MA Mustapha Amyere, PhD - Université catholique de Louvain - Project Manager

MA Mustapha Amyere

PhD

Université catholique de Louvain

Project Manager

Brussels, brussels | Belgium

Main Specialties: Advanced Heart Failure & Transplant Cardiology, Biochemical Genetics, Biology, Blood Banking - Transfusion Medicine, Cardiovascular Disease, Dermatology, Family Medicine, Molecular Genetic Pathology, Vascular Surgery

MA Mustapha Amyere, PhD - Université catholique de Louvain - Project Manager

MA Mustapha Amyere

PhD

Publications

18Publications

516Reads

-Profile Views

530PubMed Central Citations

Germline Loss-of-Function Mutations in EPHB4 Cause a Second Form of Capillary Malformation-Arteriovenous Malformation (CM-AVM2) Deregulating RAS-MAPK Signaling.

Circulation 2017 Sep 7;136(11):1037-1048. Epub 2017 Jul 7.

From Human Molecular Genetics, de Duve Institute, Université catholique de Louvain, Brussels, Belgium (M.A., R.H., M.V.); Center for Human Genetics, Cliniques Universitaires St Luc, Université catholique de Louvain, Brussels, Belgium (N.R.); Université catholique de Louvain, Brussels, Belgium (E.P.); Department of Dermatology, Hospital de la Santa Creu I Sant Pau, Barcelona, Spain (E.B.); Department of Dermatology, Hospital Garrahan, Buenos Aires, Argentina (M.C.); Strong Hospital, University of Rochester School of Medicine and Dentistry, Rochester, NY (M.C.); Departments of Pediatrics and Medicine, Columbia University, New York (W.C., A.B.); Department of Medical Imaging, Sainte-Justine Mother- Child University Hospital, Montreal, Canada (J.D.); Service de Dermatologie, Centre Hospitalo-Universitaire de Nice, France (J.-P.L.); Genética Molecular, Hospital Sant Joan de Déu, Barcelona, Spain (L.M.); Service de Dermatologie, Centre de Référence des Maladies rares de la peau, Hôpital Larrey, Toulouse, France (J.M.-H.); Departments of Medicine and Genetics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia (R.E.P.); Victorian Clinical Genetics Services, Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia (D.J.A.); Department of Neuroradiology, Lariboisière Hospital, Paris, France (A.B.); Vascular Anomalies Program, Lenox Hill Hospital, New York (F.B.); Vascular Birthmark Institute of New York, Roosevelt Hospital (F.B.); Department of Pediatrics, Medical Genetics University of Iowa Carver College of Medicine, Iowa City (H.B.); Department of Dermatology, Université de Caen Basse Normandie, CHU Caen, France (A.D.); Department of Urology, Wake Forest School of Medicine, Winston Salem, NC (D.B.); Genetics Service, Paediatric Department, University Hospital Santa Maria, Lisbon, Portugal (J.D.); Department of Dermatology, Hospital Sant Joan de Deu, Barcelona, Spain (M.A.G.-E.); Departement of Dermatology, School of Medicine, University of California, San Francisco (I.P.); Department of Genetics, University Hospital, Caen, France (M.G.); Department of Molecular Medicine and Surgery, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden (M.K.); Department of Pediatrics, Division of Medical Genetics, Stanford University School of Medicine, CA (A.K.H.-K., L.H.); Hopital Pellegrin Enfants, Bordeaux, France (C.L.-L.); Hôpital Sainte-Justine, Montréal, Quebec, Canada (C.M.); Department of Dermatology, Texas Children's Hospital, Houston (D.M.); Département de Pédiatrie et Génétique Médicale, CHRU Hôpital Morvan, Brest, France (P.P.); Department of Dermatology, Paul Sabatier University, Toulouse, France (C.P.); Service de Génétique Clinique, Hôpital Jeanne de Flandre, Lille, France (F.P.); Pediatric Dermatology Unit, Claude Bernard-Lyon, University and Hospices Civils de Lyon, Hôpital Femme-Mère-Enfant, France (A.P.); Centre Hospitalier Universitaire, Montpellier, France (I.Q.); Dermatolgie, Faculté de Médecine d'Alger, Algeria (A.S.); Department of Medical Genetics, Sydney Children's Hospital, Randwick, New South Wales, Australia (A.T.); Service de Dermatologie, Centre Hospitalo-Universitaire Dijon-Bourgogne, France (P.V.); Department of Dermatology, Hospital Sant Joan de Deu, Barcelona, Spain (A.V.); Department of Paediatric Dermatology, Sydney Children's Hospital, School of Women's and Children's Health University of New South Wales, Sydney, Australia (O.W.); Department of Plastic and Reconstructive Surgery, University of Tokyo, Hongo, Japan (S.W.); Department of Pediatric Dermatology, University Children's Hospital Zurich, Switzerland (L.W.); Children's Hospital of New York (A.W.); University of Iowa Hospitals and Clinics, Iowa City (M.W.); Department of Pediatrics, Washington University, St. Louis, MO (M.W.); and Vascular Anomalies Center, Boston Children's Hospital, Harvard Medical School, Boston, MA (L.M.B.).

