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M. Hulihan · SciRah

Researcher profile · Semantic Scholar

M. Hulihan

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M. Hulihan — researcher profile on SciRah

h-index: 42
Works: 98
Citations: 19K

Most-cited papers

α-Synuclein Locus Triplication Causes Parkinson's Disease
Andrew B. Singleton, M. Farrer, Joshua C. Johnson, AB Singleton +18 more
2003Science3,998 citations
Semantic Scholar
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology.
A. Zimprich, S. Biskup, Petra Leitner, P. Lichtner +18 more
2004Neuron3,083 citations Open access
Semantic Scholar
alpha-Synuclein locus triplication causes Parkinson's disease.
A. Singleton, M. Farrer, J. Johnson, A. Singleton +18 more
2003Science2,120 citations
Semantic Scholar
α-synuclein locus duplication as a cause of familial Parkinson's disease
M. Chartier-Harlin, J. Kachergus, C. Roumier, V. Mouroux +11 more
20041,740 citations
Semantic Scholar
Alpha-synuclein locus duplication as a cause of familial Parkinson's disease.
M. Chartier-Harlin, J. Kachergus, C. Roumier, V. Mouroux +11 more
2004The Lancet988 citations
Semantic Scholar
Comparison of kindreds with parkinsonism and α‐synuclein genomic multiplications
M. Farrer, J. Kachergus, L. Forno, S. Lincoln +7 more
2004642 citations
Semantic Scholar
Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations.
J. Kachergus, Ignacio F. Mata, M. Hulihan, Julie P. Taylor +14 more
2005American Journal of Human Genetics574 citations Open access
Semantic Scholar
Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease.
D. Maraganore, M. de Andrade, A. Elbaz, M. Farrer +24 more
2006Journal of the American Medical Association (JAMA)532 citations Open access
Semantic Scholar
Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication
Julia Fuchs, C. Nilsson, J. Kachergus, M. Munz +8 more
2007Neurology444 citations
Semantic Scholar
Comparison of kindreds with parkinsonism and alpha-synuclein genomic multiplications.
M. Farrer, J. Kachergus, L. Forno, S. Lincoln +7 more
2004Annals of Neurology367 citations
Semantic Scholar
Translation initiator EIF4G1 mutations in familial Parkinson disease.
M. Chartier-Harlin, J. Dachsel, C. Vilariño-Güell, S. Lincoln +46 more
2011American Journal of Human Genetics326 citations Open access
Semantic Scholar
DCTN1 mutations in Perry syndrome
M. Farrer, M. Hulihan, J. Kachergus, J. Dächsel +18 more
2009Nature Genetics320 citations Open access
Semantic Scholar
Lrrk2 pathogenic substitutions in Parkinson's disease
I. Mata, J. Kachergus, Julie P. Taylor, S. Lincoln +9 more
2005Neurogenetics253 citations
Semantic Scholar
Genomic investigation of α‐synuclein multiplication and parkinsonism
O. Ross, A. Braithwaite, L. Skipper, J. Kachergus +14 more
2008Annals of Neurology233 citations Open access
Semantic Scholar
The PARK8 locus in autosomal dominant parkinsonism: confirmation of linkage and further delineation of the disease-containing interval.
A. Zimprich, B. Müller-Myhsok, M. Farrer, Petra Leitner +17 more
2004American Journal of Human Genetics215 citations Open access
Semantic Scholar
Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia.
M. Farrer, J. T. Stone, Chin-Hsien Lin, J. Dächsel +4 more
2007Parkinsonism & Related Disorders212 citations
Semantic Scholar
α‐Synuclein promoter confers susceptibility to Parkinson's disease
P. Pals, S. Lincoln, Jonathan J. Manning, M. Heckman +8 more
2004200 citations
Semantic Scholar
