M. A. Pericak‐Vance

10.8k citations

57 papers · 7.1k indexed · 3 hit papers · h-index 24

Physiology top 0.5%
Molecular Biology top 2%
Genetics top 0.5%
Pulmonary and Respiratory Medicine top 2%
Cellular and Molecular Neuroscience top 2%

Co-authors: Ann M. Saunders Guy S. Salvesen A D Roses Jan J. Enghild Warren J. Strittmatter D. E. Schmechel Douglas A. Marchuk Alan E. Guttmacher
Topics: Alzheimer's disease research and treatments (9 papers)Glaucoma and retinal disorders (7 papers)Muscle Physiology and Disorders (5 papers)
Cited by: Genetics Physiology Neurology
Journals: Science Proceedings of the National Academy of Sciences The Lancet
Partner nations: United States United Kingdom Netherlands

In The Last Decade

M. A. Pericak‐Vance

56 papers receiving 6.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease.

1993 3.3k citations Ann M. Saunders, M. A. Pericak‐Vance et al. profile →
Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1

1994 1.1k citations Kimberly A. McAllister, David W. Johnson et al. Nature Genetics profile →
Mutations in the activin receptor–like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2

1996 846 citations David W. Johnson, Carol J. Gallione et al. Nature Genetics profile →

Peers

Countries citing papers authored by M. A. Pericak‐Vance

Since Specialization

Citations

This map shows the geographic impact of M. A. Pericak‐Vance'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 M. A. Pericak‐Vance with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. A. Pericak‐Vance more than expected).

Fields of papers citing papers by M. A. Pericak‐Vance

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M. A. Pericak‐Vance. 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 M. A. Pericak‐Vance. The network helps show where M. A. Pericak‐Vance may publish in the future.

