Hadas Lahat

1.6k total citations
15 papers, 1.1k citations indexed

About

Hadas Lahat is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Hadas Lahat has authored 15 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 10 papers in Cardiology and Cardiovascular Medicine and 3 papers in Genetics. Recurrent topics in Hadas Lahat's work include Cardiac electrophysiology and arrhythmias (8 papers), Ion channel regulation and function (7 papers) and Cardiac Arrhythmias and Treatments (6 papers). Hadas Lahat is often cited by papers focused on Cardiac electrophysiology and arrhythmias (8 papers), Ion channel regulation and function (7 papers) and Cardiac Arrhythmias and Treatments (6 papers). Hadas Lahat collaborates with scholars based in Israel, United States and Germany. Hadas Lahat's co-authors include Etgar Levy‐Nissenbaum, Michael Eldar, Elon Pras, Elon Pras, Boleslaw Goldman, Doron Lancet, Edna Ben‐Asher, Nili Avidan, Orna Man and Daniel L. Kastner and has published in prestigious journals such as Circulation, Nature Genetics and The American Journal of Human Genetics.

In The Last Decade

Hadas Lahat

15 papers receiving 1.1k citations

Peers

Hadas Lahat

CCM

GENET

CMN

Achim Plum Germany

Giedrius Kanaporis United States

T. Jarry‐Guichard France

Yun‐Qian Gao China

Michelle L. Milstein United States

Diana Faria Germany

Evgeny Loukianov United States

Jost Schönberger Germany

Veronika Karcagi Hungary

Corinna Friedrich Germany

Achim Plum Germany

Hadas Lahat

62 ×0.1

CCM

974 ×1.3

114 ×1.1

GENET

38 ×0.4

88 ×1.0

CMN

Citations per year, relative to Hadas Lahat Hadas Lahat (= 1×) peers Achim Plum

Countries citing papers authored by Hadas Lahat

Since Specialization

Citations

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

Fields of papers citing papers by Hadas Lahat

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hadas Lahat

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

All Works

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15 of 15 papers shown

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

Yoskovitz, Guy, Yael Peled, Michael Gramlich, et al.. (2012). A Novel Titin Mutation in Adult-Onset Familial Dilated Cardiomyopathy. The American Journal of Cardiology. 109(11). 1644–1650. 28 indexed citations

Nof, Eyal, David Luria, Hadas Lahat, et al.. (2007). Point Mutation in the HCN4 Cardiac Ion Channel Pore Affecting Synthesis, Trafficking, and Functional Expression Is Associated With Familial Asymptomatic Sinus Bradycardia. Circulation. 116(5). 463–470. 113 indexed citations

Arad, Michael, Hadas Lahat, & Dov Freimark. (2005). Genetic ideology of dilated cardiompathy.. PubMed. 7(6). 392–6. 2 indexed citations

Lahat, Hadas, Elon Pras, & Michael Eldar. (2004). A missense mutation in CASQ2 is associated with autosomal recessive catecholamine‐induced polymorphic ventricular tachycardia in Bedouin families from Israel. Annals of Medicine. 36(sup1). 87–91. 27 indexed citations

Nof, Eyal, Hadas Lahat, Naama Constantini, et al.. (2004). A novel form of familial bidirectional ventricular tachycardia. The American Journal of Cardiology. 93(2). 231–234. 3 indexed citations

Levy‐Nissenbaum, Etgar, Regina C. Betz, Moshe Frydman, et al.. (2003). Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin. Nature Genetics. 34(2). 151–153. 108 indexed citations

Eldar, M., Elon Pras, & Hadas Lahat. (2002). A Missense Mutation in a Highly Conserved Region of CASQ2 Is Associated with Autosomal Recessive Catecholamine-induced Polymorphic Ventricular Tachycardia in Bedouin Families from Israel. Cold Spring Harbor Symposia on Quantitative Biology. 67(0). 333–338. 20 indexed citations

Ben‐Zeev, Bruria, Etgar Levy‐Nissenbaum, Hadas Lahat, et al.. (2002). Megalencephalic leukoencephalopathy with subcortical cysts; a founder effect in Israeli patients and a higher than expected carrier rate among Libyan Jews. Human Genetics. 111(2). 214–218. 27 indexed citations

10.

Pras, Eran, Etgar Levy‐Nissenbaum, Hadas Lahat, et al.. (2002). A Missense Mutation in the LIM2 Gene Is Associated with Autosomal Recessive Presenile Cataract in an Inbred Iraqi Jewish Family. The American Journal of Human Genetics. 70(5). 1363–1367. 92 indexed citations

11.

Lahat, Hadas, et al.. (2002). Autosomal recessive catecholamine-induced polymorphic ventricular tachycardia.. PubMed. 4(12). 1095–30. 1 indexed citations

12.

Levy‐Nissenbaum, Etgar, Michael Eldar, Qing Wang, et al.. (2001). Genetic Analysis of Brugada Syndrome in Israel: Two Novel Mutations and Possible Genetic Heterogeneity. Genetic Testing. 5(4). 331–334. 13 indexed citations

13.

Lahat, Hadas, Elon Pras, Nili Avidan, et al.. (2001). A Missense Mutation in a Highly Conserved Region of CASQ2 Is Associated with Autosomal Recessive Catecholamine-Induced Polymorphic Ventricular Tachycardia in Bedouin Families from Israel. The American Journal of Human Genetics. 69(6). 1378–1384. 461 indexed citations

14.

Lahat, Hadas, Michael Eldar, Etgar Levy‐Nissenbaum, et al.. (2001). Autosomal Recessive Catecholamine- or Exercise-Induced Polymorphic Ventricular Tachycardia. Circulation. 103(23). 2822–2827. 179 indexed citations

15.

Pras, Elon, Etgar Levy‐Nissenbaum, Hadas Lahat, et al.. (2001). A gene causing autosomal recessive cataract maps to the short arm of chromosome 3.. PubMed. 3(8). 559–62. 38 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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