Clinical features of LRRK2‐associated Parkinson's disease in central Norway
J. Aasly, M. Toft, Ignacio Fernandez-Mata, J. Kachergus +3 more
2005Annals of Neurology196 citations
Semantic Scholar
LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic study.
M. Hulihan, L. Ishihara-Paul, J. Kachergus, L. Warren +14 more
2008Lancet Neurology187 citations
Semantic Scholar
Incidence of Sickle Cell Trait — United States, 2010
J. Ojodu, M. Hulihan, Shammara N. Pope, Althea M. Grant
2014MMWR. Morbidity and mortality weekly report167 citations
Semantic Scholar
Linkage disequilibrium and association of MAPT H1 in Parkinson disease.
L. Skipper, Kristen Wilkes, M. Toft, M. Baker +6 more
2004American Journal of Human Genetics158 citations Open access
Semantic Scholar
LRRK2 mutations in Parkinson disease
M. Farrer, J. T. Stone, Ignacio F. Mata, Sarah J. Lincoln +4 more
2005Neurology157 citations
Semantic Scholar
Pallidonigral TDP-43 pathology in Perry syndrome
C. Wider, D. Dickson, A. Stoessl, Y. Tsuboi +15 more
2008Parkinsonism & Related Disorders112 citations Open access
Semantic Scholar
alpha-Synuclein promoter confers susceptibility to Parkinson's disease.
P. Pals, S. Lincoln, Jonathan J. Manning, M. Heckman +8 more
2004Annals of Neurology100 citations
Semantic Scholar
DJ-1 mutations are a rare cause of recessively inherited early onset parkinsonism mediated by loss of protein function
P. Lockhart, Sarah J. Lincoln, M. Hulihan, J. Kachergus +4 more
2004Journal of Medical Genetics95 citations Open access
Semantic Scholar
LRRK2 R1441G in Spanish patients with Parkinson's disease.
I. Mata, Julie P. Taylor, J. Kachergus, M. Hulihan +9 more
2005Neuroscience Letters91 citations
Semantic Scholar
Defining Sickle Cell Disease Mortality Using a Population-Based Surveillance System, 2004 through 2008
Susan T. Paulukonis, J. Eckman, A. Snyder, Ward Hagar +4 more
2016Public health reports (1974)86 citations Open access
Semantic Scholar
Increased oxidative stress in patients with amyotrophic lateral sclerosis/Parkinsonism‐dementia complex in the Kii peninsula, Japan
Ming-Jen Lee, Ignacio F. Mata, Chin-Hsien Lin, K. Tzen +6 more
2009Movement Disorders81 citations
Semantic Scholar
Multiple alpha‐synuclein gene polymorphisms are associated with Parkinson’s disease in a Norwegian population
Ronny Myhre, Mathias Toft, J. Kachergus, M. Hulihan +3 more
2008Acta Neurologica Scandinavica80 citations Open access
Semantic Scholar
Parkin mutations and early-onset parkinsonism in a Taiwanese cohort.
Ruey-Meei Wu, R. Bounds, S. Lincoln, M. Hulihan +5 more
2005Archives of Neurology73 citations
Semantic Scholar
Genetic variation of Omi/HtrA2 and Parkinson’s disease
Owen A. Ross, A. Soto, C. Vilariño-Güell, M. Heckman +13 more
2008Parkinsonism & Related Disorders71 citations Open access
Semantic Scholar
The use of US health insurance data for surveillance of rare disorders: hereditary hemorrhagic telangiectasia
S. Grosse, S. Boulet, Althea M. Grant, M. Hulihan +1 more
2013Genetics in Medicine67 citations Open access
Semantic Scholar
Characterization of DCTN1 genetic variability in neurodegeneration
C. Vilariño-Güell, C. Wider, A. Soto-Ortolaza, S. A. Cobb +22 more
2009Neurology65 citations Open access
Semantic Scholar
Genomewide association, Parkinson disease, and PARK10.
M. Farrer, K. Haugarvoll, O. Ross, J. T. Stone +14 more
2006American Journal of Human Genetics63 citations Open access
Semantic Scholar
PINK1 mutations and parkinsonism
L. Ishihara-Paul, M. Hulihan, J. Kachergus, R. Upmanyu +15 more
