Mustapha Amyere

3.0k citations

19 papers · 1.9k indexed · 1 hit paper · h-index 13

Nephrology top 2%
Genetics top 5%
- Genomic variations and chromosomal abnormalities 3
Cell Biology top 5%
- Cellular transport and secretion 4
- Cellular Mechanics and Interactions 3
- melanin and skin pigmentation 2
- Microtubule and mitosis dynamics 2
Pediatrics, Perinatology and Child Health top 5%
- Prenatal Screening and Diagnostics 3
Molecular Biology top 10%
Physiology
- Erythrocyte Function and Pathophysiology 3
Oncology
- Bone health and treatments 2

Co-authors: Miikka Vikkula Pierre J. Courtoy Patrick Van Deŕ Smissen Alex Veithen Bernard Payrastre Joris Vermeesch Jean‐Pierre Fryns Yves Moreau
Cited by: Nephrology Genetics Cell Biology
Partner nations: Belgium France United States

In The Last Decade

Mustapha Amyere

19 papers receiving 1.8k citations

Hit Papers

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Peers

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

The 25 scholars most cited alongside Mustapha Amyere, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Mustapha Amyere Line = papers co-authored together Mustapha Amyere links everyone, so they are left out of the graph.

All Works

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19 of 19 papers shown

#	Work
1	Isolated bilateral transverse agenesis of the distal segments of the lower limbs at the level of the knee joint in a human fetus Antoine Christiaens,Pierre Deprez,Mustapha Amyere,Antonella Mendola,Pierre Bernard,Y. Gillerot,Philippe Clapuyt,Catherine Godfraind,Benoît Lengelé,Miikka Vikkula,Catherine Behets	2015	1
2	Common Somatic Alterations Identified in Maffucci Syndrome by Molecular Karyotyping Mustapha Amyere,A. Dompmartin,Vinciane Wouters,O Enjolras,Ilkka Kaitila,Pierre‐Louis Docquier,Catherine Godfraind,John B. Mulliken,Laurence M. Boon,Miikka Vikkula	2014	8
3	Somatic Uniparental Isodisomy Explains Multifocality of Glomuvenous Malformations Mustapha Amyere,Virginie Aerts,Pascal Brouillard,Brendan A.S. McIntyre,François P. Duhoux,Michel Wassef,O Enjolras,John B. Mulliken,Olivier Devuyst,Hélène Antoine‐Poirel,Laurence M. Boon,Miikka Vikkula	2013	59
4	TMEM165 Deficiency Causes a Congenital Disorder of Glycosylation François Foulquier,Mustapha Amyere,Jaak Jaeken,Renate Zeevaert,Els Schollen,Valérie Race,Riet Bammens,Willy Morelle,Claire Rosnoblet,Dominique Legrand,Didier Demaegd,Neil R.M. Buist,David Cheillan,Nathalie Guffon,Pierre Morsomme,Willem Annaert,Hudson H. Freeze,Emile Van Schaftingen,Miikka Vikkula,Gert Matthijs	2012	163
5	Chromosome Instability Is Common in Human Cleavage-Stage Embryos Evelyne Vanneste,Thierry Voet,Cedric Le Caginec,Michèle Ampe,Peter Könings,Cindy Melotte,Sophie Debrock,Mustapha Amyere,Miikka Vikkula,Frans Schuit,Jean‐Pierre Fryns,Geert Verbeke,Thomas D’Hooghe,Yves Moreau,Joris Vermeesch	2012	1
6	Giant cell tumor occurring in familial Paget's disease of bone: Report of clinical characteristics and linkage analysis of a large pedigree Fernando Gianfrancesco,Domenico Rendina,Daniela Merlotti,Teresa Esposito,Mustapha Amyere,Daniela Formicola,Riccardo Muscariello,Gianpaolo De Filippo,Pasquale Strazzullo,Ranuccio Nuti,Miikka Vikkula,Luigi Gennari	2012	13
7	KITLG Mutations Cause Familial Progressive Hyper- and Hypopigmentation Mustapha Amyere,Thomas Vogt,Joe J. Hoo,F Brandrup,Anette Bygum,Laurence M. Boon,Miikka Vikkula	2011	35
8	Chromosome instability is common in human cleavage-stage embryosbreakdown → Evelyne Vanneste,Thierry Voet,Cédric Le Caignec,Michèle Ampe,Peter Könings,Cindy Melotte,Sophie Debrock,Mustapha Amyere,Miikka Vikkula,Frans Schuit,Jean‐Pierre Fryns,Geert Verbeke,Thomas D’Hooghe,Yves Moreau,Joris Vermeesch	2009	601
9	Molecular identification of aspartate N-acetyltransferase and its mutation in hypoacetylaspartia Elsa Wiame,Donatienne Tyteca,Nathalie Pierrot,François Collard,Mustapha Amyere,G. Noël,Jonathan Desmedt,Marie‐Cécile Nassogne,Miikka Vikkula,Jean-Noël Octave,Marie‐Françoise Vincent,Pierre J. Courtoy,Eugen Boltshauser,Emile Van Schaftingen	2009	99
