Leah Peleg

994 total citations
55 papers, 697 citations indexed

About

Leah Peleg is a scholar working on Physiology, Molecular Biology and Epidemiology. According to data from OpenAlex, Leah Peleg has authored 55 papers receiving a total of 697 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Physiology, 13 papers in Molecular Biology and 12 papers in Epidemiology. Recurrent topics in Leah Peleg's work include Lysosomal Storage Disorders Research (17 papers), Trypanosoma species research and implications (11 papers) and Circadian rhythm and melatonin (11 papers). Leah Peleg is often cited by papers focused on Lysosomal Storage Disorders Research (17 papers), Trypanosoma species research and implications (11 papers) and Circadian rhythm and melatonin (11 papers). Leah Peleg collaborates with scholars based in Israel, United States and Australia. Leah Peleg's co-authors include R. Ben‐Ishai, Eyal Raz, Israel Ashkenazi, Boleslaw Goldman, Michal Berkenstadt, Gad Barkai, Howard Cuckle, Ari Zimran, Yuval Weigl and Muriel N. Nesbitt and has published in prestigious journals such as JAMA, International Journal of Cancer and Cellular and Molecular Life Sciences.

In The Last Decade

Leah Peleg

55 papers receiving 671 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Leah Peleg Israel	14	270	236	181	89	82	55	697
Milena Laure‐Kamionowska Poland	13	342 1.3×	103 0.4×	287 1.6×	58 0.7×	53 0.6×	46	782
G. Stefano Brigidi Canada	11	442 1.6×	245 1.0×	100 0.6×	89 1.0×	151 1.8×	11	940
Xuequn Chen China	15	215 0.8×	135 0.6×	138 0.8×	147 1.7×	51 0.6×	25	688
William J. DeVito United States	20	295 1.1×	79 0.3×	98 0.5×	137 1.5×	33 0.4×	52	986
Nadège Briançon United States	8	246 0.9×	154 0.7×	88 0.5×	301 3.4×	20 0.2×	8	745
Camila Scorticati Argentina	14	222 0.8×	66 0.3×	131 0.7×	58 0.7×	83 1.0×	28	709
L S Jacobs United States	14	225 0.8×	102 0.4×	61 0.3×	110 1.2×	112 1.4×	18	793
Loredana Zocchi United States	12	327 1.2×	164 0.7×	83 0.5×	290 3.3×	42 0.5×	14	756
D. Dondi Italy	22	437 1.6×	108 0.5×	402 2.2×	119 1.3×	59 0.7×	52	1.4k
Mohammed Selloum France	12	362 1.3×	147 0.6×	140 0.8×	36 0.4×	93 1.1×	22	724

Countries citing papers authored by Leah Peleg

Since Specialization

Citations

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

Fields of papers citing papers by Leah Peleg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Leah Peleg

This figure shows the co-authorship network connecting the top 25 collaborators of Leah Peleg. A scholar is included among the top collaborators of Leah Peleg 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 Leah Peleg. Leah Peleg 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

Peleg, Leah, et al.. (2014). An update of Gaucher mutations distribution in the Ashkenazi Jewish population: prevalence and country of origin of the mutation R496H.. PubMed. 16(11). 683–5. 11 indexed citations

Cohen, Yoram, et al.. (2010). The GALT rush: High carrier frequency of an unusual deletion mutation of the GALT gene in the Ashkenazi population. Molecular Genetics and Metabolism. 102(2). 157–160. 7 indexed citations

Feldman, Baruch, et al.. (2010). The single cell as a tool for genetic testing: credibility, precision, implication. Journal of Assisted Reproduction and Genetics. 27(6). 335–341. 5 indexed citations

Gazit, Ephraim, et al.. (2008). Thrombophilic polymorphisms in Israel. Blood Cells Molecules and Diseases. 41(2). 230–233. 8 indexed citations

Berkenstadt, Michal, et al.. (2007). Preconceptional and prenatal screening for fragile X syndrome: Experience with 40 000 tests. Prenatal Diagnosis. 27(11). 991–994. 69 indexed citations

Lahad, Amnon, Amir Shmueli, Ari Zimran, et al.. (2007). Carrier Screening for Gaucher Disease. JAMA. 298(11). 1281–1281. 59 indexed citations

Amichai, Boaz, et al.. (2006). Novel mutations in two families with Darier's disease. International Journal of Dermatology. 46(1). 64–67. 6 indexed citations

Frisch, Amos, et al.. (2004). Origin and spread of the 1278insTATC mutation causing Tay-Sachs disease in Ashkenazi Jews: genetic drift as a robust and parsimonious hypothesis. Human Genetics. 114(4). 366–376. 20 indexed citations

Drory, Vivian E., et al.. (2003). Hexosaminidase A deficiency is an uncommon cause of a syndrome mimicking amyotrophic lateral sclerosis. Muscle & Nerve. 28(1). 109–112. 18 indexed citations

10.

Tunçtan, Bahar, Yuval Weigl, Leah Peleg, et al.. (2002). Circadian variation of nitric oxide synthase activity in mouse tissue. Chronobiology International. 19(2). 393–404. 49 indexed citations

11.

Liron, M, et al.. (2002). Protein electrophoretic markers in Israel: compilation of data and genetic affinities. Annals of Human Biology. 29(2). 142–175. 4 indexed citations

12.

Peleg, Leah, et al.. (2000). A novel mutation in the HEXA gene specific to Tay–Sachs disease carriers of Jewish Iraqi origin. Clinical Genetics. 57(5). 398–400. 4 indexed citations

13.

Zelnik, Nathanel, et al.. (2000). Clinical Manifestations of Psychiatric Patients Who Are Carriers of Tay-Sachs Disease. Neuropsychobiology. 41(3). 127–131. 10 indexed citations

14.

Aviram‐Goldring, Ayala, Boleslav Goldman, Rakefet Chen‐Shtoyerman, et al.. (2000). Deletion patterns of the STS gene and flanking sequences in Israeli X-linked ichthyosis patients and carriers: analysis by polymerase chain reaction and fluorescence in situ hybridization techniques. International Journal of Dermatology. 39(3). 182–187. 22 indexed citations

15.

Peleg, Leah, et al.. (1998). Lower frequency of Gaucher disease carriers among Tay-Sachs disease carriers. European Journal of Human Genetics. 6(2). 185–186. 3 indexed citations

16.

Peleg, Leah, et al.. (1995). Genetic control of biological rhythms: Independent expression of each rhythm parameter. Life Sciences. 56(13). 1143–1149. 6 indexed citations

17.

Peleg, Leah & Boleslaw Goldman. (1994). Detection of Tay-Sachs Disease Carriers among Individuals with Thermolabile Hexosaminidase B. Clinical Chemistry and Laboratory Medicine (CCLM). 32(2). 65–70. 6 indexed citations

18.

Goldman, Boleslaw, et al.. (1993). Prenatal and postnatal studies of a late infantile GM2 gangliosidosis in a family of Syrian origin: a possible B1 variant.. PubMed. 29(10). 623–8. 3 indexed citations

19.

Peleg, Leah, M. N. Nesbitt, & Israel Ashkenazi. (1989). Strain dependent response of circadian rhythms during exposure to continuous illumination. Life Sciences. 44(13). 893–900. 9 indexed citations

20.

Peleg, Leah, et al.. (1986). Circadian Rhythms of Enzymes' Activity in Mice Tissues During Exposure to Continuous Illumination. Chronobiology International. 3(1). 39–45. 4 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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