FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Azzedine Aboura

Research Profile

Procedures

Physiology

Disorders

Anatomy

Living Beings

Occupations

Cytogenetics

Co-author Network

Publications

TOP 3
Fabien Guimiot; S Khung-Savatovsky; I Tillous-Borde; Azzedine Aboura; A Bazin; Anne-Lise Delezoide; Céline Dupont; A Fuentes-Duarte; Annabelle Azancot
Maternal transmission of interstitial 8p23.1 deletion detected during prenatal diagnosis.
Francesca R Grati; Fabien Guimiot; Laurence Loeuillet; Federico Maggi; Francesca Malvestiti; Livia Marcato; Anna Maria Ruggeri; Giuseppe Simoni; Howard R Slater; AC Tabet; Azzedine Aboura; Eleonore Blondeel; Simona De Toffol; Celine Dupont; Devika Ganesamoorthy; Denise Molina Gomes; Robert Wainer; François Vialard
Application of a new molecular technique for the genetic evaluation of products of conception.
Andrée Delahaye; Anne-Lise Delezoide; Séverine Drunat; Jacques Elion; Marion Gérard; Pierre Gressens; Romain Guilherme; Fabien Guimiot; Chan Huel; Suonavy Khung-Savatovsky; Azzedine Aboura; Jean-Luc Alessandri; Brigitte Benzacken; Pierre Bitoun; Julien Boumendil; Stéphanie Robin; Stéphane Serero; Alain Verloes; Eva Pipiras
Pre- and postnatal phenotype of 6p25 deletions involving the FOXC1 gene.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Azzedine Aboura (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2013: Fabien Guimiot; S Khung-Savatovsky; I Tillous-Borde; Azzedine Aboura; A Bazin; Anne-Lise Delezoide; Céline Dupont; A Fuentes-Duarte; Annabelle Azancot
Maternal transmission of interstitial 8p23.1 deletion detected during prenatal diagnosis.
American journal of medical genetics. Part A 2013;161A(1):208-13.
2013: Francesca R Grati; Fabien Guimiot; Laurence Loeuillet; Federico Maggi; Francesca Malvestiti; Livia Marcato; Anna Maria Ruggeri; Giuseppe Simoni; Howard R Slater; AC Tabet; Azzedine Aboura; Eleonore Blondeel; Simona De Toffol; Celine Dupont; Devika Ganesamoorthy; Denise Molina Gomes; Robert Wainer; François Vialard
Application of a new molecular technique for the genetic evaluation of products of conception.
Prenatal diagnosis 2013;33(1):32-41.
2012: Andrée Delahaye; Anne-Lise Delezoide; Séverine Drunat; Jacques Elion; Marion Gérard; Pierre Gressens; Romain Guilherme; Fabien Guimiot; Chan Huel; Suonavy Khung-Savatovsky; Azzedine Aboura; Jean-Luc Alessandri; Brigitte Benzacken; Pierre Bitoun; Julien Boumendil; Stéphanie Robin; Stéphane Serero; Alain Verloes; Eva Pipiras
Pre- and postnatal phenotype of 6p25 deletions involving the FOXC1 gene.
American journal of medical genetics. Part A 2012;158A(10):2430-8.
2012: Jérôme Rambaud; AC Tabet; Alain Verloes; Isabelle Marey; Laurence Perrin-Sabourin; Azzedine Aboura; Brigitte Benzacken; Yline Capri; Céline Dupont; Marion Gérard
Nail and phalangeal agenesis in a patient with 4pter and 9pter duplication.
American journal of medical genetics. Part A 2012;158A(9):2277-82.
2012: Emmanuel Spaggiari; Philippe Mabboux; Martine Sinico; Azzedine Aboura; Anne-Lise Delezoide; Céline Dupont; Fabien Guimiot
Prenatal diagnosis of a 7p15-p21 deletion encompassing the TWIST1 gene involved in Saethre-Chotzen syndrome.
