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Françoise Clerget-Darpoux

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Physiology

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Genes & Molecular Sequences

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Procedures

Chromosome Mapping

Chemicals & Drugs

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France

Occupations

Population Genetics

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Publications

TOP 3
Couturier Nicolas; Gourraud Pierre-Antoine; Cournu-Rebeix Isabelle; Gout Claire; Bucciarelli Florence; Edan Gilles; Babron Marie-Claude; Clerget-Darpoux Françoise; Clanet Michel; Fontaine Bertrand; Brassat David
IFIH1-GCA-KCNH7 locus is not associated with genetic susceptibility to multiple sclerosis in French patients.
Perdry Hervé; Babron Marie-Claude; Clerget-Darpoux Françoise
The ordered transmission disequilibrium test: detection of modifier genes.
Génin Emmanuelle; Feingold Josué; Clerget-Darpoux Françoise
Identifying modifier genes of monogenic disease: strategies and difficulties.

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All Publications

2009: Couturier Nicolas; Gourraud Pierre-Antoine; Cournu-Rebeix Isabelle; Gout Claire; Bucciarelli Florence; Edan Gilles; Babron Marie-Claude; Clerget-Darpoux Françoise; Clanet Michel; Fontaine Bertrand; Brassat David
IFIH1-GCA-KCNH7 locus is not associated with genetic susceptibility to multiple sclerosis in French patients.
European journal of human genetics : EJHG 2009;17(6):844-7.
2009: Perdry Hervé; Babron Marie-Claude; Clerget-Darpoux Françoise
The ordered transmission disequilibrium test: detection of modifier genes.
Genetic epidemiology 2009;33(1):1-5.
2008: Génin Emmanuelle; Feingold Josué; Clerget-Darpoux Françoise
Identifying modifier genes of monogenic disease: strategies and difficulties.
Human genetics 2008;124(4):357-68.
2007: Pickrell Joseph; Clerget-Darpoux Françoise; Bourgain Catherine
Power of genome-wide association studies in the presence of interacting loci.
Genetic epidemiology 2007;31(7):748-62.
2007: Bourgey Mathieu; Calcagno Giuseppe; Tinto Nadia; Gennarelli Daniela; Margaritte-Jeannin Patricia; Greco Luigi; Limongelli Maria Giovanna; Esposito Oscar; Marano Caterina; Troncone Riccardo; Spampanato Antonella; Clerget-Darpoux Françoise; Sacchetti Lucia
HLA related genetic risk for coeliac disease.
Gut 2007;56(8):1054-9.
2007: Fontaine B; Sémana G; Clerget-Darpoux F
[What's new in multiple sclerosis genetics?]
Revue neurologique 2007;163(6-7):677-81.
2007: Bourgain Catherine; Génin Emmanuelle; Cox Nancy; Clerget-Darpoux Françoise
Are genome-wide association studies all that we need to dissect the genetic component of complex human diseases?
European journal of human genetics : EJHG 2007;15(3):260-3.
2007: Perdry Hervé; Maher Brion S; Babron Marie-Claude; McHenry Toby; Clerget-Darpoux Françoise; Marazita Mary L
An ordered subset approach to including covariates in the transmission disequilibrium test.
BMC proceedings 2007;1 Suppl 1():S77.
2007: Kotti Salma; Bourgey Mathieu; Clerget-Darpoux Françoise
Power of the 2-locus TDT for testing the interaction of two susceptibility genes.
BMC proceedings 2007;1 Suppl 1():S65.
2007: Bourgey Mathieu; Perdry Hervé; Clerget-Darpoux Françoise
Modeling the effect of PTPN22 in rheumatoid arthritis.
BMC proceedings 2007;1 Suppl 1():S37.
2007: Margaritte-Jeannin Patricia; Babron Marie-Claude; Clerget-Darpoux Françoise
On the choice of linkage statistics.
BMC proceedings 2007;1 Suppl 1():S102.
2007: Bartlett Christopher W; Vieland Veronica J; Bartlett Jacquelaine; Bell Jordana T; Bhattacharjee Samsiddhi; Clerget-Darpoux Françoise; Bush William S; Edwards Todd L; Gao Guimin; Halder Indrani; Huang Yungui; Kotti Salma; Larkin Emma K; Li Hua; Motsinger Alison A; Mukhopadhyay Nandita; Namkung Junghyun; Park Taesung; Ritchie Marylyn D; Stein Catherine M; Zhou Ji-Yuan
Discussing gene-gene interaction: warning--translating equations to English may result in jabberwocky.
Genetic epidemiology 2007;31 Suppl 1():S61-7.
