Adi Mory

1.8k citations

40 papers · 592 indexed · h-index 15

Co-authors: Alina Kurolap Ruth Gershoni‐Baruch Efrat Dagan Hagit Baris Feldman Amos Etzioni Tamar Paperna Tova Hershkovitz Hagit Baris
Topics: Genomics and Rare Diseases (6 papers)Mitochondrial Function and Pathology (6 papers)Genomic variations and chromosomal abnormalities (6 papers)
Cited by: Immunology and Allergy Immunology Genetics
Journals: New England Journal of Medicine Blood Neurology
Partner nations: Israel United States France

In The Last Decade

Adi Mory

35 papers receiving 583 citations

Peers

Countries citing papers authored by Adi Mory

Since Specialization

Citations

This map shows the geographic impact of Adi Mory's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Adi Mory with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Adi Mory more than expected).

Fields of papers citing papers by Adi Mory

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Adi Mory. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Adi Mory. The network helps show where Adi Mory may publish in the future.

Co-authorship network of co-authors of Adi Mory

This figure shows the co-authorship network connecting the top 25 collaborators of Adi Mory. A scholar is included among the top collaborators of Adi Mory based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Adi Mory. Adi Mory is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Deletion of RAI1 noncoding exons 1–2 causes Smith–Magenis syndrome 2025 ·Journal of Genetics ·Uri Hamiel,Alina Kurolap,(unknown),Adi Mory,Anat Bar Shira,Hagit Baris Feldman,Daphna Marom	0
2	Diagnostic Value of Exome Sequencing in Isolated Polyhydramnios 2025 ·Prenatal Diagnosis ·(unknown),(unknown),Adi Mory,Adi Reches,Karina Krajden Haratz,(unknown),Hagit Baris Feldman,Lena Sagi‐Dain,Mordechai Shohat,(unknown),Yuval Yaron,Michal Levy	0
3	Prenatal Diagnosis of a KIDINS220 De Novo Heterozygous Variant in a Fetus With a Complex CNS Anomaly 2024 ·Prenatal Diagnosis ·Hadas Miremberg,R. Birnbaum,(unknown),(unknown),Yuval Yaron,Adi Mory,G. Malinger,Karina Krajden Haratz	0
4	SMARCC1 is a susceptibility gene for congenital hydrocephalus with an autosomal dominant inheritance mode and incomplete penetrance 2023 ·Prenatal Diagnosis ·(unknown),Alina Kurolap,Adi Mory,Karina Krajden Haratz,Dvora Kidron,G. Malinger,Hagit Baris Feldman,Yuval Yaron	3
5	A common benign intronic deletion masking a pathogenic deep intronic PCCB variant - genome sequencing and RNA studies to the rescue 2023 ·Molecular Genetics and Metabolism ·Alina Kurolap,(unknown),(unknown),Isaiah D. Wexler,(unknown),Adi Mory,Ortal Barel,Shlomo Almashanu,Hagit Baris Feldman	1
6	Upgrading an intronic TMEM67 variant of unknown significance to likely pathogenic through RNA studies and community data sharing 2022 ·Prenatal Diagnosis ·Alina Kurolap,Adi Mory,(unknown),Karina Krajden Haratz,G. Malinger,R. Birnbaum,Hagit Baris Feldman,Yuval Yaron	3
7	Exome sequencing as first‐tier test for fetuses with severe central nervous system structural anomalies 2022 ·Ultrasound in Obstetrics and Gynecology ·Yuval Yaron,(unknown),Adi Mory,(unknown),Alina Kurolap,Anat Bar Shira,(unknown),Daphna Marom,(unknown),Hagit Baris Feldman,G. Malinger,Karina Krajden Haratz,Adi Reches	48
8	Unique Ataxia-Oculomotor Apraxia 2 (AOA2) in Israel with Novel Variants, Atypical Late Presentation, and Possible Identification of a Poison Exon 2022 ·Journal of Molecular Neuroscience ·(unknown),Alina Kurolap,Israela Lerer,Judith Dagan,(unknown),Adi Mory,Yael Wilnai,(unknown),Nir Giladi,Tanya Gurevich,Vardiella Meiner,Alexander Lossos,Hagit Baris Feldman	2
9	A novel TUFM homozygous variant in a child with mitochondrial cardiomyopathy expands the phenotype of combined oxidative phosphorylation deficiency 4 2019 ·Journal of Human Genetics ·Tova Hershkovitz,Alina Kurolap,Claudia Gonzaga‐Jauregui,Tamar Paperna,Adi Mory,Sarah E. Wolf,John D. Overton,Alan R. Shuldiner,Ann Saada,Hanna Mandel,Hagit Baris Feldman	21
