Patricia L. Kramer

3.7k citations

31 papers · 2.3k indexed · 1 hit paper · h-index 20

Neurology top 0.5%
Cellular and Molecular Neuroscience top 1%
Molecular Biology
Neurology top 5%
Physiology top 10%

Co-authors: Xandra O. Breakefield Laurie J. Ozelius Susan Bressman Deborah de Leon Mitchell F. Brin Stanley Fahn Neil Risch James F. Gusella
Topics: Neurological disorders and treatments (12 papers)Parkinson's Disease Mechanisms and Treatments (8 papers)Genetic Neurodegenerative Diseases (8 papers)
Cited by: Neurology Cellular and Molecular Neuroscience
Journals: Proceedings of the National Academy of Sciences Neuron Nature Genetics
Partner nations: United States Germany Italy

In The Last Decade

Patricia L. Kramer

31 papers receiving 2.3k 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.

The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein

1997 770 citations Laurie J. Ozelius, Jeffrey Hewett et al. Nature Genetics profile →

Peers

Countries citing papers authored by Patricia L. Kramer

Since Specialization

Citations

This map shows the geographic impact of Patricia L. Kramer'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 Patricia L. Kramer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Patricia L. Kramer more than expected).

Fields of papers citing papers by Patricia L. Kramer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Patricia L. Kramer. 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 Patricia L. Kramer. The network helps show where Patricia L. Kramer may publish in the future.

