N. Gérard

发表

Mutation frequencies of the cytochrome CYP2D6 gene in Parkinson disease patients and in families.

S. Panserat, R. Krishnamoorthy, G. Lucotte, 1996, American journal of medical genetics.

Allele and genotype frequency of CYP2C9 in Tamilnadu population

C. Adithan, R. Krishnamoorthy, N. Gérard, 2003, European Journal of Clinical Pharmacology.

Allele and genotype frequency of CYP2C19 in a Tamilian population.

C. Adithan, J. Rosemary, R. Krishnamoorthy, 2003, British journal of clinical pharmacology.

Glutathione S-transferase M1 and T1 null genotype distribution in South Indians

C. Adithan, R. Krishnamoorthy, N. Padmaja, 2004, European Journal of Clinical Pharmacology.

North African Berber and Arab Influences in the Western Mediterranean Revealed by Y-Chromosome DNA Haplotypes

G. Lucotte, F. Diéterlen, N. Gérard, 2006, Human biology.

CYP2D6 polymorphism in a Gabonese population: contribution of the CYP2D6*2 and CYP2D6*17 alleles to the high prevalence of the intermediate metabolic phenotype.

S. Panserat, R. Krishnamoorthy, É. Jacqz-Aigrain, 1999, British journal of clinical pharmacology.

Localization of the gene for fibrodysplasia ossificans progressiva (FOP) to chromosome 17q21-22.

G. Lenoir, K. Fontaine, G. Lucotte, 2000, Genetic counseling.

Molecular Spectrum of β-Thalassemia Mutations in the admixed Venezuelan population, and their linkage to β-Globin Gene Haplotypes

T. Berbar, R. Krishnamoorthy, O. García, 2012, Hemoglobin.

Spectrum of β thalassemia mutations and their linkage to β‐globin gene haplotypes in the Indo‐Mauritians

R. Nagel, R. Ducrocq, N. Kotea, 2000 .

A Novel Deletional β-Thalassemic Variant in an Ethnic Qatari Patient

A. Pathare, R. Krishnamoorthy, S. Pravin, 2009, Hemoglobin.

Molecular Basis of Thalassemia in Qatar

R. Krishnamoorthy, Mowafak M Hamodat, N. Gérard, 2007, Hemoglobin.

Haplotypes of the Y chromosome in some populations of west Africa

G. Lucotte, N. Gérard, 2002 .

Roles of Gender, Age at Onset and Environmental Risk in the Frequency of CYP2D6-Deficient Alleles in Patients with Parkinson’s Disease

S. Panserat, G. Lucotte, N. Gérard, 2002, European Neurology.

Implications of the Genetic Epidemiology of Globin Haplotypes Linked to the Sickle Cell Gene in Southern Iran

Z. Rahimi, R. Nagel, R. Krishnamoorthy, 2006, Human biology.

Molecular Basis of α-Thalassemia in Bahrain

S. Al-Arrayed, N. Gérard, Nagel Rl, 2001 .

THALASSEMIC MUTATIONS IN SOUTHERN IRAN

Z. Rahimi, R. Nagel, R. Krishnamoorthy, 2006 .

A pharmacological study on pegylated asparaginase used in front-line treatment of children with acute lymphoblastic leukemia

M. Zago, A. Savoia, J. Elion, 1998 .

A mismatched-primer polymerase chain reaction-restriction fragment length polymorphism strategy for rapid screening of the polyadenylation signal mutation alpha(T-Saudi) (AATAAA-->AATAAG) in the alpha2-globin gene.

