P. C. Gaskell

15.2k citations

45 papers · 10.7k indexed · 3 hit papers · h-index 23

Impact in

Physiology top 0.1%
- Alzheimer's disease research and treatments
Neurology top 0.2%
- Neuroinflammation and Neurodegeneration Mechanisms

Papers in

Cellular and Molecular Neuroscience 18
- Hereditary Neurological Disorders 10
- Genetic Neurodegenerative Diseases 5
Neurology 8
- Neurological diseases and metabolism 8
- Parkinson's Disease Mechanisms and Treatments 5

Co-authors: Jeffery M. Vance Allen D. Roses Ann M. Saunders Elizabeth H. Corder Warren J. Strittmatter D. E. Schmechel Gary W. Small J. L. Haines
Journals: Neurogenetics (5 papers)Neurology (4 papers)Neurobiology of Aging (3 papers)The American Journal of Human Genetics (3 papers)Genomics (3 papers)
Partner nations: United States United Kingdom Cyprus

In The Last Decade

P. C. Gaskell

43 papers receiving 10.4k citations

Hit Papers

align trajectories log scale

Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease 1994 · 1.4k citations

Peers

Countries citing papers authored by P. C. Gaskell

Since Specialization

Citations

This map shows the geographic impact of P. C. Gaskell's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by P. C. Gaskell with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites P. C. Gaskell more than expected).

Fields of papers citing papers by P. C. Gaskell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by P. C. Gaskell. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by P. C. Gaskell. The network helps show where P. C. Gaskell may publish in the future.