2007: Yang Qiong; Biernacka Joanna M; Chen Ming-Huei; Houwing-Duistermaat Jeanine J; Bergemann Tracy L; Basu Saonli; Fan Ruzong; Liu Lian; Bourgey Mathieu; Clerget-Darpoux Françoise; Lin Wan-Yu; Elston Robert C; Cupples L Adrienne; Apprey Victor; Cui Jing; Dupuis Josée; Ionita-Laza Iuliana; Li Rui; Lou Xuemei; Perdry Hervé; Sherva Richard; Shugart Yin Yao; Suarez Brian; Wang Hongling; Wormald Hanna; Xing Guan; Xing Chao
Using linkage and association to identify and model genetic effects: summary of GAW15 Group 4.
Genetic epidemiology 2007;31 Suppl 1():S34-42.
2007: Clerget-Darpoux Françoise; Elston Robert C
Are linkage analysis and the collection of family data dead? Prospects for family studies in the age of genome-wide association.
Human heredity 2007;64(2):91-6.
2006: Giordano M; Marano C; Mellai M; Limongelli M G; Bolognesi E; Clerget-Darpoux F; Momigliano-Richiardi P; Greco L
A family-based study does not confirm the association of MYO9B with celiac disease in the Italian population.
Genes and immunity 2006;7(7):606-8.
2006: Leutenegger Anne-Louise; Labalme Audrey; Genin Emmanuelle; Toutain Annick; Steichen Elisabeth; Clerget-Darpoux Francoise; Edery Patrick
Using genomic inbreeding coefficient estimates for homozygosity mapping of rare recessive traits: application to Taybi-Linder syndrome.
American journal of human genetics 2006;79(1):62-6.
2006: Michou Laëtitia; Croiseau Pascal; Petit-Teixeira Elisabeth; du Montcel Sophie Tezenas; Lemaire Isabelle; Pierlot Céline; Osorio José; Frigui Wafa; Lasbleiz Sandra; Quillet Patrick; Bardin Thomas; Prum Bernard; Clerget-Darpoux Françoise; Cornélis François;
Validation of the reshaped shared epitope HLA-DRB1 classification in rheumatoid arthritis.
Arthritis research & therapy 2006;8(3):R79.
2005: Jannot Anne-Sophie; Meziani Roubila; Bertrand Guylene; Gérard Benedicte; Descamps Vincent; Archimbaud Alain; Picard Catherine; Ollivaud Laurence; Basset-Seguin Nicole; Kerob Delphine; Lanternier Guy; Lebbe Celeste; Saiag P; Crickx Beatrice; Clerget-Darpoux Françoise; Grandchamp Bernard; Soufir Nadem; Melan-Cohort
Allele variations in the OCA2 gene (pink-eyed-dilution locus) are associated with genetic susceptibility to melanoma.
European journal of human genetics : EJHG 2005;13(8):913-20.
2005: du Montcel Sophie Tezenas; Michou Laetitia; Petit-Teixeira Elisabeth; Osorio José; Lemaire Isabelle; Lasbleiz Sandra; Pierlot Céline; Quillet Patrick; Bardin Thomas; Prum Bernard; Cornelis François; Clerget-Darpoux Françoise
New classification of HLA-DRB1 alleles supports the shared epitope hypothesis of rheumatoid arthritis susceptibility.
Arthritis and rheumatism 2005;52(4):1063-8.
2004: Margaritte-Jeannin P; Babron M C; Bourgey M; Louka A S; Clot F; Percopo S; Coto I; Hugot J P; Ascher H; Sollid L M; Greco L; Clerget-Darpoux F
HLA-DQ relative risks for coeliac disease in European populations: a study of the European Genetics Cluster on Coeliac Disease.
Tissue antigens 2004;63(6):562-7.
2004: Holopainen P; Naluai A T; Moodie S; Percopo S; Coto I; Clot F; Ascher H; Sollid L; Ciclitira P; Greco L; Clerget-Darpoux F; Partanen J;
Candidate gene region 2q33 in European families with coeliac disease.
Tissue antigens 2004;63(3):212-22.
2004: Pericak-Vance Margaret A; Rimmler Jackie B; Haines Jonathan L; Garcia Melissa E; Oksenberg Jorge R; Barcellos Lisa F; Lincoln Robin; Hauser Stephen L; Cournu-Rebeix Isabelle; Azoulay-Cayla Ariele; Lyon-Caen Olivier; Fontaine Bertrand; Duhamel Emmanuelle; Coppin Helene; Brassat David; Roth Marie-Paule; Clanet Michel; Alizadeh Mehdi; Yaouanq Jacqueline; Quelvennec Erwann; Semana Gilbert; Edan Gilles; Babron Marie-Claude; Genin Emmanuelle; Clerget-Darpoux Francoise
Investigation of seven proposed regions of linkage in multiple sclerosis: an American and French collaborative study.
Neurogenetics 2004;5(1):45-8.