European journal of medical genetics 2012;55(8-9):498-501.
2012: Céline Dupont; Azzedine Aboura; C Baumann; Brigitte Benzacken; P Bourdoncle; Fabien Guimiot; Dominique Le Tessier; C Lebugle; I Marey; L Perrin; D Smiljkovski; AC Tabet; Jean-Michel Dupont
3D position of pericentromeric heterochromatin within the nucleus of a patient with ICF syndrome.
Clinical genetics 2012;82(2):187-92.
2012: Marie Devernay; Emmanuel Ecosse; Bénédicte Gérard; Lamia Kerdjana; AC Tabet; Azzedine Aboura; Brigitte Benzacken; Diana Bolca; Joël Coste; Jean-Claude Carel
Parental origin of the X-chromosome does not influence growth hormone treatment effect in Turner syndrome.
The Journal of clinical endocrinology and metabolism 2012;97(7):E1241-8.
2012: Andrée Delahaye; Séverine Drunat; Céline Dupont; Jacques Elion; Laurence Faivre; Frédérique Gatelais; Marion Gérard-Blanluet; Pierre Gressens; Sophie Kaltenbach; Marie Legendre; Sandrine Passemard; Eva Pipiras; Samuel Quentin; AC Tabet; Annick Toutain; Alain Verloes; Azzedine Aboura; Serge Amselem; Pierre Bitoun; Nicolas Chassaing; Brigitte Benzacken
Genomic imbalances detected by array-CGH in patients with syndromal ocular developmental anomalies.
European journal of human genetics : EJHG 2012;20(5):527-33.
2012: Véronique Haddad; Aurore Coulomb L'Herminé; Anne-Elisabeth Mas; Olivier Picone; Azzedine Aboura; Sophie Brisset; Luc Druart; Narjes Guediche; Lucie Tosca; Gérard Tachdjian
Tetrasomy 13q31.1qter due to an inverted duplicated neocentric marker chromosome in a fetus with multiple malformations.
American journal of medical genetics. Part A 2012;158A(4):894-900.
2010: Manuel Schiff; Andrée Delahaye; Joris Andrieux; Damien Sanlaville; Catherine Vincent-Delorme; Azzedine Aboura; Brigitte Benzacken; Sonia Bouquillon; Monique Elmaleh-Berges; Audrey Labalme; Sandrine Passemard; Laurence Perrin; Sylvie MANOUVRIER; Patrick Edery; Alain Verloes; Séverine Drunat
Further delineation of the 17p13.3 microdeletion involving YWHAE but distal to PAFAH1B1: four additional patients.
European journal of medical genetics 2010;53(5):303-8.
2010: Anne-Claude Tabet; Azzedine Aboura; Marion Gérard; Marion Pilorge; Céline Dupont; Jean-François Gadisseux; Nadège Hervy; Eva Pipiras; Andrée Delahaye; Samia Kanafani; Alain Verloes; Brigitte Benzacken; Catalina Betancur
Molecular characterization of a de novo 6q24.2q25.3 duplication interrupting UTRN in a patient with arthrogryposis.
American journal of medical genetics. Part A 2010;152A(7):1781-8.
2010: Sylvie Jaillard; Séverine Drunat; Claude Bendavid; Azzedine Aboura; Amandine Etcheverry; Hubert Journel; Andrée Delahaye; Laurent Pasquier; Dominique Bonneau; Annick Toutain; Lydie Burglen; Agnès Guichet; Eva Pipiras; Brigitte Gilbert-Dussardier; Brigitte Benzacken; Dominique Martin-Coignard; Catherine Henry; Albert David; Josette Lucas; Jean Mosser; Véronique David; Sylvie Odent; Alain Verloes; Christèle Dubourg
Identification of gene copy number variations in patients with mental retardation using array-CGH: Novel syndromes in a large French series.
European journal of medical genetics 2010;53(2):66-75.
