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
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| Format: | Article |
| Language: | English |
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KeAi Communications Co., Ltd.
2025-03-01
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| Series: | Genes and Diseases |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2352304224000771 |
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| author | Ronen Schneider Shirlee Shril Florian Buerger Konstantin Deutsch Kirollos Yousef Camille N. Frank Ana C. Onuchic-Whitford Thomas M. Kitzler Youying Mao Verena Klämbt Muhammad Y. Zahoor Katharina Lemberg Amar J. Majmundar Bshara Mansour Ken Saida Steve Seltzsam Caroline M. Kolvenbach Lea Maria Merz Nils D. Mertens Tobias Hermle Nina Mann Dalia Pantel Abdul A. Halawi Aaron Bao Luca Schierbaum Sophia Schneider Daanya Salmanullah Iddo Z. Ben-Dov Itamar Sagiv Loai A. Eid Hazem Subhi H. Awad Muna Al Saffar Neveen A. Soliman Marwa M. Nabhan Jameela A. Kari Sherif El Desoky Mohamed A. Shalaby Said Ooda Hanan M. Fathy Shrikant Mane Richard P. Lifton Michael J.G. Somers Friedhelm Hildebrandt |
| author_facet | Ronen Schneider Shirlee Shril Florian Buerger Konstantin Deutsch Kirollos Yousef Camille N. Frank Ana C. Onuchic-Whitford Thomas M. Kitzler Youying Mao Verena Klämbt Muhammad Y. Zahoor Katharina Lemberg Amar J. Majmundar Bshara Mansour Ken Saida Steve Seltzsam Caroline M. Kolvenbach Lea Maria Merz Nils D. Mertens Tobias Hermle Nina Mann Dalia Pantel Abdul A. Halawi Aaron Bao Luca Schierbaum Sophia Schneider Daanya Salmanullah Iddo Z. Ben-Dov Itamar Sagiv Loai A. Eid Hazem Subhi H. Awad Muna Al Saffar Neveen A. Soliman Marwa M. Nabhan Jameela A. Kari Sherif El Desoky Mohamed A. Shalaby Said Ooda Hanan M. Fathy Shrikant Mane Richard P. Lifton Michael J.G. Somers Friedhelm Hildebrandt |
| author_sort | Ronen Schneider |
| collection | DOAJ |
| format | Article |
| id | doaj-art-3c08ede7e1a648f58d6ed6a63a0436b6 |
| institution | Kabale University |
| issn | 2352-3042 |
| language | English |
| publishDate | 2025-03-01 |
| publisher | KeAi Communications Co., Ltd. |
| record_format | Article |
| series | Genes and Diseases |
| spelling | doaj-art-3c08ede7e1a648f58d6ed6a63a0436b62024-12-26T08:56:24ZengKeAi Communications Co., Ltd.Genes and Diseases2352-30422025-03-01122101280Expanding 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 syndromeRonen Schneider0Shirlee Shril1Florian Buerger2Konstantin Deutsch3Kirollos Yousef4Camille N. Frank5Ana C. Onuchic-Whitford6Thomas M. Kitzler7Youying Mao8Verena Klämbt9Muhammad Y. Zahoor10Katharina Lemberg11Amar J. Majmundar12Bshara Mansour13Ken Saida14Steve Seltzsam15Caroline M. Kolvenbach16Lea Maria Merz17Nils D. Mertens18Tobias Hermle19Nina Mann20Dalia Pantel21Abdul A. Halawi22Aaron Bao23Luca Schierbaum24Sophia Schneider25Daanya Salmanullah26Iddo Z. Ben-Dov27Itamar Sagiv28Loai A. Eid29Hazem Subhi H. Awad30Muna Al Saffar31Neveen A. Soliman32Marwa M. Nabhan33Jameela A. Kari34Sherif El Desoky35Mohamed A. Shalaby36Said Ooda37Hanan M. Fathy38Shrikant Mane39Richard P. Lifton40Michael J.G. Somers41Friedhelm Hildebrandt42Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USADepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USADepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USADepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USADepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USADepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USADepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA; Division of Renal Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USADepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USADepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USADepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USADepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA; Institute of Biochemistry & Biotechnology, University of Veterinary & Animal Sciences, Lahore 54000, PakistanDepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USADepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USADepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USADepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USADepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USADepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA; Institute of Anatomy, Medical Faculty, University of Bonn, Bonn