Patricia Kramer

6.4k total citations · 1 hit paper
21 papers, 1.9k citations indexed

About

Patricia Kramer is a scholar working on Neurology, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, Patricia Kramer has authored 21 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Neurology, 9 papers in Cellular and Molecular Neuroscience and 7 papers in Molecular Biology. Recurrent topics in Patricia Kramer's work include Neurological disorders and treatments (8 papers), Genetic Neurodegenerative Diseases (8 papers) and Parkinson's Disease Mechanisms and Treatments (6 papers). Patricia Kramer is often cited by papers focused on Neurological disorders and treatments (8 papers), Genetic Neurodegenerative Diseases (8 papers) and Parkinson's Disease Mechanisms and Treatments (6 papers). Patricia Kramer collaborates with scholars based in United States, Italy and Germany. Patricia Kramer's co-authors include M. Litt, John G. Nutt, E. R. Brunt, D.L. Browne, Stephen T. Gancher, Eric A. Smith, Laurie J. Ozelius, Susan Bressman, Stanley Fahn and Deborah de Leon and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Annals of Neurology.

In The Last Decade

Patricia Kramer

21 papers receiving 1.9k 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.

Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1

1994 561 citations D.L. Browne, Stephen T. Gancher et al. Nature Genetics profile →

Peers

Countries citing papers authored by Patricia Kramer

Since Specialization

Citations

This map shows the geographic impact of Patricia 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 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 Kramer more than expected).

Fields of papers citing papers by Patricia Kramer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patricia Kramer

