1999 - Potamkin Prize for Research in Pick's, Alzheimer's, and Related Diseases, American Academy of Neurology
Kirk C. Wilhelmsen mainly investigates Genetics, Genetic linkage, Parkinsonism, Frontotemporal dementia and parkinsonism linked to chromosome 17 and Dementia. His work in Genetics addresses issues such as Dystonia, which are connected to fields such as Idiopathic Torsion Dystonia. Kirk C. Wilhelmsen interconnects Microsatellite, Chromosome and Pathology in the investigation of issues within Genetic linkage.
His Pathology study deals with Genetic heterogeneity intersecting with Spinal muscular atrophies, SMA*, Spinal muscular atrophy and Chromosomal region. As a part of the same scientific study, Kirk C. Wilhelmsen usually deals with the Parkinsonism, concentrating on Tau protein and frequently concerns with Microtubule, Alternative splicing and Neurodegeneration. The Dementia study combines topics in areas such as Amyotrophy and Neuroscience.
Kirk C. Wilhelmsen focuses on Genetics, Genetic linkage, Disease, Genome-wide association study and Locus. His work is dedicated to discovering how Genetics, Alcohol dependence are connected with Psychiatry and Heritability and other disciplines. Kirk C. Wilhelmsen has researched Genetic linkage in several fields, including Substance dependence, Pathology, Microsatellite, Chromosome and Linkage.
His Disease study integrates concerns from other disciplines, such as Biomarker, Computational biology and Pathogenesis. His Locus research includes elements of Parkinsonism and Gene mapping. His studies in Parkinsonism integrate themes in fields like Amyotrophy and Chromosome 17.
Kirk C. Wilhelmsen mostly deals with Genome-wide association study, Genetics, Exome sequencing, Gene and Bioinformatics. His research in Genome-wide association study intersects with topics in Cardiology, Allele frequency, Quantitative trait locus, Internal medicine and Genetic association. In his research on the topic of Genetics, Heritability and Allele is strongly related with Meta-analysis.
His Exome sequencing research is multidisciplinary, incorporating perspectives in Computational biology, Disease and Candidate gene. His work on Phenotype, Whole genome sequencing and Missense mutation as part of general Gene research is frequently linked to EBI3, thereby connecting diverse disciplines of science. His Bioinformatics study combines topics in areas such as Causative gene, Disease gene, Medical record and Myopathy.
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Mutation-Specific Functional Impairments in Distinct Tau Isoforms of Hereditary FTDP-17
Ming Hong;Victoria Zhukareva;Vanessa Vogelsberg-Ragaglia;Zbigniew Wszolek.
Frontotemporal dementia and parkinsonism linked to chromosome 17: A consensus conference
Norman L. Foster;Kirk C. Wilhelmsen;Anders A. F. Sima;Anders A. F. Sima;Margaret Z. Jones.
Annals of Neurology (1997)
Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.2–13.3
L. M. Brzustowicz;L. M. Brzustowicz;T. Lehner;T. Lehner;L. H. Castilla;L. H. Castilla;G. K. Penchaszadeh;G. K. Penchaszadeh.
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
Rebecca Sims;Sven J. Van Der Lee;Adam C. Naj;Céline Bellenguez;Céline Bellenguez.
Nature Genetics (2017)
Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17
Lorraine N. Clark;Parvoneh Poorkaj;Zbigniew Wszolek;Daniel H. Geschwind.
Proceedings of the National Academy of Sciences of the United States of America (1998)
Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22
K. C. Wilhelmsen;T. Lynch;E. Pavlou;M. Higgins.
American Journal of Human Genetics (1994)
Localization of a gene for partial epilepsy to chromosome 10q
Ruth Ottman;Ruth Ottman;Neil Risch;W. Allen Hauser;Timothy A. Pedley.
Nature Genetics (1995)
Clinical characteristics of a family with chromosome 17‐linked disinhibition‐dementia‐ parkinsonism‐amyotrophy complex
T. Lynch;M. Sano;K. S. Marder;K. L. Bell.
Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome
Dawn H. Siegel;Gabrielle H.S. Ashton;Homero G. Penagos;James V. Lee.
American Journal of Human Genetics (2003)
Nucleic acid sequences of the oncogene v-rel in reticuloendotheliosis virus strain T and its cellular homolog, the proto-oncogene c-rel.
K C Wilhelmsen;K Eggleton;H M Temin.
Journal of Virology (1984)
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