D-53113, GermanyDepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA; Department of Pediatrics, University Hospital Leipzig, Leipzig 04103, GermanyDepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USADepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USADepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USADepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA; Institute of Human Genetics, Heidelberg University, Heidelberg 69117, GermanyDepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USADepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USADepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USADepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USADepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USADepartment of Nephrology and Hypertension, Hadassah Medical Center and the Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem 91120, IsraelDepartment of Nephrology and Hypertension, Hadassah Medical Center and the Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem 91120, IsraelPediatric Nephrology Department, Dubai Hospital, Dubai 14660, United Arab EmiratesPediatric Nephrology Department, Dubai Hospital, Dubai 14660, United Arab EmiratesDepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA; Department of Pediatrics, United Arab Emirates University, Abu Dhabi 15551, United Arab EmiratesDepartment of Pediatrics, Center of Pediatric Nephrology & Transplantation, Kasr Al Ainy School of Medicine, Cairo University, Cairo 11562, Egypt; Egyptian Group for Orphan Renal Diseases (EGORD), Cairo 11451, EgyptDepartment of Pediatrics, Faculty of Medicine, King Abdulaziz University, Jeddah 21589, Saudi Arabia; Pediatric Nephrology Center of Excellence, King Abdulaziz University Hospital, Jeddah 21589, Saudi ArabiaDepartment of Pediatrics, Faculty of Medicine, King Abdulaziz University, Jeddah 21589, Saudi Arabia; Pediatric Nephrology Center of Excellence, King Abdulaziz University Hospital, Jeddah 21589, Saudi ArabiaDepartment of Pediatrics, Faculty of Medicine, King Abdulaziz University, Jeddah 21589, Saudi Arabia; Pediatric Nephrology Center of Excellence, King Abdulaziz University Hospital, Jeddah 21589, Saudi ArabiaDepartment of Pediatrics, Faculty of Medicine, King Abdulaziz University, Jeddah 21589, Saudi Arabia; Pediatric Nephrology Center of Excellence, King Abdulaziz University Hospital, Jeddah 21589, Saudi ArabiaExperimental and Clinical Internal Medicine Department, Medical Research Institute, Alexandria University, Alexandria 21511, EgyptDepartment of Pediatrics, Faculty of Medicine, Alexandria University, Alexandria 21526, EgyptDepartment of Genetics, Yale University School of Medicine, New Haven, CT 06510, USADepartment of Genetics, Yale University School of Medicine, New Haven, CT 06510, USADepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA; Corresponding author.Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA; Corresponding author. Division of Nephrology, Boston Children's Hospital, 300 Longwood Avenue, Boston, MA 02115, USA.http://www.sciencedirect.com/science/article/pii/S2352304224000771 |
| spellingShingle | Ronen Schneider Shirlee Shril Florian Buerger Konstantin Deutsch Kirollos Yousef Camille N. Frank Ana C. Onuchic-Whitford Thomas M. Kitzler Youying Mao Verena Klämbt Muhammad Y. Zahoor Katharina Lemberg Amar J. Majmundar Bshara Mansour Ken Saida Steve Seltzsam Caroline M. Kolvenbach Lea Maria Merz Nils D. Mertens Tobias Hermle Nina Mann Dalia Pantel Abdul A. Halawi Aaron Bao Luca Schierbaum Sophia Schneider Daanya Salmanullah Iddo Z. Ben-Dov Itamar Sagiv Loai A. Eid Hazem Subhi H. Awad Muna Al Saffar Neveen A. Soliman Marwa M. Nabhan Jameela A. Kari Sherif El Desoky Mohamed A. Shalaby Said Ooda Hanan M. Fathy Shrikant Mane Richard P. Lifton Michael J.G. Somers Friedhelm Hildebrandt 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 Genes and Diseases |
| title | 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 |
| title_full | 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 |
| title_fullStr | 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 |
| title_full_unstemmed | 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 |
| title_short | 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 |
| title_sort | 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 |
| url | http://www.sciencedirect.com/science/article/pii/S2352304224000771 |
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