2004: Jannot A-S; Essioux L; Clerget-Darpoux F
Association in multifactorial traits: how to deal with rare observations?
Human heredity 2004;58(2):73-81.
2003: Babron Marie-Claude; Nilsson Staffan; Adamovic Svetlana; Naluai Asa Torinsson; Wahlström Jan; Ascher Henry; Ciclitira Paul J; Sollid Ludvig M; Partanen Jukka; Greco Luigi; Clerget-Darpoux Françoise;
Meta and pooled analysis of European coeliac disease data.
European journal of human genetics : EJHG 2003;11(11):828-34.
2003: Alizadeh Mehdi; Génin Emmanuelle; Babron Marie-Claude; Birebent Brigitte; Cournu-Rebeix Isabelle; Yaouanq Jacqueline; Dréano Stéphane; Sawcer Stephen; Compston Alastair; Clanet Michel; Edan Gilles; Fontaine Bertrand; Clerget-Darpoux Françoise; Semana Gilbert;
Genetic analysis of multiple sclerosis in Europeans: French data.
Journal of neuroimmunology 2003;143(1-2):74-8.
2003: Cournu-Rebeix I; Génin E; Lesca G; Azoulay-Cayla A; Tubridy N; Noé E; Clanet M; Edan G; Clerget-Darpoux F; Sémana G; Fontaine B
Intercellular adhesion molecule-1: a protective haplotype against multiple sclerosis.
Genes and immunity 2003;4(7):518-23.
2003: Jannot A-S; Essioux L; Reese M G; Clerget-Darpoux F
Improved use of SNP information to detect the role of genes.
Genetic epidemiology 2003;25(2):158-67.
2003: Leutenegger Anne-Louise; Prum Bernard; Génin Emmanuelle; Verny Christophe; Lemainque Arnaud; Clerget-Darpoux Françoise; Thompson Elizabeth A
Estimation of the inbreeding coefficient through use of genomic data.
American journal of human genetics 2003;73(3):516-23.
2003: Dizier M-H; Quesneville H; Besse-Schmittler C; Guilloud-Bataille M; Selinger-Leneman H; Clerget-Darpoux F; Demenais F
Indication of linkage and genetic heterogeneity for asthma and atopy on chromosomes 8p and 12q in 107 French EGEA families.
European journal of human genetics : EJHG 2003;11(8):590-6.
2003: Alizadeh Mehdi; Babron Marie-Claude; Birebent Brigitte; Matsuda Fumihiko; Quelvennec Erwann; Liblau Roland; Cournu-Rebeix Isabelle; Momigliano-Richiardi Patricia; Sequeiros Jorge; Yaouanq Jacqueline; Genin Emmanuelle; Vasilescu Alexandre; Bougerie Héloise; Trojano Maria; Martins Silva Berta; Maciel Patricia; Clerget-Darpoux Françoise; Clanet Michel; Edan Gilles; Fontaine Bertrand; Semana Gilbert
Genetic interaction of CTLA-4 with HLA-DR15 in multiple sclerosis patients.
Annals of neurology 2003;54(1):119-22.
2003: Percopo S; Babron M-C; Whalen M; De Virgiliis S; Coto I; Clerget-Darpoux F; Landolfo F; Greco L
Saturation of the 5q31-q33 candidate region for coeliac disease.
Annals of human genetics 2003;67(Pt 3):265-8.
2002: Verpillat Patrice; Ricard Sylvain; Hannequin Didier; Dubois Bruno; Bou Jacqueline; Camuzat Agnès; Pradier Laurent; Frebourg Thierry; Brice Alexis; Clerget-Darpoux Françoise; Deleuze Jean-François; Campion Dominique;
Is the saitohin gene involved in neurodegenerative diseases?
Annals of neurology 2002;52(6):829-32.
2002: Leutenegger Anne-Louise; Génin Emmanuelle; Thompson Elizabeth A; Clerget-Darpoux Françoise
Impact of parental relationships in maximum lod score affected sib-pair method.
Genetic epidemiology 2002;23(4):413-25.
2002: Verpillat Patrice; Camuzat Agnès; Hannequin Didier; Thomas-Anterion Catherine; Puel Michèle; Belliard Serge; Dubois Bruno; Didic Mira; Lacomblez Lucette; Moreaud Olivier; Golfier Véronique; Campion Dominique; Brice Alexis; Clerget-Darpoux Françoise
Apolipoprotein E gene in frontotemporal dementia: an association study and meta-analysis.
European journal of human genetics : EJHG 2002;10(7):399-405.
2002: Verpillat Patrice; Camuzat Agnès; Hannequin Didier; Thomas-Anterion Catherine; Puel Michèle; Belliard Serge; Dubois Bruno; Didic Mira; Michel Bernard-François; Lacomblez Lucette; Moreaud Olivier; Sellal François; Golfier Véronique; Campion Dominique; Clerget-Darpoux Françoise; Brice Alexis
Association between the extended tau haplotype and frontotemporal dementia.