Co-authorship network

The 25 scholars most cited alongside P. C. Gaskell, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with P. C. Gaskell Line = papers co-authored together P. C. Gaskell links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Maternal lineages and Alzheimer disease risk in the Old Order Amish Human Genetics ·Joelle M. van der Walt, William K. Scott, Susan Slifer, P. C. Gaskell, Eden R. Martin, Kathleen A. Welsh‐Bohmer, Costa dos Passos Colling, Amy Crunk, Ihab Abu Rahal, Lynne L. McFarland, Nabil Abassy, Charles E. Jackson, Jonathan L. Haines, Margaret A. Pericak‐Vance	2005	24
2	Covariate analysis of late-onset Alzheimer disease refines the chromosome 12 locus Molecular Psychiatry ·Catherine Russell, Nathalie Schnetz‐Boutaud, S J Kenealy, Lan Jiang, V. Jeevagan, Zhizhong Guo, P. C. Gaskell, Harry E. Gwirtsman, Lynne L. McFarland, Сигаев И.Ю., Paola G. Bronson, John R. Gilbert, Eden R. Martin, M. A. Pericak‐Vance, Jonathan L. Haines	2005	18
3	Intragenic modifiers of hereditary spastic paraplegia due to spastin gene mutations Neurogenetics ·Ingrid K. Svenson, Mark Kloos, P. C. Gaskell, Martha Nance, James Garbern, Shin‐ichi Hisanaga, Margaret A. Pericak‐Vance, Allison E. Ashley‐Koch, Douglas A. Marchuk	2004	61
4	Lewy body pathology is a frequent co-pathology in familial Alzheimer's disease Acta Neuropathologica ·Brian Zalma, M. Murray Carson, John F. Ervin, Donald E. Schmechel, P. C. Gaskell, Margaret A. Pericak‐Vance, Jeffery M. Vance, Christine M. Hulette	2003	30
5	Reduction in the minimum candidate interval in the dominant-intermediate form of Charcot-Marie-Tooth neuropathy to D19S586 to D19S432 Neurogenetics ·Marcy C. Speer, Felicia L. Graham, Mao Yong Cao, ore Psodorov, Jeffrey M. Stajich, P. C. Gaskell, Margaret A Pericak‐Vance, Jeffery M. Vance	2002	7
6	A Kinesin Heavy Chain (KIF5A) Mutation in Hereditary Spastic Paraplegia (SPG10) The American Journal of Human Genetics ·Evan Reid, Mark Kloos, Allison E. Ashley‐Koch, L.A. Hughes, María Rivadeneira-Ruiz, Ingrid K. Svenson, Felicia L. Graham, P. C. Gaskell, Andrew Dearlove, Margaret A. Pericak‐Vance, David C. Rubinsztein, Douglas A. Marchuk	2002	377
7	Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia Neurogenetics ·Allison E. Ashley‐Koch, Mao Yong Cao, P. C. Gaskell, Sandra G. West, Richard W. Tim, Chantelle M. Wolpert, Rodney H. Jones, Carolyn Farrell, Martha Nance, Ingrid K. Svenson, Douglas A. Marchuk, Rose-Mary N. Boustany, Jeffery M. Vance, William K. Scott, Margaret A. Pericak‐Vance	2001	8
8	Identification and Expression Analysis of Spastin Gene Mutations in Hereditary Spastic Paraplegia The American Journal of Human Genetics ·Ingrid K. Svenson, Allison E. Ashley‐Koch, P. C. Gaskell, سیمین دخت طهماسبی, Yulya Bataeva, Helen Kingston, Edward L. Hogan, Rose-Mary N. Boustany, Jeffery M. Vance, Martha Nance, Margaret A. Pericak‐Vance, Douglas A. Marchuk	2001	112
9	Lewy body and Alzheimer pathology in a family with the amyloid-β precursor protein APP717 gene mutation Acta Neuropathologica ·Carlyn K. Rosenberg, Jeffery M. Vance, Ann M. Saunders, John R. Gilbert, P. C. Gaskell, Christine M. Hulette	2000	49
10	Neuropathological Features of Frontotemporal Dementia and Parkinsonism Linked to Chromosome 17q21–22 (FTDP-17) Journal of Neuropathology & Experimental Neurology ·Christine M. Hulette, Jeffery M. Vance, A.D. Roses, D.E. Schmechel, Larry H. Yamaoka, P. C. Gaskell, Kathleen A. Welsh‐Bohmer, R. Anthony Crowther, Maria Grazia Spillantini	1999	42
11	Complete Genomic Screen in Late-Onset Familial Alzheimer’s Disease Neurobiology of Aging ·Jeffery M. Vance, Yeimy Natalia Buitrón-Chávez, Larry H. Yamaoka, P. C. Gaskell, William K. Scott, Henry Terwedow, Marisa M. Menold, P.M. Conneally, Gary W. Small, Ann M. Saunders, Allen D. Roses, J. L. Haines	1998	44
12	No association or linkage between an intronic polymorphism of presenilin-1 and sporadic or late-onset familial Alzheimer disease Genetic Epidemiology ·William K. Scott, Larry H. Yamaoka, P. A. Locke, B.L. Rosi, P. C. Gaskell, Ann M. Saunders, P.M. Conneally, Gary W. Small, Lindsay A. Farrer, John H. Growdon, Allen D. Roses, Margaret A. Pericak‐Vance, Jonathan L. Haines	1997	28
13	Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13 in American families suggests the existence of a second causal mutation Neuromuscular Disorders ·Jeffrey M. Stajich, James M. Gilchrist, Felicia Lennon, Arnold Lee, Larry H. Yamaoka, B.L. Rosi, P. C. Gaskell, Roizman Ei, 光男山田, Allen D. Roses, Jeffery M. Vance, Margaret A. Pericak-Vance	1997	6
14	No Genetic Effect of α1-Antichymotrypsin in Alzheimer Disease Genomics ·Jonathan L. Haines, Roizman Ei, Ann M. Saunders, J.M. Schildkraut, John H. Growdon, P. C. Gaskell, Lindsay A. Farrer, Sanford A. Auerbach, James F. Gusella, P. A. Locke, B.L. Rosi, Larry H. Yamaoka, Gary W. Small, P. M. Conneally, Allen D. Roses, M. A. Pericak‐Vance	1996	77
15	Confirmation of linkage of oculopharyngel muscular dystrophy to chromosome 14q 11.2‐q13 Annals of Neurology ·Jeffrey M. Stajich, Felicia Lennon, Arnold Lee, Larry H. Yamaoka, James H. Chapman, P. C. Gaskell, Allen D. Roses, Jeffery M. Vance, Margaret A. Pericak‐Vance, James M. Gilchrist, 光男山田	1996	9
16	Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease Nature Genetics ·Elizabeth H. Corder, Ann M. Saunders, Neil Risch, Warren J. Strittmatter, D. E. Schmechel, P. C. Gaskell, Jacqueline Rimmler, P. A. Locke, P. M. Conneally, Ken Schmader, G. W. Small, Allen D. Roses, Jonathan L. Haines, Jeffery M. Vance Hit paper breakdown →	1994	1414
17	Development of a microsatellite genetic map spanning 5q31–q33 and subsequent placement of the LGMD1A locus between D5S178 and IL9 Neuromuscular Disorders ·Larry H. Yamaoka, Carol A. Westbrook, Marcy C. Speer, James M. Gilchrist, Ethylin Wang Jabs, Adina Chasan, Von K. Weissermel, P. C. Gaskell, Allen D. Roses, Margaret A. Pericak-Vance	1994	25
18	Gene Dose of Apolipoprotein E Type 4 Allele and the Risk of Alzheimer's Disease in Late Onset Families Science ·Elizabeth H. Corder, Ann M. Saunders, Warren J. Strittmatter, D. E. Schmechel, P. C. Gaskell, Gary W. Small, Allen D. Roses, J. L. Haines, Jeffery M. Vance Hit paper breakdown →	1993	7044
19	Localization of a Gene (CMT2A) for Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 to Chromosome 1p and Evidence of Genetic Heterogeneity Genomics ·Kamel Ben Othmane, Lefkos Middleton, Zhou Fanglong, Charles W. Holtzer, Felicia Lennon, Marvin P. Rozear, M. Chrobak, P. C. Gaskell, Allen D. Roses, Margaret A. Pericak‐Vance, Jeffery M. Vance	1993	120
20	Linkage studies in peripheral neurofibromatosis. Journal of Medical Genetics ·Jeffery M. Vance, Larry H. Yamaoka, Arthur S. Aylsworth, Ethan F. T. Hoff, P. C. Gaskell, Mark J. Alberts, W.‐Y. Hung, Carol Haynes, Allen D. Roses	1987	3

