Amir Peleg - Genetics Institute, Carmel Medical Center

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论文共 36 篇作者统计合作学者相似作者

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National Rapid Genome Sequencing in Neonatal Intensive Care

Daphna Marom,Adi Mory, Sivan Reytan-Miron,Yam Amir,Alina Kurolap, Julia Grinshpun Cohen, Yocheved Morhi,Tatiana Smolkin,Lior Cohen,Shmuel Zangen,Adel Shalata,Arieh Riskin,Amir Peleg,Karen Lavie-Nevo,Dror Mandel,Elana Chervinsky, Clari Felszer Fisch,Vered Fleisher Sheffer,Tzipora C. Falik-Zaccai,Jonathan Rips,Noa Ofek Shlomai,Smadar Eventov Friedman, Calanit Hershkovich Shporen, Sagie Josefsberg Ben-Yehoshua,Aryeh Simmonds, Racheli Goldfarb Yaacobi,Sofia Bauer-Rusek, Hussam Omari,Karin Weiss,Ori Hochwald,Arie Koifman,Omer Globus,Nurit Assia Batzir, Naveh Yaron,Reeval Segel,Iris Morag,Orit Reish,Aviva Eliyahu,Leah Leibovitch, Marina Eskin Schwartz,Ramy Abramsky,Amit Hochberg,Anat Oron,Ehud Banne,Igor Portnov,Nadra Nasser Samra,Amihood Singer,Hagit Baris Feldman

JAMA NETWORK OPENno. 2 (2024)

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The Effect of Opting-in Versus Opting-out Forming on the Rate of Reported Variants of Questionable Significance in Prenatal Microarray

Jumana Haddad-Halloun, Ava Wexler,Moran Echar, Amalia Harari-Shaham, Shirley Polager-Modan, Rawan Zaatry, Rasha Maayouf, Maisa Assadi, Olga Krivoruk,Amir Peleg,Lena Sagi-Dain

INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS (2024)

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[HOW SIMPLE IS "SIMPLE" GENETIC COUNSELING?]

Moran Echar,Amir Peleg,Amalia Harari-Shacham,Shirley Modan,Lena Sagi-Dain

Harefuahno. 6 (2023): 381-385

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Diagnostic yield and recognized barriers of a pediatric endogenetics clinic

Amir Peleg,Ilana Koren

EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 118-118

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Non-indicated invasive tests yield higher percentage of Ashkenazi Jewish patients

Moran Echar,Amir Peleg,Jumana Haddad-Halloun,Lena Sagi-Dain

EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 105-105

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How simple is a simple genetic counseling

Moran Echar,Amir Peleg,Amalia Harari-Shacham,Shirley Modan,Lena Sagi-Dain

EUROPEAN JOURNAL OF HUMAN GENETICS（2022）

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Changing a single word in prenatal microarray agreement form significantly decreases the rate of reported variants of questionable significance

Lena Sagi-Dain,Moran Echar, Amalia Harari-Shaham, Shirley Polager-Modan, Rawan Zaatry, Olga Krivoruk,Jumana Haddad-Halloun,Amir Peleg

EUROPEAN JOURNAL OF HUMAN GENETICS（2022）

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Genetic counseling during COVID19 pandemic. One center experience

Amir Peleg,Lena Sagi-Dain

EUROPEAN JOURNAL OF HUMAN GENETICS（2022）

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The anxiety caused by abnormal results of Down syndrome screening tests

Lena Sagi-Dain,Amir Peleg,Shlomi Sagi,Amihood Singer

JOURNAL OF OBSTETRICS AND GYNAECOLOGY（2022）

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Biallelic ADAM22 Pathogenic Variants Cause Progressive Encephalopathy and Infantile-Onset Refractory Epilepsy

Marieke M. van der Knoop,Reza Maroofian,Yuko Fukata,Yvette van Ierland,Ehsan G. Karimiani,Anna Elina Lehesjoki,Mikko Muona,Anders Paetau,Yuri Miyazaki,Yoko Hirano,Laila Selim, Marina de Franca,Rodrigo Ambrosio Fock, Christian Beetz,Claudia A. L. Ruivenkamp,Alison J. Eaton,Francois D. Morneau-Jacob,Lena Sagi-Dain,Lilach Shemer-Meiri,Amir Peleg,Jumana Haddad-Halloun,Daan J. Kamphuis,Cacha M. P. C. D. Peeters-Scholte,Semra Hiz Kurul,Rita Horvath,Hanns Lochmueller,David Murphy,Stephan Waldmueller,Stephanie Spranger, David Overberg,Alison M. Muir,Aboulfazl Rad,Barbara Vona, Firdous Abdulwahad,Sateesh Maddirevula,Inna S. Povolotskaya,Victoria Y. Voinova, Vykuntaraju K. Gowda,Varunvenkat M. Srinivasan,Fowzan S. Alkuraya,Heather C. Mefford,Majid Alfadhel,Tobias B. Haack,Pasquale Striano,Mariasavina Severino,Masaki Fukata,Yvonne Hilhorst-Hofstee,Henry Houlden

Brain（2022）

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