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Jacqueline Rimmler

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Publications

TOP 3
Yi-Ju Li; Mollie A Minear; Jacqueline B Rimmler; Bei Zhao; Elmer Balajonda; Michael A Hauser; R Rand Allingham; Allen O Eghrari; Sheikh Amer Riazuddin; Nicholas Katsanis; John D Gottsch; Simon G Gregory; Gordon K Klintworth; Natalie A Afshari
Replication of TCF4 through association and linkage studies in late-onset Fuchs endothelial corneal dystrophy.
Allison E Ashley-Koch; Yujun Shao; Jacqueline B Rimmler; Perry C Gaskell; Kathleen A Welsh-Bohmer; Charles E Jackson; William Scott; Jonathan L Haines; Margaret Pericak-Vance
An autosomal genomic screen for dementia in an extended Amish family.
Shannon J Kenealy; Marie-Claude Babron; Yuki Bradford; Nathalie Schnetz-Boutaud; Jonathan L Haines; Jacqueline B Rimmler; Silke Schmidt; Margaret Pericak-Vance; Lisa F Barcellos; Robin R Lincoln; Jorge R Oksenberg; Stephen L Hauser; Michel Clanet; David Brassat; G Edan; Jacqueline Yaouanq; Gilbert Semana; Isabelle Cournu-Rebeix; O Lyon-Caen; Bertrand Fontaine
A second-generation genomic screen for multiple sclerosis.

