Mustapha Amyere

3.0k total citations · 1 hit paper
19 papers, 1.9k citations indexed

About

Mustapha Amyere is a scholar working on Cell Biology, Molecular Biology and Genetics. According to data from OpenAlex, Mustapha Amyere has authored 19 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Cell Biology, 7 papers in Molecular Biology and 6 papers in Genetics. Recurrent topics in Mustapha Amyere's work include Cellular transport and secretion (4 papers), Erythrocyte Function and Pathophysiology (3 papers) and Prenatal Screening and Diagnostics (3 papers). Mustapha Amyere is often cited by papers focused on Cellular transport and secretion (4 papers), Erythrocyte Function and Pathophysiology (3 papers) and Prenatal Screening and Diagnostics (3 papers). Mustapha Amyere collaborates with scholars based in Belgium, France and United States. Mustapha Amyere's co-authors include Miikka Vikkula, Pierre J. Courtoy, Patrick Van Deŕ Smissen, Alex Veithen, Bernard Payrastre, Joris Vermeesch, Jean‐Pierre Fryns, Yves Moreau, Cindy Melotte and Thomas D’Hooghe and has published in prestigious journals such as Nature Medicine, Nature Genetics and Biochemical Journal.

In The Last Decade

Mustapha Amyere

19 papers receiving 1.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Chromosome instability is common in human cleavage-stage embryos

2009 601 citations Evelyne Vanneste, Thierry Voet et al. Nature Medicine profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mustapha Amyere Belgium	13	854	563	349	322	285	19	1.9k
Evelyne Fischer France	23	1.6k 1.9×	823 1.5×	226 0.6×	390 1.2×	165 0.6×	43	2.7k
Somayyeh Fahiminiya Canada	27	1.2k 1.4×	811 1.4×	106 0.3×	146 0.5×	76 0.3×	52	2.2k
Misao Ohki Japan	19	2.3k 2.7×	416 0.7×	136 0.4×	134 0.4×	32 0.1×	26	2.9k
Masahiro Muto Japan	18	1.4k 1.7×	405 0.7×	90 0.3×	78 0.2×	48 0.2×	54	1.9k
Alexander P.A. Stegmann Netherlands	24	839 1.0×	375 0.7×	104 0.3×	52 0.2×	87 0.3×	52	2.0k
Manas K. Ray United States	26	1.4k 1.7×	577 1.0×	42 0.1×	126 0.4×	39 0.1×	52	2.1k
K Yamamura Japan	22	1.1k 1.3×	530 0.9×	32 0.1×	121 0.4×	55 0.2×	39	2.5k
Stuart J. Swiedler United States	21	1.2k 1.4×	146 0.3×	44 0.1×	556 1.7×	49 0.2×	30	2.9k
J J Cassiman Belgium	34	1.9k 2.2×	573 1.0×	60 0.2×	1.5k 4.7×	26 0.1×	66	3.4k
Masahiro Tahara Japan	26	839 1.0×	142 0.3×	106 0.3×	362 1.1×	13 0.0×	75	1.9k

Countries citing papers authored by Mustapha Amyere

Since Specialization

Citations

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

Fields of papers citing papers by Mustapha Amyere

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mustapha Amyere

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

All Works

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19 of 19 papers shown

Deprez, Pierre, Mustapha Amyere, Antonella Mendola, et al.. (2015). Isolated bilateral transverse agenesis of the distal segments of the lower limbs at the level of the knee joint in a human fetus. American Journal of Medical Genetics Part A. 170(2). 523–530. 1 indexed citations

Amyere, Mustapha, A. Dompmartin, Vinciane Wouters, et al.. (2014). Common Somatic Alterations Identified in Maffucci Syndrome by Molecular Karyotyping. Molecular Syndromology. 5(6). 259–267. 8 indexed citations

Amyere, Mustapha, Pascal Brouillard, Brendan A.S. McIntyre, et al.. (2013). Somatic Uniparental Isodisomy Explains Multifocality of Glomuvenous Malformations. The American Journal of Human Genetics. 92(2). 188–196. 59 indexed citations

Vanneste, Evelyne, Thierry Voet, Michèle Ampe, et al.. (2012). Chromosome Instability Is Common in Human Cleavage-Stage Embryos. Obstetrical & Gynecological Survey. 67(12). 787–788. 1 indexed citations