Archives of neurology 2002;59(6):935-9.
2002: Bourgain Catherine; Genin Emmanuelle; Clerget-Darpoux Françoise
Comparison of family based haplotype methods using intragenic SNPs in candidate genes.
European journal of human genetics : EJHG 2002;10(5):313-9.
2002: Génin Emmanuelle; Todorov Alexandre A; Clerget-Darpoux Françoise
Properties of the transmission-disequilibrium test in the presence of inbreeding.
Genetic epidemiology 2002;22(2):116-27.
2002: Bourgain C; Genin E; Ober C; Clerget-Darpoux F
Missing data in haplotype analysis: a study on the MILC method.
Annals of human genetics 2002;66(Pt 1):99-108.
2001: Dizier M H; Besse-Schmittler C; Guilloud-Bataille M; Selinger-Leneman H; Kauffmann F; Clerget-Darpoux F; Demenais F;
Indication of linkage and genetic heterogeneity of asthma according to age at onset on chromosome 7q in 107 French EGEA families.
European journal of human genetics : EJHG 2001;9(11):867-72.
2001: Valdes A M; Noble J A; Génin E; Clerget-Darpoux F; Erlich H A; Thomson G
Modeling of HLA class II susceptibility to Type I diabetes reveals an effect associated with DPB1.
Genetic epidemiology 2001;21(3):212-23.
2001: Verpillat P; Bouley S; Campion D; Hannequin D; Dubois B; Belliard S; Puel M; Thomas-Antérion C; Agid Y; Brice A; Clerget-Darpoux F
Use of haplotype information to test involvement of the LRP gene in Alzheimer's disease in the French population.
European journal of human genetics : EJHG 2001;9(6):464-8.
2001: Greco L; Babron M C; Corazza G R; Percopo S; Sica R; Clot F; Fulchignoni-Lataud M C; Zavattari P; Momigliano-Richiardi P; Casari G; Gasparini P; Tosi R; Mantovani V; De Virgiliis S; Iacono G; D'Alfonso A; Selinger-Leneman H; Lemainque A; Serre J L; Clerget-Darpoux F
Existence of a genetic risk factor on chromosome 5q in Italian coeliac disease families.
Annals of human genetics 2001;65(Pt 1):35-41.
2001: Bourgain C; Génin E; Holopainen P; Mustalahti K; Mäki M; Partanen J; Clerget-Darpoux F
Use of closely related affected individuals for the genetic study of complex diseases in founder populations.
American journal of human genetics 2001;68(1):154-159.
2001: Bourgain C; Génin E; Margaritte-Jeannin P; Clerget-Darpoux F
Maximum identity length contrast: a powerful method for susceptibility gene detection in isolated populations.
Genetic epidemiology 2001;21 Suppl 1():S560-4.
2001: Babron M C; Selinger-Leneman H; Dizier M H; Clerget-Darpoux F
Homogeneity of asthma genome scan results.
Genetic epidemiology 2001;21 Suppl 1():S44-8.
2000: Tézenas du Montcel S; Reviron D; Genin E; Roudier J; Mercier P; Clerget-Darpoux F
Modeling the HLA component in rheumatoid arthritis: sensitivity to DRB1 allele frequencies.
Genetic epidemiology 2000;19(4):422-8.
2000: Dizier M H; Quesneville H; Prum B; Selinger-Leneman H; Clerget-Darpoux F
The triangle test statistic (TTS): a test of genetic homogeneity using departure from the triangle constraints in IBD distribution among affected sib-pairs.
Annals of human genetics 2000;64(Pt 5):433-42.
2000: Zurutuza L; Verpillat P; Raux G; Hannequin D; Puel M; Belliard S; Michon A; Pothin Y; Camuzat A; Penet C; Martin C; Brice A; Campion D; Clerget-Darpoux F; Frebourg T
APOE promoter polymorphisms do not confer independent risk for Alzheimer's disease in a French population.
European journal of human genetics : EJHG 2000;8(9):713-6.
2000: Verpillat P; Bouley S; Hannequin D; Belliard S; Puel M; Thomas-Anterion C; Dubois B; Agid Y; Campion D; Clerget-Darpoux F; Brice A
Alpha2-macroglobulin gene and Alzheimer's disease: confirmation of association by haplotypes analyses.
Annals of neurology 2000;48(3):400-2.
2000: Bourgain C; Genin E; Quesneville H; Clerget-Darpoux F
Search for multifactorial disease susceptibility genes in founder populations.
Annals of human genetics 2000;64(Pt 3):255-65.
2000: Clot F; Babron M C; Percopo S; Giordano M; Bouguerra F; Clerget-Darpoux F; Greco L; Serre J L; Fulchignoni-Lataud M C
Study of two ectopeptidases in the susceptibility to celiac disease: two newly identified polymorphisms of dipeptidylpeptidase IV.
