Wendy H. Raskind

13.3k total citations · 2 hit papers
144 papers, 8.4k citations indexed

About

Wendy H. Raskind is a scholar working on Molecular Biology, Genetics and Developmental and Educational Psychology. According to data from OpenAlex, Wendy H. Raskind has authored 144 papers receiving a total of 8.4k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Molecular Biology, 47 papers in Genetics and 30 papers in Developmental and Educational Psychology. Recurrent topics in Wendy H. Raskind's work include Genetics and Neurodevelopmental Disorders (31 papers), Reading and Literacy Development (26 papers) and Cognitive and developmental aspects of mathematical skills (15 papers). Wendy H. Raskind is often cited by papers focused on Genetics and Neurodevelopmental Disorders (31 papers), Reading and Literacy Development (26 papers) and Cognitive and developmental aspects of mathematical skills (15 papers). Wendy H. Raskind collaborates with scholars based in United States, Australia and Japan. Wendy H. Raskind's co-authors include Virginia W. Berninger, Mark Matsushita, Ellen M. Wijsman, E U Conrad, Gregory A. Schmale, Robert D. Abbott, Thomas D. Bird, Brian J. Reid, Zoran Brkanac and Kathleen Nielsen and has published in prestigious journals such as Science, New England Journal of Medicine and Cell.

In The Last Decade

Wendy H. Raskind

142 papers receiving 8.2k citations

Hit Papers

align trajectories sort by overperformance

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.

A p53-Dependent Mouse Spindle Checkpoint

1995 592 citations Wendy H. Raskind et al. profile →
The natural history of hereditary multiple exostoses.

1994 441 citations Wendy H. Raskind et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Wendy H. Raskind United States	50	3.2k	1.6k	1.4k	1.1k	1.1k	144	8.4k
Eric Legius Belgium	57	4.6k 1.5×	3.1k 2.0×	102 0.1×	591 0.5×	1.2k 1.2×	296	12.1k
William J. Kimberling United States	54	6.3k 2.0×	3.5k 2.2×	614 0.4×	542 0.5×	121 0.1×	186	11.6k
Maximilian Muenke United States	67	10.5k 3.3×	8.1k 5.1×	111 0.1×	571 0.5×	755 0.7×	277	15.6k
Han G. Brunner Netherlands	65	11.9k 3.8×	9.2k 5.8×	103 0.1×	1.6k 1.4×	632 0.6×	278	20.9k
Jane A. Hurst United Kingdom	34	2.6k 0.8×	3.1k 2.0×	648 0.5×	187 0.2×	236 0.2×	85	7.7k
Matthias Groszer United States	31	3.1k 1.0×	915 0.6×	399 0.3×	842 0.7×	27 0.0×	37	5.3k
André Reis Germany	60	7.7k 2.4×	4.4k 2.8×	49 0.0×	1.4k 1.2×	444 0.4×	320	13.6k
Cor W. R. J. Cremers Netherlands	54	3.8k 1.2×	1.4k 0.9×	340 0.2×	266 0.2×	302 0.3×	361	11.8k
Kay E. Davies United Kingdom	79	19.3k 6.1×	6.9k 4.4×	230 0.2×	3.8k 3.3×	306 0.3×	380	24.4k
Koenraad Devriendt Belgium	56	6.8k 2.2×	6.0k 3.8×	70 0.0×	380 0.3×	240 0.2×	444	12.6k

Countries citing papers authored by Wendy H. Raskind

Since Specialization

Citations

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

Fields of papers citing papers by Wendy H. Raskind

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Wendy H. Raskind. 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 Wendy H. Raskind. The network helps show where Wendy H. Raskind may publish in the future.

Co-authorship network of co-authors of Wendy H. Raskind

This figure shows the co-authorship network connecting the top 25 collaborators of Wendy H. Raskind. A scholar is included among the top collaborators of Wendy H. Raskind 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 Wendy H. Raskind. Wendy H. Raskind 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

Kiianitsa, Kostantin, Brian Hayes, Paul N. Valdmanis, et al.. (2024). TREM2 variants that cause early dementia and increase Alzheimer’s disease risk affect gene splicing. Brain. 147(7). 2368–2383. 9 indexed citations

Kiianitsa, Kostantin, Tuhin Virmani, Refugio A. Martinez, et al.. (2022). Reduced gene dosage is a common mechanism of neuropathologies caused by ATP6AP2 splicing mutations. Parkinsonism & Related Disorders. 101. 31–38. 3 indexed citations

