Adi Mory

1.8k citations

40 papers · 592 · h-index 15

Impact in

Immunology and Allergy top 10%
- Cell Adhesion Molecules Research
Immunology
- Immunodeficiency and Autoimmune Disorders

Papers in

Molecular Biology 18
- Mitochondrial Function and Pathology 6
- RNA Research and Splicing 3
Genetics 17
- Genomic variations and chromosomal abnormalities 6
- Genomics and Rare Diseases 6
- Genetics and Neurodevelopmental Disorders 4

Co-authors: Alina Kurolap (26 shared papers)Ruth Gershoni‐Baruch (8 shared papers)Efrat Dagan (8 shared papers)Hagit Baris Feldman (20 shared papers)Amos Etzioni (2 shared papers)Tamar Paperna (14 shared papers)Tova Hershkovitz (8 shared papers)Hagit Baris (7 shared papers)
Journals: Prenatal Diagnosis (4 papers)European Journal of Human Genetics (2 papers)The American Journal of Human Genetics (2 papers)Molecular Genetics and Metabolism (2 papers)Journal of Medical Genetics (2 papers)
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-authors

The 25 scholars most cited alongside Adi Mory, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Adi Mory Line = papers co-authored together Adi Mory links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 40 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Loss of Kindlin-3 in LAD-III eliminates LFA-1 but not VLA-4 adhesiveness developed under shear flow conditions Blood ·Eugenia Manevich-Mendelson, 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	2009	82
2	Leukocyte Adhesion Deficiency Type II: Long-Term Follow-Up and Review of the Literature Journal of Clinical Immunology ·Yael Gazit, Adi Mory, Amos Etzioni, Moshe Frydman, Oded Scheuerman, Ruth Gershoni‐Baruch, Ben‐Zion Garty	2010	50
3	Exome sequencing as first‐tier test for fetuses with severe central nervous system structural anomalies Ultrasound in Obstetrics and Gynecology ·Yuval Yaron, Vered Ofen Glassner, Adi Mory, Noa Zunz Henig, Alina Kurolap, Anat Bar Shira, D. Brabbing Goldstein, Daphna Marom, (unknown), Hagit Baris Feldman, G. Malinger, Karina Krajden Haratz, Adi Reches	2022	48
4	The LRRK2 G2019S mutation is associated with Parkinson disease and concomitant non-skin cancers Neurology ·Rivka Inzelberg, Ohad Cohen, J. Aharon‐Peretz, Ilana Schlesinger, Ruth Gershoni‐Baruch, Ruth Djaldetti, Zeev Nitsan, L. Ephraty, Olga Tunkel, Evgenia Kozlova, Lilah Inzelberg, N. Kaplan, Tariq Mehr, Adi Mory, Efrat Dagan, Edna Schechtman, Eitan Friedman, Sharon Hassin‐Baer	2012	47
5	The contribution of Niemann-Pick SMPD1 mutations to Parkinson disease in Ashkenazi Jews Parkinsonism & Related Disorders ·Efrat Dagan, Ilana Schlesinger, M. Ayoub, Adi Mory, Maria Nassar, Alina Kurolap, Judith Peretz-Aharon, Ruth Gershoni‐Baruch	2015	44
6	Mutations in the mitochondrial ribosomal protein MRPS22 lead to primary ovarian insufficiency Human Molecular Genetics ·Anlu Chen, Dov Tiosano, Tülay Güran, Hagit Baris, Yavuz Bayram, Adi Mory, Laura Shapiro-Kulnane, Craig A. Hodges, Zeynep Coban‐Akdemir, Serap Turan, Shalini N. Jhangiani, Focco van den Akker, Charles L. Hoppel, Helen K. Salz, James R. Lupski, David A. Buchner	2018	41
7	Loss of Glycine Transporter 1 Causes a Subtype of Glycine Encephalopathy with Arthrogryposis and Mildly Elevated Cerebrospinal Fluid Glycine The American Journal of Human Genetics ·Alina Kurolap, Anja Armbruster, Tova Hershkovitz, Katharina Hauf, Adi Mory, Tamar Paperna, Ewald Hannappel, Galit Tal, Yusif Nijem, Ella Sella, Muhammad Mahajnah, Anat Ilivitzki, Dov Hershkovitz, Nina Ekhilevitch, Hanna Mandel, Volker Eulenburg, Hagit Baris	2016	25
8	A Nonsense Mutation in the Human Homolog of Drosophila rogdi Causes Kohlschutter–Tonz Syndrome The American Journal of Human Genetics ·Adi Mory, Efrat Dagan, Barbara Illi, Philippe Duquesnoy, Shikma Mordechai, Ishai Shahor, Sveva Romani, Nivin Hawash-Moustafa, Hanna Mandel, Enza Maria Valente, Serge Amselem, Ruth Gershoni‐Baruch	2012	23
9	A missense mutation in ALDH1A3 causes isolated microphthalmia/anophthalmia in nine individuals from an inbred Muslim kindred European Journal of Human Genetics ·Adi Mory, Francesc X. Ruiz, Efrat Dagan, Evgenia A Yakovtseva, Alina Kurolap, Xavier Parés, Jaume Farrés, Ruth Gershoni‐Baruch	2013	22
10	A novel TUFM homozygous variant in a child with mitochondrial cardiomyopathy expands the phenotype of combined oxidative phosphorylation deficiency 4 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	2019	21
