Karen Krajewski

2.0k total citations
17 papers, 1.3k citations indexed

About

Karen Krajewski is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Karen Krajewski has authored 17 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Cellular and Molecular Neuroscience, 7 papers in Neurology and 5 papers in Molecular Biology. Recurrent topics in Karen Krajewski's work include Hereditary Neurological Disorders (15 papers), Genetic Neurodegenerative Diseases (12 papers) and Neurological diseases and metabolism (7 papers). Karen Krajewski is often cited by papers focused on Hereditary Neurological Disorders (15 papers), Genetic Neurodegenerative Diseases (12 papers) and Neurological diseases and metabolism (7 papers). Karen Krajewski collaborates with scholars based in United States, Italy and Canada. Karen Krajewski's co-authors include Michael E. Shy, Richard A. Lewis, Jun Li, John Kamholz, James Garbern, Pedro Mancías, James R. Lupski, Ian J. Butler, Agnes Jani‐Acsadi and Mena Scavina and has published in prestigious journals such as Brain, Neurology and The Journal of Comparative Neurology.

In The Last Decade

Karen Krajewski

17 papers receiving 1.2k citations

Peers

Countries citing papers authored by Karen Krajewski

Since Specialization

Citations

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

Fields of papers citing papers by Karen Krajewski

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karen Krajewski

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

All Works

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17 of 17 papers shown

#	Work	Indexed citations
1	A Review of Genetic Counseling for Charcot Marie Tooth Disease (CMT) 2013 ·Journal of Genetic Counseling ·Carly E. Siskind, Seema Panchal, (unknown), Shawna Feely, Joline Dalton, Alice B. Schindler, Karen Krajewski	19
2	Charcot-Marie-Tooth Neuropathies: Diagnosis and Management 2008 ·Seminars in Neurology ·Agnes Jani‐Acsadi, Karen Krajewski, Michael E. Shy	55
3	Mutations in PRPS1, Which Encodes the Phosphoribosyl Pyrophosphate Synthetase Enzyme Critical for Nucleotide Biosynthesis, Cause Hereditary Peripheral Neuropathy with Hearing Loss and Optic Neuropathy (CMTX5) 2007 ·The American Journal of Human Genetics ·Hee‐Jin Kim, (unknown), Michael E. Shy, Karen Krajewski, (unknown), (unknown), (unknown), Hong‐Hee Won, Byung‐Ok Choi, Sung Hwa Hong, (unknown), Yeon‐Lim Suh, Chang‐Seok Ki, Soo‐Youn Lee, Sun-Hee Kim, Jong‐Won Kim	94
4	Stoichiometric Alteration of PMP22 Protein Determines the Phenotype of Hereditary Neuropathy With Liability to Pressure Palsies 2007 ·Archives of Neurology ·Jun Li, (unknown), (unknown), Rosemary Shy, Karen Krajewski, Michael E. Shy, Garth A. Nicholson	27
5	T118M PMP22 mutation causes partial loss of function and HNPP‐like neuropathy 2006 ·Annals of Neurology ·Michael E. Shy, Mena Scavina, (unknown), Karen Krajewski, Jun Li, John Kamholz, Edwin H. Kolodny, Kinga Szigeti, Richard A. Fischer, Gulam Mustafa Saifi, Steven S. Scherer, James R. Lupski	47
6	Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2 2006 ·Annals of Neurology ·Stephan Züchner, Peter De Jonghe, Albena Jordanova, Kristl G. Claeys, Velina Guergueltcheva, Sylvia Cherninkova, Steven R. Hamilton, (unknown), Karen Krajewski, (unknown), (unknown), Kristien Verhoeven, C. T. Langerhorst, Marianne de Visser, Frank Baas, Thomas D. Bird, Vincent Timmerman, Michael E. Shy, Jeffery M. Vance	268
7	Major myelin protein gene (P0) mutation causes a novel form of axonal degeneration 2006 ·The Journal of Comparative Neurology ·(unknown), Yunhong Bai, (unknown), Marina Grandis, (unknown), Anna Trostinskaia, Karen Krajewski, James Garbern, William J. Kupsky, Michael E. Shy	38
8	SIMPLEmutations in Charcot-Marie-Tooth disease and the potential role of its protein product in protein degradation 2005 ·Human Mutation ·Gulam Mustafa Saifi, Kinga Szigeti, Wojciech Wiszniewski, Michael E. Shy, Karen Krajewski, I Hausmanowa-Pétrusewicz, Andrzej Kochański, (unknown), Pedro Mancías, Ian J. Butler, James R. Lupski	73
9	Genetic testing in neuromuscular disease 2004 ·Neurologic Clinics ·Karen Krajewski, Michael E. Shy	8
10	Schwann cell expression of PLP1 but not DM20 is necessary to prevent neuropathy 2003 ·Annals of Neurology ·Michael E. Shy, Grace M. Hobson, (unknown), Odile Boespflug‐Tanguy, James Garbern, Karen Sperle, Wen Li, Alexander Gow, Diana Rodriguez, Enrico Bertini, Pedro Mancías, Karen Krajewski, Richard A. Lewis, John Kamholz	50
11	Loss‐of‐function phenotype of hereditary neuropathy with liability to pressure palsies 2003 ·Muscle & Nerve ·Jun Li, Karen Krajewski, Richard A. Lewis, Michael E. Shy	49
12	Motor unit number estimate of distal and proximal muscles in Charcot–Marie–Tooth disease 2003 ·Muscle & Nerve ·Richard A. Lewis, Jun Li, Darren R. Fuerst, Michael E. Shy, Karen Krajewski	43
13	Transient central nervous system white matter abnormality in X‐linked Charcot‐Marie‐Tooth disease 2002 ·Annals of Neurology ·Henry L. Paulson, James Garbern, Timothy F. Hoban, Karen Krajewski, Richard A. Lewis, Kenneth H. Fischbeck, Robert I. Grossman, Robert E. Lenkinski, John Kamholz, Michael E. Shy	127
14	Hereditary neuropathy with liability to pressure palsy 2002 ·Neurology ·Jun Li, Karen Krajewski, Michael E. Shy, Richard A. Lewis	107
15	Charcot‐Marie‐Tooth disease and related neuropathies: Mutation distribution and genotype‐phenotype correlation 2001 ·Annals of Neurology ·Cornelius F. Boerkoel, Hiroshi Takashima, Carlos García, Richard K. Olney, John P. Johnson, Katherine Berry, Paul Russo, Shelley Kennedy, Ahmad S. Teebi, Mena Scavina, Lowell L. Williams, Pedro Mancías, Ian J. Butler, Karen Krajewski, Michael E. Shy, James R. Lupski	198
16	Charcot–Marie–Tooth disease type 1 2000 ·Brain ·John Kamholz, Daniela M. Menichella, Ágnes Jáni, James Garbern, Richard A. Lewis, Karen Krajewski, Jack Lilien, Steven S. Scherer, Michael E. Shy	64
17	Correlation between Weakness and Axonal Loss in Patients with CMT1A 1999 ·Annals of the New York Academy of Sciences ·Karen Krajewski, (unknown), Richard A. Lewis, James Garbern, (unknown), John Kamholz, Michael E. Shy	23

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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