Journal of pediatric gastroenterology and nutrition 2000;30(4):464-6.
2000: Reboul J; Mertens C; Levillayer F; Eichenbaum-Voline S; Vilkoren T; Cournu I; Babron M C; Lyon-Caen O; Clerget-Darpoux F; Edan G; Clanet M; Brahic M; Bureau J F; Fontaine B; Liblau R
Cytokines in genetic susceptibility to multiple sclerosis: a candidate gene approach. French Multiple Sclerosis Genetics Group.
Journal of neuroimmunology 2000;102(1):107-12.
1999: Fontaine B; Cournu I; Arnaud I; Babron M C; Eichenbaum-Voline S; Oksenberg J R; Pericak-Vance M A; Haines J L; Semama G; Liblau R; Lyon-Caen O; Clerget-Darpoux F; Clanet M; Hauser S L
Chromosome 17q22-q24 and multiple sclerosis genetic susceptibility. American-French Multiple Sclerosis Genetic Group.
Genes and immunity 1999;1(2):149-50.
1999: Clot F; Fulchignoni-Lataud M C; Renoux C; Percopo S; Bouguerra F; Babron M C; Djilali-Saiah I; Caillat-Zucman S; Clerget-Darpoux F; Greco L; Serre J L
Linkage and association study of the CTLA-4 region in coeliac disease for Italian and Tunisian populations.
Tissue antigens 1999;54(5):527-30.
1999: Campion D; Dumanchin C; Hannequin D; Dubois B; Belliard S; Puel M; Thomas-Anterion C; Michon A; Martin C; Charbonnier F; Raux G; Camuzat A; Penet C; Mesnage V; Martinez M; Clerget-Darpoux F; Brice A; Frebourg T
Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum.
American journal of human genetics 1999;65(3):664-70.
1999: Bouguerra F; Dugoujon J M; Babron M C; Greco L; Khaldi F; Debbabi A; Bennaceur B; Clerget-Darpoux F
Susceptibility to coeliac disease in Tunisian children and GM immunoglobulin allotypes.
European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics 1999;26(4):293-7.
1999: Clot F; Gianfrani C; Babron M C; Bouguerra F; Southwood S; Kagnoff M F; Troncone R; Percopo S; Eliaou J F; Clerget-Darpoux F; Sette A; Greco L
HLA-DR53 molecules are associated with susceptibility to celiac disease and selectively bind gliadin-derived peptides.
Immunogenetics 1999;49(9):800-7.
1999: Quesneville H; Dizier M H; Clerget-Darpoux F
Departure from the triangle constraints in discordant sib pairs: a test for genetic heterogeneity.
Genetic epidemiology 1999;17 Suppl 1():S685-9.
1999: Génin E; Guyon F; Margaritte-Jeannin P; Quesneville H; Clerget-Darpoux F
Detection and modeling of disease susceptibility locus effects: how much can be learned from contrast of populations?
Genetic epidemiology 1999;17 Suppl 1():S569-74.
1999: Babron M C; Barillot E; Margaritte-Jeannin P; Clerget-Darpoux F
Strategies for detecting susceptibility genes in a complex disease.
Genetic epidemiology 1999;17 Suppl 1():S479-83.
1998: Roume J; Genin E; Cormier-Daire V; Ma H W; Mehaye B; Attie T; Razavi-Encha F; Fallet-Bianco C; Buenerd A; Clerget-Darpoux F; Munnich A; Le Merrer M
A gene for Meckel syndrome maps to chromosome 11q13.
American journal of human genetics 1998;63(4):1095-101.
1998: Génin E; Todorov A A; Clerget-Darpoux F
Optimization of genome search strategies for homozygosity mapping: influence of marker spacing on power and threshold criteria for identification of candidate regions.
Annals of human genetics 1998;62(Pt 5):419-29.
1998: Mertens C; Brassat D; Reboul J; Eichenbaum-Voline S; Vuillemin-Azais C; Cournu I; Babron M C; Semana G; Edan G; Clanet M; Clerget-Darpoux F; Baron-Van Evercooren A; Lyon-Caen O; Liblau R; Fontaine B
A systematic study of oligodendrocyte growth factors as candidates for genetic susceptibility to MS. French Multiple Sclerosis Genetics Group.
Neurology 1998;51(3):748-53.
1998: Dumanchin C; Brice A; Campion D; Hannequin D; Martin C; Moreau V; Agid Y; Martinez M; Clerget-Darpoux F; Frebourg T
De novo presenilin 1 mutations are rare in clinically sporadic, early onset Alzheimer's disease cases. French Alzheimer's Disease Study Group.
Journal of medical genetics 1998;35(8):672-3.