10	A novel heterozygous loss‐of‐function DCC Netrin 1 receptor variant in prenatal agenesis of corpus callosum and review of the literature 2019 ·American Journal of Medical Genetics Part A ·Lena Sagi‐Dain,Alina Kurolap,Anat Ilivitzki,Adi Mory,Tamar Paperna,(unknown),Claudia Gonzaga‐Jauregui,Amir Peleg,Hagit Baris Feldman	8
11	Identification of a novel PCNT founder pathogenic variant in the Israeli Druze population 2019 ·European Journal of Medical Genetics ·Karin Weiss,Nina Ekhilevitch,Lior Cohen,(unknown),Rachel Bello,Ariel F. Martinez,Yarin Hadid,Liran I. Shlush,Alina Kurolap,Tamar Paperna,Adi Mory,Hagit Baris,Maximilian Muenke	6
12	A Unique Presentation of Infantile-Onset Colitis and Eosinophilic Disease without Recurrent Infections Resulting from a Novel Homozygous CARMIL2 Variant 2019 ·Journal of Clinical Immunology ·Alina Kurolap,(unknown),Liza Konnikova,Lael Werner,Claudia Gonzaga‐Jauregui,(unknown),Vanessa Mitsialis,Adi Mory,(unknown),Sarah Wall,Ron Shaoul,John D. Overton,Alan R. Shuldiner,Yaniv Zohar,Tamar Paperna,Scott B. Snapper,Dror S. Shouval,Hagit Baris Feldman	15
13	Rare Disease Diagnostics: A Single-center Experience and Lessons Learnt 2018 ·Rambam Maimonides Medical Journal ·Karin Weiss,Alina Kurolap,Tamar Paperna,Adi Mory,(unknown),Tova Hershkovitz,Nina Ekhilevitch,Hagit Baris	4
14	Loss of Glycine Transporter 1 Causes a Subtype of Glycine Encephalopathy with Arthrogryposis and Mildly Elevated Cerebrospinal Fluid Glycine 2016 ·The American Journal of Human Genetics ·Alina Kurolap,(unknown),Tova Hershkovitz,(unknown),Adi Mory,Tamar Paperna,Ewald Hannappel,Galit Tal,(unknown),(unknown),Muhammad Mahajnah,Anat Ilivitzki,Dov Hershkovitz,Nina Ekhilevitch,Hanna Mandel,Volker Eulenburg,Hagit Baris	25
15	A Novel Missense Mutation in FLT4 Causes Autosomal Recessive Hereditary Lymphedema 2015 ·Lymphatic Research and Biology ·(unknown),Alina Kurolap,Efrat Dagan,Adi Mory,Ruth Gershoni‐Baruch	8
16	The contribution of Niemann-Pick SMPD1 mutations to Parkinson disease in Ashkenazi Jews 2015 ·Parkinsonism & Related Disorders ·Efrat Dagan,Ilana Schlesinger,(unknown),Adi Mory,Maria Nassar,Alina Kurolap,(unknown),Ruth Gershoni‐Baruch	44
17	Kohlschutter-Tonz Syndrome: Clinical and Genetic Insights Gained From 16 Cases Deriving From a Close-Knit Village in Northern Israel 2014 ·Pediatric Neurology ·Adi Mory,Efrat Dagan,(unknown),Hanna Mandel,Barbara Illi,(unknown),Alina Kurolap,(unknown),Enza Maria Valente,Serge Amselem,Ruth Gershoni‐Baruch	16
18	A missense mutation in ALDH1A3 causes isolated microphthalmia/anophthalmia in nine individuals from an inbred Muslim kindred 2013 ·European Journal of Human Genetics ·Adi Mory,Francesc X. Ruiz,Efrat Dagan,(unknown),Alina Kurolap,Xavier Parés,Jaume Farrés,Ruth Gershoni‐Baruch	22
19	Leukocyte Adhesion Deficiency Type II: Long-Term Follow-Up and Review of the Literature 2010 ·Journal of Clinical Immunology ·Yael Gazit,Adi Mory,Amos Etzioni,Moshe Frydman,Oded Scheuerman,Ruth Gershoni‐Baruch,Ben‐Zion Garty	50
20	Loss of Kindlin-3 in LAD-III eliminates LFA-1 but not VLA-4 adhesiveness developed under shear flow conditions 2009 ·Blood ·(unknown),Sara W. Feigelson,Ronit Pasvolsky,Memet Aker,Valentin Grabovsky,Ziv Shulman,Sara Şebnem Kılıç,Maria Alessandra Rosenthal‐Allieri,Shifra Ben‐Dor,Adi Mory,Alain Bernard,Markus Moser,Amos Etzioni,R. Alon	82

About Adi Mory

Adi Mory is a scholar working on Genetics, Clinical Biochemistry and Immunology and Allergy, having authored 40 papers that have together received 592 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (6 papers), Mitochondrial Function and Pathology (6 papers) and Genomic variations and chromosomal abnormalities (6 papers). The work is most often cited by research in Immunology and Allergy (86 citations), Immunology (124 citations) and Genetics (147 citations). Adi Mory has collaborated with scholars based in Israel, United States and France. Frequent co-authors include Alina Kurolap, Ruth Gershoni‐Baruch, Efrat Dagan, Hagit Baris Feldman, Amos Etzioni, Tamar Paperna, Tova Hershkovitz, Hagit Baris, Hanna Mandel and Ilana Schlesinger. Their work appears in journals such as New England Journal of Medicine, Blood and Neurology.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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