Publications by authors named "Gerard Lucotte"

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Near fixation of 374l allele frequencies of the skin pigmentation gene SLC45A2 in Africa.
Gérard Lucotte, Isao Yuasa

Biochem Genet· October 2013

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The relationship between vascular endothelial growth factor -2578C/A polymorphism and age-related macular degeneration.
Gérard Lucotte, Nathalie Change

Ophthalmic Genet· August 2013

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A rare variant of the mtDNA HVS1 sequence in the hairs of Napoléon's family.
Gérard Lucotte

Investig Genet· October 2010

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A decreasing gradient of 374F allele frequencies in the skin pigmentation gene SLC45A2, from the north of West Europe to North Africa.
Gérard Lucotte, Géraldine Mercier, Florent Diéterlen, Isao Yuasa

Biochem Genet· February 2010

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Molecular basis of complement factor I (CFI) polymorphism: one of two polymorphic suballeles responsible for CFI A is Japanese-specific.
Isao Yuasa, Mayumi Nakagawa, Kazuo Umetsu, Shinji Harihara, Aya Matsusue, Gérard Lucotte

J Hum Genet· February 2009

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Genetic screening of the G2019S mutation of the LRRK2 gene in Southwest European, North African, and Sephardic Jewish subjects.
Nathalie Change, Géraldine Mercier, Gérard Lucotte

Genet Test· September 2008

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Population distribution of the methionine allele at the PRNP codon 129 polymorphism in Europe and the Middle East.
Géraldine Mercier, Florent Diéterlen, Gérard Lucotte

Hum Biol· April 2008

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OCA2 481Thr, a hypofunctional allele in pigmentation, is characteristic of northeastern Asian populations.
Isao Yuasa, Kazuo Umetsu, Shinji Harihara, Aya Miyoshi, Naruya Saitou, Gérard Lucotte

J Hum Genet· September 2007

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High prevalences of carriers of the 35delG mutation of connexin 26 in the Mediterranean area.
Gérard Lucotte

Int J Pediatr Otorhinolaryngol· May 2007

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Genetic screening for two LRRK2 mutations in French patients with idiopathic Parkinson's disease.
Benoît Funalot, William C Nichols, Jordi Pérez-Tur, Géraldine Mercier, Gérard Lucotte

Genet Test· April 2007

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A functional variant of the dopamine D3 receptor is associated with risk and age-at-onset of essential tremor.
Freddy Jeanneteau, Benoît Funalot, Joseph Jankovic, Hao Deng, Jean-Pierre Lagarde, Gérard Lucotte

Proc Natl Acad Sci U S A· July 2006

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North African Berber and Arab influences in the western Mediterranean revealed by Y-chromosome DNA haplotypes.
Nathalie Gérard, Sala Berriche, Annie Aouizérate, Florent Diéterlen, Gérard Lucotte

Hum Biol· June 2006

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Connexin 26 mutation 35delG: prevalence of carriers in various regions in France.
Géraldine Mercier, Christian Bathelier, Gérard Lucotte

Int J Pediatr Otorhinolaryngol· September 2005

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The 35delG mutation in the connexin 26 gene (GJB2) associated with congenital deafness: European carrier frequencies and evidence for its origin in ancient Greece.
Gérard Lucotte, Florent Diéterlen

Genet Test· July 2005

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Haplotype XV of the Y-chromosome is the main haplotype in West-Europe.
Florent Diéterlen, Gérard Lucotte

Biomed Pharmacother· June 2005

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The population distribution of the Met allele at the PRNP129 polymorphism (a high risk factor for Creutzfeldt-Jakob disease) in various regions of France and in West Europe.
Gérard Lucotte, Géraldine Mercier

Infect Genet Evol· March 2005

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A European allele map of the C282Y mutation of hemochromatosis: Celtic versus Viking origin of the mutation?
Gérard Lucotte, Florent Dieterlen

Blood Cells Mol Dis· May 2004

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The endogenous retroviral locus ERVWE1 is a bona fide gene involved in hominoid placental physiology.
François Mallet, Olivier Bouton, Sarah Prudhomme, Valérie Cheynet, Guy Oriol, Gérard Lucotte

Proc Natl Acad Sci U S A· February 2004

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Y-chromosome DNA haplotypes in Jews: comparisons with Lebanese and Palestinians.
Gérard Lucotte, Géraldine Mercier

Genet Test· November 2003

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More about the Viking hypothesis of origin of the delta32 mutation in the CCR5 gene conferring resistance to HIV-1 infection.
Gérard Lucotte, Florent Dieterlen

Infect Genet Evol· November 2003

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Y-chromosome DNA haplotype XI in Eastern Europe.
Gérard Lucotte, Géraldine Mercier, Florent Dieterlen

Hum Biol· June 2003

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Paternal European ancestry in French Polynesia detected by Y-chromosome haplotypes.
Gérard Lucotte

Hum Biol· February 2003

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Roles of gender, age at onset and environmental risk in the frequency of CYP2D6-deficient alleles in patients with Parkinson's disease.
Nathalie Gérard, Stéphane Panserat, Gérard Lucotte

Eur Neurol· October 2002

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Frequencies of 32 base pair deletion of the (Delta 32) allele of the CCR5 HIV-1 co-receptor gene in Caucasians: a comparative analysis.
Gérard Lucotte

Infect Genet Evol· May 2002

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[Y-chromosome haplotypes in Corsica].
Gérard Lucotte, Antoine Pinna, Géraldine Mercier

C R Biol· March 2002

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