Vijiaratnam, Nirosen, Kailash P. Bhatia, Anthony E. Lang, Wendy H. Raskind, & Alberto J. Espay. (2019). ADCY5–Related Dyskinesia: Improving Clinical Detection of an Evolving Disorder. Movement Disorders Clinical Practice. 6(7). 512–520. 34 indexed citations

Korvatska, Olena, Nicholas S. Strand, Jason D. Berndt, et al.. (2013). Altered splicing of ATP6AP2 causes X-linked parkinsonism with spasticity (XPDS). Human Molecular Genetics. 22(16). 3259–3268. 101 indexed citations

Chen, Dong-Hui, Wendy H. Raskind, William W. Parson, et al.. (2010). A novel mutation in FHL1 in a family with X-linked scapuloperoneal myopathy: Phenotypic spectrum and structural study of FHL1 mutations. Journal of the Neurological Sciences. 296(1-2). 22–29. 32 indexed citations

Michaud, Joëlle, Ken Simpson, Robert Escher, et al.. (2008). Integrative analysis of RUNX1 downstream pathways and target genes. BMC Genomics. 9(1). 363–363. 97 indexed citations

Brkanac, Zoran, Nicola H. Chapman, Mark Matsushita, et al.. (2007). Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 144B(4). 556–560. 78 indexed citations

Richards, Todd L., Elizabeth Aylward, Katherine Field, et al.. (2006). Converging Evidence for Triple Word Form Theory in Children With Dyslexia. Developmental Neuropsychology. 30(1). 547–589. 74 indexed citations

Igo, Robert P., Nicola H. Chapman, Virginia W. Berninger, et al.. (2005). Genomewide scan for real‐word reading subphenotypes of dyslexia: Novel chromosome 13 locus and genetic complexity. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 141B(1). 15–27. 39 indexed citations

10.

Chapman, Nicola H., Robert P. Igo, Jennifer B. Thomson, et al.. (2004). Linkage analyses of four regions previously implicated in dyslexia: Confirmation of a locus on chromosome 15q. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 131B(1). 67–75. 73 indexed citations

11.

Chen, Dong-Hui, Zoran Brkanac, Christophe L. M. J. Verlinde, et al.. (2003). Missense Mutations in the Regulatory Domain of PKCγ: A New Mechanism for Dominant Nonepisodic Cerebellar Ataxia. The American Journal of Human Genetics. 72(4). 839–849. 174 indexed citations

12.

Wijsman, Ellen M., et al.. (2003). Familial Aggregation Patterns in Mathematical Ability. Behavior Genetics. 34(1). 51–62. 7 indexed citations

13.

Brkanac, Zoran, Magali Fernandez, Mark Matsushita, et al.. (2002). Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22‐q32. American Journal of Medical Genetics. 114(4). 450–457. 47 indexed citations

14.

Allikmets, Rando, et al.. (1999). Mutation of a Putative Mitochondrial Iron Transporter Gene (ABC7) in X-Linked Sideroblastic Anemia and Ataxia (XLSA/A). Human Molecular Genetics. 8(5). 743–749. 313 indexed citations

15.

Fink, John K., Terry Heiman‐Patterson, Thomas D. Bird, et al.. (1996). Hereditary Spastic Paraplegia. Neurology. 46(6). 1507–1514. 147 indexed citations

16.

Raskind, Wendy H., Ernest U. Conrad, & Mark Matsushita. (1996). Frequent loss of heterozygosity for markers on chromosome arm 10q in chondrosarcomas. Genes Chromosomes and Cancer. 16(2). 138–143. 27 indexed citations

17.

Klemsz, Michael J., Robert Hromas, Wendy H. Raskind, E Bruno, & Robert S. Hoffman. (1994). PE-1, a Novel ETS Oncogene Family Member, Localizes to Chromosome 1q21-q23. Genomics. 20(2). 291–294. 12 indexed citations

18.

Hromas, Robert, Steven Collins, Wendy H. Raskind, Larry L. Deaven, & K Kaushansky. (1991). Hem-1, a potential membrane protein, with expression restricted to blood cells. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1090(2). 241–244. 18 indexed citations

19.

Starkebaum, Gordon, Paul J. Martin, Jack W. Singer, et al.. (1983). Chronic lymphocytosis with neutropenia: Evidence for a novel, abnormal T-cell population associated with antibody-mediated neutrophil destruction. Clinical Immunology and Immunopathology. 27(1). 110–123. 40 indexed citations

20.

Raskind, Wendy H., et al.. (1979). X chromosome inactivation and SV40 transformation of mammalian cells. Somatic Cell and Molecular Genetics. 5(6). 945–955. 7 indexed citations

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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