Najim Lahrouchi

3.0k total citations
16 papers, 231 citations indexed

About

Najim Lahrouchi is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Genetics. According to data from OpenAlex, Najim Lahrouchi has authored 16 papers receiving a total of 231 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Cardiology and Cardiovascular Medicine, 9 papers in Molecular Biology and 3 papers in Genetics. Recurrent topics in Najim Lahrouchi's work include Cardiac electrophysiology and arrhythmias (7 papers), Cardiomyopathy and Myosin Studies (5 papers) and Ion channel regulation and function (4 papers). Najim Lahrouchi is often cited by papers focused on Cardiac electrophysiology and arrhythmias (7 papers), Cardiomyopathy and Myosin Studies (5 papers) and Ion channel regulation and function (4 papers). Najim Lahrouchi collaborates with scholars based in Netherlands, Canada and Denmark. Najim Lahrouchi's co-authors include Connie R. Bezzina, Arthur A.M. Wilde, Hanno L. Tan, Ahmad S. Amin, Rafik Tadros, Elijah R. Behr, Pieter G. Postema, Leander Beekman, Milena Radivojkov‐Blagojevic and Jacob Tfelt‐Hansen and has published in prestigious journals such as JAMA, European Heart Journal and Cardiovascular Research.

In The Last Decade

Najim Lahrouchi

12 papers receiving 228 citations

Peers

Najim Lahrouchi

CCM

GENET

EPIDE

Sarah Costa Switzerland

Emioli Randazzo Italy

Silvia Passantino Italy

Paramdeep Baweja United States

Efstathios Papatheodorou United Kingdom

Jonah P. Zuflacht United States

Waseem Hindieh Canada

Satoki Fukae Japan

Xochitl Jimenez United States

Nobue Yagihara Japan

Sarah Costa Switzerland

Najim Lahrouchi

179 ×1.1

CCM

47 ×0.4

13 ×0.5

GENET

5 ×0.3

EPIDE

0 ×0.0

Citations per year, relative to Najim Lahrouchi Najim Lahrouchi (= 1×) peers Sarah Costa

Countries citing papers authored by Najim Lahrouchi

Since Specialization

Citations

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

Fields of papers citing papers by Najim Lahrouchi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Najim Lahrouchi

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

All Works

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16 of 16 papers shown

Jordà, Paloma, Yiwei Lai, Louis‐Philippe Lemieux Perreault, et al.. (2025). Genetic analyses across cardiovascular traits: leveraging genetic correlations to empower locus discovery and prediction in common cardiovascular diseases. npj Genomic Medicine. 10(1). 65–65.

Jordà, Paloma, et al.. (2023). Assessment of multi-trait analysis of GWAS (MTAG) for discovery of novel genetic variants and mechanistic insight in common cardiovascular diseases. European Heart Journal. 44(Supplement_2).

Glinge, Charlotte, Najim Lahrouchi, Reza Jabbari, Jacob Tfelt‐Hansen, & Connie R. Bezzina. (2020). Genome-wide association studies of cardiac electrical phenotypes. Cardiovascular Research. 116(9). 1620–1634. 19 indexed citations

Walsh, Roddy, Najim Lahrouchi, Charlotte Glinge, et al.. (2020). Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of 5182 cases from long QT syndrome and Brugada syndrome consortia cohorts and gnomAD population controls. European Heart Journal. 41(Supplement_2).

Tadros, Rafik, Hanno L. Tan, Jan A. Kors, et al.. (2019). Predicting cardiac electrical response to sodium-channel blockade and Brugada syndrome using polygenic risk scores. European Heart Journal. 40(37). 3097–3107. 51 indexed citations

Vandenwijngaert, Sara, Najim Lahrouchi, Mohsin A.F. Khan, et al.. (2019). Blood Pressure-Associated Genetic Variants in the Natriuretic Peptide Receptor 1 Gene Modulate Guanylate Cyclase Activity. Circulation Genomic and Precision Medicine. 12(8). e002472–e002472. 13 indexed citations

Škorić‐Milosavljević, Doris, Fleur V.Y. Tjong, Julien Barc, et al.. (2019). GATA6 mutations: Characterization of two novel patients and a comprehensive overview of the GATA6 genotypic and phenotypic spectrum. American Journal of Medical Genetics Part A. 179(9). 1836–1845. 20 indexed citations

Lahrouchi, Najim, Rachida Amri, Mariëlle Alders, et al.. (2017). Clinical and molecular findings in a Moroccan family with Jervell and Lange-Nielsen syndrome: a case report. Journal of Medical Case Reports. 11(1). 88–88. 3 indexed citations

Lahrouchi, Najim, Elisabeth M. Lodder, Rafik Tadros, et al.. (2017). Exome sequencing identifies primary carnitine deficiency in a family with cardiomyopathy and sudden death. European Journal of Human Genetics. 25(6). 783–787. 20 indexed citations

10.

Tadros, Rafik, Eline A. Nannenberg, Krystien V.V. Lieve, et al.. (2017). Yield and Pitfalls of Ajmaline Testing in the Evaluation of Unexplained Cardiac Arrest and Sudden Unexplained Death. JACC. Clinical electrophysiology. 3(12). 1400–1408. 30 indexed citations

11.

Lahrouchi, Najim, Elijah R. Behr, & Connie R. Bezzina. (2016). Next-Generation Sequencing in Post-mortem Genetic Testing of Young Sudden Cardiac Death Cases. Frontiers in Cardiovascular Medicine. 3. 13–13. 19 indexed citations

12.

Mizusawa, Yuka, Hiroshi Morita, Arnon Adler, et al.. (2016). Prognostic significance of fever-induced Brugada syndrome. Heart Rhythm. 13(7). 1515–1520. 49 indexed citations

13.

Crotti, Lia, Carla Spazzolini, Nicole J. Boczek, et al.. (2016). Abstract 14840: International Calmodulinopathy Registry (ICaMR). 134. 2 indexed citations

14.

Lahrouchi, Najim & Connie R. Bezzina. (2015). Cardiac dyssynchrony and response to cardiac resynchronisation therapy in heart failure: can genetic predisposition play a role?. Netherlands Heart Journal. 24(1). 11–15.

15.

Lahrouchi, Najim, Machteld I. Bosscha, & Annette C. Moll. (2014). A Child With a White Pupil. JAMA. 311(17). 1799–1799. 1 indexed citations

16.

Lahrouchi, Najim, Lukas Rammeloo, David R. Koolbergen, & J Hruda. (2013). Ruptured aneurysm of the right coronary sinus of Valsalva in a child with Down syndrome. Cardiology in the Young. 24(2). 376–378. 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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