Adi Mory

1.8k total citations
40 papers, 592 citations indexed

About

Adi Mory is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Adi Mory has authored 40 papers receiving a total of 592 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 17 papers in Genetics and 6 papers in Immunology. Recurrent topics in Adi Mory's work include Genomics and Rare Diseases (6 papers), Mitochondrial Function and Pathology (6 papers) and Genomic variations and chromosomal abnormalities (6 papers). Adi Mory is often cited by papers focused on Genomics and Rare Diseases (6 papers), Mitochondrial Function and Pathology (6 papers) and Genomic variations and chromosomal abnormalities (6 papers). Adi Mory collaborates with scholars based in Israel, United States and France. Adi Mory's 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 and has published in prestigious journals such as New England Journal of Medicine, Blood and Neurology.

In The Last Decade

Adi Mory

35 papers receiving 583 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Adi Mory Israel	15	245	147	124	86	78	40	592
Ortal Barel Israel	15	450 1.8×	247 1.7×	189 1.5×	16 0.2×	31 0.4×	63	868
Hiroaki Miyahara Japan	16	317 1.3×	53 0.4×	63 0.5×	28 0.3×	142 1.8×	67	682
Lauréane Mittaz Switzerland	10	211 0.9×	180 1.2×	133 1.1×	33 0.4×	34 0.4×	10	586
Morad Khayat Israel	16	422 1.7×	162 1.1×	33 0.3×	21 0.2×	18 0.2×	50	664
Mieko Matsushima Japan	9	468 1.9×	178 1.2×	39 0.3×	53 0.6×	24 0.3×	11	852
Mark Malin Australia	11	373 1.5×	122 0.8×	766 6.2×	22 0.3×	51 0.7×	13	1.4k
Manuela Fanciulli Italy	11	241 1.0×	367 2.5×	150 1.2×	19 0.2×	24 0.3×	13	726
Atsuko Maeda Japan	12	307 1.3×	36 0.2×	200 1.6×	127 1.5×	39 0.5×	14	801
Jerry C. Cheng United States	14	387 1.6×	66 0.4×	100 0.8×	10 0.1×	61 0.8×	28	707
Martina Klempt Germany	12	235 1.0×	86 0.6×	28 0.2×	59 0.7×	20 0.3×	18	397

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

Hamiel, Uri, Alina Kurolap, Adi Mory, et al.. (2025). Deletion of RAI1 noncoding exons 1–2 causes Smith–Magenis syndrome. Journal of Genetics. 104(1).

Mory, Adi, Adi Reches, Karina Krajden Haratz, et al.. (2025). Diagnostic Value of Exome Sequencing in Isolated Polyhydramnios. Prenatal Diagnosis.

Miremberg, Hadas, R. Birnbaum, Yuval Yaron, et al.. (2024). Prenatal Diagnosis of a KIDINS220 De Novo Heterozygous Variant in a Fetus With a Complex CNS Anomaly. Prenatal Diagnosis. 44(12). 1518–1521.

Kurolap, Alina, Adi Mory, Karina Krajden Haratz, et al.. (2023). SMARCC1 is a susceptibility gene for congenital hydrocephalus with an autosomal dominant inheritance mode and incomplete penetrance. Prenatal Diagnosis. 43(10). 1374–1377. 3 indexed citations

Kurolap, Alina, Isaiah D. Wexler, Adi Mory, et al.. (2023). A common benign intronic deletion masking a pathogenic deep intronic PCCB variant - genome sequencing and RNA studies to the rescue. Molecular Genetics and Metabolism. 140(3). 107702–107702. 1 indexed citations

Kurolap, Alina, Adi Mory, Karina Krajden Haratz, et al.. (2022). Upgrading an intronic TMEM67 variant of unknown significance to likely pathogenic through RNA studies and community data sharing. Prenatal Diagnosis. 42(12). 1484–1487. 3 indexed citations

