Sung-hae L. Kang

Medical Genetics

1010 Veteran Ave
West Medical Building - Cytogenetics Lab (#22-26)
Los Angeles, CA 90095

Last Updated: 09/26/2026

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Found 23 publications

ELOC-Mutated Renal Cell Carcinoma is a Rare Indolent Tumor With Distinctive Genomic Characteristics.

ELOC-Mutated Renal Cell Carcinoma is a Rare Indolent Tumor With Distinctive Genomic Characteristics.

Journal: Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc

Published: November 17, 2024

3D genome organization shapes DNA damage susceptibility to platinum-based drugs.

3D genome organization shapes DNA damage susceptibility to platinum-based drugs.

Journal: Nucleic acids research

Published: June 25, 2024

Fetal and neonatal outcomes after "atypical findings" on cell-free fetal DNA screening.

Fetal and neonatal outcomes after "atypical findings" on cell-free fetal DNA screening.

Journal: American journal of obstetrics & gynecology MFM

Published: February 21, 2024

The Role of Preprocedure Genetic Counseling in Pregnancies Interrupted for Fetal Abnormalities.

The Role of Preprocedure Genetic Counseling in Pregnancies Interrupted for Fetal Abnormalities.

Journal: American journal of perinatology

Published: December 28, 2023

Human T cell generation is restored in CD3δ severe combined immunodeficiency through adenine base editing.

Human T cell generation is restored in CD3δ severe combined immunodeficiency through adenine base editing.

Journal: Cell

Published: December 06, 2022

Evidence-based review of genomic aberrations in diffuse large B cell lymphoma, not otherwise specified (DLBCL, NOS): Report from the cancer genomics consortium lymphoma working group.

Evidence-based review of genomic aberrations in diffuse large B cell lymphoma, not otherwise specified (DLBCL, NOS): Report from the cancer genomics consortium lymphoma working group.

Journal: Cancer genetics

Published: May 02, 2022

Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies.

Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: August 17, 2018

Identification of novel candidate disease genes from de novo exonic copy number variants.

Identification of novel candidate disease genes from de novo exonic copy number variants.

Journal: Genome medicine

Published: April 12, 2017

Pathologic Predictors of Treatment Response to Neo-adjuvant Chemotherapy for Invasive Lobular Breast Carcinoma.

Pathologic Predictors of Treatment Response to Neo-adjuvant Chemotherapy for Invasive Lobular Breast Carcinoma.

Journal: The breast journal

Published: March 23, 2017

Utility of Oncotype DX Risk Assessment in Patients With Invasive Lobular Carcinoma.

Utility of Oncotype DX Risk Assessment in Patients With Invasive Lobular Carcinoma.

Journal: Clinical breast cancer

Published: April 27, 2015

USP7 Acts as a Molecular Rheostat to Promote WASH-Dependent Endosomal Protein Recycling and Is Mutated in a Human Neurodevelopmental Disorder.

USP7 Acts as a Molecular Rheostat to Promote WASH-Dependent Endosomal Protein Recycling and Is Mutated in a Human Neurodevelopmental Disorder.

Journal: Molecular cell

Published: April 17, 2015

Parental somatic mosaicism is underrecognized and influences recurrence risk of genomic disorders.

Parental somatic mosaicism is underrecognized and influences recurrence risk of genomic disorders.

Journal: American journal of human genetics

Published: May 15, 2014

Showing 1-12 of 23

Last Updated: 09/26/2026