Moran Gal

832 total citations
9 papers, 439 citations indexed

About

Moran Gal is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Moran Gal has authored 9 papers receiving a total of 439 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Molecular Biology and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Moran Gal's work include Genomics and Rare Diseases (1 paper), Ion channel regulation and function (1 paper) and Mitochondrial Function and Pathology (1 paper). Moran Gal is often cited by papers focused on Genomics and Rare Diseases (1 paper), Ion channel regulation and function (1 paper) and Mitochondrial Function and Pathology (1 paper). Moran Gal collaborates with scholars based in Israel, Switzerland and Canada. Moran Gal's co-authors include Paul Renbaum, Ephrat Levy‐Lahad, Rachel Beeri, Mary‐Claire King, Uziel Beller, Ming K. Lee, Julia Grinshpun‐Cohen, Bella Kaufman, Raphael Catane and Eitan Friedman and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Gene and Cell Research.

In The Last Decade

Moran Gal

9 papers receiving 435 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Moran Gal Israel	7	251	188	73	61	50	9	439
Yael Laitman Israel	12	241 1.0×	181 1.0×	69 0.9×	75 1.2×	19 0.4×	39	489
Diane Allingham‐Hawkins Canada	10	371 1.5×	283 1.5×	122 1.7×	64 1.0×	32 0.6×	21	607
Shehla Mohammed United Kingdom	12	248 1.0×	497 2.6×	92 1.3×	76 1.2×	54 1.1×	25	680
J. Couturier France	10	142 0.6×	247 1.3×	56 0.8×	46 0.8×	24 0.5×	17	404
N. Weinberg Israel	7	334 1.3×	281 1.5×	69 0.9×	41 0.7×	55 1.1×	8	512
Bartłomiej Budny Poland	14	396 1.6×	376 2.0×	30 0.4×	41 0.7×	71 1.4×	45	706
Gayle Patel United States	7	420 1.7×	285 1.5×	104 1.4×	92 1.5×	35 0.7×	9	569
Ruen Yao China	15	334 1.3×	385 2.0×	61 0.8×	27 0.4×	44 0.9×	64	657
Rebecca I. Torene United States	10	206 0.8×	165 0.9×	36 0.5×	45 0.7×	56 1.1×	20	506
Hyon J. Kim South Korea	14	292 1.2×	191 1.0×	51 0.7×	28 0.5×	112 2.2×	28	532

Countries citing papers authored by Moran Gal

Since Specialization

Citations

This map shows the geographic impact of Moran Gal'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 Moran Gal with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Moran Gal more than expected).

Fields of papers citing papers by Moran Gal

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Moran Gal. 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 Moran Gal. The network helps show where Moran Gal may publish in the future.

Co-authorship network of co-authors of Moran Gal

This figure shows the co-authorship network connecting the top 25 collaborators of Moran Gal. A scholar is included among the top collaborators of Moran Gal 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 Moran Gal. Moran Gal is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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9 of 9 papers shown

Jacob‐Hirsch, Jasmine, Eran Eyal, Binyamin A. Knisbacher, et al.. (2018). Whole-genome sequencing reveals principles of brain retrotransposition in neurodevelopmental disorders. Cell Research. 28(2). 187–203. 51 indexed citations

Gal, Moran, Daniella Magen, Sarit Ravid, et al.. (2016). A novel homozygous splice site mutation in NALCN identified in siblings with cachexia, strabismus, severe intellectual disability, epilepsy and abnormal respiratory rhythm. European Journal of Medical Genetics. 59(4). 204–209. 25 indexed citations

Gal, Moran, Michal Barák, Min Lin, et al.. (2016). Expanding preconception carrier screening for the Jewish population using high throughput microfluidics technology and next generation sequencing. BMC Medical Genomics. 9(1). 24–24. 2 indexed citations

Gal, Moran, et al.. (2016). Which Anthropometric Measure Best Correlates with Neonatal Fat Mass at Birth?. American Journal of Perinatology. 33(9). 826–830. 3 indexed citations

Leibowitz‐Amit, Raya, Ariel Israel, Moran Gal, et al.. (2016). Association between the Absolute Baseline Lymphocyte Count and Response to Neoadjuvant Platinum-based Chemotherapy in Muscle-invasive Bladder Cancer. Clinical Oncology. 28(12). 790–796. 20 indexed citations

Gal, Moran, et al.. (2014). Novel mutation in TSPAN12 leads to autosomal recessive inheritance of congenital vitreoretinal disease with intra‐familial phenotypic variability. American Journal of Medical Genetics Part A. 164(12). 2996–3002. 19 indexed citations

Lahad, Amnon, Bella Kaufman, Eitan Friedman, et al.. (2014). Population-based screening for breast and ovarian cancer risk due toBRCA1andBRCA2. Proceedings of the National Academy of Sciences. 111(39). 14205–14210. 234 indexed citations

Shalitin, Shlomit, et al.. (2011). Endocrine Outcome in Long-Term Survivors of Childhood Brain Tumors. Hormone Research in Paediatrics. 76(2). 113–122. 43 indexed citations

Renbaum, Paul, et al.. (2003). Egr-1 upregulates the Alzheimer's disease presenilin-2 gene in neuronal cells. Gene. 318. 113–124. 42 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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