Jamal Ghoumid

1.4k total citations
34 papers, 352 citations indexed

About

Jamal Ghoumid is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Jamal Ghoumid has authored 34 papers receiving a total of 352 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 18 papers in Genetics and 3 papers in Surgery. Recurrent topics in Jamal Ghoumid's work include Genetics and Neurodevelopmental Disorders (8 papers), Congenital heart defects research (6 papers) and RNA modifications and cancer (6 papers). Jamal Ghoumid is often cited by papers focused on Genetics and Neurodevelopmental Disorders (8 papers), Congenital heart defects research (6 papers) and RNA modifications and cancer (6 papers). Jamal Ghoumid collaborates with scholars based in France, United Kingdom and United States. Jamal Ghoumid's co-authors include Sylvie Manouvrier‐Hanu, Florence Petit, Anne‐Sophie Jourdain, Muriel Holder‐Espinasse, Thomas Smol, Audrey Briand‐Suleau, Irina Giurgea, Fabienne Escande, Nicole Porchet and Frédéric Frénois and has published in prestigious journals such as Human Molecular Genetics, Molecular Psychiatry and Epilepsia.

In The Last Decade

Jamal Ghoumid

27 papers receiving 348 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jamal Ghoumid France 11 209 160 62 30 22 34 352
Magdalena Badura‐Stronka Poland 12 183 0.9× 141 0.9× 77 1.2× 18 0.6× 40 1.8× 32 357
Gabriela Stangoni Italy 9 122 0.6× 166 1.0× 32 0.5× 18 0.6× 7 0.3× 24 257
Marije Meuwissen Belgium 11 153 0.7× 186 1.2× 31 0.5× 40 1.3× 25 1.1× 23 368
Gevork N. Mnatzakanian Canada 8 216 1.0× 267 1.7× 50 0.8× 10 0.3× 20 0.9× 15 409
Ruolan Guo China 11 158 0.8× 120 0.8× 31 0.5× 17 0.6× 14 0.6× 41 332
Jennifer Lee United States 8 95 0.5× 94 0.6× 18 0.3× 12 0.4× 14 0.6× 11 319
Gundula Povysil United States 9 131 0.6× 141 0.9× 13 0.2× 15 0.5× 11 0.5× 18 314
Francesco Benedicenti Italy 10 165 0.8× 123 0.8× 66 1.1× 28 0.9× 23 1.0× 21 417
Dana Gabriková Slovakia 10 126 0.6× 108 0.7× 24 0.4× 23 0.8× 9 0.4× 22 297
Dhanya Lakshmi Narayanan India 10 135 0.6× 88 0.6× 19 0.3× 19 0.6× 27 1.2× 42 261