2010: Laila Rifai; Marylin Port-Lis; Anne-Claude Tabet; Isabelle Bailleul-Forestier; Brigitte Benzacken; Séverine Drunat; Suzanne Kuzbari; Sandrine Passemard; Alain Verloes; Azzedine Aboura
Ectodermal dysplasia-like syndrome with mental retardation due to contiguous gene deletion: further clinical and molecular delineation of del(2q32) syndrome.
American journal of medical genetics. Part A 2010;152A(1):111-7.
2009: Romain Guilherme; Fabien Guimiot; Anne-Claude Tabet; Suonavy Khung-Savatovsky; Evelyne Gauthier; Marc Nouchy; Brigitte Benzacken; Alain Verloes; Jean-François Oury; Anne-Lise Delezoide; Azzedine Aboura
Abnormal muscle development of the diaphragm in a fetus with 2p14-p16 duplication.
American journal of medical genetics. Part A 2009;149A(12):2892-7.
2009: Azzedine Aboura; Claire Dupas; Gérard Tachdjian; Marie-France Portnoï; Nathalie Bourcigaux; Didier Dewailly; René Frydman; Bart Fauser; Nathalie Ronci-Chaix; Bruno Donadille; Philippe Bouchard; Sophie Christin-Maitre
Array comparative genomic hybridization profiling analysis reveals deoxyribonucleic acid copy number variations associated with premature ovarian failure.
The Journal of clinical endocrinology and metabolism 2009;94(11):4540-6.
2009: Fabien Guimiot; Pascale Marcorelles; Azzedine Aboura; Georges Bonyhay; Sophie Patrier; Françoise Menez; Valérie Drouin-Garraud; Valentine Icowick; Danièle Eurin; Catherine Garel; Hélène Moirot; Eric Verspyck; Pascale Saugier-Veber; Tania Attie-Bitach; Olivier Picone; Jean François Oury; Alain Verloes; Anne-Lise Delezoide; Annie Laquerrière
Giant diencephalic harmartoma and related anomalies: a newly recognized entity distinct from the Pallister-Hall syndrome.
American journal of medical genetics. Part A 2009;149A(6):1108-15.
2008: Celine Dupont; Andree Delahaye; Lydie Burglen; Anne-Claude Tabet; Azzedine Aboura; Samia Kanafani; Françoise Baverel; Thierry Billette de Villemeur; Brigitte Benzacken; Eva Pipiras
First cryptic balanced reciprocal translocation mosaicism and familial transmission.
American journal of medical genetics. Part A 2008;146A(22):2971-4.
2008: Valérie Bélien; Marion Gérard-Blanluet; Stéphane Serero; Nathalie Le Dû; Clarisse Baumann; Marie-Line Jacquemont; Céline Dupont; Kada Krabchi; Séverine Drunat; Annie Elbez; Jean-Claude Janaud; Brigitte Benzacken; Alain Verloes; Anne-Claude Tabet; Azzedine Aboura
Partial trisomy of chromosome 22 resulting from a supernumerary marker chromosome 22 in a child with features of cat eye syndrome.
American journal of medical genetics. Part A 2008;146A(14):1871-4.
2008: Gérard Tachdjian; Azzedine Aboura; Marie-France Portnoï; Maud Pasquier; Nathalie Bourcigaux; Tabassome Simon; Ghislaine Rousseau; Lina Finkel; Moncef Benkhalifa; Sophie Christin-Maitre
Cryptic Xp duplication including the SHOX gene in a woman with 46,X, del(X)(q21.31) and premature ovarian failure.
Human reproduction (Oxford, England) 2008;23(1):222-6.
2007: P Mabboux; Sophie Brisset; Azzedine Aboura; D Pineau; V Koubi; S Joannidis; Philippe Labrune; Gérard Tachdjian
Pure and complete trisomy 18p due to a supernumerary marker chromosome associated with moderate mental retardation.
American journal of medical genetics. Part A 2007;143(7):727-33.
