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G David

Research Profile

Anatomy

Chromosomes, Human, Pair 3

Disorders

Chemicals & Drugs

Concepts & Ideas

Genes & Molecular Sequences

Procedures

Chromosome Mapping

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Infants

Physiology

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Publications

TOP 3
Giovanni Stevanin; G David; Alexandra Dürr; Paola Giunti; Ali Benomar; M Abada-Bendib; M S Lee; Yves Agid; Alexis Brice
Multiple origins of the spinocerebellar ataxia 7 (SCA7) mutation revealed by linkage disequilibrium studies with closely flanking markers, including an intragenic polymorphism (G3145TG/A3145TG).
G David; Alexandra Dürr; Giovanni Stevanin; G Cancel; Nacer Abbas; Ali Benomar; Samir Belal; Anne-Sophie Lebre; M Abada-Bendib; Djamel Grid; M Holmberg; Mohamed Yahyaoui; Faycal Hentati; Taïeb Chkili; Yves Agid; Alexis Brice
Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7).
Giovanni Stevanin; Alexandra Dürr; G David; O Didierjean; G Cancel; Sophie Rivaud; Ayman Tourbah; J M Warter; Yves Agid; Alexis Brice
Clinical and molecular features of spinocerebellar ataxia type 6.

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All Publications

1999: Giovanni Stevanin; G David; Alexandra Dürr; Paola Giunti; Ali Benomar; M Abada-Bendib; M S Lee; Yves Agid; Alexis Brice
Multiple origins of the spinocerebellar ataxia 7 (SCA7) mutation revealed by linkage disequilibrium studies with closely flanking markers, including an intragenic polymorphism (G3145TG/A3145TG).
European journal of human genetics : EJHG 1999;7(8):889-96.
1998: G David; Alexandra Dürr; Giovanni Stevanin; G Cancel; Nacer Abbas; Ali Benomar; Samir Belal; Anne-Sophie Lebre; M Abada-Bendib; Djamel Grid; M Holmberg; Mohamed Yahyaoui; Faycal Hentati; Taïeb Chkili; Yves Agid; Alexis Brice
Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7).
Human molecular genetics 1998;7(2):165-70.
1997: Giovanni Stevanin; Alexandra Dürr; G David; O Didierjean; G Cancel; Sophie Rivaud; Ayman Tourbah; J M Warter; Yves Agid; Alexis Brice
Clinical and molecular features of spinocerebellar ataxia type 6.
Neurology 1997;49(5):1243-6.
1997: G David; Nacer Abbas; Giovanni Stevanin; Alexandra Dürr; Gaël Yvert; G Cancel; C Weber; G Imbert; Frédéric Saudou; E Antoniou; Harry A Drabkin; Robert M Gemmill; Paola Giunti; Ali Benomar; Nicholas W Wood; Merle Ruberg; Yves Agid; Jean-Louis Mandel; Alexis Brice
Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion.
Nature genetics 1997;17(1):65-70.
1996: Giovanni Stevanin; Yvon Trottier; G Cancel; Alexandra Dürr; G David; O Didierjean; Katrin Bürk; G Imbert; Frédéric Saudou; M Abada-Bendib; Isabelle Gourfinkel-An; Ali Benomar; Nacer Abbas; Thomas Klockgether; Djamel Grid; Yves Agid; Jean-Louis Mandel; Alexis Brice
Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxias.
Human molecular genetics 1996;5(12):1887-92.
1996: G David; Paola Giunti; Nacer Abbas; Philippe Coullin; Giovanni Stevanin; W Horta; Robert M Gemmill; Jean Weissenbach; Nicholas W Wood; S Cunha; Harry A Drabkin; A E Harding; Yves Agid; Alexis Brice
The gene for autosomal dominant cerebellar ataxia type II is located in a 5-cM region in 3p12-p13: genetic and physical mapping of the SCA7 locus.
American journal of human genetics 1996;59(6):1328-36.
1996: Kerstin Lindblad; M L Savontaus; Giovanni Stevanin; M Holmberg; Kathleen B Digre; Cecilia Zander; H Ehrsson; G David; Ali Benomar; E Nikoskelainen; Yvon Trottier; G Holmgren; L J Ptacek; A Anttinen; Alexis Brice; Martin Schalling
An expanded CAG repeat sequence in spinocerebellar ataxia type 7.
Genome research 1996;6(10):965-71.
1995: Yvon Trottier; Yves Lutz; Giovanni Stevanin; G Imbert; Didier Devys; G Cancel; Frédéric Saudou; C Weber; G David; Làszlò Tora
Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias.
Nature 1995;378(6555):403-6.
1995: Ali Benomar; Luc Krols; Giovanni Stevanin; G Cancel; Eric LeGuern; G David; H Ouhabi; Jean-Jacques Martin; Alexandra Dürr; A Zaim
The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12-p21.1.
Nature genetics 1995;10(1):84-8.