1998: Martinez M; Campion D; Brice A; Hannequin D; Dubois B; Didierjean O; Michon A; Thomas-Anterion C; Puel M; Frebourg T; Agid Y; Clerget-Darpoux F
Apolipoprotein E epsilon4 allele and familial aggregation of Alzheimer disease.
Archives of neurology 1998;55(6):810-6.
1998: Verpillat P; Margaritte-Jeannin P; Clerget-Darpoux F
About the use of APOE in Alzheimer's disease studies.
American journal of medical genetics 1998;81(2):195.
1998: Greco L; Percopo S; Clot F; Bouguerra F; Babron M C; Eliaou J F; Franzese C; Troncone R; Clerget-Darpoux F
Lack of correlation between genotype and phenotype in celiac disease.
Journal of pediatric gastroenterology and nutrition 1998;26(3):286-90.
1998: Génin E; Quesneville H; Clerget-Darpoux F
On the probability of identity states in permutable populations: reply to Cannings.
American journal of human genetics 1998;62(3):726-7.
1998: Greco L; Corazza G; Babron M C; Clot F; Fulchignoni-Lataud M C; Percopo S; Zavattari P; Bouguerra F; Dib C; Tosi R; Troncone R; Ventura A; Mantavoni W; Magazzù G; Gatti R; Lazzari R; Giunta A; Perri F; Iacono G; Cardi E; de Virgiliis S; Cataldo F; De Angelis G; Musumeci S; Clerget-Darpoux F
Genome search in celiac disease.
American journal of human genetics 1998;62(3):669-75.
1998: Hannequin D; Campion D; Dumanchin C; Martinez M; Agid Y; Clerget-Darpoux F; Frebourg T; Brice A
[Genetics of Alzheimer's disease]
Revue neurologique 1998;154 Suppl 2():S65-74.
1998: Génin E; Babron M C; McDermott M F; Mulcahy B; Waldron-Lynch F; Adams C; Clegg D O; Ward R H; Shanahan F; Molloy M G; O'Gara F; Clerget-Darpoux F
Modelling the major histocompatibility complex susceptibility to RA using the MASC method.
Genetic epidemiology 1998;15(4):419-30.
1997: Didierjean O; Martinez M; Campion D; Hannequin D; Dubois B; Martin C; Puel M; Thomas Anterion C; Pasquier F; Moreau O; Babron M C; Penet C; Agid Y; Clerget-Darpoux F; Frebourg T; Brice A
No effect of the alpha1-antichymotrypsin A allele in Alzheimer's disease.
Journal of neurology, neurosurgery, and psychiatry 1997;63(1):103-5.
1997: Yaouanq J; Semana G; Eichenbaum S; Quelvennec E; Roth M P; Clanet M; Edan G; Clerget-Darpoux F
Evidence for linkage disequilibrium between HLA-DRB1 gene and multiple sclerosis. The French Research Group on Genetic Susceptibility to MS.
Science (New York, N.Y.) 1997;276(5313):664-5.
1997: Legeai-Mallet L; Margaritte-Jeannin P; Lemdani M; Le Merrer M; Plauchu H; Maroteaux P; Munnich A; Clerget-Darpoux F
An extension of the admixture test for the study of genetic heterogeneity in hereditary multiple exostoses.
Human genetics 1997;99(3):298-302.
1997: Bickeböller H; Campion D; Brice A; Amouyel P; Hannequin D; Didierjean O; Penet C; Martin C; Pérez-Tur J; Michon A; Dubois B; Ledoze F; Thomas-Anterion C; Pasquier F; Puel M; Demonet J F; Moreaud O; Babron M C; Meulien D; Guez D; Chartier-Harlin M C; Frebourg T; Agid Y; Martinez M; Clerget-Darpoux F
Apolipoprotein E and Alzheimer disease: genotype-specific risks by age and sex.
American journal of human genetics 1997;60(2):439-46.
1997: Génin E; Bellis G; Clerget-Darpoux F
Information provided by pairs of distantly affected relatives to search for genes involved in rare autosomal dominant diseases.
Annals of human genetics 1997;61(Pt 1):25-36.
1997: Eichenbaum-Voline S; Génin E; Babron M C; Margaritte-Jeannin P; Prum B; Clerget-Darpoux F
Caution in the interpretation of MLS.
Genetic epidemiology 1997;14(6):1079-83.
1997: Margaritte-Jeannin P; Babron M C; Génin E; Eichenbaum-Voline S; Clerget-Darpoux F
Heterogeneity of marker allele frequencies hinders interpretation of linkage analysis: illustration on chromosome 18 markers.
Genetic epidemiology 1997;14(6):669-74.
1997: Bouguerra F; Babron M C; Eliaou J F; Debbabi A; Clot J; Khaldi F; Greco L; Clerget-Darpoux F
Synergistic effect of two HLA heterodimers in the susceptibility to celiac disease in Tunisia.
