Bibliografia UJ CM

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Catherine Labbe, Kotaro Ogaki, Oswaldo Lorenzo-Betancor, Minerva M. Carrasquillo, Michael G. Heckman, Allan McCarthy, Alexandra I. Soto-Ortolaza, Ronald L. Walton, Timothy Lynch, Joanna Siuda, Grzegorz Opala, Anna Krygowska-Wajs, Maria Barcikowska, Krzysztof Czyzewski, Dennis W. Dickson, Ryan J. Uitti, Zbigniew K. Wszolek, Owen A. Ross.
Exonic Re-Sequencing of the Chromosome 2q24.3 Parkinson's Disease Locus.
PLoS One
2015 : Vol. 10, nr 6 art. no. e0128586, s. 1-10, il., bibliogr. 23 poz., abstr.
Open Access Creative Commons Attribution License CC-BY 4.0.
p-ISSN: 1932-6203
AZ
ORG
AIF
IF: 3.057
Adres url:
Streszczenie w PubMed:
2/9
Catherine Labbe, Kotaro Ogaki, Lorenzo Lorenzo-Betancor,, Alexandra Soto-Ortolaza, Antony S. Walton, Sruti Rayaprolu, Shinsuke Fujioka, Melissa E. Murray, Michael G. Heckman, Andreas Puschmann, Allan McCarthy, Timothy Lynch, Joanna Siuda, Grzegorz Opala, Monika Rudzinska, Anna Krygowska-Wajs, Maria Barcikowska, Krzysztof Czyzewski, Yanosh Sanotsky, Irena Rektorova, Pamela J. McLean, Rosa Rademakers, Nilufer Ertekin-Taner, Anhar Hassan, J.Eric Ahlskog, Bradley F. Boeve, Ronald C. Petersen, Demetrius M. Maraganore, Charles H. Adler, Tanis J. Ferman, Joseph E. Parisi, Neill R. Graff-Radford, Ryan J. Uitti, Zbigniew K. Wszolek, Dennis W. Dickson, Owen A. Ross.
Role for the microtubule-associated protein tau variant p.A152T in risk of Α-synucleinopathies.
Neurology
2015 : Vol. 85, nr 19, s. 1680-1686
p-ISSN: 0028-3878
AZ
ORG
AIF
IF: 8.166
Adres url:
Streszczenie w PubMed:
3/9
Barbara Shannon, Alexandra Soto-Ortolaza, Sruti Rayaprolu, Heather D. Cannon, Catherine Labbe, Bruno A. Benitez, Jiyoon Choi, Timothy Lynch, Magdalena Boczarska-Jedynak, Grzegorz Opala, Anna Krygowska-Wajs, Maria Barcikowska, Jay A. Van Gerpen, Ryan J. Uitti, Wolfdieter Springer, Carlos Cruchaga, Zbigniew K. Wszolek, Owen A. Ross.
Genetic variation of the retromer subunits VPS26A/B-VPS29 in Parkinson's disease.
Neurobiol. Aging
2014 : Vol. 35, nr 8, s. 1958.e1-1958.e2, bibliogr., abstr.
p-ISSN: 0197-4580
AZ
ORG
AIF
IF: 5.013
Adres url:
4/9
Michael G. Heckman, Alexis Elbaz, Alexandra I. Soto-Ortolaza, Daniel J. Serie, Jan O. Aasly, Grazia Annesi, Georg Auburger, Justin A. Bacon, Magdalena Boczarska-Jedynak, Maria Bozi, Laura Brighina, Marie-Christine Chartier-Harlin, Efthimios Dardiotis, Alain Destee, Carlo Ferrarese, Alessandro Ferraris, Brian Fiske, Suzana Gispert, Georgios M. Hadjigeorgiou, Nobutaka Hattori, John P.A. Ioannidis, Barbara Jasinska-Myga, Beom S Jeon, Yun Joong Kim, Christine Klein, Rejko Kruger, Elli Kyratzi, Chin-Hsien Lin, Katja Lohmann, Marie-Anne Loriot, Timothy Lynch, George D. Mellick, Eugenie Mutez, Grzegorz Opala, Sung Sup Park, Simona Petrucci, Aldo Quattrone, Manu Sharma, Peter A. Silburn, Young Ho Sohn, Leonidas Stefanis, Vera Tadic, Hiroyuki Tomiyama, Ryan J. Uitti, Enza Maria Valente, Demetrios K. Vassilatis, Carles Vilarino-Guell, Linda R. White, Karin Wirdefeldt, Zbigniew Wszolek, Ruey-Meei Wu, Georgia Xiromerisiou, Demetrius M. Maraganore, Matthew J. Farrer, Owen A. Ross, Genetic Epidemiology Of Parkinson's Disease (GEO-PD) Consortium.
Protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants.