Yaron, Yuval, Adi Mory, Alina Kurolap, et al.. (2022). Exome sequencing as first‐tier test for fetuses with severe central nervous system structural anomalies. Ultrasound in Obstetrics and Gynecology. 60(1). 59–67. 48 indexed citations

Kurolap, Alina, Israela Lerer, Judith Dagan, et al.. (2022). Unique Ataxia-Oculomotor Apraxia 2 (AOA2) in Israel with Novel Variants, Atypical Late Presentation, and Possible Identification of a Poison Exon. Journal of Molecular Neuroscience. 72(8). 1715–1723. 2 indexed citations

Hershkovitz, Tova, Alina Kurolap, Claudia Gonzaga‐Jauregui, et al.. (2019). A novel TUFM homozygous variant in a child with mitochondrial cardiomyopathy expands the phenotype of combined oxidative phosphorylation deficiency 4. Journal of Human Genetics. 64(6). 589–595. 21 indexed citations

10.

Sagi‐Dain, Lena, Alina Kurolap, Anat Ilivitzki, et al.. (2019). A novel heterozygous loss‐of‐function DCC Netrin 1 receptor variant in prenatal agenesis of corpus callosum and review of the literature. American Journal of Medical Genetics Part A. 182(1). 205–212. 8 indexed citations

11.

Weiss, Karin, Nina Ekhilevitch, Lior Cohen, et al.. (2019). Identification of a novel PCNT founder pathogenic variant in the Israeli Druze population. European Journal of Medical Genetics. 63(2). 103643–103643. 6 indexed citations

12.

Kurolap, Alina, Liza Konnikova, Lael Werner, et al.. (2019). A Unique Presentation of Infantile-Onset Colitis and Eosinophilic Disease without Recurrent Infections Resulting from a Novel Homozygous CARMIL2 Variant. Journal of Clinical Immunology. 39(4). 430–439. 15 indexed citations

13.

Weiss, Karin, Alina Kurolap, Tamar Paperna, et al.. (2018). Rare Disease Diagnostics: A Single-center Experience and Lessons Learnt. Rambam Maimonides Medical Journal. 9(3). e0018–e0018. 4 indexed citations

14.

Kurolap, Alina, Tova Hershkovitz, Adi Mory, et al.. (2016). 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. 99(5). 1172–1180. 25 indexed citations

15.

Kurolap, Alina, et al.. (2015). A Novel Missense Mutation in FLT4 Causes Autosomal Recessive Hereditary Lymphedema. Lymphatic Research and Biology. 13(2). 107–111. 8 indexed citations

16.

Dagan, Efrat, Ilana Schlesinger, Adi Mory, et al.. (2015). The contribution of Niemann-Pick SMPD1 mutations to Parkinson disease in Ashkenazi Jews. Parkinsonism & Related Disorders. 21(9). 1067–1071. 44 indexed citations

17.

Mory, Adi, Efrat Dagan, Hanna Mandel, et al.. (2014). Kohlschutter-Tonz Syndrome: Clinical and Genetic Insights Gained From 16 Cases Deriving From a Close-Knit Village in Northern Israel. Pediatric Neurology. 50(4). 421–426. 16 indexed citations

18.

Mory, Adi, Francesc X. Ruiz, Efrat Dagan, et al.. (2013). A missense mutation in ALDH1A3 causes isolated microphthalmia/anophthalmia in nine individuals from an inbred Muslim kindred. European Journal of Human Genetics. 22(3). 419–422. 22 indexed citations

19.

Gazit, Yael, Adi Mory, Amos Etzioni, et al.. (2010). Leukocyte Adhesion Deficiency Type II: Long-Term Follow-Up and Review of the Literature. Journal of Clinical Immunology. 30(2). 308–313. 50 indexed citations

20.

Feigelson, Sara W., Ronit Pasvolsky, Memet Aker, et al.. (2009). Loss of Kindlin-3 in LAD-III eliminates LFA-1 but not VLA-4 adhesiveness developed under shear flow conditions. Blood. 114(11). 2344–2353. 82 indexed citations

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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