Publications by authors named "Ghaleb Daouk"

Claim this Profile
T
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

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
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

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
B
Beyond the tubule: pathological variants of , encoding the megalin receptor, result in glomerular loss and early progressive chronic kidney disease.
Jennifer R Charlton, Weizhen Tan, Ghaleb Daouk, Lisa Teot, Seymour Rosen

Am J Physiol Renal Physiol· December 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
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

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genetic variants in the LAMA5 gene in pediatric nephrotic syndrome.
Daniela A Braun, Jillian K Warejko, Shazia Ashraf, Weizhen Tan, Ankana Daga, Ghaleb Daouk

Nephrol Dial Transplant· March 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
W
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

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
W
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

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A Multi-layered Quantitative In Vivo Expression Atlas of the Podocyte Unravels Kidney Disease Candidate Genes.
Markus M Rinschen, Markus Gödel, Florian Grahammer, Stefan Zschiedrich, Martin Helmstädter, Ghaleb Daouk

Cell Rep· May 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
W
Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic Syndrome.
Jillian K Warejko, Markus Schueler, Asaf Vivante, Weizhen Tan, Ankana Daga, Ghaleb Daouk

Hypertension· April 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Analysis of 24 genes reveals a monogenic cause in 11.1% of cases with steroid-resistant nephrotic syndrome at a single center.
Weizhen Tan, Svjetlana Lovric, Shazia Ashraf, Jia Rao, David Schapiro, Ghaleb Daouk

Pediatr Nephrol· February 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
W
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

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
W
Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome.
Jillian K Warejko, Weizhen Tan, Ankana Daga, David Schapiro, Jennifer A Lawson, Ghaleb Daouk

Clin J Am Soc Nephrol· January 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Exome Sequencing Discerns Syndromes in Patients from Consanguineous Families with Congenital Anomalies of the Kidneys and Urinary Tract.
Asaf Vivante, Daw-Yang Hwang, Stefan Kohl, Jing Chen, Shirlee Shril, Ghaleb Daouk

J Am Soc Nephrol· January 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Recent advances in the pathogenesis of hypertension in children.
Ghaleb H Daouk, Julie R Ingelfinger

J Med Liban· May 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
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

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
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

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis