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Items: 1 to 50 of 226

1.

Bioinformatics for precision medicine in oncology: principles and application to the SHIVA clinical trial.

Servant N, Roméjon J, Gestraud P, La Rosa P, Lucotte G, Lair S, Bernard V, Zeitouni B, Coffin F, Jules-Clément G, Yvon F, Lermine A, Poullet P, Liva S, Pook S, Popova T, Barette C, Prud'homme F, Dick JG, Kamal M, Le Tourneau C, Barillot E, Hupé P.

Front Genet. 2014 May 30;5:152. doi: 10.3389/fgene.2014.00152. eCollection 2014. Review.

2.

Near fixation of 374l allele frequencies of the skin pigmentation gene SLC45A2 in Africa.

Lucotte G, Yuasa I.

Biochem Genet. 2013 Oct;51(9-10):655-65. doi: 10.1007/s10528-013-9595-8. Epub 2013 May 10.

PMID:
23660638
3.

The relationship between vascular endothelial growth factor -2578C/A polymorphism and age-related macular degeneration.

Lucotte G, Change N.

Ophthalmic Genet. 2013 Mar-Jun;34(1-2):112-4. doi: 10.3109/13816810.2012.707272. Epub 2012 Aug 20. No abstract available.

PMID:
22906062
4.

Screening for the M694V mutation of the familial Mediterranean fever (FMF) gene in 604 French patients.

Bathelier C, Lenoir G, Lucotte G.

Genet Couns. 2010;21(4):461-6. No abstract available.

PMID:
21290976
5.

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

Lucotte G.

Investig Genet. 2010 Oct 4;1(1):7. doi: 10.1186/2041-2223-1-7.

6.

A decreasing gradient of 374F allele frequencies in the skin pigmentation gene SLC45A2, from the north of West Europe to North Africa.

Lucotte G, Mercier G, Diéterlen F, Yuasa I.

Biochem Genet. 2010 Feb;48(1-2):26-33. doi: 10.1007/s10528-009-9289-4.

PMID:
19916045
8.

Molecular basis of complement factor I (CFI) polymorphism: one of two polymorphic suballeles responsible for CFI A is Japanese-specific.

Yuasa I, Nakagawa M, Umetsu K, Harihara S, Matsusue A, Nishimukai H, Fukumori Y, Saitou N, Park KS, Jin F, Lucotte G, Chattopadhyay PK, Henke L, Henke J.

J Hum Genet. 2008;53(11-12):1016-21. doi: 10.1007/s10038-008-0337-4. Epub 2008 Sep 30.

PMID:
18825487
9.
10.

Genetic screening of the G2019S mutation of the LRRK2 gene in Southwest European, North African, and Sephardic Jewish subjects.

Change N, Mercier G, Lucotte G.

Genet Test. 2008 Sep;12(3):333-9. doi: 10.1089/gte.2007.0098.

PMID:
18666856
11.

Mutations of the noggin and of the activin A type I receptor genes in fibrodysplasia ossificans progressiva (FOP).

Lucotte G, Lagarde JP; FOP European Research Group.

Genet Couns. 2007;18(3):349-52. No abstract available.

PMID:
18019378
12.

Distribution of two Asian-related coding SNPs in the MC1R and OCA2 genes.

Yuasa I, Umetsu K, Harihara S, Kido A, Miyoshi A, Saitou N, Dashnyam B, Jin F, Lucotte G, Chattopadhyay PK, Henke L, Henke J.

Biochem Genet. 2007 Aug;45(7-8):535-42. Epub 2007 Jun 15.

PMID:
17570052
13.

OCA2 481Thr, a hypofunctional allele in pigmentation, is characteristic of northeastern Asian populations.

Yuasa I, Umetsu K, Harihara S, Miyoshi A, Saitou N, Park KS, Dashnyam B, Jin F, Lucotte G, Chattopadhyay PK, Henke L, Henke J.

J Hum Genet. 2007;52(8):690-3. Epub 2007 Jun 14.

PMID:
17568986
14.

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

Lucotte G.

Int J Pediatr Otorhinolaryngol. 2007 May;71(5):741-6. Epub 2007 Feb 20.

PMID:
17316834
15.

Genetic screening for two LRRK2 mutations in French patients with idiopathic Parkinson's disease.

Funalot B, Nichols WC, Pérez-Tur J, Mercier G, Lucotte G.

Genet Test. 2006 Winter;10(4):290-3.

PMID:
17253937
16.

North African Berber and Arab influences in the western Mediterranean revealed by Y-chromosome DNA haplotypes.

Gérard N, Berriche S, Aouizérate A, Diéterlen F, Lucotte G.

Hum Biol. 2006 Jun;78(3):307-16.

PMID:
17216803
17.

Distribution of the F374 allele of the SLC45A2 (MATP) gene and founder-haplotype analysis.

Yuasa I, Umetsu K, Harihara S, Kido A, Miyoshi A, Saitou N, Dashnyam B, Jin F, Lucotte G, Chattopadhyay PK, Henke L, Henke J.

Ann Hum Genet. 2006 Nov;70(Pt 6):802-11.

18.

A functional variant of the dopamine D3 receptor is associated with risk and age-at-onset of essential tremor.

Jeanneteau F, Funalot B, Jankovic J, Deng H, Lagarde JP, Lucotte G, Sokoloff P.

Proc Natl Acad Sci U S A. 2006 Jul 11;103(28):10753-8. Epub 2006 Jun 29.

19.

Linkage with the Ser9Gly DRD3 polymorphism in essential tremor families.

Lucotte G, Lagarde JP, Funalot B, Sokoloff P.

Clin Genet. 2006 May;69(5):437-40. No abstract available.