Co-authorship network of co-authors of Patricia L. Kramer

This figure shows the co-authorship network connecting the top 25 collaborators of Patricia L. Kramer. A scholar is included among the top collaborators of Patricia L. Kramer 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 Patricia L. Kramer. Patricia L. Kramer 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	Review of selected databases of longitudinal aging studies 2012 ·Alzheimer s & Dementia ·Deniz Erten‐Lyons,(unknown),Andrea M. Piccinin,Scott M. Hofer,Hiroko H. Dodge,Joseph F. Quinn,Randy Woltjer,Patricia L. Kramer,Jeffrey Kaye	12
2	Reconstructability Analysis as a Tool for Identifying Gene-Gene Interactions in Studies of Human Diseases 2010 ·Statistical Applications in Genetics and Molecular Biology ·(unknown),Patricia L. Kramer,Shawn K. Westaway,Nancy J. Cox,Martin Zwick	8
3	Alzheimer disease pathology in cognitively healthy elderly: A genome-wide study 2010 ·Neurobiology of Aging ·Patricia L. Kramer,Haiyan Xu,Randall L. Woltjer,Shawn K. Westaway,David Clark,Deniz Erten‐Lyons,Jeffrey Kaye,Kathleen A. Welsh‐Bohmer,Juan C. Troncoso,William R. Markesbery,Ronald C. Petersen,Raymond Scott Turner,Walter A. Kukull,David A. Bennett,Douglas Galasko,John C. Morris,Jürg Ott	82
4	The Path to Open-Angle Glaucoma Gene Discovery: Endophenotypic Status of Intraocular Pressure, Cup-to-Disc Ratio, and Central Corneal Thickness 2010 ·Investigative Ophthalmology & Visual Science ·Jac Charlesworth,Patricia L. Kramer,Tom Dyer,(unknown),John R. Samples,Jamie E. Craig,David A. Mackey,Alex W. Hewitt,John Blangero,Mary K. Wirtz	72
5	A loss-of-function nonsynonymous polymorphism in the osmoregulatory TRPV4 gene is associated with human hyponatremia 2009 ·Proceedings of the National Academy of Sciences ·Wei Tian,Yi Fu,Anna García-Elías,José M. Fernández‐Fernández,Rubén Vicente,Patricia L. Kramer,Robert F. Klein,Robert Hitzemann,Eric Orwoll,Beth Wilmot,Shannon K. McWeeney,Miguel A. Valverde,David Cohen	79
6	Childhood‐onset restless legs syndrome: Clinical and genetic features of 22 families 2008 ·Movement Disorders ·Hiltrud Muhle,Anja Neumann,K. Lohmann-Hedrich,Thora Lohnau,Yang Lü,Susen Winkler,Stephan Waltz,(unknown),Patricia L. Kramer,Christine Klein,Ulrich Stephani	52
7	Linear trend tests for case–control genetic association that incorporate random phenotype and genotype misclassification error 2007 ·Genetic Epidemiology ·Derek Gordon,Chad Haynes,Yaning Yang,Patricia L. Kramer,Stephen J. Finch	25
8	Translational gene mapping of cognitive decline 2006 ·Neurobiology of Aging ·Beth Wilmot,Shannon K. McWeeney,Randal R. Nixon,Thomas J. Montine,(unknown),Christina A. Harrington,Jeffrey Kaye,Patricia L. Kramer	29
9	Lewy body Parkinson's disease in a large pedigree with 77Parkin mutation carriers 2005 ·Annals of Neurology ·Peter P. Pramstaller,Michael G. Schlossmacher,Thomas S. Jacques,Francesco Scaravilli,(unknown),(unknown),Katja Hedrich,(unknown),(unknown),Rüdiger Hilker,Patricia L. Kramer,Christine Klein	187
10	Co‐occurrence of restless legs syndrome and Parkin mutations in two families 2005 ·Movement Disorders ·(unknown),Ana Djarmati,Kemal Kabakci,Irene Pichler,(unknown),Thora Lohnau,Norman Kock,Johann Hagenah,Katja Hedrich,E. Schwinger,Patricia L. Kramer,Peter P. Pramstaller,Christine Klein	26
11	ε‐sarcoglycan mutations found in combination with other dystonia gene mutations 2002 ·Annals of Neurology ·Christine Klein,Liu Liu,Dana Doheny,Norman Kock,B. Müller,Patrícia de Carvalho Aguiar,Joanne Leung,Deborah de Leon,Susan Bressman,Jeremy M. Silverman,Christopher J. Smith,Fabio Danisi,Chris Morrison,Ruth H. Walker,Miodrag Velickovic,E. Schwinger,Patricia L. Kramer,Xandra O. Breakefield,Mitchell F. Brin,Laurie J. Ozelius	69
12	Genetic linkage of autosomal dominant primary open angle glaucoma to chromosome 3q in a Greek pedigree 2001 ·European Journal of Human Genetics ·George Kitsos,Hans Eiberg,E Economou-Petersen,Mary K. Wirtz,Patricia L. Kramer,Miltiadis Aspiotis,Niels Tommerup,Michael B. Petersen,K. Psilas	23
13	A new locus for autosomal dominant congenital cataracts maps to chromosome 3. 2000 ·PubMed ·Patricia L. Kramer,(unknown),(unknown),(unknown),Richard G. Weleber,M. Litt	18
14	Rapid-onset dystonia-parkinsonism: Linkage to chromosome 19q13 1999 ·Annals of Neurology ·Patricia L. Kramer,Mari Mineta,Christine Klein,Karla Schilling,Deborah de Leon,Martin R. Farlow,Xandra O. Breakefield,Susan Bressman,William B. Dobyns,Laurie J. Ozelius,Allison Brashear	52
15	The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding proteinbreakdown → 1997 ·Nature Genetics ·Laurie J. Ozelius,Jeffrey Hewett,(unknown),Susan Bressman,Patricia L. Kramer,Christo Shalish,Deborah de Leon,Mitchell F. Brin,Deborah Raymond,David P. Corey,Stanley Fahn,Neil Risch,Alan Buckler,James F. Gusella,Xandra O. Breakefield	770
16	Exclusion of the DYT1 locus in a non‐Jewish family with early‐onset dystonia 1994 ·Movement Disorders ·Susan Bressman,Ann Hunt,Gary A. Heiman,Mitchell F. Brin,Robert E. Burke,Stanley Fahn,Joel M. Trugman,Deborah de Leon,Patricia L. Kramer,Kirk C. Wilhelmsen,Torbjoern G. Nygaard	29
17	Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32–34 1990 ·Annals of Neurology ·Patricia L. Kramer,Deborah de Leon,Laurie J. Ozelius,Neil Risch,Susan Bressman,Mitchell F. Brin,Deborah E. Schuback,Robert E. Burke,David J. Kwiatkowski,Heidi Shale,James F. Gusella,Xandra O. Breakefield,Stanley Fahn	109
18	Human gene for torsion dystonia located on chromosome 9q32-q34 1989 ·Neuron ·Laurie J. Ozelius,Patricia L. Kramer,Carol Moskowitz,David J. Kwiatkowski,Mitchell F. Brin,Susan Bressman,Deborah E. Schuback,Catherine T. Falk,Neil Risch,Deborah de Leon,Robert E. Burke,Jonathan L. Haines,James F. Gusella,Stanley Fahn,Xandra O. Breakefield	186
19	Development of a map of chromosome 11p 1986 ·Genetic Epidemiology ·Patricia L. Kramer,Lindsay A. Farrer,A.J. Pakstis,Kenneth K. Kídd	5
20	Adolescent growth patterns in a northern Italian community. 1983 ·PubMed ·Patricia L. Kramer	3

About Patricia L. Kramer

Patricia L. Kramer is a scholar working on Neurology, Neuropsychology and Physiological Psychology and Ophthalmology, having authored 31 papers that have together received 2.3k indexed citations. Recurring topics across this work include Neurological disorders and treatments (12 papers), Parkinson's Disease Mechanisms and Treatments (8 papers) and Genetic Neurodegenerative Diseases (8 papers). The work is most often cited by research in Neurology (1.6k citations), Cellular and Molecular Neuroscience (1.3k citations) and Neurology (264 citations). Patricia L. Kramer has collaborated with scholars based in United States, Germany and Italy. Frequent co-authors include Xandra O. Breakefield, Laurie J. Ozelius, Susan Bressman, Deborah de Leon, Mitchell F. Brin, Stanley Fahn, Neil Risch, James F. Gusella, Christo Shalish and Alan Buckler. Their work appears in journals such as Proceedings of the National Academy of Sciences, Neuron and Nature Genetics.

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