α-Synuclein Locus Triplication Causes Parkinson's Disease
Singleton, A. B., Farrer, M., Johnson, J., Singleton, A., Hague, S., Kachergus, J., Hulihan, M., Peuralinna, T., Dutra, A., Nussbaum, R., Lincoln, S., Crawley, A., Hanson, M., Maraganore, D., Adler, C., Cookson, M. R., Muenter, M., Baptista, M., Miller, D., Blancato, J., Hardy, J., Gwinn-Hardy, K.
Published in Science (American Association for the Advancement of Science) (31.10.2003)
Published in Science (American Association for the Advancement of Science) (31.10.2003)
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Journal Article
Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication
Fuchs, J, Nilsson, C, Kachergus, J, Munz, M, Larsson, E-M, Schüle, B, Langston, J W, Middleton, F A, Ross, O A, Hulihan, M, Gasser, T, Farrer, M J
Published in Neurology (20.03.2007)
Published in Neurology (20.03.2007)
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Journal Article
LRRK2 Gly2019Ser penetrance in Arab–Berber patients from Tunisia: a case-control genetic study
Hulihan, Mary M, MPH, Ishihara-Paul, Lianna, PhD, Kachergus, Jennifer, BSc, Warren, Liling, PhD, Amouri, Rim, PhD, Elango, Ramu, PhD, Prinjha, Rab K, PhD, Upmanyu, Ruchi, MSc, Kefi, Mounir, MD, Zouari, Mourad, MD, Sassi, Samia Ben, MD, Yahmed, Samia Ben, MD, El Euch-Fayeche, Ghada, MD, Matthews, Paul M, PhD, Middleton, Lefkos T, MD, Gibson, Rachel A, PhD, Hentati, Fayçal, MD, Farrer, Matthew J, PhD
Published in Lancet neurology (01.07.2008)
Published in Lancet neurology (01.07.2008)
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Journal Article
PINK1 mutations and parkinsonism
Ishihara-Paul, L, Hulihan, M M, Kachergus, J, Upmanyu, R, Warren, L, Amouri, R, Elango, R, Prinjha, R K, Soto, A, Kefi, M, Zouari, M, Sassi, S B, Yahmed, S B, El Euch-Fayeche, G, Matthews, P M, Middleton, L T, Gibson, R A, Hentati, F, Farrer, M J
Published in Neurology (16.09.2008)
Published in Neurology (16.09.2008)
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Journal Article
Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia
Farrer, Matthew J, Stone, Jeremy T, Lin, Chin-Hsien, Dächsel, Justus C, Hulihan, Mary M, Haugarvoll, Kristoffer, Ross, Owen A, Wu, Ruey-Meei
Published in Parkinsonism & related disorders (01.03.2007)
Published in Parkinsonism & related disorders (01.03.2007)
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Journal Article
Lrrk2 pathogenic substitutions in Parkinson's disease
MATA, Ignacio F, KACHERGUS, Jennifer M, LAHOZ, Carlos, WSZOLEK, Zbigniew K, FARRER, Matthew J, TAYLOR, Julie P, LINCOLN, Sarah, AASLY, Jan, LYNCH, Timothy, HULIHAN, Mary M, COBB, Stephanie A, WU, Ruey-Meei, LU, Chin-Song
Published in Neurogenetics (01.12.2005)
Published in Neurogenetics (01.12.2005)
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Journal Article
278 Emergency Department Utilization by Californians With Sickle Cell Disease, 2005-2014
Paulukonis, S, Vichinsky, E, Neumayr, L, Treadwell, M, Coates, T, Feuchtbaum, L, Hulihan, M
Published in Annals of emergency medicine (01.10.2016)
Published in Annals of emergency medicine (01.10.2016)
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Journal Article
LRRK2 mutations in Parkinson disease
Farrer, M, Stone, J, Mata, I F, Lincoln, S, Kachergus, J, Hulihan, M, Strain, K J, Maraganore, D M
Published in Neurology (13.09.2005)
Published in Neurology (13.09.2005)
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Journal Article
Public Health Surveillance of Nonmalignant Blood Disorders