R. Krishnamoorthy, N Jassim, S Al-Arrayed, 1999, Hemoglobin.

Hb H Disease Among Tunisians: Molecular Characterization of α‐Thalassemia Determinants and Hematological Findings

S. Abbès, F. Guémira, S. Omar, 2003, Hemoglobin.

A NOVEL β-THALASSEMIA MUTATION IN AN ASIAN INDIAN

M. Chandy, A. Srivastava, R. Krishnamoorthy, 2002 .

A novel C→A transversion within the distal CCAAT motif of the Gγ-globin gene in the algerian Gγβ+-hereditary persistence of fetal hemoglobin

T. Merghoub, S. Zertal-Zidani, D. Satta, 1999 .

Contribution to the Description of the β‐Thalassemia Spectrum in Tunisia and the Origin of Mutation Diversity

K. Dellagi, S. Abbès, M. Bejaoui, 2004, Hemoglobin.

-Globin Gene Cluster Haplotypes in Iranian Patients with - Thalassemia

Z. Rahimi, R. Nagel, M. Haghshenass, 2005 .

Worldwide distribution of NAT2 diversity: Implications for NAT2 evolutionary history

A. Langaney, A. Sabbagh, P. Darlu, 2008, BMC Genetics.

A New High A2‐β‐Thalassemia Due to a 468 bp Deletion (− 475 to − 8) in the β‐Globin Gene Promoter of the Intact β‐Globin Structural Gene

J. Elion, R. Ducrocq, R. Krishnamoorthy, 2004 .

A novel C-->A transversion within the distal CCAAT motif of the Ggamma-globin gene in the Algerian Ggammabeta+-hereditary persistence of fetal hemoglobin.

T. Merghoub, S. Zertal-Zidani, D. Satta, 1999, Hemoglobin.

Allele doses of apolipoprotein E type epsilon 4 in sporadic late-onset Alzheimer's disease.

P. Landais, G. Lucotte, J. Turpin, 1995, American journal of medical genetics.

Genotype and allele frequency of CYP2D6 in Tamilian population

C. Adithan, K. Koumaravelou, R. Krishnamoorthy, 2003, European Journal of Clinical Pharmacology.

A Novel α‐Thalassemia Nonsense Mutation in Codon 23 of the α2‐Globin Gene (GAG→TAG) in a Tunisian Family

R. Krishnamoorthy, H. Siala, T. Messaoud, 2004 .

The effect of the CYP2C19 genotype on the hydroxylation index of omeprazole in South Indians

C. Adithan, J. Rosemary, R. Krishnamoorthy, 2005, European Journal of Clinical Pharmacology.

DNA haplotype-dependent differences in the amino acid sequence of debrisoquine 4-hydroxylase (CYP2D6): evidence for two major allozymes in extensive metabolisers

M. Galteau, S. Panserat, R. Krishnamoorthy, 1994, Human Genetics.

Molecular heterogeneity of the XbaI defined 44kb allele of the CYP2D locus within the Caucasian population.

M. Galteau, É. Jacqz-Aigrain, C. Mura, 1993, British journal of clinical pharmacology.

CYP2D6 genetic polymorphism in South Indian populations.

C. Adithan, R. Krishnamoorthy, S. Soya, 2006, Biological & pharmaceutical bulletin.

An unequal cross-over event within the CYP2D gene cluster generates a chimeric CYP2D7/CYP2D6 gene which is associated with the poor metabolizer phenotype.

M M Galteau, M. Galteau, S. Panserat, 1995, British journal of clinical pharmacology.

High frequency of the apolipoprotein E *4 allele in African pygmies and most of the African populations in sub-Saharan Africa.

G. Lucotte, J. Lagarde, A. Raisonnier, 1997, Human biology.

CYP2C9 and CYP2C19 genetic polymorphisms: frequencies in the south Indian population

A. Chandrasekaran, A. Peter, S. Sam, 2005, Fundamental & clinical pharmacology.

North African Genes in Iberia Studied by Y-Chromosome DNA Haplotype 5

G. Lucotte, N. Gérard, G. Mercier, 2001, Human biology.

Relationships of the 2642 deletion polymorphism (delta 2642) in the huntingtin gene with the CAG repeat expansion length and age at onset of the disease.

P. Roubertoux, I. Schmitt, G. Lucotte, 1996, Genetic counseling.

Trinucleotide repeat elongation in the huntingtin gene in Huntington's disease patients from 85 French families. The French HD Research Group.

O. Loreille, G. Lucotte, J. Turpin, 1994, Genetic counseling.