2008Neurology58 citations Open access
Semantic Scholar
The impact of chelation therapy on survival in transfusional iron overload: a meta-analysis of myelodysplastic syndrome
A. Mainous, R. Tanner, M. Hulihan, Mirna P. Amaya +1 more
2014British Journal of Haematology56 citations Open access
Semantic Scholar
Attitudes toward Management of Sickle Cell Disease and Its Complications: A National Survey of Academic Family Physicians
A. Mainous, R. Tanner, Christopher A. Harle, R. Baker +2 more
2015Anemia55 citations Open access
Semantic Scholar
Public health implications of sickle cell trait: a report of the CDC meeting.
Althea M. Grant, Christopher S. Parker, Lanetta B. Jordan, M. Hulihan +4 more
2011American Journal of Preventive Medicine50 citations Open access
Semantic Scholar
State-based surveillance for selected hemoglobinopathies
M. Hulihan, L. Feuchtbaum, Lanetta B. Jordan, R. Kirby +10 more
2014Genetics in Medicine46 citations Open access
Semantic Scholar
Sickle cell disease incidence among newborns in New York State by maternal race/ethnicity and nativity
Ying Wang, J. Kennedy, M. Caggana, R. Zimmerman +8 more
2012Genetics in Medicine46 citations Open access
Semantic Scholar
ATP13A2 variability in Parkinson disease
C. Vilariño-Güell, A. Soto, Sarah J. Lincoln, Samia Ben Yahmed +13 more
2009Human Mutation44 citations Open access
Semantic Scholar
Glucosidase-beta variations and Lewy Body Disorders
M. Farrer, L. Williams, A. Algom, J. Kachergus +6 more
2008Parkinsonism & Related Disorders44 citations Open access
Semantic Scholar
Rett Syndrome : An Overlooked Diagnosis in Women with Stereotypic Hand Movements , Psychomotor Retardation , Parkinsonism , and Dystonia ?
I. Mata, O. Ross, J. Kachergus, M. Hulihan +9 more
200742 citations
Semantic Scholar
Leucine-rich repeat kinase 1: a paralog of LRRK2 and a candidate gene for Parkinson’s disease
Julie P. Taylor, M. Hulihan, J. Kachergus, H. Melrose +10 more
2007Neurogenetics40 citations
Semantic Scholar
Lrrk2 R1441 substitution and progressive supranuclear palsy
Owen A Ross, Andrew J. Whittle, S. A. Cobb, M. Hulihan +4 more
2006Neuropathology and Applied Neurobiology40 citations
Semantic Scholar
The accuracy of hospital ICD-9-CM codes for determining Sickle Cell Disease genotype
A. Snyder, P. Lane, Mei Zhou, Susan T. Paulukonis +1 more
2017Journal of Rare Diseases Research & Treatment39 citations Open access
Semantic Scholar
Birth Prevalence of Sickle Cell Disease and County-Level Social Vulnerability — Sickle Cell Data Collection Program, 11 States, 2016–2020
Mariam Kayle, A. Blewer, Wei Pan, Jennifer A. Rothman +26 more
2024MMWR. Morbidity and mortality weekly report37 citations Open access
Semantic Scholar
Surveillance for Sickle Cell Disease — Sickle Cell Data Collection Program, Two States, 2004–2018
A. Snyder, Sangeetha Lakshmanan, M. Hulihan, Susan T. Paulukonis +5 more
2022Morbidity and mortality weekly report. Surveillance summaries34 citations Open access
Semantic Scholar
Clinical traits of LRRK2-associated Parkinson's disease in Ireland: a link between familial and idiopathic PD.
D. Gosal, O. Ross, Joseph C. Wiley, G. Irvine +10 more
2005Parkinsonism & Related Disorders34 citations
Semantic Scholar
Fine-mapping and candidate gene investigation within the PARK10 locus
K. Haugarvoll, M. Toft, L. Skipper, M. Heckman +13 more
2009European Journal of Human Genetics33 citations Open access
Semantic Scholar

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