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R. Schreiber · SciRah

Researcher profile · Semantic Scholar

R. Schreiber

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R. Schreiber — researcher profile on SciRah

h-index: 9
Works: 21
Citations: 452

Most-cited papers

SLC30A9 mutation affecting intracellular zinc homeostasis causes a novel cerebro-renal syndrome
Y. Perez, Z. Shorer, K. Liani-Leibson, Pauline Chabosseau +12 more
2017Brain : a journal of neurology89 citations Open access
Semantic Scholar
Familial biliary atresia in three siblings including twins.
B. M. Smith, J. Laberge, R. Schreiber, A. Weber +1 more
1991Journal of Pediatric Surgery71 citations
Semantic Scholar
Meconium stained amniotic fluid in preterm delivery is an independent risk factor for perinatal complications.
M. Mazor, R. Hershkovitz, A. Bashiri, E. Maymon +4 more
1998European Journal of Obstetrics, Gynecology, and Reproductive Biology58 citations
Semantic Scholar
Partial lipodystrophy, C3 nephritic factor and clinically inapparent mesangiocapillary glomerulonephritis.
William M. Bennett, E. Bardana, K. Wuepper, D. Houghton +3 more
1977American Journal of Medicine49 citations
Semantic Scholar
Dominant PAX2 mutations may cause steroid resistant neprotic syndrome and FSGS in children
A. Vivante, O. Chacham, S. Shril, R. Schreiber +7 more
2019Pediatric nephrology (Berlin, West)48 citations Open access
Semantic Scholar
Determinants of Aciclovir-Induced Nephrotoxicity in Children
R. Schreiber, J. Wolpin, G. Koren
2008Paediatric drugs40 citations
Semantic Scholar
Inherited renal tubular dysgenesis may not be universally fatal
R. Schreiber, M. Gubler, O. Gribouval, Hanna Shalev +1 more
2010Pediatric nephrology (Berlin, West)31 citations
Semantic Scholar
Nerve Growth Factor-Tyrosine Kinase A Pathway Is Involved in Thermoregulation and Adaptation to Stress: Studies on Patients with Hereditary Sensory and Autonomic Neuropathy Type IV
N. Loewenthal, J. Levy, R. Schreiber, V. Pinsk +3 more
2005Pediatric Research21 citations
Semantic Scholar
Diagnostic Utility of Exome Sequencing Among Israeli Children With Kidney Failure
Yishay Ben-Moshe, Omer Shlomovitz, Danit Atias-Varon, Orly Haskin +24 more
2023Kidney International Reports12 citations Open access
Semantic Scholar
X-linked C1GALT1C1 mutation causes atypical hemolytic uremic syndrome
N. Hadar, R. Schreiber, M. Eskin-Schwartz, Eyal Kristal +7 more
2023European Journal of Human Genetics6 citations Open access
Semantic Scholar
Glomerular involvement in children with H syndrome
Odeya David, Michael Geylis, Eyal Kristal, G. Ling +1 more
2021Pediatric nephrology (Berlin, West)6 citations
Semantic Scholar
A novel SLC12A1 mutation in Bedouin kindred with antenatal Bartter syndrome type I
D. Halperin, V. Dolgin, Michael Geylis, M. Drabkin +6 more
2019Annals of Human Genetics5 citations
Semantic Scholar
Hypoparathyroidism-retardation-dysmorphism syndrome—Clinical insights from a large longitudinal cohort in a single medical center
Odeya David, Rotem Agur, R. Novoa, David Shaki +9 more
2022Frontiers in Pediatrics4 citations Open access
Semantic Scholar
Listeria Meningitis in an Immunocompetent Adolescent.
Ori Hassin, D. Danino, R. Schreiber, E. Leibovitz +1 more
2020The Israel Medical Association journal : IMAJ4 citations
Semantic Scholar
Pediatric chronic kidney disease rates in Southern Israel are higher than reported
D. Landau, R. Schreiber, A. Kleinman, Alina Vodonos +1 more
2013F1000Research4 citations Open access
Semantic Scholar
Hemolytic uremic syndrome after pediatric liver transplantation.
D. Turner, R. Schreiber, D. Grant, D. Hébert +1 more
2006Journal of Pediatric Gastroenterology and Nutrition - JPGN3 citations Open access
Semantic Scholar
Hodgkin's lymphoma, nephrotic syndrome, and echinococcosis cysts: an unusual association and literature review
Michael Geylis, Guy Beck Rosen, D. Danino, R. Schreiber +3 more
2019Pediatric Hematology & Oncology1 citations
Semantic Scholar
Alternative Pathway Complement Dysregulation in Atypical HUS: A Case Communication.
Eyal Kristal, Shani Arotzker, Michael Geylis, Siham Elamour +2 more
2026The Israel Medical Association journal : IMAJ0 citations
Semantic Scholar
FC035: Exome Sequencing of the Israeli Dialysis-Treated Pediatric Population Reveals Monogenic Etiology in ∼44% of Cases
Maayan Kagan, Yishay Ben Moshe, Omer Shlomovitz, Danit Atias-Varon +17 more
2022Nephrology, Dialysis and Transplantation0 citations
Semantic Scholar
Renal Vein Thrombosis as a Presenting Sign in a Boy with Lupus Nephritis- Case Report
Ester Forer, R. Nassar, E. Ling, R. Schreiber +3 more
20210 citations
Semantic Scholar
GASTROESOPHAGEAL REFLUX AND LARYNGEAL DISORDERS IN CHILDREN:169
W. Al-Oabandi, K. Al-Sebeih, J. Manoukian, É. Drouin +1 more
1997Journal of Pediatric Gastroenterology and Nutrition - JPGN0 citations
Semantic Scholar

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