Co-authorship network of co-authors of M. A. Pericak‐Vance

This figure shows the co-authorship network connecting the top 25 collaborators of M. A. Pericak‐Vance. A scholar is included among the top collaborators of M. A. Pericak‐Vance based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with M. A. Pericak‐Vance. M. A. Pericak‐Vance is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Examination of association of genes in the serotonin system to autism 2009 ·Neurogenetics ·(unknown),Nathalie Schnetz‐Boutaud,Jonathan D. Bartlett,(unknown),H Wright,Ruth K. Abramson,(unknown),John R. Gilbert,M. A. Pericak‐Vance,J.L. Haines	55
2	Polymorphisms of the Tumor Suppressor GeneLSAMPare Associated with Left Main Coronary Artery Disease 2008 ·Annals of Human Genetics ·(unknown),Elizabeth R. Hauser,Svati H. Shah,David Seo,P. Sivashanmugam,Sabrina T. Exum,Simon G. Gregory,C. B. Granger,J. L. Haines,Christopher J. Jones,David C. Crossman,Carol Haynes,William E. Kraus,Neil J. Freedman,M. A. Pericak‐Vance,Pascal J. Goldschmidt‐Clermont,Jeffery M. Vance	23
3	Linkage and Association Study of Late‐Onset Alzheimer Disease Families Linked to 9p21.3 2008 ·Annals of Human Genetics ·Stephan Züchner,John R. Gilbert,Eden R. Martin,Christopher R. Leon Guerrero,(unknown),(unknown),Paola G. Bronson,(unknown),D.E. Schmechel,J. L. Haines,M. A. Pericak‐Vance	35
4	Phenotype Analysis of Patients With the Risk Variant LOC387715 (A69S) in Age-related Macular Degeneration 2007 ·American Journal of Ophthalmology ·R. Keith Shuler,Silke Schmidt,Paul J. Gallins,Michael A. Hauser,William K. Scott,Jennifer Caldwell,Anita Agarwal,Jonathan L. Haines,M. A. Pericak‐Vance,Eric A. Postel	7
5	Distribution of WDR36 DNA Sequence Variants in Primary Open Angle Glaucoma Patients 2006 ·Investigative Ophthalmology & Visual Science ·(unknown),Michael A. Hauser,(unknown),Dayse F Sena,(unknown),E. DelBono,M. A. Pericak‐Vance,Jonathan L. Haines,R. Rand Allingham,Janey L. Wiggs	1
6	Analysis of nitric oxide synthase genes in age–related macular degeneration 2004 ·Investigative Ophthalmology & Visual Science ·Stefanie J. Schmidt,(unknown),(unknown),Eric A. Postel,Anita Agarwal,J. Donald M. Gass,(unknown),Catherine Bowes Rickman,J.L. Haines,M. A. Pericak‐Vance	1
7	Evaluation of NOS3 polymorphisms in patients with primary open angle glaucoma 2004 ·Investigative Ophthalmology & Visual Science ·Dayse F Sena,Louis R. Pasquale,R. Rand Allingham,Michael A. Hauser,M. A. Pericak‐Vance,E. DelBono,Jonathan L. Haines,Janey L. Wiggs	2
8	A Second-Generation Genomic Screen for Multiple Sclerosis 2004 ·The American Journal of Human Genetics ·S J Kenealy,Marie‐Claude Babron,Yvonne M. Bradford,Nathalie Schnetz‐Boutaud,J. L. Haines,Jacqueline Rimmler,Silke Schmidt,M. A. Pericak‐Vance,Lisa F. Barcellos,Robin Lincoln,Jorge R. Oksenberg,Stephen L. Hauser,Michel Clanet,David Brassat,Gilles Edan,Jacqueline Yaouanq,G. Sémana,Isabelle Cournu‐Rebeix,O. Lyon‐Caen,Bertrand Fontaine	40
9	Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder 2001 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Yujun Shao,Kimberly L. Raiford,Chantelle M. Wolpert,Allison E. Ashley‐Koch,Michael L. Cuccaro,John R. Gilbert,M. A. Pericak‐Vance	1
10	Sequence variation in the transforming growth factor-β1 (TGFB1) gene and multiple sclerosis susceptibility 2001 ·Journal of Neuroimmunology ·A. J. Green,Lisa F. Barcellos,Jacqueline Rimmler,M. Garcia,Stacy J. Caillier,Robin Lincoln,Patricia Bucher,M. A. Pericak‐Vance,J. L. Haines,Stephen L. Hauser,Jorge R. Oksenberg	26
11	Physical and cDNA Mapping in the <i>DBH</i> Region of Human Chromosome 9q34 2000 ·Human Heredity ·John R. Gilbert,Arun Kumar,Sarah E. Newey,Nagesh Rao,P.A. Ioannou,Hongyu Qiu,(unknown),Pu Xu,Mark J. Pettenati,M. A. Pericak‐Vance	5
12	Gln368STOP myocilin mutation in families with late-onset primary open-angle glaucoma. 1998 ·PubMed ·R. Rand Allingham,Janey L. Wiggs,(unknown),Douglas Vollrath,(unknown),Bob Broomer,(unknown),Elizabeth A. Del Bono,John W. Kern,Kate Patterson,(unknown),M. A. Pericak‐Vance	92
13	Adult-Onset Primary Open Angle Glaucoma Does Not Localize to Chromosome 2cen-q13 in North American Families 1998 ·Human Heredity ·R. Rand Allingham,Janey L. Wiggs,K. F. Damji,Leon W. Herndon,(unknown),(unknown),(unknown),Elizabeth A. Del Bono,(unknown),Jonathan L. Haines,M. A. Pericak‐Vance	3
14	Further exclusion of FSHD1B from the telomeric region of 10q 1997 ·Neurogenetics ·(unknown),M. A. Pericak‐Vance,Jeffrey M. Stajich,(unknown),Mark C. Jordan,Allen D. Roses,Jeffery M. Vance,(unknown)	2
15	No Association between α1‐Antichymotrypsin and Familial Alzheimer's Diseasesa 1996 ·Annals of the New York Academy of Sciences ·Jonathan L. Haines,(unknown),Ann M. Saunders,Joellen M. Schildkraut,John H. Growdon,(unknown),Lindsay A. Farrer,Sanford A. Auerbach,James F. Gusella,P. A. Locke,B.L. Rosi,Larry H. Yamaoka,Gary W. Small,P. Michael Conneally,Allen D. Roses,M. A. Pericak‐Vance	10
16	No Genetic Effect of α1-Antichymotrypsin in Alzheimer Disease 1996 ·Genomics ·Jonathan L. Haines,(unknown),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	77
17	Genes linked to systemic hypertension (HTN) and Maturity Onset Diabetes of the Young (MODY) are not associated with Primary Open Angle Glaucoma (POAG) 1996 ·Investigative Ophthalmology & Visual Science ·R. Rand Allingham,Janey L. Wiggs,K. F. Damji,(unknown),(unknown),(unknown),Elizabeth A. Del Bono,(unknown),Monica Ter‐Minassian,J. L. Haines,M. A. Pericak‐Vance	1
18	Genetic heterogeneity in hereditary haemorrhagic telangiectasia: possible correlation with clinical phenotype. 1994 ·Journal of Medical Genetics ·Kimberly A. McAllister,Felicia Lennon,(unknown),Wendy McKinnon,E.A. Helmbold,Dorene S. Markel,Charles E. Jackson,Alan E. Guttmacher,M. A. Pericak‐Vance,Douglas A. Marchuk	79
19	Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1breakdown → 1994 ·Nature Genetics ·Kimberly A. McAllister,(unknown),David W. Johnson,Carol J. Gallione,(unknown),Charles E. Jackson,E.A. Helmbold,Dorene S. Markel,Wendy McKinnon,(unknown),Mary Kay McCormick,M. A. Pericak‐Vance,Peter Heutink,Ben A. Oostra,T. Haitjema,(unknown),Mary Porteous,Alan E. Guttmacher,Michelle Letarte,Douglas A. Marchuk	1137
20	Genetic epidemiology of the susceptibility to leprosy. 1987 ·Journal of Clinical Investigation ·E D Shields,D. A. Russell,M. A. Pericak‐Vance	78

About M. A. Pericak‐Vance

M. A. Pericak‐Vance is a scholar working on Ophthalmology, Cellular and Molecular Neuroscience and Genetics, having authored 57 papers that have together received 7.1k indexed citations. Recurring topics across this work include Alzheimer's disease research and treatments (9 papers), Glaucoma and retinal disorders (7 papers) and Muscle Physiology and Disorders (5 papers). The work is most often cited by research in Genetics (1.3k citations), Physiology (2.7k citations) and Neurology (598 citations). M. A. Pericak‐Vance has collaborated with scholars based in United States, United Kingdom and Netherlands. Frequent co-authors include Ann M. Saunders, Guy S. Salvesen, A D Roses, Jan J. Enghild, Warren J. Strittmatter, D. E. Schmechel, Douglas A. Marchuk, Alan E. Guttmacher, Charles E. Jackson and Carol J. Gallione. Their work appears in journals such as Science, Proceedings of the National Academy of Sciences and The Lancet.

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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