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All Publications

2011: Yi-Ju Li; Mollie A Minear; Jacqueline B Rimmler; Bei Zhao; Elmer Balajonda; Michael A Hauser; R Rand Allingham; Allen O Eghrari; Sheikh Amer Riazuddin; Nicholas Katsanis; John D Gottsch; Simon G Gregory; Gordon K Klintworth; Natalie A Afshari
Replication of TCF4 through association and linkage studies in late-onset Fuchs endothelial corneal dystrophy.
PloS one 2011;6(4):e18044.
2005: Allison E Ashley-Koch; Yujun Shao; Jacqueline B Rimmler; Perry C Gaskell; Kathleen A Welsh-Bohmer; Charles E Jackson; William Scott; Jonathan L Haines; Margaret Pericak-Vance
An autosomal genomic screen for dementia in an extended Amish family.
Neuroscience letters 2005;379(3):199-204.
2004: Shannon J Kenealy; Marie-Claude Babron; Yuki Bradford; Nathalie Schnetz-Boutaud; Jonathan L Haines; Jacqueline B Rimmler; Silke Schmidt; Margaret Pericak-Vance; Lisa F Barcellos; Robin R Lincoln; Jorge R Oksenberg; Stephen L Hauser; Michel Clanet; David Brassat; G Edan; Jacqueline Yaouanq; Gilbert Semana; Isabelle Cournu-Rebeix; O Lyon-Caen; Bertrand Fontaine
A second-generation genomic screen for multiple sclerosis.
American journal of human genetics 2004;75(6):1070-8.
2004: Margaret Pericak-Vance; Jacqueline B Rimmler; Jonathan L Haines; Melissa E Garcia; Jorge R Oksenberg; Lisa F Barcellos; Robin R Lincoln; Stephen L Hauser; Isabelle Cournu-Rebeix; Ariele Azoulay-Cayla; Olivier Lyon-Caen; Bertrand Fontaine; Emmanuelle Duhamel; helene coppin; David Brassat; Marie-Paule Roth; Michel Clanet; Mehdi Alizadeh; Jacqueline Yaouanq; Erwann Quelvennec; Gilbert Semana; Gilles Edan; Marie-Claude Babron; Emmanuelle Genin; Françoise Clerget-Darpoux
Investigation of seven proposed regions of linkage in multiple sclerosis: an American and French collaborative study.
Neurogenetics 2004;5(1):45-8.
2002: Jonathan L Haines; Yuki Bradford; Melissa E Garcia; Allison D Reed; Elizabeth Neumeister; Margaret Pericak-Vance; Jacqueline B Rimmler; Marisa M Menold; Eden R Martin; Jorge R Oksenberg; Lisa F Barcellos; Robin R Lincoln; Stephen L Hauser
Multiple susceptibility loci for multiple sclerosis.
Human molecular genetics 2002;11(19):2251-6.
2002: Silke Schmidt; Lisa F Barcellos; Karen DeSombre; Jacqueline B Rimmler; Robin R Lincoln; Patricia Bucher; Ann M Saunders; Eric Lai; Eden R Martin; Jeffery Vance; Jorge R Oksenberg; Stephen L Hauser; Margaret Pericak-Vance; Jonathan L Haines
Association of polymorphisms in the apolipoprotein E region with susceptibility to and progression of multiple sclerosis.
American journal of human genetics 2002;70(3):708-17.
2002: Lisa F Barcellos; Jorge R Oksenberg; A J Green; Patricia Bucher; Jacqueline B Rimmler; Silke Schmidt; Melissa E Garcia; Robin R Lincoln; Margaret Pericak-Vance; Jonathan L Haines; Stephen L Hauser
Genetic basis for clinical expression in multiple sclerosis.
Brain : a journal of neurology 2002;125(Pt 1):150-8.
2001: Margaret Pericak-Vance; Jacqueline B Rimmler; Eden R Martin; Jonathan L Haines; Melissa E Garcia; Jorge R Oksenberg; Lisa F Barcellos; Robin R Lincoln; Donald Goodkin; Stephen L Hauser
Linkage and association analysis of chromosome 19q13 in multiple sclerosis.
Neurogenetics 2001;3(4):195-201.
2001: A J Green; Lisa F Barcellos; Jacqueline B Rimmler; Melissa E Garcia; Stacy J Caillier; Robin R Lincoln; Patricia Bucher; Margaret Pericak-Vance; Jonathan L Haines; Stephen L Hauser; Jorge R Oksenberg
Sequence variation in the transforming growth factor-beta1 (TGFB1) gene and multiple sclerosis susceptibility.
Journal of neuroimmunology 2001;116(1):116-24.
2000: Lisa F Barcellos; AM Schito; Jacqueline B Rimmler; E Vittinghoff; A Shih; Robin R Lincoln; S Callier; Mary K Elkins; Donald Goodkin; Jonathan L Haines; Margaret Pericak-Vance; Stephen L Hauser; Jorge R Oksenberg
CC-chemokine receptor 5 polymorphism and age of onset in familial multiple sclerosis. Multiple Sclerosis Genetics Group.
Immunogenetics 2000;51(4-5):281-8.
1999: Eric Seboun; Jorge R Oksenberg; A Rombos; K Usuku; Donald Goodkin; Robin R Lincoln; M Wong; Danielle Pham-Dinh; O Boesplug-Tanguy; R Carsique; R Fitoussi; C Gartioux; C Reyes; F Ribierre; S Faure; C Fizames; Gabor Gyapay; Jean Weissenbach; André Dautigny; Jacqueline B Rimmler; Melissa E Garcia; Margaret Pericak-Vance; Jonathan L Haines; Stephen L Hauser
Linkage analysis of candidate myelin genes in familial multiple sclerosis.
Neurogenetics 1999;2(3):155-62.
1998: A Hentati; Karim Ouahchi; Margaret Pericak-Vance; D Nijhawan; A Ahmad; Y Yang; Jacqueline B Rimmler; W Hung; B Schlotter; A Ahmed; Mongi Ben Hamida; Faycal Hentati; Teepu Siddique
Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers.
Neurogenetics 1998;2(1):55-60.
1998: Jonathan L Haines; H A Terwedow; K Burgess; Margaret Pericak-Vance; Jacqueline B Rimmler; Eden R Martin; Jorge R Oksenberg; Robin R Lincoln; D Y Zhang; D R Banatao; N Gatto; D E Goodkin; Stephen L Hauser
Linkage of the MHC to familial multiple sclerosis suggests genetic heterogeneity. The Multiple Sclerosis Genetics Group.
Human molecular genetics 1998;7(8):1229-34.
1998: Teepu Siddique; Margaret Pericak-Vance; J Caliendo; S T Hong; Wu-Yen Hung; J Kaplan; Diane McKenna-Yasek; Jacqueline B Rimmler; Peter C Sapp; Ann M Saunders; William Scott; Nailah Siddique; Jonathan L Haines; Robert H Brown
Lack of association between apolipoprotein E genotype and sporadic amyotrophic lateral sclerosis.
Neurogenetics 1998;1(3):213-6.
1996: Jonathan L Haines; M Ter-Minassian; A Bazyk; James Gusella; D J Kim; H Terwedow; Margaret Pericak-Vance; Jacqueline B Rimmler; C S Haynes; Allen D Roses; A Lee; B Shaner; M Menold; Eric Seboun; R P Fitoussi; C Gartioux; C Reyes; F Ribierre; Gabor Gyapay; Jean Weissenbach; Stephen L Hauser; D E Goodkin; R Lincoln; K Usuku; J R Oksenberg
A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group.
Nature genetics 1996;13(4):469-71.