2007: S Kanafani; Azzedine Aboura; Eva Pipiras; Lionel Carbillon; AC Tabet; C Largillière; C Garel; P Gressens; Martine Bucourt; Isabelle Cedrin-Durnerin; Eric Lachassinne; C Roumegoux; Michèle Uzan; Jean-Noel Hugues; Jean-Philippe Wolf; Brigitte Benzacken
Semilobar holoprosencephaly prenatal diagnosis: an unexpected complex rearrangement in a de novo apparently balanced reciprocal translocation on karyotype.
Prenatal diagnosis 2007;27(3):279-84.
2006: M-L Maurin; Sophie Brisset; Marc Le Lorc'h; V Poncet; Pascale Trioche; Azzedine Aboura; Philippe Labrune; Gérard Tachdjian
Terminal 14q32.33 deletion: genotype-phenotype correlation.
American journal of medical genetics. Part A 2006;140(21):2324-9.
2006: Marie-France Portnoï; Azzedine Aboura; Gérard Tachdjian; Philippe Bouchard; Didier Dewailly; Nathalie Bourcigaux; René Frydman; Anne-Céline Reyss; Sophie Brisset; Sophie Christin-Maitre
Molecular cytogenetic studies of Xq critical regions in premature ovarian failure patients.
Human reproduction (Oxford, England) 2006;21(9):2329-34.
2006: Luigi Titomanlio; Irina Giurgea; Clarisse Baumann; Monique Elmaleh; Philippe Sachs; François Chalard; Azzedine Aboura; Alain Verloes
A locus for sacral/anorectal malformations maps to 6q25.3 in a 0.3 Mb interval region.
European journal of human genetics : EJHG 2006;14(8):971-4.
2006: Gérard Tachdjian; Azzedine Aboura; Sophie Brisset; Marc Dommergues; Vincent Gajdos; Philippe Labrune
Early and rapid prenatal diagnosis of monosomy 2q36.1 in trophoblast cells.
Fetal diagnosis and therapy 2006;21(5):428-32.
2005: E Gonzales; L Caeymaex; Azzedine Aboura; M Vial; Jocelyne De Laveaucoupet; Philippe Labrune; Gérard Tachdjian
[Cocaine and trisomy 8 associated with prenatal diagnosis of corpus callosum agenesis].
Journal de gynécologie, obstétrique et biologie de la reproduction 2005;34(8):803-6.
2005: Franck Viguié; Azzedine Aboura; Didier Bouscary; Sylvie Ramond; Alain Delmer; Gérard Tachdjian; Jean-Pierre Marie; Nicole Casadevall
Common 4q24 deletion in four cases of hematopoietic malignancy: early stem cell involvement?
Leukemia 2005;19(8):1411-5.
2005: Sophie Brisset; Vincent Izard; M Misrahi; Azzedine Aboura; S Madoux; Sophie Ferlicot; D Schoevaert; Jean-Claude Soufir; René Frydman; Gérard Tachdjian
Cytogenetic, molecular and testicular tissue studies in an infertile 45,X male carrying an unbalanced (Y;22) translocation: case report.
Human reproduction (Oxford, England) 2005;20(8):2168-72.
2005: François M Petit; Frydman Nelly; Moncef Benkhalifa; Anne Le Du; Azzedine Aboura; Renato Fanchin; René Frydman; Gérard Tachdjian
Could sperm aneuploidy rate determination be used as a predictive test before intracytoplasmic sperm injection?
Journal of andrology 2005;26(2):235-41.
2005: François M Petit; Vincent Gajdos; Frédéric Parisot; Liliane Capel; Azzedine Aboura; Alain Lachaux; Gérard Tachdjian; Christian Pous; Philippe Labrune
Paternal isodisomy for chromosome 2 as the cause of Crigler-Najjar type I syndrome.
European journal of human genetics : EJHG 2005;13(3):278-82.
2004: Gérard Tachdjian; Azzedine Aboura; Moncef Benkhalifa; Isabelle Creveaux; L Foix-Hélias; J F Gadisseux; Odile Boespflug-Tanguy; M Mohammed; Philippe Labrune