10	Autosomal-Dominant Microtia Linked to Five Tandem Copies of a Copy-Number-Variable Region at Chromosome 4p16 Irina Balikova,Kevin Martens,Cindy Melotte,Mustapha Amyere,Steven Van Vooren,Yves Moreau,David Vetrie,Heike Fiegler,Nigel P. Carter,Thomas Liehr,Miikka Vikkula,Gert Matthijs,Jean‐Pierre Fryns,Ingele Casteels,Koenraad Devriendt,Joris Vermeesch	2008	30
11	Rare presentation of familial paraganglioma without evidence of mutation in the SDH, RET and VHL genes: towards further genetic heterogeneity Alexandre Persu,Mustapha Amyere,Ilse Gutierrez-Roelens,Pierre Rustin,Christine Sempoux,Frédéric Lecouvet,Bernard E. Van Beers,Yves Horsmans,Jean-François De Plaen,MarcHamoir,Miikka Vikkula	2008	3
12	Identification of candidate regions for a novel Usher syndrome type II locus. Imen Ben Rebeh,Z. Benzina,Houria Dhouib,Imen Hadjamor,Mustapha Amyere,Leila Ayadi,Khalil Turki,B. Hammami,Noureddine Kmiha,H. Kammoun,Bochra Hakim,Ilhem Charfedine,Miikka Vikkula,Abdelmonem Ghorbel,Hammadi Ayadi,Saber Masmoudi	2008	6
13	Src Triggers Circular Ruffling and Macropinocytosis at the Apical Surface of Polarized MDCK Cells Marcel Mettlen,Anna E. Płatek,Patrick Van Deŕ Smissen,Sarah Carpentier,Mustapha Amyere,Letizia Lanzetti,Philippe de Diesbach,Donatienne Tyteca,Pierre J. Courtoy	2006	79
14	DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis Bettina Lorenz‐Depiereux,Murat Bastepe,Anna Benet‐Pagès,Mustapha Amyere,Janine Wagenstaller,Ursula Müller-Barth,Klaus Badenhoop,Stéphanie Kaiser,Roger S. Rittmaster,Alan H Shlossberg,José L. Olivares,C Loris,Feliciano J. Ramos,Francis H. Glorieux,Miikka Vikkula,Harald Jüppner,Tim M. Strom	2006	373
15	Localization of candidate regions for a novel gene for Kartagener syndrome Ilse Gutierrez-Roelens,Thierry Sluysmans,Mark Jorissen,Mustapha Amyere,Miikka Vikkula	2006	5
16	v-Src accelerates spontaneous motility via phosphoinositide 3-kinase, phospholipase C and phospholipase D, but abrogates chemotaxis in Rat-1 and MDCK cells Anna E. Płatek,Marcel Mettlen,Isabelle Camby,Róbert Kiss,Mustapha Amyere,Pierre J. Courtoy	2004	19
17	Origin, originality, functions, subversions and molecular signalling of macropinocytosis Mustapha Amyere,Marcel Mettlen,Patrick Van Deŕ Smissen,Anna E. Płatek,Bernard Payrastre,Alex Veithen,Pierre J. Courtoy	2001	136
18	Constitutive Macropinocytosis in Oncogene-transformed Fibroblasts Depends on Sequential Permanent Activation of Phosphoinositide 3-Kinase and Phospholipase C Mustapha Amyere,Bernard Payrastre,U. Krause,Patrick Van Deŕ Smissen,Alex Veithen,Pierre J. Courtoy	2000	194
19	Regulation of macropinocytosis in v-Src-transformed fibroblasts: cyclic AMP selectively promotes regurgitation of macropinosomes Alex Veithen,Mustapha Amyere,Patrick Van Deŕ Smissen,Philippe Cupers,Pierre J. Courtoy	1998	28

About Mustapha Amyere

Mustapha Amyere is a scholar working on Cell Biology, Developmental Biology and Genetics, having authored 19 papers that have together received 1.9k indexed citations. Recurring topics across this work include Cellular transport and secretion (4 papers), Erythrocyte Function and Pathophysiology (3 papers), Prenatal Screening and Diagnostics (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Cellular Mechanics and Interactions (3 papers), Bone health and treatments (2 papers), melanin and skin pigmentation (2 papers) and Microtubule and mitosis dynamics (2 papers). The work is most often cited by research in Nephrology (285 citations), Genetics (563 citations) and Cell Biology (322 citations). Mustapha Amyere has collaborated with scholars based in Belgium, France and United States. Frequent 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.

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