Countries citing papers authored by Jamal Ghoumid

Since Specialization
Citations

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

Fields of papers citing papers by Jamal Ghoumid

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jamal Ghoumid

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

All Works

20 of 20 papers shown
1.
Caumes, Roseline, Emilie Ait‐Yahya, C. Thuillier, et al.. (2025). Combining long-read DNA and RNA sequencing to enhance molecular understanding of structural variations leading to copy gains. Computational and Structural Biotechnology Journal. 27. 1732–1740. 1 indexed citations
2.
Caumes, Roseline, C. Thuillier, Odile Boute‐Bénéjean, et al.. (2024). NONO-related X-linked intellectual disability syndrome: Further clinical and molecular delineation. European Journal of Medical Genetics. 73. 104987–104987.
3.
Mansour‐Hendili, Lamisse, Cyril Gitiaux, Céline Latouche, et al.. (2024). Recurrent “outsider” intronic variation in the SLC5A6 gene causes severe mixed axonal and demyelinating neuropathy, cyclic vomiting and optic atrophy in 3 families from Maghreb. Frontiers in Genetics. 15. 1352006–1352006. 1 indexed citations
4.
Vanlerberghe, Clémence, Frédéric Frénois, Thomas Smol, et al.. (2024). RPL26 variants: A rare cause of Diamond-Blackfan anemia syndrome with multiple congenital anomalies at the forefront. Genetics in Medicine. 26(12). 101266–101266.
5.
Vanlerberghe, Clémence, Frédéric Frénois, Emilie Ait‐Yahya, et al.. (2024). Functional characterization vs in silico prediction for TBX5 missense and splice variants in Holt-Oram syndrome. Genetics in Medicine. 26(12). 101267–101267.
6.
Barbotin, Anne‐Laure, Anne‐Sophie Jourdain, Alexandre Moerman, et al.. (2024). Identification of a novel CFAP61 homozygous splicing variant associated with multiple morphological abnormalities of the flagella. Journal of Assisted Reproduction and Genetics. 41(6). 1499–1505. 3 indexed citations
7.
Brunelle, Perrine, C. Thuillier, Clémence Vanlerberghe, et al.. (2024). Expanded phenotypic spectrum of UDP‐glucose‐6‐dehydrogenase recessive neurodevelopmental disorder: Two novel descriptions with or without epileptic encephalopathy. American Journal of Medical Genetics Part A. 194(12). e63820–e63820. 1 indexed citations
8.
Smol, Thomas, Perrine Brunelle, Roseline Caumes, et al.. (2022). TRIT1 deficiency: Two novel patients with four novel variants. European Journal of Medical Genetics. 65(11). 104603–104603. 2 indexed citations
9.
Dessein, Anne‐Frédérique, Jòseph Vamecq, Aurore Devos, et al.. (2022). A novel HADHA variant associated with an atypical moderate and late-onset LCHAD deficiency. Molecular Genetics and Metabolism Reports. 31. 100860–100860. 4 indexed citations
10.
Ghoumid, Jamal, Thomas Smol, Perrine Brunelle, et al.. (2021). Le test de concordance de script à l’heure de la réforme du second cycle des études médicales en France : étude pilote en génétique médicale. Pédagogie médicale. 22(2). 67–72.
11.
Khouri, Elma El, Jamal Ghoumid, Damien Haye, et al.. (2021). Wnt/β-catenin pathway and cell adhesion deregulation in CSDE1-related intellectual disability and autism spectrum disorders. Molecular Psychiatry. 26(7). 3572–3585. 11 indexed citations
12.
Smol, Thomas, et al.. (2019). Mayer-Rokitansky-Künster-Hauser syndrome due to 2q12.1q14.1 deletion: PAX8 the causing gene?. European Journal of Medical Genetics. 63(4). 103812–103812. 10 indexed citations
13.
Ghoumid, Jamal, Florence Petit, Odile Boute‐Bénéjean, et al.. (2017). Cerebellar hypoplasia with endosteal sclerosis is a POLR3-related disorder. European Journal of Human Genetics. 25(8). 1011–1014. 10 indexed citations
14.
Lebrun, Nicolas, Irina Giurgea, Alice Goldenberg, et al.. (2017). Molecular and cellular issues of KMT2A variants involved in Wiedemann-Steiner syndrome. European Journal of Human Genetics. 26(1). 107–116. 25 indexed citations
15.
Ghoumid, Jamal, Florence Petit, Muriel Holder‐Espinasse, et al.. (2015). Nail–Patella Syndrome: clinical and molecular data in 55 families raising the hypothesis of a genetic heterogeneity. European Journal of Human Genetics. 24(1). 44–50. 33 indexed citations
16.
Mégarbané, André, Bénédicte Demeer, Paule Bénit, et al.. (2013). KBP–cytoskeleton interactions underlie developmental anomalies in Goldberg–Shprintzen syndrome. Human Molecular Genetics. 22(12). 2387–2399. 24 indexed citations
17.
Perrin, Laurence, Odile Fenneteau, Brice Ilharreborde, et al.. (2012). A new lysosomal storage disorder resembling Morquio syndrome in sibs. European Journal of Medical Genetics. 55(3). 157–162. 1 indexed citations
18.
Ghoumid, Jamal, Joris Andrieux, Bernard Sablonnière, et al.. (2011). Duplication at chromosome 2q31.1-q31.2 in a family presenting syndactyly and nystagmus. European Journal of Human Genetics. 19(11). 1198–1201. 6 indexed citations
19.
Ghoumid, Jamal, D. Subtil, Louise Devisme, et al.. (2009). Hypertelorism‐microtia‐clefting syndrome (HMC syndrome): prenatal diagnosis in two siblings. Prenatal Diagnosis. 29(11). 1064–1065.
20.
Houfflin‐Debarge, V., Jamal Ghoumid, Louise Devisme, et al.. (2009). Prenatal diagnosis of Nager syndrome in a monochorionic‐diamniotic twin pregnancy. Prenatal Diagnosis. 29(2). 187–189. 8 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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