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Alice Rudolph

Research Profile

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Nathan Pankratz; D K Kissell; Michael W Pauciulo; Cheryl A Halter; Alice Rudolph; Ronald F Pfeiffer; Karen Marder; Tatiana Foroud; William C Nichols
Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations.
Nathan Pankratz; William C Nichols; Veronika E Elsaesser; Michael W Pauciulo; Diane K Marek; Cheryl A Halter; Joanne Wojcieszek; Alice Rudolph; Ronald F Pfeiffer; Tatiana Foroud
Alpha-synuclein and familial Parkinson's disease.
William C Nichols; D K Kissell; Nathan Pankratz; Michael W Pauciulo; Veronika E Elsaesser; K A Clark; Cheryl A Halter; Alice Rudolph; Joanne Wojcieszek; Ronald F Pfeiffer; Tatiana Foroud
Variation in GIGYF2 is not associated with Parkinson disease.

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All Publications

2009: Nathan Pankratz; D K Kissell; Michael W Pauciulo; Cheryl A Halter; Alice Rudolph; Ronald F Pfeiffer; Karen Marder; Tatiana Foroud; William C Nichols
Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations.
Neurology 2009;73(4):279-86.
2009: Nathan Pankratz; William C Nichols; Veronika E Elsaesser; Michael W Pauciulo; Diane K Marek; Cheryl A Halter; Joanne Wojcieszek; Alice Rudolph; Ronald F Pfeiffer; Tatiana Foroud
Alpha-synuclein and familial Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2009;24(8):1125-31.
2009: William C Nichols; D K Kissell; Nathan Pankratz; Michael W Pauciulo; Veronika E Elsaesser; K A Clark; Cheryl A Halter; Alice Rudolph; Joanne Wojcieszek; Ronald F Pfeiffer; Tatiana Foroud
Variation in GIGYF2 is not associated with Parkinson disease.
Neurology 2009;72(22):1886-92.
2009: William C Nichols; Nathan Pankratz; Diane K Marek; Michael W Pauciulo; Veronika E Elsaesser; Cheryl A Halter; Alice Rudolph; Joanne Wojcieszek; Ronald F Pfeiffer; Tatiana Foroud
Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onset.
Neurology 2009;72(4):310-6.
2007: William C Nichols; Veronika E Elsaesser; Nathan Pankratz; Michael W Pauciulo; Diane K Marek; Cheryl A Halter; Alice Rudolph; Clifford W Shults; Tatiana Foroud
LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8.
Neurology 2007;69(18):1737-44.
2007: William C Nichols; Diane K Marek; Michael W Pauciulo; Nathan Pankratz; Cheryl A Halter; Alice Rudolph; Clifford W Shults; Joanne Wojcieszek; Tatiana Foroud
R1514Q substitution in Lrrk2 is not a pathogenic Parkinson's disease mutation.
Movement disorders : official journal of the Movement Disorder Society 2007;22(2):254-7.
2006: Nathan Pankratz; Michael W Pauciulo; Veronika E Elsaesser; Diane K Marek; Cheryl A Halter; Alice Rudolph; Clifford W Shults; Tatiana Foroud; William C Nichols
Mutations in LRRK2 other than G2019S are rare in a north American-based sample of familial Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2006;21(12):2257-60.
2006: Nathan Pankratz; Michael W Pauciulo; Veronika E Elsaesser; Diane K Marek; Cheryl A Halter; Joanne Wojcieszek; Alice Rudolph; Clifford W Shults; Tatiana Foroud; William C Nichols
Mutations in DJ-1 are rare in familial Parkinson disease.
Neuroscience letters 2006;408(3):209-13.
2006: Nathan Pankratz; Lisa Byder; Cheryl A Halter; Alice Rudolph; Clifford W Shults; P Michael Conneally; Tatiana Foroud; William C Nichols
Presence of an APOE4 allele results in significantly earlier onset of Parkinson's disease and a higher risk with dementia.
Movement disorders : official journal of the Movement Disorder Society 2006;21(1):45-9.
2005: William C Nichols; Nathan Pankratz; Dena Hernandez; Coro Paisan-Ruiz; Shushant Jain; Cheryl A Halter; Veronika E Michaels; Terry Reed; Alice Rudolph; Clifford W Shults; Andrew Singleton; Tatiana Foroud
Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease.
Lancet 2005;365(9457):410-2.
2004: William C Nichols; Sean K Uniacke; Nathan Pankratz; Terry Reed; David K Simon; Cheryl A Halter; Alice Rudolph; Clifford W Shults; P Michael Conneally; Tatiana Foroud
Evaluation of the role of Nurr1 in a large sample of familial Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2004;19(6):649-55.
2004: Nathan Pankratz; Sean K Uniacke; Cheryl A Halter; Alice Rudolph; Clifford W Shults; P Michael Conneally; Tatiana Foroud; William C Nichols
Genes influencing Parkinson disease onset: replication of PARK3 and identification of novel loci.
Neurology 2004;62(9):1616-8.
2003: Nathan Pankratz; William C Nichols; Sean K Uniacke; Cheryl A Halter; Jill Murrell; Alice Rudolph; Clifford W Shults; P Michael Conneally; Tatiana Foroud
Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease families.
Human molecular genetics 2003;12(20):2599-608.
2003: Nathan Pankratz; William C Nichols; Sean K Uniacke; Cheryl A Halter; Alice Rudolph; Clifford W Shults; P Michael Conneally; Tatiana Foroud
Significant linkage of Parkinson disease to chromosome 2q36-37.
American journal of human genetics 2003;72(4):1053-7.
2003: Tatiana Foroud; Sean K Uniacke; L Liu; Nathan Pankratz; Alice Rudolph; Cheryl A Halter; Clifford W Shults; Karen Marder; P Michael Conneally; William C Nichols
Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease.
Neurology 2003;60(5):796-801.
2002: William C Nichols; Nathan Pankratz; Sean K Uniacke; Michael W Pauciulo; Cheryl A Halter; Alice Rudolph; P Michael Conneally; Tatiana Foroud
Linkage stratification and mutation analysis at the Parkin locus identifies mutation positive Parkinson's disease families.
Journal of medical genetics 2002;39(7):489-92.
2002: Nathan Pankratz; William C Nichols; Sean K Uniacke; Cheryl A Halter; Alice Rudolph; Clifford W Shults; P Michael Conneally; Tatiana Foroud
Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations.
American journal of human genetics 2002;71(1):124-35.