This figure shows the co-authorship network connecting the top 25 collaborators of Patricia Kramer. A scholar is included among the top collaborators of Patricia 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 Kramer. Patricia Kramer is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Prospective Study Investigating the Prevalence and Evolution of Malnourishment in the Acute Orthopaedic Trauma Patient. 2022 ·PubMed ·Reza Firoozabadi, Benjamin Hamilton, (unknown), Julie Agel, Stephen K. Benirschke, Patricia Kramer, (unknown)	2
2	Neuropathologic Basis of Age-Associated Brain Atrophy 2013 ·JAMA Neurology ·Deniz Erten‐Lyons, Hiroko H. Dodge, Randall L. Woltjer, Lisa C. Silbert, Diane B. Howieson, Patricia Kramer, Jeffrey Kaye	81
3	Microcephaly Genes and Risk of Late-onset Alzheimer Disease 2011 ·Alzheimer Disease & Associated Disorders ·Deniz Erten‐Lyons, Beth Wilmot, Pavana Anur, Shannon K. McWeeney, Shawn K. Westaway, Lisa C. Silbert, Patricia Kramer, Jeffrey Kaye	5
4	Exceptional Brain Aging in a Rural Population‐Based Cohort 2009 ·The Journal of Rural Health ·Jeffrey Kaye, (unknown), James F. Calvert, (unknown), Debbie Crawford, Patricia Kramer	13
5	Pediatric calcaneal fractures 2009 ·Orthopedic Reviews ·Hobie Summers, Patricia Kramer, Stephen K. Benirschke	12
6	The FAS gene, brain volume, and disease progression in Alzheimer's disease 2009 ·Alzheimer s & Dementia ·Deniz Erten‐Lyons, Anne Jacobson, Patricia Kramer, Andrew Grupe, Jeffrey Kaye	28
7	Narrowing the DYT6 dystonia region and evidence for locus heterogeneity in the Amish–Mennonites 2007 ·American Journal of Medical Genetics Part A ·Rachel Saunders‐Pullman, Deborah Raymond, Geetha Senthil, Patricia Kramer, Erin Ohmann, Amanda Deligtisch, Vicki Shanker, Paul Greene, (unknown), Neng Huang, Michele Tagliati, Patricia L. Kavanagh, Jeannie Soto‐Valencia, Patrícia de Carvalho Aguiar, Neil Risch, Laurie J. Ozelius, Susan Bressman	48
8	Parkinson's disease and LRRK2: Frequency of a common mutation in U.S. movement disorder clinics 2005 ·Movement Disorders ·Denise M. Kay, Cyrus P. Zabetian, Stewart A. Factor, John G. Nutt, Ali Samii, Alida Griffith, T. Bird, Patricia Kramer, Donald S. Higgins, Haydeh Payami	73
9	Rapid‐onset dystonia–parkinsonism: A fourth family consistent with linkage to chromosome 19q13 2004 ·Movement Disorders ·Jacek Zaremba, Hanna Mierzewska, (unknown), Patricia Kramer, Laurie J. Ozelius, Allison Brashear	24
10	Distribution, type, and origin of Parkin mutations: Review and case studies 2004 ·Movement Disorders ·Katja Hedrich, (unknown), Beth Wilmot, Karen Marder, Juliette Harris, Jennifer Garrels, (unknown), P. Vieregge, Helfried Jacobs, Susan Bressman, Anthony E. Lang, Martin Kann, Giovanni Abbruzzese, Paolo Martinelli, E. Schwinger, Laurie J. Ozelius, Peter P. Pramstaller, Christine Klein, Patricia Kramer	165
11	Complementary and Alternative Medicines in the Treatment of Dementia 2003 ·Drugs & Aging ·Bruce J. Diamond, Susan K. Johnson, (unknown), (unknown), (unknown), (unknown), Patricia Kramer	27
12	Novel mutation in the TOR1A (DYT1) gene in atypical, early onset dystonia and polymorphisms in dystonia and early onset parkinsonism 2001 ·Neurogenetics ·Joanne Leung, Christine Klein, Jennifer Friedman, P. Vieregge, Helfried Jacobs, Dana Doheny, Christoph Kamm, (unknown), Peter P. Pramstaller, John B. Penney, (unknown), Joseph Jankovic, Thomas Gasser, Susan Bressman, David P. Corey, Patricia Kramer, Mitchell F. Brin, Laurie J. Ozelius, Xandra O. Breakefield	126
13	Autosomal-Dominant Congenital Cataract Associated with a Deletion Mutation in the Human Beaded Filament Protein Gene BFSP2 2000 ·The American Journal of Human Genetics ·Petra Jakobs, John F. Hess, Paul G. Fitzgerald, Patricia Kramer, Richard G. Weleber, M. Litt	137
14	Localization of a gene for myoclonus-dystonia to chromosome 7q21-q31 1999 ·Annals of Neurology ·Torbjoern G. Nygaard, Deborah Raymond, Caiping Chen, Ichizo Nishino, Paul Greene, Danna Jennings, Gary A. Heiman, (unknown), (unknown), Patricia Kramer, Laurie J. Ozelius, Susan Bressman	71
15	Association of a missense change in the D2 dopamine receptor with myoclonus dystonia 1999 ·Proceedings of the National Academy of Sciences ·Christine Klein, Mitchell F. Brin, Patricia Kramer, Miguel Sena‐Esteves, Deborah de Leon, Dana Doheny, Susan Bressman, Stanley Fahn, Xandra O. Breakefield, Laurie J. Ozelius	90
16	Fine Localization of the Torsion Dystonia Gene (DYT1) on Human Chromosome 9q34: YAC Map and Linkage Disequilibrium 1997 ·Genome Research ·Laurie J. Ozelius, Jeffrey Hewett, Patricia Kramer, Susan Bressman, Christo Shalish, Deborah de Leon, M. Rutter, Neil Risch, Mitchell F. Brin, Elena D. Markova, Limborskaia Sa, I. A. Ivanova‐Smolenskaya, Mary Kay McCormick, Stanley Fahn, Alan Buckler, James F. Gusella, Xandra O. Breakefield	50
17	Homozygosity mapping of Hallervorden–Spatz syndrome to chromosome 20p12.3–p13 1996 ·Nature Genetics ·Todd D. Taylor, M. Litt, Patricia Kramer, Massimo Pandolfo, Lucia Angelini, Nardo Nardocci, Sean Davis, Marta Pineda, Haruo Hattori, (unknown), Maria Roberta Cilio, Enrico Bertini, Susan J. Hayflick	103
18	Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population 1995 ·Nature Genetics ·Neil Risch, Deborah de Leon, Laurie J. Ozelius, Patricia Kramer, Laura Almasy, Burton H. Singer, Stanley Fahn, Xandra O. Breakefield, Susan Bressman	318
19	Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1 breakdown → 1994 ·Nature Genetics ·D.L. Browne, Stephen T. Gancher, John G. Nutt, E. R. Brunt, Eric A. Smith, Patricia Kramer, M. Litt	561
20	Inhibition between spatially tuned mechanisms: temporal influences (A) 1984 ·Lynn A. Olzak, Patricia Kramer	2

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.

Explore authors with similar magnitude of impact