D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Genetics D-index 53 Citations 11,962 170 World Ranking 2944 National Ranking 1285

Research.com Recognitions

Awards & Achievements

1999 - Potamkin Prize for Research in Pick's, Alzheimer's, and Related Diseases, American Academy of Neurology

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Mutation
  • Genetics

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.

His most cited work include:

  • Mutation-Specific Functional Impairments in Distinct Tau Isoforms of Hereditary FTDP-17 (802 citations)
  • Frontotemporal dementia and parkinsonism linked to chromosome 17: A consensus conference (551 citations)
  • Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q1 1.2–13.3 (456 citations)

What are the main themes of his work throughout his whole career to date?

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.

He most often published in these fields:

  • Genetics (45.75%)
  • Genetic linkage (21.23%)
  • Disease (15.09%)

What were the highlights of his more recent work (between 2016-2021)?

  • Genome-wide association study (15.09%)
  • Genetics (45.75%)
  • Exome sequencing (8.96%)

In recent papers he was focusing on the following fields of study:

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.

Between 2016 and 2021, his most popular works were:

  • Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease (429 citations)
  • Dissecting the Causal Mechanism of X-Linked Dystonia-Parkinsonism by Integrating Genome and Transcriptome Assembly (82 citations)
  • Prenatal exome sequencing in anomalous fetuses: new opportunities and challenges. (81 citations)

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

Mutation-Specific Functional Impairments in Distinct Tau Isoforms of Hereditary FTDP-17

Ming Hong;Victoria Zhukareva;Vanessa Vogelsberg-Ragaglia;Zbigniew Wszolek.
Science (1998)

1110 Citations

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)

765 Citations

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.
Nature (1990)

710 Citations

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)

683 Citations

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)

592 Citations

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)

485 Citations

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)

417 Citations

Clinical characteristics of a family with chromosome 17‐linked disinhibition‐dementia‐ parkinsonism‐amyotrophy complex

T. Lynch;M. Sano;K. S. Marder;K. L. Bell.
Neurology (1994)

378 Citations

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)

369 Citations

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)

347 Citations

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