Anne-Louise Leutenegger

Anne-Louise Leutenegger

UNVERIFIED PROFILE

Are you Anne-Louise Leutenegger?   Register this Author

Register author
Anne-Louise Leutenegger

Anne-Louise Leutenegger

Publications by authors named "Anne-Louise Leutenegger"

Are you Anne-Louise Leutenegger?   Register this Author

39Publications

1326Reads

46Profile Views

Strategies for phasing and imputation in a population isolate.

Genet Epidemiol 2018 03 10;42(2):201-213. Epub 2018 Jan 10.

Université Paris-Diderot, Sorbonne Paris Cité, U946, Paris, France.

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1002/gepi.22109
Publisher Site
http://dx.doi.org/10.1002/gepi.22109DOI Listing
March 2018

Clinical and demographic factors and outcome of amyotrophic lateral sclerosis in relation to population ancestral origin.

Eur J Epidemiol 2016 Mar 12;31(3):229-45. Epub 2015 Oct 12.

Laboratorio di Malattie Neurologiche, Dipartimento di Neuroscienze, IRCCS Istituto di Ricerche Farmacologiche Mario Negri, Milan, Italy.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s10654-015-0090-xDOI Listing
March 2016

Relationship inference from the genetic data on parents or offspring: A comparative study.

Theor Popul Biol 2016 Feb 30;107:31-8. Epub 2015 Sep 30.

Inserm, U946, Genetic Variation and Human Diseases Lab, Paris, France; Université Paris Diderot, Sorbonne Paris Cité, Institut Universitaire d'Hématologie, UMR 946, Paris, France. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.tpb.2015.09.002DOI Listing
February 2016

High level of inbreeding in final phase of 1000 Genomes Project.

Sci Rep 2015 Dec 2;5:17453. Epub 2015 Dec 2.

INSERM, Genetic variability and human diseases, UMR 946, F-75010 Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/srep17453DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4667178PMC
December 2015

Genome-wide inbreeding estimation within Lebanese communities using SNP arrays.

Eur J Hum Genet 2015 Oct 26;23(10):1364-9. Epub 2014 Nov 26.

EA 2493 « pathologie cellulaire & génétique, de la conception à la naissance », Université de Versailles-Saint Quentin en Yvelines, Yvelines, France.

View Article

Download full-text PDF

Source
http://www.nature.com/articles/ejhg2014246
Publisher Site
http://dx.doi.org/10.1038/ejhg.2014.246DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4592074PMC
October 2015

Inbreeding coefficient estimation with dense SNP data: comparison of strategies and application to HapMap III.

Hum Hered 2014 29;77(1-4):49-62. Epub 2014 Jul 29.

Genetic Variability and Human Diseases, Inserm, U946, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1159/000358224DOI Listing
March 2015

FSuite: exploiting inbreeding in dense SNP chip and exome data.

Bioinformatics 2014 Jul 14;30(13):1940-1. Epub 2014 Mar 14.

Inserm, U946, Genetic variability and human diseases, Paris, 75010, Université Paris Sud, Kremlin-Bicêtre, 94270, Fondation Jean Dausset CEPH, Paris, 75010, Université Paris-Diderot, UMR 946, Institut Universitaire d'Hématologie, Paris, 75475, Inserm, U1078, Génétique, Génomique fonctionnelle et Biotechnologies, Brest, 29218 and Centre Hospitalier Régional Universitaire de Brest, Brest, 29200, France Inserm, U946, Genetic variability and human diseases, Paris, 75010, Université Paris Sud, Kremlin-Bicêtre, 94270, Fondation Jean Dausset CEPH, Paris, 75010, Université Paris-Diderot, UMR 946, Institut Universitaire d'Hématologie, Paris, 75475, Inserm, U1078, Génétique, Génomique fonctionnelle et Biotechnologies, Brest, 29218 and Centre Hospitalier Régional Universitaire de Brest, Brest, 29200, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/bioinformatics/btu149DOI Listing
July 2014

Does anonymous sperm donation increase the risk for unions between relatives and the incidence of autosomal recessive diseases due to consanguinity?

Hum Reprod 2014 Mar 16;29(3):394-9. Epub 2013 Dec 16.

EA 2493 'Pathologie Cellulaire and Génétique, de la Conception à la Naissance', Université de Versailles, Saint Quentin en Yvelines, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/humrep/det452DOI Listing
March 2014

Could inbred cases identified in GWAS data succeed in detecting rare recessive variants where affected sib-pairs have failed?

Hum Hered 2012 11;74(3-4):142-52. Epub 2013 Apr 11.

Inserm UMR-946, Genetic Variability and Human Diseases, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1159/000346790DOI Listing
October 2013

Does inbreeding affect N-glycosylation of human plasma proteins?

Mol Genet Genomics 2011 May 13;285(5):427-32. Epub 2011 Apr 13.

Department of Public Health, Medical School, University of Split, Šoltanska 2, 210000 Split, Croatia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00438-011-0620-5DOI Listing
May 2011

LRRK2 exon 41 mutations in sporadic Parkinson disease in Europeans.

Arch Neurol 2007 Mar;64(3):425-30

Institut National de la Santé et de la Recherche Médicale Unité 679, Neurology and Experimental Therapeutics, and Faculté de Médecine, Université Pierre et Marie Curie, 75651 Paris CEDEX 13, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1001/archneur.64.3.425DOI Listing
March 2007

Juvenile-onset Parkinsonism as a result of the first mutation in the adenosine triphosphate orientation domain of PINK1.

Arch Neurol 2006 Sep;63(9):1257-61

Institut National de la Santé et de la Recherche Médicale U679, Assistance Publique, Hôpitaux de Paris, Faculté de Médecine, Université Paris 6-Pierre et Marie Curie, Hôpital de la Pitié-Salpêtrière, 47 Blvd. de l'Hôpital, 75651 Paris CEDEX 13, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1001/archneur.63.9.1257DOI Listing
September 2006

Detection of susceptibility loci by genome-wide linkage analysis.

BMC Genet 2005 Dec 30;6 Suppl 1:S18. Epub 2005 Dec 30.

INSERM U535, 94817 Villejuif Cedex, Villejuif, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1186/1471-2156-6-S1-S18DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866769PMC
December 2005

G2019S LRRK2 mutation in French and North African families with Parkinson's disease.

Ann Neurol 2005 Nov;58(5):784-7

Institut National de la Sante et de la Recherche Médicale U679 (formerly U289), Neurologie et Thérapeutique Expérimentale, Hôpital de la Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ana.20636DOI Listing
November 2005

Estimation of the inbreeding coefficient through use of genomic data.

Am J Hum Genet 2003 Sep 29;73(3):516-23. Epub 2003 Jul 29.

Unité de Recherche en Génétique Epidémiologique et Structure des Populations Humaines, INSERM U535, Villejuif, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1086/378207DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1180677PMC
September 2003

Impact of parental relationships in maximum lod score affected sib-pair method.

Genet Epidemiol 2002 Nov;23(4):413-25

Unité de Recherche d'Epidémiologie Génétique, INSERM U535, Kremlin-Bicêtre, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/gepi.10190DOI Listing
November 2002

Presence of large deletions in kindreds with autism.

Am J Hum Genet 2002 Jul 7;71(1):100-15. Epub 2002 Jun 7.

Geriatrics Research Education and Clinical Center, Puget Sound Veterans Affairs Medical Center, University of Washington, Seattle 98108, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1086/341291DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC384967PMC
July 2002