Publications by authors named "Stephanie Cobb"

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The man who mistook his neuropsychologist for a popstar: when configural processing fails in acquired prosopagnosia.
Ashok Jansari, Scott Miller, Laura Pearce, Stephanie Cobb, Noam Sagiv

Front Hum Neurosci· August 2015

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EIF4G1 gene mutations are not a common cause of Parkinson's disease in the Japanese population.
Kenya Nishioka, Manabu Funayama, Carles Vilariño-Güell, Kotaro Ogaki, Yuanzhe Li, Stephanie A Cobb

Parkinsonism Relat Disord· June 2014

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PARK2 variability in Polish Parkinson's disease patients--interaction with mitochondrial haplogroups.
Katarzyna Gaweda-Walerych, Krzysztof Safranow, Barbara Jasinska-Myga, Monika Bialecka, Gabriela Klodowska-Duda, Stephanie A Cobb

Parkinsonism Relat Disord· June 2012

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First neuropathological description of a patient with Parkinson's disease and LRRK2 p.N1437H mutation.
Andreas Puschmann, Elisabet Englund, Owen A Ross, Carles Vilariño-Güell, Sarah J Lincoln, Stephanie A Cobb

Parkinsonism Relat Disord· May 2012

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Translation initiator EIF4G1 mutations in familial Parkinson disease.
Marie-Christine Chartier-Harlin, Justus C Dachsel, Carles Vilariño-Güell, Sarah J Lincoln, Frédéric Leprêtre, Stephanie A Cobb

Am J Hum Genet· September 2011

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VPS35 mutations in Parkinson disease.
Carles Vilariño-Güell, Christian Wider, Owen A Ross, Justus C Dachsel, Jennifer M Kachergus, Stephanie A Cobb

Am J Hum Genet· July 2011

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Glucocerebrosidase mutations in diffuse Lewy body disease.
Kenya Nishioka, Owen A Ross, Carles Vilariño-Güell, Stephanie A Cobb, Jennifer M Kachergus

Parkinsonism Relat Disord· January 2011

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Genetic variation of the mitochondrial complex I subunit NDUFV2 and Parkinson's disease.
Kenya Nishioka, Carles Vilariño-Güell, Stephanie A Cobb, Jennifer M Kachergus, Owen A Ross

Parkinsonism Relat Disord· December 2010

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LINGO1 and LINGO2 variants are associated with essential tremor and Parkinson disease.
Carles Vilariño-Güell, Christian Wider, Owen A Ross, Barbara Jasinska-Myga, Jennifer Kachergus, Stephanie A Cobb

Neurogenetics· October 2010

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Novel pathogenic LRRK2 p.Asn1437His substitution in familial Parkinson's disease.
Jan O Aasly, Carles Vilariño-Güell, Justus C Dachsel, Philip J Webber, Andrew B West, Stephanie A Cobb

Mov Disord· October 2010

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LRRK2 variation and Parkinson's disease in African Americans.
Owen A Ross, Greggory J Wilhoite, Justin A Bacon, Alexandra Soto-Ortolaza, Jennifer Kachergus, Stephanie A Cobb

Mov Disord· September 2010

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Glucocerebrosidase mutations are not a common risk factor for Parkinson disease in North Africa.
Kenya Nishioka, Carles Vilariño-Güell, Stephanie A Cobb, Jennifer M Kachergus, Owen A Ross

Neurosci Lett· June 2010

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LINGO1 rs9652490 is associated with essential tremor and Parkinson disease.
Carles Vilariño-Güell, Owen A Ross, Christian Wider, Barbara Jasinska-Myga, Stephanie A Cobb

Parkinsonism Relat Disord· February 2010

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Alpha-synuclein polymorphisms are associated with Parkinson's disease in a Saskatchewan population.
Alex Rajput, Carles Vilariño-Güell, Michele L Rajput, Owen A Ross, Alexandra I Soto-Ortolaza, Stephanie A Cobb

Mov Disord· December 2009

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A Swedish family with de novo alpha-synuclein A53T mutation: evidence for early cortical dysfunction.
Andreas Puschmann, Owen A Ross, Carles Vilariño-Güell, Sarah J Lincoln, Jennifer M Kachergus, Stephanie A Cobb

Parkinsonism Relat Disord· November 2009

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GCH1 in early-onset Parkinson's disease.
Stephanie A Cobb, Christian Wider, Owen A Ross, Ignacio F Mata, Charles H Adler

Mov Disord· October 2009

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Lrrk2 mutations in South America: A study of Chilean Parkinson's disease.
Carolina Perez-Pastene, Stephanie A Cobb, Fernando Díaz-Grez, Mary M Hulihan, Marcelo Miranda

Neurosci Lett· July 2007

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Genomewide association, Parkinson disease, and PARK10.
Matthew J Farrer, Kristoffer Haugarvoll, Owen A Ross, Jeremy T Stone, Nicole M Milkovic, Stephanie A Cobb

Am J Hum Genet· June 2006

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Effective interventions for lifestyle change after myocardial infarction or coronary artery revascularization.
Stephanie L Cobb, Debra J Brown, Leslie L Davis

J Am Acad Nurse Pract· January 2006

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Lrrk2 pathogenic substitutions in Parkinson's disease.
Ignacio F Mata, Jennifer M Kachergus, Julie P Taylor, Sarah Lincoln, Jan Aasly, Stephanie A Cobb

Neurogenetics· December 2005

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Intestinal expression of mutant and wild-type progastrin significantly increases colon carcinogenesis in response to azoxymethane in transgenic mice.
Stephanie Cobb, Thomas Wood, Jeffrey Ceci, Andrea Varro, Marco Velasco

Cancer· March 2004

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Deletion of functional gastrin gene markedly increases colon carcinogenesis in response to azoxymethane in mice.
Stephanie Cobb, Thomas Wood, Lino Tessarollo, Marco Velasco, Randall Given

Gastroenterology· August 2002

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