann, Hironori Hojo, Lijin Dong, Paul Roschger, Bijal Kikani +6 more

Effect of stimulants on final adult height

Journal of Pediatric Endocrinology and Metabolism(2022)10.1515/jpem-2022-0344

N/A

0DataRank · unranked

6 citations

Elaine Zhou, Youn Hee Jee, Natalia M. Wojnowski

The Association of Accelerated Early Growth, Timing of Puberty, and Metabolic Consequences in Children

The Journal of Clinical Endocrinology & Metabolism(2023)10.1210/clinem/dgad202

N/A

0DataRank · unranked

25 citations

Sanjay Jumani, Verónica Mericq, Youn Hee Jee

Loss-of-function variant in SPIN4 causes an X-linked overgrowth syndrome

JCI Insight(2023)10.1172/jci.insight.167074

N/A

0DataRank · unranked

16 citations

Jacob P. Wagner, Elaine Zhou, Lijin Dong, Kevin M. Barnes, Youn Hee Jee +2 more

Variants in WASHC3, a component of the WASH complex, cause short stature, variable neurodevelopmental abnormalities, and distinctive facial dysmorphism

Genetics in Medicine Open(2024)10.1016/j.gimo.2024.101915

N/A

0DataRank · unranked

1 citations

Julian C. Lui, Dana Marafi, Zhi‐Jie Xia, Ruchika Bhatia, Elaine Zhou +21 more

A Novel Variant in an Intron Splicing Enhancer Associated with Familial Growth Hormone Deficiency

Hormone Research in Paediatrics(2025)10.1159/000545037

N/A

0DataRank · unranked

0 citations

Mariam Gangat, Bethany L. Murphy, Jennifer L. Miller, Youn Hee Jee, Sally Radovick