Genetic epidemiology 1997;14(4):413-22.
1996: Génin E; Clerget-Darpoux F
Consanguinity and the sib-pair method: an approach using identity by descent between and within individuals.
American journal of human genetics 1996;59(5):1149-62.
1996: Campion D; Brice A; Hannequin D; Charbonnier F; Dubois B; Martin C; Michon A; Penet C; Bellis M; Calenda A; Martinez M; Agid Y; Clerget-Darpoux F; Frebourg T
No founder effect in three novel Alzheimer's disease families with APP 717 Val-->Ile mutation. Clerget-darpoux. French Alzheimer's Disease Study Group.
Journal of medical genetics 1996;33(8):661-4.
1996: Campion D; Brice A; Dumanchin C; Puel M; Baulac M; De La Sayette V; Hannequin D; Duyckaerts C; Michon A; Martin C; Moreau V; Penet C; Martinez M; Clerget-Darpoux F; Agid Y; Frebourg T
A novel presenilin 1 mutation resulting in familial Alzheimer's disease with an onset age of 29 years.
Neuroreport 1996;7(10):1582-4.
1996: Dizier M H; Babron M C; Clerget-Darpoux F
Conclusion of LOD-score analysis for family data generated under two-locus models.
American journal of human genetics 1996;58(6):1338-46.
1996: Génin E; Clerget-Darpoux F
Association studies in consanguineous populations.
American journal of human genetics 1996;58(4):861-6.
1996: Martinez M; Campion D; Babron M C; Hannequin D; Agid Y; Bellis M; Brice A; Mallet J; Michon A; Thomas-Anterion C; Clerget-Darpoux F
Segregation analysis of Alzheimer pedigrees: rare Mendelian dominant mutation(s) explain a minority of early-onset cases. French Alzheimer Collaborative Group.
American journal of medical genetics 1996;67(1):9-12.
1995: Pérez-Tur J; Campion D; Martinez M; Brice A; Tardieu S; Hannequin D; Agid Y; Delacourte A; Clerget-Darpoux F; Chartier-Harlin M C
Evidence for apolipoprotein E epsilon 4 association in early-onset Alzheimer's patients with late-onset relatives.
American journal of medical genetics 1995;60(6):550-3.
1995: Hannequin D; Campion D; Tardieu S; Auzou P; Martinez M; Dubois B; Clerget-Darpoux F; Agid Y; Brice A
[Phenotype of familial forms of early-onset Alzheimer's disease linked to chromosome 14. Clinical and neuropsychological characteristics of a large group]
Revue neurologique 1995;151(12):682-90.
1995: Margaritte-Jeannin P; Clerget-Darpoux F; Hors J; Deschamps I
Testing parental imprinting in insulin-dependent diabetes mellitus by the marker-association-segregation-chi 2 method.
American journal of human genetics 1995;56(5):1080-7.
1995: Génin E; Martinez M; Clerget-Darpoux F
Posterior probability of linkage and maximal lod score.
Annals of human genetics 1995;59(Pt 1):123-32.
1995: Bickeböller H; Clerget-Darpoux F
Statistical properties of the allelic and genotypic transmission/disequilibrium test for multiallelic markers.
Genetic epidemiology 1995;12(6):865-70.
1995: Dizier M H; Babron M C; Clerget-Darpoux F
Modeling the role of two susceptibility loci by the MASC method.
Genetic epidemiology 1995;12(6):589-93.
1995: Clerget-Darpoux F; Babron M C; Bickeböller H
Comparing the power of linkage detection by the transmission disequilibrium test and the identity-by-descent test.
Genetic epidemiology 1995;12(6):583-8.
1995: Bickeböller H; Margaritte-Jeannin P; Babron M C; Clerget-Darpoux F
Systematic search of susceptibility loci with methods using gametic disequilibrium.
Genetic epidemiology 1995;12(6):577-82.
1995: Margaritte-Jeannin P; Essioux L; Bonaïti-Pellié C; Clerget-Darpoux F
Genetic counselling in breast cancer: sensitivity to parameter values and to available information.
Annales de génétique 1995;38(1):19-25.
1994: Dizier M H; Babron M C; Clerget-Darpoux F
Interactive effect of two candidate genes in a disease: extension of the marker-association-segregation chi(2) method.
American journal of human genetics 1994;55(5):1042-9.
1994: Clerget-Darpoux F; Bouguerra F; Kastally R; Semana G; Babron M C; Debbabi A; Bennaceur B; Eliaou J F
High risk genotypes for celiac disease.
Comptes rendus de l'Académie des sciences. Série III, Sciences de la vie 1994;317(10):931-6.
1993: Dizier M H; Bonaïti-Pellié C; Clerget-Darpoux F
Conclusions of segregation analysis for family data generated under two-locus models.