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http://dx.doi.org/10.1161/CIRCULATIONAHA.116.026886DOI Listing
September 2017
107 Reads
4 Citations
14.430 Impact Factor

Isolated bilateral transverse agenesis of the distal segments of the lower limbs at the level of the knee joint in a human fetus.

Am J Med Genet A 2016 Feb 6;170A(2):523-530. Epub 2015 Nov 6.

Pôle de Morphologie, Institut de Recherche Expérimentale et Clinique, Université Catholique de Louvain, Brussels, Belgium.

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http://dx.doi.org/10.1002/ajmg.a.37462DOI Listing
February 2016
53 Reads
2.160 Impact Factor

Common somatic alterations identified in maffucci syndrome by molecular karyotyping.

Mol Syndromol 2014 Dec 26;5(6):259-67. Epub 2014 Aug 26.

Laboratory of Human Molecular Genetics, de Duve Institute, Université catholique de Louvain, Brussels, Belgium ; Walloon Excellence in Lifesciences and Biotechnology (WELBIO), Université catholique de Louvain, Brussels, Belgium.

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http://dx.doi.org/10.1159/000365898DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4281579PMC
December 2014
27 Reads
2 Citations

TMEM165 deficiency causes a congenital disorder of glycosylation.

Am J Hum Genet 2012 Jul 7;91(1):15-26. Epub 2012 Jun 7.

Centre National de la Recherche Scientifique UMR, Structural and Functional Glycobiology Unit, University of Lille, Institut Fédératif de Recherche, Villeneuve D'Ascq, France.

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http://dx.doi.org/10.1016/j.ajhg.2012.05.002DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3397274PMC
July 2012
35 Reads
39 Citations
10.931 Impact Factor

KITLG mutations cause familial progressive hyper- and hypopigmentation.

J Invest Dermatol 2011 Jun 3;131(6):1234-9. Epub 2011 Mar 3.

Laboratory of Human Molecular Genetics, de Duve Institute, Université Catholique de Louvain, Brussels, Belgium.

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http://dx.doi.org/10.1038/jid.2011.29DOI Listing
June 2011
17 Reads
7 Citations
7.220 Impact Factor

Molecular identification of aspartate N-acetyltransferase and its mutation in hypoacetylaspartia.

Biochem J 2009 Dec 14;425(1):127-36. Epub 2009 Dec 14.

Laboratory of Physiological Chemistry, Université Catholique de Louvain and de Duve Institute, B-1200 Brussels, Belgium.

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http://dx.doi.org/10.1042/BJ20091024DOI Listing
December 2009
22 Reads
28 Citations
4.400 Impact Factor

Chromosome instability is common in human cleavage-stage embryos.

Nat Med 2009 May 26;15(5):577-83. Epub 2009 Apr 26.

Center for Human Genetics, K.U.Leuven, Belgium.

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http://dx.doi.org/10.1038/nm.1924DOI Listing
May 2009
31 Reads
168 Citations
27.363 Impact Factor

Identification of candidate regions for a novel Usher syndrome type II locus.

Mol Vis 2008 Sep 19;14:1719-26. Epub 2008 Sep 19.

Unité Cibles pour le Diagnostic et la Thérapie, Centre de Biotechnologie de Sfax, Tunisie

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2538493PMC
September 2008
22 Reads
5 Citations
1.990 Impact Factor

Localization of candidate regions for a novel gene for Kartagener syndrome.

Eur J Hum Genet 2006 Jul 26;14(7):809-15. Epub 2006 Apr 26.

Laboratory of Human Molecular Genetics, Christian de Duve Institute of Cellular Pathology, Brussels, Belgium.

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http://dx.doi.org/10.1038/sj.ejhg.5201631DOI Listing
July 2006
5 Reads
4 Citations
4.350 Impact Factor

Src triggers circular ruffling and macropinocytosis at the apical surface of polarized MDCK cells.

Traffic 2006 May;7(5):589-603

CELL Unit, Université catholique de Louvain and Christian de Duve Institute of Cellular Pathology, 1200 Brussels, Belgium.

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http://dx.doi.org/10.1111/j.1600-0854.2006.00412.xDOI Listing
May 2006
6 Reads
40 Citations
4.350 Impact Factor

v-Src accelerates spontaneous motility via phosphoinositide 3-kinase, phospholipase C and phospholipase D, but abrogates chemotaxis in Rat-1 and MDCK cells.

J Cell Sci 2004 Sep 31;117(Pt 20):4849-61. Epub 2004 Aug 31.

CELL Unit, Christian de Duve Institute of Cellular Pathology, Université catholique de Louvain, UCL 75.41, Avenue Hippocrate, 75, 1200 Bruxelles, Belgium.

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http://dx.doi.org/10.1242/jcs.01359DOI Listing
September 2004
8 Reads
7 Citations
5.432 Impact Factor

Origin, originality, functions, subversions and molecular signalling of macropinocytosis.

Int J Med Microbiol 2002 Feb;291(6-7):487-94

Cell biology Unit, UCL and ICP, Brussels, Belgium.

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February 2002
15 Reads
60 Citations
3.614 Impact Factor