Myriam Srour

5.4k total citations
88 papers, 1.9k citations indexed

About

Myriam Srour is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Myriam Srour has authored 88 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Molecular Biology, 28 papers in Genetics and 22 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Myriam Srour's work include Genomics and Rare Diseases (13 papers), Fetal and Pediatric Neurological Disorders (13 papers) and Genetics and Neurodevelopmental Disorders (13 papers). Myriam Srour is often cited by papers focused on Genomics and Rare Diseases (13 papers), Fetal and Pediatric Neurological Disorders (13 papers) and Genetics and Neurodevelopmental Disorders (13 papers). Myriam Srour collaborates with scholars based in Canada, Italy and United States. Myriam Srour's co-authors include Michael Shevell, Guy A. Rouleau, Jacques L. Michaud, Fadi F. Hamdan, Andrea Accogli, Barbara Mazer, Maryam Oskoui, Lysanne Patry, Annette Majnemer and José‐Mario Capo‐Chichi and has published in prestigious journals such as Science, Nature Communications and Journal of Neuroscience.

In The Last Decade

Myriam Srour

82 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Myriam Srour Canada	20	703	653	466	320	197	88	1.9k
Kimberly A. Aldinger United States	25	1.3k 1.8×	613 0.9×	358 0.8×	344 1.1×	365 1.9×	48	2.3k
Mihovil Pletikos United States	18	680 1.0×	358 0.5×	430 0.9×	297 0.9×	458 2.3×	21	1.8k
Zygmunt Galdzicki United States	27	1.1k 1.6×	1.0k 1.5×	246 0.5×	382 1.2×	282 1.4×	60	2.7k
Meral Topçu Türkiye	24	1.4k 2.0×	718 1.1×	509 1.1×	399 1.2×	195 1.0×	85	2.5k
Dawna D. Armstrong United States	21	730 1.0×	754 1.2×	195 0.4×	231 0.7×	510 2.6×	33	1.6k
Petter Strømme Norway	28	1.2k 1.7×	1.1k 1.8×	296 0.6×	296 0.9×	311 1.6×	76	2.7k
Carlos Cardoso France	24	1.2k 1.7×	871 1.3×	282 0.6×	302 0.9×	211 1.1×	37	2.0k
Michael R. Pranzatelli United States	30	471 0.7×	450 0.7×	204 0.4×	770 2.4×	112 0.6×	144	2.9k
Stephen L. Kinsman United States	18	663 0.9×	177 0.3×	435 0.9×	565 1.8×	111 0.6×	30	1.8k
Déborah Morris-Rosendahl Germany	25	931 1.3×	654 1.0×	133 0.3×	463 1.4×	192 1.0×	65	1.8k

Countries citing papers authored by Myriam Srour

Since Specialization

Citations

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

Fields of papers citing papers by Myriam Srour

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Myriam Srour

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

Chaudhari, Karina, Kai-Yue Zhang, Patricia T. Yam, et al.. (2024). A human DCC variant causing mirror movement disorder reveals that the WAVE regulatory complex mediates axon guidance by netrin-1–DCC. Science Signaling. 17(856). eadk2345–eadk2345. 3 indexed citations

Yam, Patricia T., Baoyu Chen, Alfonso Fasano, et al.. (2023). Genetics of mirror movements identifies a multifunctional complex required for Netrin-1 guidance and lateralization of motor control. Science Advances. 9(19). eadd5501–eadd5501. 11 indexed citations

Srour, Myriam, et al.. (2023). Holoprosencephaly: Review of Embryology, Clinical Phenotypes, Etiology and Management. Children. 10(4). 647–647. 12 indexed citations

Shevell, Michael, et al.. (2023). Evaluation of Individuals with Non-Syndromic Global Developmental Delay and Intellectual Disability. Children. 10(3). 414–414. 6 indexed citations