Neurobiol. Aging
2014 : Vol. 35, nr 1, s. 266.e5-266.e14, il., bibliogr., abstr.
p-ISSN: 0197-4580
AZ
ORG
AIF
IF: 5.013
5/9
Alexandra I. Soto-Ortolaza, Michael G. Heckman, Catherine Labbe, Daniel J. Serie, Andreas Puschmann, Sruti Rayaprolu, Audrey Strongosky, Magdalena Boczarska-Jedynak, Grzegorz Opala, Anna Krygowska-Wajs, Maria Barcikowska, Krzysztof Czyzewski, Timothy Lynch, Ryan J. Uitti, Zbigniew K. Wszolek, Owen A. Ross.
GWAS risk factors in Parkinson's disease: LRRK2 coding variation and genetic interaction with PARK16.
American Journal of Neurodegenerative Disease
2013 : Vol. 2, nr 4, s. 287-299, bibliogr. 23 poz., abstr.
p-ISSN: 2165-591X
AZ
ORG
APZ
Adres url:
6/9
Dorota Hoffman-Zacharska, Dariusz Koziorowski, Owen A. Ross, Michał Milewski, Jarosław Poznański, Marta Jurek, Zbigniew K. Wszolek, Alexandra Soto-Ortolaza, Jarosław Sławek, Piotr Janik, Zygmunt Jamrozik, Anna Potulska-Chromik, Barbara Jasińska-Myga, Grzegorz Opala, Anna Krygowska-Wajs, Krzysztof Czyżewski, Dennis W. Dickson, Jerzy Bal, Andrzej Friedman.
Novel A18T and pA29S substitutions in Α-synuclein may be associated with sporadic Parkinson's disease.
Parkinsonism & Related Disorders
2013 : Vol. 19, nr 11, s. 1057-1060, il., bibliogr. 12 poz., abstr.
p-ISSN: 1353-8020
AZ
ORG
AIF
IF: 4.126
Adres url:
7/9
Andreas Puschmann, Christophe Verbeeck, Michael G. Heckman, Alexandra I. Soto-Ortolaza, Timothy Lynch, Barbara Jasinska-Myga, Grzegorz Opala, Anna Krygowska-Wajs, Maria Barcikowska, Ryan J. Uitti, Zbigniew K. Wszolek, Owen A. Ross.
Human leukocyte antigen variation and Parkinson's disease.
Parkinsonism & Related Disorders
2011 : Vol. 17, nr 5, s. 376-378, bibliogr. 12 poz., abstr.
p-ISSN: 1353-8020
AZ
ORG
AIF
IF: 3.795
8/9
Marie-Christine Chartier-Harlin, Justus C. Dachsel, Carles Vilarino-Guell, Sarah J. Lincoln, Frederic Lepretre, Mary M. Hulihan, Jennifer Kachergus, Austen J. Milnerwood, Lucia Tapia, Mee-Sook Song, Emilie Le Rhun, Eugenie Mutez, Lydie Larvor, Aurelie Duflot, Christel Vanbesien-Mailliot, Alexandre Kreisler, Owen A. Ross, Kenya Nishioka, Alexandra I. Soto-Ortolaza, Stephanie A. Cobb, Heather A. Melrose, Bahareh Behrouz, Brett H. Keeling, Justin A. Bacon, Emna Hentati, Lindsey Williams, Akiko Yanagiya, Nahum Sonenberg, Paul J. Lockhart, Abba C. Zubair, Ryan J. Uitti, Jan O. Aasly, Anna Krygowska-Wajs, Grzegorz Opala, Zbigniew K. Wszolek, Roberta Frigerio, Demetrius M. Maraganore, David Gosal, Tim Lynch, Michael Hutchinson, Anna Rita Bentivoglio, Enza Maria Valente, William C. Nichols, Nathan Pankratz, Tatiana Foroud, Rachel A. Gibson, Faycal Hentati, Dennis W. Dickson, Alain Destee, Matthew J. Farrer.
Translation initiator EIF4G1 mutations in familial Parkinson disease.
American Journal of Human Genetics
2011 : Vol. 89, nr 3, s. 398-406, bibliogr. 25 poz.
p-ISSN: 0002-9297
AZ
ORG
AIF
IF: 10.603
9/9
Carles Vilarino-Guell, C. Wider, Owen A. Ross, Justus C. Dachsel, Jennifer M. Kachergus, Sarah J. Lincoln, Alexandra I. Soto-Ortolaza, Stephanie A. Cobb, Greggory J. Wilhoite, Justin A. Bacon, Bahareh Behrouz, Heather A. Melrose, Emna Hentati, Andreas Puschmann, Daniel M. Evans, Elizabeth Conibear, Wyeth W. Wasserman, Jan O. Aasly, Pierre R. Burkhard, Ruth Djaldetti, Joseph Ghika, Faycal Hentati, Anna Krygowska-Wajs, Tim Lynch, Eldad Melamed, Alex Rajput, Ali H. Rajput, Alessandra Solida, Ruey-Meei Wu, Ryan J. Uitti, Zbigniew K. Wszolek, Francois Vingerhoets, Matthew J. Farrer.
VPS35 mutations in Parkinson disease.
American Journal of Human Genetics
2011 : Vol. 89, nr 1, s. 162-167, bibliogr. 24 poz.
p-ISSN: 0002-9297
AZ
ORG
AIF
IF: 10.603
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