Foulquier, François, Mustapha Amyere, Jaak Jaeken, et al.. (2012). TMEM165 Deficiency Causes a Congenital Disorder of Glycosylation. The American Journal of Human Genetics. 91(1). 15–26. 163 indexed citations

Gianfrancesco, Fernando, Domenico Rendina, Daniela Merlotti, et al.. (2012). Giant cell tumor occurring in familial Paget's disease of bone: Report of clinical characteristics and linkage analysis of a large pedigree. Journal of Bone and Mineral Research. 28(2). 341–350. 13 indexed citations

Amyere, Mustapha, Thomas Vogt, Joe J. Hoo, et al.. (2011). KITLG Mutations Cause Familial Progressive Hyper- and Hypopigmentation. Journal of Investigative Dermatology. 131(6). 1234–1239. 35 indexed citations

Vanneste, Evelyne, Thierry Voet, Cédric Le Caignec, et al.. (2009). Chromosome instability is common in human cleavage-stage embryos. Nature Medicine. 15(5). 577–583. 601 indexed citations breakdown →

Wiame, Elsa, Donatienne Tyteca, Nathalie Pierrot, et al.. (2009). Molecular identification of aspartate N-acetyltransferase and its mutation in hypoacetylaspartia. Biochemical Journal. 425(1). 127–139. 99 indexed citations

10.

Benzina, Z., Mustapha Amyere, B. Hammami, et al.. (2008). Identification of candidate regions for a novel Usher syndrome type II locus.. PubMed. 14. 1719–26. 6 indexed citations

11.

Balikova, Irina, Kevin Martens, Cindy Melotte, et al.. (2008). Autosomal-Dominant Microtia Linked to Five Tandem Copies of a Copy-Number-Variable Region at Chromosome 4p16. The American Journal of Human Genetics. 82(1). 181–187. 30 indexed citations

12.

Persu, Alexandre, Mustapha Amyere, Ilse Gutierrez-Roelens, et al.. (2008). Rare presentation of familial paraganglioma without evidence of mutation in the SDH, RET and VHL genes: towards further genetic heterogeneity. Journal of Hypertension. 27(1). 76–82. 3 indexed citations

13.

Lorenz‐Depiereux, Bettina, Murat Bastepe, Anna Benet‐Pagès, et al.. (2006). DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis. Nature Genetics. 38(11). 1248–1250. 373 indexed citations

14.

Mettlen, Marcel, Anna E. Płatek, Patrick Van Deŕ Smissen, et al.. (2006). Src Triggers Circular Ruffling and Macropinocytosis at the Apical Surface of Polarized MDCK Cells. Traffic. 7(5). 589–603. 79 indexed citations

15.

Gutierrez-Roelens, Ilse, Thierry Sluysmans, Mark Jorissen, Mustapha Amyere, & Miikka Vikkula. (2006). Localization of candidate regions for a novel gene for Kartagener syndrome. European Journal of Human Genetics. 14(7). 809–815. 5 indexed citations

16.

Płatek, Anna E., Marcel Mettlen, Isabelle Camby, et al.. (2004). v-Src accelerates spontaneous motility via phosphoinositide 3-kinase, phospholipase C and phospholipase D, but abrogates chemotaxis in Rat-1 and MDCK cells. Journal of Cell Science. 117(20). 4849–4861. 19 indexed citations

17.

Amyere, Mustapha, Marcel Mettlen, Patrick Van Deŕ Smissen, et al.. (2001). Origin, originality, functions, subversions and molecular signalling of macropinocytosis. International Journal of Medical Microbiology. 291(6-7). 487–494. 136 indexed citations

18.

Amyere, Mustapha, Bernard Payrastre, U. Krause, et al.. (2000). Constitutive Macropinocytosis in Oncogene-transformed Fibroblasts Depends on Sequential Permanent Activation of Phosphoinositide 3-Kinase and Phospholipase C. Molecular Biology of the Cell. 11(10). 3453–3467. 194 indexed citations

19.

Veithen, Alex, Mustapha Amyere, Patrick Van Deŕ Smissen, Philippe Cupers, & Pierre J. Courtoy. (1998). Regulation of macropinocytosis in v-Src-transformed fibroblasts: cyclic AMP selectively promotes regurgitation of macropinosomes. Journal of Cell Science. 111(16). 2329–2335. 28 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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