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Morasha Plesser Duvdevani
Morasha Plesser Duvdevani
Hebrew University of Jerusalem
Exome sequencing
Genetics
Biology
DNA sequencing
Molecular biology
4
Papers
75
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Whole‐genome sequencing reveals complex chromosome rearrangement disrupting NIPBL in infant with Cornelia de Lange syndrome
2020
American Journal of Medical Genetics Part A
Morasha Plesser Duvdevani
Maria Pettersson
Jesper Eisfeldt
Ortal Avraham
Judith Dagan
Ayala Frumkin
James R. Lupski
Anna Lindstrand
Tamar Harel
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Citations (7)
Mutated MCM9 is associated with predisposition to hereditary mixed polyposis and colorectal cancer in addition to primary ovarian failure
2015
Cancer Genetics and Cytogenetics
Yael Goldberg
Naama Halpern
Ayala Hubert
Samuel N. Adler
Sherri Cohen
Morasha Plesser Duvdevani
Orit Pappo
Avraham Shaag
Vardiella Meiner
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Citations (45)
Transaldolase Deficiency: A New Case Expands the Phenotypic Spectrum
2015
Ehud Banne
Vardiella Meiner
Avraham Shaag
Rachel Katz-Brull
Ayelet Gamliel
Stanley H. Korman
Smadar Horowitz Cederboim
Morasha Plesser Duvdevani
Ayala Frumkin
Amir Zilkha
Vadim Kapuller
Dan Arbell
Elite Cohen
Smadar Eventov Friedman
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Citations (9)
"The Most Important Test You’ll Ever Take"?: Attitudes toward confidential carrier matching and open individual testing among modern-religious Jews in Israel
2011
Social Science & Medicine
Ayala Frumkin
Aviad E. Raz
Morasha Plesser Duvdevani
Sari Lieberman
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Citations (14)
1