American journal of human genetics 1993;53(6):1338-46.
1993: Dizier M H; Eliaou J F; Babron M C; Combe B; Sany J; Clot J; Clerget-Darpoux F
Investigation of the HLA component involved in rheumatoid arthritis (RA) by using the marker association-segregation chi-square (MASC) method: rejection of the unifying-shared-epitope hypothesis.
American journal of human genetics 1993;53(3):715-21.
1992: Dizier M H; Bonaiti-Pellié C; Clerget-Darpoux F
POINTER correctly estimates the transmission probabilities under the general transmission model in the case of incomplete selection.
American journal of human genetics 1992;51(6):1449-50.
1992: Margaritte P; Bonaiti-Pellie C; King M C; Clerget-Darpoux F
Linkage of familial breast cancer to chromosome 17q21 may not be restricted to early-onset disease.
American journal of human genetics 1992;50(6):1231-4.
1991: Clerget-Darpoux F; Babron M C; Deschamps I; Hors J
Complementation and maternal effect in insulin-dependent diabetes.
American journal of human genetics 1991;49(1):42-8.
1991: Müller B; Clerget-Darpoux F
A test based on the exact probability distribution of the chi 2 statistic--incorporation into the MASC method.
Annals of human genetics 1991;55(Pt 1):69-75.
1991: Dizier M H; Silman A J; Ollier W; Grennan D M; Clerget-Darpoux F
Interactive effect of HLA and Gm and genetic heterogeneity tested in 79 rheumatoid arthritis families.
Disease markers 1991;9(1):27-34.
1990: Bonaïti-Pellié C; Clerget-Darpoux F; Babron M C
Hereditary retinoblastoma: can balanced insertion entirely explain the differences of expressivity among families?
Human genetics 1990;86(2):203-8.
1990: Prum B; Guilloud-Bataille M; Clerget-Darpoux F
On the use of chi 2 tests for nested categorized data.
Annals of human genetics 1990;54(Pt 4):315-20.
1990: Dizier M H; Clerget-Darpoux F; Hochez J
Two-disease-locus model: segregation analysis using information on two markers in nuclear families. Application to IDDM.
Tissue antigens 1990;36(1):1-7.
1990: Clerget-Darpoux F; Babron M C; Bonaïti-Pellié C
Assessing the effect of multiple linkage tests in complex diseases.
Genetic epidemiology 1990;7(4):245-53.
1989: Dizier M H; Clerget-Darpoux F; Hochez J
Segregation analysis of two genetic markers in IDDM families under two-locus models.
Genetic epidemiology 1989;6(1):71-5.
1989: Clerget-Darpoux F; Babron M C
Testing genetic models for IDDM by the MASC method.
Genetic epidemiology 1989;6(1):59-64.
1988: Clerget-Darpoux F; Babron M C; Prum B; Lathrop G M; Deschamps I; Hors J
A new method to test genetic models in HLA associated diseases: the MASC method.
Annals of human genetics 1988;52(Pt 3):247-58.
1986: Dizier M H; Deschamps I; Hors J; Blanc M; Rivat L; Clerget-Darpoux F
Interactive effect of HLA and Gm tested in a study of 135 juvenile insulin-dependent diabetic families.
Tissue antigens 1986;27(5):269-78.
1986: Dizier M H; Clerget-Darpoux F
Two-disease locus model: sib pair method using information on both HLA and Gm.
Genetic epidemiology 1986;3(5):343-56.
1986: Demenais F; Martinez M; Bonaïti-Pellié C; Clerget-Darpoux F; Feingold N
Segregation analysis of the Jacobsen data.
Genetic epidemiology. Supplement 1986;1():49-54.
1986: Clerget-Darpoux F; Dizier M H; Bonaïti-Pellié C; Babron M C; Hochez J; Martinez M
Discrimination between genetic models for insulin dependent diabetes mellitus.
Genetic epidemiology. Supplement 1986;1():313-8.
1985: Dizier M H; Deschamps I; Hors J; Blanc M; Rivat-Peran L; Feingold N; Clerget-Darpoux F
[Interaction between HLA and Gm for susceptibility to insulin-dependent diabetes]
Revue d'épidémiologie et de santé publique 1985;33(4-5):337-40.
1981: Clerget-Darpoux F; Bonaïti-Pellié C; Deschamps I; Hors J; Feingold N
Juvenile insulin-dependent diabetes: a possible susceptibility gene in interaction with HLA.
Annals of human genetics 1981;45(Pt 2):199-206.
1980: Clerget-Darpoux F; Bonaiti-Pellie C; Hors J; Deschamps I; Feingold N
Application of the lod score method to detection of linkage between HLA and juvenile insulin-dependent diabetes.
Clinical genetics 1980;18(1):51-7.

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