Beckman, Michele G., MPH, Hulihan, Mary M., MPH, Byams, Vanessa R., MPH, Oakley, Meredith A., DVM, MPH, Reyes, Nimia, MD, Trimble, Sean, MPH, Grant, Althea M., PhD, MPH
Published in American journal of preventive medicine (01.11.2014)
Published in American journal of preventive medicine (01.11.2014)
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Journal Article
Characterization of DCTN1 genetic variability in neurodegeneration
Vilariño-Güell, C, Wider, C, Soto-Ortolaza, A I, Cobb, S A, Kachergus, J M, Keeling, B H, Dachsel, J C, Hulihan, M M, Dickson, D W, Wszolek, Z K, Uitti, R J, Graff-Radford, N R, Boeve, B F, Josephs, K A, Miller, B, Boylan, K B, Gwinn, K, Adler, C H, Aasly, J O, Hentati, F, Destée, A, Krygowska-Wajs, A, Chartier-Harlin, M-C, Ross, O A, Rademakers, R, Farrer, M J
Published in Neurology (09.06.2009)
Published in Neurology (09.06.2009)
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Transferrin Saturation and Hospital Length of Stay and Mortality in Medicare Beneficiaries
Mainous III, Arch G., Diaz, Vanessa A., Knoll, Michele E., Hulihan, Mary M., Grant, Althea M., Wright, Robert U.
Published in Journal of the American Geriatrics Society (JAGS) (01.01.2013)
Published in Journal of the American Geriatrics Society (JAGS) (01.01.2013)
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Journal Article
Lrrk2 R1441 substitution and progressive supranuclear palsy
Ross, O. A., Whittle, A. J., Cobb, S. A., Hulihan, M. M., Lincoln, S. J., Toft, M., Farrer, M. J., Dickson, D. W.
Published in Neuropathology and applied neurobiology (01.02.2006)
Published in Neuropathology and applied neurobiology (01.02.2006)
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Journal Article
Genomewide Association, Parkinson Disease, and PARK10
Farrer, Matthew J., Haugarvoll, Kristoffer, Ross, Owen A., Stone, Jeremy T., Milkovic, Nicole M., Cobb, Stephanie A., Whittle, Andrew J., Lincoln, Sarah J., Hulihan, Mary M., Heckman, Michael G., White, Linda R., Aasly, Jan O., Gibson, J. Mark, Gosal, David, Lynch, Timothy, Wszolek, Zbigniew K., Uitti, Ryan J., Toft, Mathias
Published in American journal of human genetics (01.06.2006)
Published in American journal of human genetics (01.06.2006)
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Journal Article
DJ-1 mutations are a rare cause of recessively inherited early onset parkinsonism mediated by loss of protein function
Lockhart, P J, Lincoln, S, Hulihan, M, Kachergus, J, Wilkes, K, Bisceglio, G, Mash, D C, Farrer, M J
Published in Journal of medical genetics (01.03.2004)
Published in Journal of medical genetics (01.03.2004)
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Journal Article
Fine-mapping and candidate gene investigation within the PARK10 locus
HAUGARVOLL, Kristoffer, TOFT, Mathias, WHITE, Linda R, LYNCH, Timothy, GIBSON, J. Mark, UITTI, Ryan J, WSZOLEK, Zbigniew K, AASLY, Jan O, FARRER, Matthew J, SKIPPER, Lisa, HECKMAN, Michael G, CROOK, Julia E, SOTO, Alexandra, ROSS, Owen A, HULIHAN, Mary M, KACHERGUS, Jennifer M, SANDO, Sigrid B
Published in European journal of human genetics : EJHG (01.03.2009)
Published in European journal of human genetics : EJHG (01.03.2009)
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Journal Article
A national survey of hemochromatosis patients
Mainous, 3rd, Arch G, Knoll, Michele E, Everett, Charles J, Hulihan, Mary M, Grant, Althea M, Garrison, Cheryl, Koenig, Gerald, Sayers, Cynthia, Allen, Kelsey W
Published in Journal of the American Board of Family Medicine (01.07.2012)
Published in Journal of the American Board of Family Medicine (01.07.2012)
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