De novo interstitial direct duplication of Xq21.1q25 associated with skewed X-inactivation pattern.
American journal of medical genetics. Part A 2004;131(3):273-80.
2004: Aurore L'herminé-Coulomb; LUCILE HOUYEL; Azzedine Aboura; François Audibert; Dorothée Dal Soglio; Gérard Tachdjian
Double-outlet right ventricle with absent left ventricle and mitral atresia in a fetus with a deletion 22q12.
Prenatal diagnosis 2004;24(9):708-12.
2003: Aurore Coulomb L'Herminé; Azzedine Aboura; Sophie Brisset; L Cuisset; V Castaigne; Philippe Labrune; René Frydman; Gérard Tachdjian
Fetal phenotype of Prader-Willi syndrome due to maternal disomy for chromosome 15.
Prenatal diagnosis 2003;23(11):938-43.
2003: Sophie Brisset; Azzedine Aboura; François Audibert; Jean-Marc Costa; Aurore Coulomb L'Herminé; Valérie Gautier; René Frydman; Gérard Tachdjian
Discordant prenatal diagnosis of trisomy 21 due to mosaic structural rearrangements of chromosome 21.
Prenatal diagnosis 2003;23(6):461-9.
2003: Azzedine Aboura; Philippe Labrune; Francis Perreaux; V Poncet; Sophie Brisset; L Foix-L'Helias; Gérard Tachdjian
Deletion in the ABL gene resulting from a meiotic recombination of a maternal (3;22;9)(q22;q12;q34.1) translocation.
Journal of medical genetics 2003;40(1):e6.
2002: Franck Viguié; Azzedine Aboura; Didier Bouscary; Martine Guesnu; Elisabeth Baumelou; François Dreyfus; Nicole Casadevall; Gérard Tachdjian
Isodicentric/pseudoisodicentric chromosome 21 amplification in four cases of acute myelocytic leukemia or myelodysplasia.
Cancer genetics and cytogenetics 2002;138(1):80-4.
2002: Aurore Coulomb L'Herminé; Azzedine Aboura; B Simon-Bouy; F Robin; François Audibert; N Strouk; F Capron; René Frydman; Gérard Tachdjian
Female pseudohermaphroditism in a fetus with a deletion 9(q22.2q31.1).
Prenatal diagnosis 2002;22(8):652-5.
2002: Azzedine Aboura; A Coulomb-L'Herminé; François Audibert; F Capron; R Frydman; Gérard Tachdjian
De novo interstitial direct duplication 1(q23.1q31.1) in a fetus with Pierre Robin sequence and camptodactyly.
American journal of medical genetics 2002;108(2):153-9.
2002: Gérard Tachdjian; Francis Perreaux; Azzedine Aboura; P Chevalier; M-F Portnoi; B Esteva; Pascale Trioche; Philippe Labrune
Molecular cytogenetic analysis of a Xp21.3-pter deletion in a family with normal and short stature.
Clinical genetics 2002;61(2):163-5.
2001: AC Tabet; Azzedine Aboura; M C Dauge; François Audibert; Aurore Coulomb; A Batallan; M H Couturier-Turpin; G Feldmann; Gérard Tachdjian
Cytogenetic analysis of trophoblasts by comparative genomic hybridization in embryo-fetal development anomalies.
Prenatal diagnosis 2001;21(8):613-8.
2000: Gérard Tachdjian; Azzedine Aboura; Jean-Michel Lapierre; Franck Viguié
Cytogenetic analysis from DNA by comparative genomic hybridization.
Annales de génétique 2000;43(3-4):147-54.
2000: Franck Viguié; Azzedine Aboura; Sylvie Ramond; Didier Bouscary; M Baudard; C Chomienne; Jean-Pierre Marie
Submicroscopic insertion of RARalpha gene into chromosome 15 in two cases of acute promyelocytic leukemia.
Cancer genetics and cytogenetics 2000;119(2):162-4.