Publications by authors named "Ghaleb H Daouk"

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Trio exome sequencing identifies de novo variants in novel candidate genes in 19.62% of CAKUT families.
Lea Maria Merz, Caroline M Kolvenbach, Chunyan Wang, Nils David Mertens, Steve Seltzsam, Ghaleb H Daouk

Genet Med· July 2025

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Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT.
Steve Seltzsam, Chunyan Wang, Bixia Zheng, Nina Mann, Dervla M Connaughton, Ghaleb H Daouk

Genet Med· February 2022

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Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations.
Dervla M Connaughton, Rufeng Dai, Danielle J Owen, Jonathan Marquez, Nina Mann, Ghaleb H Daouk

Am J Hum Genet· October 2020

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Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant Recipients.
Nina Mann, Daniela A Braun, Kassaundra Amann, Weizhen Tan, Shirlee Shril, Ghaleb H Daouk

J Am Soc Nephrol· February 2019

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Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.
Amelie T van der Ven, Dervla M Connaughton, Hadas Ityel, Nina Mann, Makiko Nakayama, Ghaleb H Daouk

J Am Soc Nephrol· September 2018

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Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis.
Ankana Daga, Amar J Majmundar, Daniela A Braun, Heon Yung Gee, Jennifer A Lawson, Ghaleb H Daouk

Kidney Int· January 2018

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Recent advances in the pathogenesis of hypertension in children.
Ghaleb H Daouk, Julie R Ingelfinger

J Med Liban· May 2011

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Tuberous sclerosis complex and renal angiomyolipoma: case report and review of the literature.
Elisabeth B Winterkorn, Ghaleb H Daouk, Sudha Anupindi, Elizabeth A Thiele

Pediatr Nephrol· August 2006

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Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 11-2004. A boy with rash, edema, and hypertension.
Michael J Somers, Ghaleb H Daouk, Robert T McCluskey

N Engl J Med· April 2004

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