Severino, Mariasavina, Domenico Tortora, Sarà Uccella, et al.. (2022). Imaging characteristics and neurosurgical outcome in subjects with agenesis of the corpus callosum and interhemispheric cysts. Neuroradiology. 64(11). 2163–2177. 3 indexed citations

Accogli, Andrea, Christine Saint‐Martin, Irma López, et al.. (2021). PCDH12 variants are associated with basal ganglia anomalies and exudative vitreoretinopathy. European Journal of Medical Genetics. 65(2). 104405–104405. 3 indexed citations

Accogli, Andrea, et al.. (2020). Neurogenesis, neuronal migration, and axon guidance. Handbook of clinical neurology. 173. 25–42. 34 indexed citations

Uccella, Sarà, Andrea Accogli, Domenico Tortora, et al.. (2019). Dissecting the neurological phenotype in children with callosal agenesis, interhemispheric cysts and malformations of cortical development. Journal of Neurology. 266(5). 1167–1181. 9 indexed citations

Zhang, Yu, Aurore Menegaux, Colleen Manitt, et al.. (2018). Mesocorticolimbic Connectivity and Volumetric Alterations inDCCMutation Carriers. Journal of Neuroscience. 38(20). 4655–4665. 19 indexed citations

10.

Accogli, Andrea, et al.. (2018). Diagnostic Yield of Intellectual Disability Gene Panels. Pediatric Neurology. 92. 32–36. 22 indexed citations

11.

Johannssen, Helge C., Matthias T. Wyss, R. Brian Roome, et al.. (2018). DCC Is Required for the Development of Nociceptive Topognosis in Mice and Humans. Cell Reports. 22(5). 1105–1114. 18 indexed citations

12.

Tétreault, Martine, Luan T. Tran, Myriam Srour, et al.. (2017). Recessive Mutations in NDUFA2 Cause Mitochondrial Leukoencephalopathy. Annals of Neurology. 82.

13.

Lacaria, Melanie, Myriam Srour, Jacques L. Michaud, et al.. (2017). Expansion of the clinical phenotype of the distal 10q26.3 deletion syndrome to include ataxia and hyperemia of the hands and feet. American Journal of Medical Genetics Part A. 173(6). 1611–1619. 15 indexed citations

14.

Tétreault, Martine, Sylvie Provost, Benjamin Béland, et al.. (2014). G.P.197. Neuromuscular Disorders. 24(9-10). 875–876.

15.

Mittal, Kirti, Taimoor I. Sheikh, Nasim Vasli, et al.. (2014). Identification of a homozygous splice site mutation in the dynein axonemal light chain 4 gene on 22q13.1 in a large consanguineous family from Pakistan with congenital mirror movement disorder. Human Genetics. 133(11). 1419–1429. 18 indexed citations

16.

Hamdan, Fadi F., Myriam Srour, José‐Mario Capo‐Chichi, et al.. (2014). De Novo Mutations in Moderate or Severe Intellectual Disability. PLoS Genetics. 10(10). e1004772–e1004772. 259 indexed citations

17.

Srour, Myriam, Fadi F. Hamdan, Jeremy Schwartzentruber, et al.. (2012). Mutations in TMEM231 cause Joubert syndrome in French Canadians. Journal of Medical Genetics. 49(10). 636–641. 49 indexed citations

18.

Lepage, Jean‐François, Vincent Beaulé, Myriam Srour, et al.. (2011). Neurophysiological investigation of congenital mirror movements in a patient with agenesis of the corpus callosum. Brain stimulation. 5(2). 137–140. 10 indexed citations

19.

Srour, Myriam, Jean‐Baptiste Rivière, Marie‐Pierre Dubé, et al.. (2010). Mutations in DCC Cause Congenital Mirror Movements. Science. 328(5978). 592–592. 128 indexed citations

20.

Srour, Myriam, et al.. (2006). SCREENING FOR DEVELOPMENTAL DELAY IN THE SETTING OF AN AMBULATORY PEDIATRIC CLINIC. Neuropediatrics. 37(S 1). 3 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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