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Margaret Ann Pericak‐Vance | ORCID 0000-0001-7283-8804 | ResearchHub

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Researchers
Margaret Ann Pericak‐Vance

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Researcher profile

Margaret Ann Pericak‐Vance

ResearchHub researcher

Duke Medical Center ORCID

13

Publications

525

Citations

10

H-index

0

Recent H-index

48

Reads

0

Followers

Overview Research Publications Projects Datasets Questions Impact Network Activity

Overview

Research identity

Research areas

Not available

Education

Not available

Research

Research outputs

Public works are drawn from admitted ResearchHub scholarly records.

Publications

Selected public works

Search public worksYearWork typeSort works

13 of 13 listed works

Exports contain available public metadata for the works currently shown.

Reduction in the minimum candidate interval in the dominant-intermediate form of Charcot-Marie-Tooth neuropathy to D19S586 to D19S432

Neurogenetics · 2002 · journal-article

8 citations · 4 reads

Genetic studies in autistic disorder and chromosome 15

Neurogenetics · 2000 · journal-article

99 citations · 4 reads

Linkage analysis of candidate myelin genes in familial multiple sclerosis

Neurogenetics · 1999 · journal-article

26 citations · 4 reads

No association between the HLA-A2 allele and Alzheimer disease

Neurogenetics · 1999 · journal-article

21 citations · 4 reads

The α-synuclein gene is not a major risk factor in familial Parkinson disease

Neurogenetics · 1999 · journal-article

29 citations · 3 reads

Fine localization of the CMT4A locus using a PAC contig and haplotype analysis

Neurogenetics · 1998 · journal-article

9 citations · 4 reads

Lack of association between apolipoprotein E genotype and sporadic amyotrophic lateral sclerosis

Neurogenetics · 1998 · journal-article

55 citations · 4 reads

Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers

Neurogenetics · 1998 · journal-article

171 citations · 4 reads

Mutation and polymorphism analysis in the tuberous sclerosis 2 ( TSC2 ) gene

Neurogenetics · 1998 · journal-article

17 citations · 3 reads

No genetic association between the LRP receptor and sporadic or late-onset familial Alzheimer disease

Neurogenetics · 1998 · journal-article

37 citations · 3 reads

Confirmation of a second locus for CMT2 and evidence for additional genetic heterogeneity

Neurogenetics · 1997 · journal-article

31 citations · 4 reads

Further exclusion of FSHD1B from the telomeric region of 10q

Neurogenetics · 1997 · journal-article

2 citations · 4 reads

Locus heterogeneity, anticipation and reduction of the chromosome 2p minimal candidate region in autosomal dominant familial spastic paraplegia

Neurogenetics · 1997 · journal-article

20 citations · 3 reads

Projects

Public projects

No public projects are available.

Datasets

Public datasets

No public datasets are available.

Questions

Questions & answers

Not available

Impact

Measured impact

Publications: 13
Citations: 525
H-index: 10
Recent H-index: 0
Reads: 48

H-index follows the standard Hirsch definition: the largest h for which h publications each have at least h citations. Recent H-index applies the same calculation to the five most recent complete calendar years (2021-2025); the current year is excluded while incomplete.

Affiliations

Institutions

DDuke Medical CenterAffiliation DDuke UniversityAffiliation

Identifiers

Scholarly links

ORCID: 0000-0001-7283-8804

Network

Research network

0 followers

Public network totals only

Activity

Recent activity

Not available

Recognition

Professional record

Not available