11	Eculizumab Is Safe and Effective as a Long‐term Treatment for Protein‐losing Enteropathy Due to CD55 Deficiency Journal of Pediatric Gastroenterology and Nutrition ·Alina Kurolap, Orly Eshach Adiv, Tova Hershkovitz, Adi Tabib, Netanel Karbian, Tamar Paperna, Adi Mory, Arcadi Vachyan, Nadav Slijper, Ran Steinberg, Yaniv Zohar, Dror Mevorach, Hagit Baris Feldman	2018	20
12	Kohlschutter-Tonz Syndrome: Clinical and Genetic Insights Gained From 16 Cases Deriving From a Close-Knit Village in Northern Israel Pediatric Neurology ·Adi Mory, Efrat Dagan, Ishai Shahor, Hanna Mandel, Barbara Illi, Jenny Zolotushko, Alina Kurolap, Emilia Chechik, Enza Maria Valente, Serge Amselem, Ruth Gershoni‐Baruch	2014	16
13	Is one diagnosis the whole story? patients with double diagnoses American Journal of Medical Genetics Part A ·Alina Kurolap, Naama Orenstein, Inbal Kedar, Monika Weisz Hubshman, Dov Tiosano, Adi Mory, Zohar Levi, Daphna Marom, Lior Cohen, Nina Ekhilevich, Jessica Douglas, C. Nowak, Wen‐Hann Tan, Hagit Baris	2016	16
14	A Unique Presentation of Infantile-Onset Colitis and Eosinophilic Disease without Recurrent Infections Resulting from a Novel Homozygous CARMIL2 Variant Journal of Clinical Immunology ·Alina Kurolap, Orly Eshach Adiv, Liza Konnikova, Lael Werner, Claudia Gonzaga‐Jauregui, Maya Steinberg, Vanessa Mitsialis, Adi Mory, M Nunberg, Sarah Wall, Ron Shaoul, John D. Overton, Alan R. Shuldiner, Yaniv Zohar, Tamar Paperna, Scott B. Snapper, Dror S. Shouval, Hagit Baris Feldman	2019	15
15	Duplication in CHIT1 gene and the risk for aspergillus lung disease in CF patients Pediatric Pulmonology ·Galit Livnat, Ronen Bar‐Yoseph, Adi Mory, Efrat Dagan, Nael Elias, Ruth Gershoni, Lea Bentur	2013	15
16	Establishing the role of PLVAP in protein-losing enteropathy: a homozygous missense variant leads to an attenuated phenotype Journal of Medical Genetics ·Alina Kurolap, Orly Eshach‐Adiv, Claudia Gonzaga‐Jauregui, Katya Dolnikov, Adi Mory, Tamar Paperna, Tova Hershkovitz, John D. Overton, Marielle Kaplan, Fabian Glaser, Yaniv Zohar, Alan R. Shuldiner, Gidon Berger, Hagit Baris	2018	14
17	Expanding the MYBPC1 phenotypic spectrum: a novel homozygous mutation causes arthrogryposis multiplex congenita Clinical Genetics ·Nina Ekhilevitch, Alina Kurolap, Danit Oz-Levi, Adi Mory, Tova Hershkovitz, Gil Ast, Hanna Mandel, Hagit Baris	2015	12
18	A recurring NFS1 pathogenic variant causes a mitochondrial disorder with variable intra-familial patient outcomes Molecular Genetics and Metabolism Reports ·Tova Hershkovitz, Alina Kurolap, Galit Tal, Tamar Paperna, Adi Mory, Jeffrey Staples, Karlla W. Brigatti, Claudia Gonzaga‐Jauregui, Elena Dumin, Ann Saada, Hanna Mandel, Hagit Baris Feldman	2020	10
19	Homozygosity for CHEK2 p.Gly167Arg leads to a unique cancer syndrome with multiple complex chromosomal translocations in peripheral blood karyotype Journal of Medical Genetics ·Tamar Paperna, Nitzan Sharon-Shwartzman, Alina Kurolap, Yael Goldberg, Nivin Moustafa, Yariv Carasso, Miora Feinstien, Adi Mory, Gili Reznick-Levi, Claudia Gonzaga‐Jauregui, Alan R. Shuldiner, Lina Basel‐Vanagaite, Yishai Ofran, Elizabeth Half, Hagit Baris Feldman	2019	9
20	A Novel Missense Mutation in FLT4 Causes Autosomal Recessive Hereditary Lymphedema Lymphatic Research and Biology ·Svetlana Melikhan-Revzin, Alina Kurolap, Efrat Dagan, Adi Mory, Ruth Gershoni‐Baruch	2015	8

About Adi Mory

Adi Mory is a scholar working on Molecular Biology, Genetics, Immunology, Pathology and Forensic Medicine and Pediatrics, Perinatology and Child Health, having authored 40 papers that have together received 592 indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (6 papers), Fetal and Pediatric Neurological Disorders (5 papers), Genetic factors in colorectal cancer (4 papers), Metabolism and Genetic Disorders (4 papers), Genetics and Neurodevelopmental Disorders (4 papers) and RNA Research and Splicing (3 papers). The work is most often cited by research in Immunology and Allergy (86 citations), Immunology (124 citations), Genetics (147 citations), Neurology (78 citations) and Clinical Biochemistry (33 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 Prenatal Diagnosis, European Journal of Human Genetics, The American Journal of Human Genetics, Molecular Genetics and Metabolism and Journal of Medical Genetics.

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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Adi Mory

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Adi Mory

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