About P. C. Gaskell

P. C. Gaskell is a scholar working on Cellular and Molecular Neuroscience, Neurology, Neurology, Physiology and Aging, having authored 45 papers that have together received 10.7k indexed citations. Recurring topics across this work include Alzheimer's disease research and treatments (14 papers), Hereditary Neurological Disorders (10 papers), Neurological diseases and metabolism (8 papers), Neurogenetic and Muscular Disorders Research (6 papers), Cholinesterase and Neurodegenerative Diseases (5 papers), Parkinson's Disease Mechanisms and Treatments (5 papers), Genetic Neurodegenerative Diseases (5 papers) and Dementia and Cognitive Impairment Research (4 papers). The work is most often cited by research in Physiology (6.3k citations), Neurology (1.7k citations), Psychiatry and Mental health (2.3k citations), Cellular and Molecular Neuroscience (2.1k citations) and Biological Psychiatry (270 citations). P. C. Gaskell has collaborated with scholars based in United States, United Kingdom and Cyprus. Frequent co-authors include Jeffery M. Vance, Allen D. Roses, Ann M. Saunders, Elizabeth H. Corder, Warren J. Strittmatter, D. E. Schmechel, Gary W. Small, J. L. Haines, Jonathan L. Haines and P. A. Locke. Their work appears in journals such as Neurogenetics, Neurology, Neurobiology of Aging, The American Journal of Human Genetics and Genomics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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