Kirk C Wilhelmsen
Kirk C Wilhelmsen
Carrol Master Schiller Distinguished Professor of Neurology and Genetics, University of North
Verified email at med.unc.edu - Homepage
Title
Cited by
Cited by
Year
Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17
M Hong, V Zhukareva, V Vogelsberg-Ragaglia, Z Wszolek, L Reed, ...
Science 282 (5395), 1914-1917, 1998
9581998
Frontotemporal dementia and parkinsonism linked to chromosome 17: a consensus conference
NL Foster, K Wilhelmsen, AAF Sima, MZ Jones, CJ D'Amato, S Gilman, ...
Annals of neurology 41 (6), 706-715, 1997
7021997
Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.2–13.3
LM Brzustowicz, T Lehner, LH Castilla, GK Penchaszadeh, ...
Nature 344 (6266), 540-541, 1990
6321990
Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17
LN Clark, P Poorkaj, Z Wszolek, DH Geschwind, ZS Nasreddine, B Miller, ...
Proceedings of the National Academy of Sciences 95 (22), 13103-13107, 1998
5351998
Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22.
KC Wilhelmsen, T Lynch, E Pavlou, M Higgins, TG Nygaard
American journal of human genetics 55 (6), 1159, 1994
4541994
Localization of a gene for partial epilepsy to chromosome 10q
R Ottman, N Risch, WA Hauser, TA Pedley, JH Lee, C Barker-Cummings, ...
Nature genetics 10 (1), 56-60, 1995
3831995
Clinical characteristics of a family with chromosome 17‐linked disinhibition‐dementia‐parkinsonism‐amyotrophy complex
T Lynch, M Sano, KS Marder, KL Bell, NL Foster, RF Defending, ...
Neurology 44 (10), 1878-1878, 1994
3371994
Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin–extracellular-matrix linker protein UNC-112, causes Kindler syndrome
DH Siegel, GHS Ashton, HG Penagos, JV Lee, HS Feiler, KC Wilhelmsen, ...
The American Journal of Human Genetics 73 (1), 174-187, 2003
3172003
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
R Sims, SJ Van Der Lee, AC Naj, C Bellenguez, N Badarinarayan, ...
Nature genetics 49 (9), 1373-1384, 2017
3102017
Nucleic acid sequences of the oncogene v-rel in reticuloendotheliosis virus strain T and its cellular homolog, the proto-oncogene c-rel.
KC Wilhelmsen, K Eggleton, HM Temin
Journal of virology 52 (1), 172-182, 1984
3041984
Comparison of family histories in FTLD subtypes and related tauopathies
JS Goldman, JM Farmer, EM Wood, JK Johnson, A Boxer, J Neuhaus, ...
Neurology 65 (11), 1817-1819, 2005
2532005
Linkage mapping of dopa–responsive dystonia (DRD) to chromosome 14q
TG Nygaard, KC Wilhelmsen, NJ Risch, DL Brown, JM Trugman, ...
Nature genetics 5 (4), 386-391, 1993
2381993
Tau gene mutation in familial progressive subcortical gliosis
M Goedert, MG Spillantini, RA Crowther, SG Chen, P Parchi, M Tabaton, ...
Nature medicine 5 (4), 454-457, 1999
2151999
Mapping of Familial Primary Pulmonary Hypertension Locus (PPH1) to Chromosome 2q31-q32
JH Morse, AC Jones, RJ Barst, SE Hodge, KC Wilhelmsen, TG Nygaard
Circulation 95 (12), 2603-2606, 1997
2041997
Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
BW Kunkle, B Grenier-Boley, R Sims, JC Bis, V Damotte, AC Naj, ...
Nature genetics 51 (3), 414-430, 2019
1882019
Hereditary dysphasic disinhibition dementia A frontotemporal dementia linked to 17 q21‐‐22
CL Lendon, T Lynch, J Norton, DW McKeel, F Busfield, N Craddock, ...
Neurology 50 (6), 1546-1555, 1998
1751998
The virus-specific intracellular RNA species of two murine coronaviruses: MHV-A59 and MHV-JHM
JL Leibowitz, KC Wilhelmsen, CW Bond
Virology 114 (1), 39-51, 1981
1741981
From genotype to phenotype: A clinical, pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP‐17) caused by the P301L tau mutation
ZS Nasreddine, M Loginov, LN Clark, J Lamarche, BL Miller, ...
Annals of Neurology: Official Journal of the American Neurological …, 1999
1461999
Localization of the gene for rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration to chromosome 17q21
M Wijker, ZK Wszolek, ECH Wolters, MA Rooimans, G Pals, RF Pfeiffer, ...
Human molecular genetics 5 (1), 151-154, 1996
1431996
An informatics approach to analyzing the incidentalome
JS Berg, M Adams, N Nassar, C Bizon, K Lee, CP Schmitt, KC Wilhelmsen, ...
Genetics in Medicine 15 (1), 36-44, 2013
1422013
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