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Pediatric Endocrinology Reviews : PER|October 28, 2014
Gaucher disease: the metabolic defect, pathophysiology, phenotypes and natural historyHagit N Baris, Ian J Cohen, Pramod K MistryAmerican Journal of Medical Genetics. Part A|October 3, 2007
Diagnostic utility of array-based comparative genomic hybridization in a clinical settingHagit N Baris, Wen-Hann Tan, Virginia E Kimonis, et al.Blood Cells, Molecules & Diseases|November 20, 2016
Trio approach reveals higher risk of PD in carriers of severe vs. mild GBA mutationsDavid Arkadir, Tama Dinur, Stephen Mullin, et al.Blood Cells, Molecules & Diseases|June 9, 2015
Re-evaluation of bone pain in patients with type 1 Gaucher disease suggests that bone crises occur in small bones as well as long bonesHagit N Baris, Monika Weisz Hubshman, Zvi Bar-Sever, et al.The Israel Medical Association Journal : IMAJ|January 24, 2008
Prevalence of breast and colorectal cancer in Ashkenazi Jewish carriers of Fanconi anemia and Bloom syndromeHagit N Baris, Inbal Kedar, Gabrielle J Halpern, et al.Rambam Maimonides Medical Journal|August 9, 2018
Rare Disease Diagnostics: A Single-center Experience and Lessons LearntKarin Weiss, Alina Kurolap, Tamar Paperna, et al.Fetal Diagnosis and Therapy|October 10, 2009
Loeys-Dietz syndrome in pregnancy: a case description and report of a novel mutationGuy Gutman, Hagit N Baris, Raphael Hirsch, et al.Journal of Perinatology : Official Journal of the California Perinatal Association|February 8, 2018
Prenatal microarray analysis in right aortic arch-a retrospective cohort study and review of the literatureIdit Maya, Amihood Singer, Hagit N Baris, et al.Journal of Applied Genetics|May 18, 2011
X inactivation testing for identifying a non-syndromic X-linked mental retardation geneHagith Yonath, Dina Marek-Yagel, Haike Resnik-Wolf, et al.Early Human Development|March 10, 2018
Microarray analysis in pregnancies with isolated echogenic bowelAmihood Singer, Idit Maya, Arie Koifman, et al.Pageof 4