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Hane Lee

14PUBLICATIONS
143CO-AUTHORS
NeurogeneticsMedical virologyGenetic immunologyGenomicsGene expression (incl. microarray and other genome-wide approaches)
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Journal

Publications (14)

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|Jun 26, 2026
Whole Exome Sequencing Reveals Promising Genes Associated with Congenital Renal Parenchymal Anomalies in Greek Children.

|Dec 30, 2025
First Latin American Case of MLASA2 Caused by a Pathogenic Variant in the Anticodon-Binding Domain of <i>YARS2</i>.

José Rafael Villafán-Bernal, Jhonatan Rosas-Hernández, Humberto García-Ortiz

|Dec 19, 2025
DE NOVO VARIANTS IN THE POLY(RC)-BINDING PROTEIN GENE <i>PCBP1</i> CAUSE A NEURODEVELOPMENTAL DISORDER.

Wallid Deb, Thomas Besnard, Florence Desprez

|Aug 28, 2025
Biparental and Androgenetic Somatic Mosaicism with Presentation of Non-Syndromic Severe Neonatal Hyperinsulinemia.

Miguel Angel Alcántara-Ortigoza, Marcela Vela-Amieva, Ariadna González-Del Angel

|Apr 14, 2025
Genome Sequencing of Rare Disease Patients Through the Korean Regional Rare Disease Diagnostic Support Program.

Rin Khang, Hane Lee, Jihye Kim

|Jan 22, 2025
Exome sequencing of 18,994 ethnically diverse patients with suspected rare Mendelian disorders.

Heonjong Han, Go Hun Seo, Seong-In Hyun

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Frequent Collaborators

3 joint publications

Go Hun Seo

2 joint publications

James R Lupski

2 joint publications

Ariadna González-Del Angel

2 joint publications

Marcela Vela-Amieva

2 joint publications

Liliana Fernández-Hernández

2 joint publications

Tobias B Haack

2 joint publications

Jeremy Woods

2 joint publications

Rebecca Buchert

2 joint publications

Kirsty McWalter

2 joint publications

Manish J Butte

Frequent Collaborators

3 joint publications

Go Hun Seo

2 joint publications

James R Lupski

2 joint publications

Ariadna González-Del Angel

2 joint publications

Marcela Vela-Amieva