PMID:
16650084
20.

A new mutation of the noggin gene in a French Fibrodysplasia ossificans progressiva (FOP) family.

Fontaine K, Sémonin O, Legarde JP, Lenoir G, Lucotte G.

Genet Couns. 2005;16(2):149-54.

PMID:
16080294
21.

Haplotype XV of the Y-chromosome is the main haplotype in West-Europe.

Diéterlen F, Lucotte G.

Biomed Pharmacother. 2005 Jun;59(5):269-72.

PMID:
15890489
22.

Connexin 26 mutation 35delG: prevalence of carriers in various regions in France.

Mercier G, Bathelier C, Lucotte G.

Int J Pediatr Otorhinolaryngol. 2005 Sep;69(9):1187-90.

PMID:
15878206
25.

Neonatal detection of the 35delG mutation of the GJB2 gene in families at risk for deafness.

Bathelier C, François M, Lucotte G.

Genet Couns. 2004;15(1):61-6.

PMID:
15083701
26.

Interaction between GSTM1-null and CYP2D6-deficient alleles in the pathogenesis of Parkinson's disease.

Santt O, Baranova H, Albuisson E, Bignon YJ, Lucotte G.

Eur J Neurol. 2004 Apr;11(4):247-51.

PMID:
15061826
27.

CCR5-Delta32 allele frequencies in Ashkenazi Jews.

Lucotte G, Smets P.

Genet Test. 2003 Winter;7(4):333-7.

PMID:
15000812
28.

Elevated frequencies of the 35delG allele of the connexin 26 gene in Corsica, France.

Lucotte G, Pinna A.

Clin Genet. 2003 Dec;64(6):517-8. No abstract available.

PMID:
14986832
29.

The endogenous retroviral locus ERVWE1 is a bona fide gene involved in hominoid placental physiology.

Mallet F, Bouton O, Prudhomme S, Cheynet V, Oriol G, Bonnaud B, Lucotte G, Duret L, Mandrand B.

Proc Natl Acad Sci U S A. 2004 Feb 10;101(6):1731-6. Epub 2004 Feb 2.

30.
31.

Duplex PCR-RFLP for simultaneous detection of factor V Leiden and prothrombin G20210A.

Lucotte G, Champenois T.

Mol Cell Probes. 2003 Oct;17(5):267-9.

PMID:
14580402
32.

Y-chromosome DNA haplotype XI in Eastern Europe.

Lucotte G, Mercier G, Dieterlen F.

Hum Biol. 2003 Jun;75(3):405-10.

PMID:
14527204
33.

A European allele map of the C282Y mutation of hemochromatosis: Celtic versus Viking origin of the mutation?

Lucotte G, Dieterlen F.

Blood Cells Mol Dis. 2003 Sep-Oct;31(2):262-7.

PMID:
12972035
34.

Molecular basis of the TaqI p49a,f polymorphism in the DYS1 locus containing DAZ genes.

Jovelin F, Berthaud S, Lucotte G.

Mol Hum Reprod. 2003 Sep;9(9):509-16.

PMID:
12900509
35.

Y-chromosome DNA haplotypes in Jews: comparisons with Lebanese and Palestinians.

Lucotte G, Mercier G.

Genet Test. 2003 Spring;7(1):67-71.

PMID:
12820706
37.
38.

Brief communication: Y-chromosome haplotypes in Egypt.

Lucotte G, Mercier G.

Am J Phys Anthropol. 2003 May;121(1):63-6.

PMID:
12687584
39.

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

Gérard N, Panserat S, Lucotte G.

Eur Neurol. 2002;48(2):114-5. No abstract available.

PMID:
12187002
40.

Confirmation of a gene for multiple sclerosis (MS) to chromosome region 19q13.3.

Lucotte GL; French MS Consortium.

Genet Couns. 2002;13(2):133-8.

PMID:
12150212
41.

[Y-chromosome haplotypes in Corsica].

Lucotte G, Pinna A, Mercier G.

C R Biol. 2002 Mar;325(3):191-6. French.

PMID:
12017766
42.

[Neonatal detection of deafness by molecular genetics in maternity hospitals: report of a 1st year concerning families at risk].

Lucotte G, François M.

Arch Pediatr. 2002 Feb;9(2):222-3. French. No abstract available.

PMID:
11915509
43.

A rare case of a patient heterozygous for the hemochromatosis mutation C282Y and homozygous for H63D.

Lucotte G, Champenois T, Sémonin O.

Blood Cells Mol Dis. 2001 Sep-Oct;27(5):892-3.

PMID:
11783952
44.

North African genes in Iberia studied by Y-chromosome DNA haplotype 5.

Lucotte G, Gérard N, Mercier G.

Hum Biol. 2001 Oct;73(5):763-9.

PMID:
11758696
45.

Meta-analysis of GJB2 mutation 35delG frequencies in Europe.

Lucotte G, Mercier G.

Genet Test. 2001 Summer;5(2):149-52.

PMID:
11551104
47.

North African genes in Iberia studied by Y-chromosome DNA haplotype V.

Lucotte G, Gérard N, Mercier G.

Hum Immunol. 2001 Sep;62(9):885-8.

PMID:
11543890
48.

Identification of three novel mutations of the noggin gene in patients with fibrodysplasia ossificans progressiva.

Sémonin O, Fontaine K, Daviaud C, Ayuso C, Lucotte G.

Am J Med Genet. 2001 Sep 1;102(4):314-7.

PMID:
11503156
49.
50.

Presymptomatic testing for autosomal dominant spinocerebellar ataxia type 1 in a French family.

Lucotte G, Sémonin O, Mercier G.

Genet Couns. 2001;12(2):173-5. No abstract available.

PMID:
11491315

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