Publications by authors named "Hanan Fathy"

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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, Hanan M Fathy

Genet Med· July 2025

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Expanding the spectrum of novel candidate genes using trio exome sequencing and identification of monogenic cause in 27.5% of 320 families with steroid-resistant nephrotic syndrome.
Ronen Schneider, Shirlee Shril, Florian Buerger, Konstantin Deutsch, Kirollos Yousef, Hanan M Fathy

Genes Dis· March 2025

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Identifying distinct phenotypes of patients with juvenile systemic lupus erythematosus: results from a cluster analysis by the Egyptian college of rheumatology (ECR) study group.
Nevin Hammam, Tamer A Gheita, Ali Bakhiet, Mohamed Bakry Mahmoud, Rasha El Owaidy, Hanan M Fathy

BMC Pediatr· October 2024

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Genetic stratification reveals COL4A variants and spontaneous remission in Egyptian children with proteinuria in the first 2 years of life.
Samar Atef Elshafey, Mohamed Alaa Eldin Hassan Thabet, Reham Abdel Haleem Abo Elwafa, Ronen Schneider, Shirlee Shril, Hanan M Fathy

Acta Paediatr· June 2023

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OXGR1 is a candidate disease gene for human calcium oxalate nephrolithiasis.
Amar J Majmundar, Eugen Widmeier, John F Heneghan, Ankana Daga, Chen-Han Wilfred Wu, Hanan M Fathy

Genet Med· March 2023

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Effect of different surface treatments on resin-matrix CAD/CAM ceramics bonding to dentin: in vitro study.
Hanan Fathy, Hamdi H Hamama, Noha El-Wassefy, Salah H Mahmoud

BMC Oral Health· December 2022

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Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract.
Chen-Han Wilfred Wu, Tze Y Lim, Chunyan Wang, Steve Seltzsam, Bixia Zheng, Hanan M Fathy

Eur Urol Open Sci· October 2022

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Dermoscopic criteria of discoid lupus erythematosus: An observational cross-sectional study of 28 patients.
Hanan Fathy, Bothaina Mahrouth Ghanim, Sherine Refat, Amany Awad

Indian J Dermatol Venereol Leprol· May 2022

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Clinical performance of resin-matrix ceramic partial coverage restorations: a systematic review.
Hanan Fathy, Hamdi H Hamama, Noha El-Wassefy, Salah H Mahmoud

Clin Oral Investig· May 2022

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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, Hanan M Fathy

Genet Med· February 2022

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Systemic lupus erythematosus children in Egypt: Homeland spectrum amid the global situation.
Nahla N Eesa, Hend Abdel Nabi, Rasha El Owaidy, Iman Khalifa, Ahmed R Radwan, Hanan M Fathy

Lupus· November 2021

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Cystin genetic variants cause autosomal recessive polycystic kidney disease associated with altered Myc expression.
Chaozhe Yang, Naoe Harafuji, Amber K O'Connor, Robert A Kesterson, Jacob A Watts, Hanan M Fathy

Sci Rep· September 2021

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Recessive Mutations in as a Candidate of Monogenic Nephrotic Syndrome.
Youying Mao, Ronen Schneider, Peter F M van der Ven, Marvin Assent, Keerthika Lohanadan, Hanan M Fathy

Kidney Int Rep· February 2021

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Lupus nephritis: correlation of immunohistochemical expression of C4d, CD163-positive M2c-like macrophages and Foxp3-expressing regulatory T cells with disease activity and chronicity.
Maram Allam, Hanan Fathy, Dina Abd Allah, Mona Abd Elkader Salem

Lupus· July 2020

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Whole exome sequencing identified ATP6V1C2 as a novel candidate gene for recessive distal renal tubular acidosis.
Tilman Jobst-Schwan, Verena Klämbt, Maureen Tarsio, John F Heneghan, Amar J Majmundar, Hanan M Fathy

Kidney Int· March 2020

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Mutations in multiple components of the nuclear pore complex cause nephrotic syndrome.
Daniela A Braun, Svjetlana Lovric, David Schapiro, Ronen Schneider, Jonathan Marquez, Hanan M Fathy

J Clin Invest· October 2018

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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, Hanan M Fathy

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, Hanan M Fathy

Kidney Int· January 2018

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Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome.
Jillian K Warejko, Weizhen Tan, Ankana Daga, David Schapiro, Jennifer A Lawson, Hanan Fathy

Clin J Am Soc Nephrol· January 2018

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Blood lead levels in a group of children: the potential risk factors and health problems.
Mones M AbuShady, Hanan A Fathy, Gihan A Fathy, Samer Abd El Fatah, Alaa Ali

J Pediatr (Rio J)· November 2017

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Tumor necrosis factor-α -308 A/G gene polymorphism in children with juvenile idiopathic arthritis: relation to disease activity, damage, and functional status.
Iman I El Gazzar, Hanan M Fathy, Tamer A Gheita, Abeer M Nour El-Din, Enas Abdel Rasheed

Clin Rheumatol· August 2017

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Relationship of Oxidant and Antioxidant Markers to Asthma Severity in Egyptian Asthmatic Children.
Inas R El-Alameey, Gihan A Fathy, Mones M Abu Shady, Alaa Ali, Hanan A Fathy

Open Access Maced J Med Sci· August 2017

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IFT81, encoding an IFT-B core protein, as a very rare cause of a ciliopathy phenotype.
Isabelle Perrault, Jan Halbritter, Jonathan D Porath, Xavier Gérard, Daniela A Braun, Hanan M Fathy

J Med Genet· October 2015

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Terra firma-forme dermatosis: Case Series and dermoscopic features.
Moheb M Abdel-Razek, Hanan Fathy

Dermatol Online J· October 2015

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Comparison of Serum IgG Antibody Test with Gastric Biopsy for the Detection of Helicobacter Pylori Infection among Egyptian Children.
Mones M Abu Shady, Hanan A Fathy, Alaa Ali, Essam M Galal, Gihan A Fathy

Open Access Maced J Med Sci· June 2015

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