Wendy H. Raskind - Concepedia

Author

Wendy H. Raskind

Also Known As

Aaron Quinlan, Amy K. Robertson, Anna Raper, Chloe M. Reuter, Chloe Reuter, Daryl A. Scott, Deborah Nickerson, Lilianna Solnica-Krezel, Minshew, Nancy, Rodriguez, Laura Lyman

230

Publications

13.2K

Citations

H-Index

213

Concepts

All Affiliations

University of Washington University of Washington Medical Center Geriatric Research Education and Clinical Center VA Puget Sound Health Care System University of Pennsylvania

About

Wendy H. Raskind is an author at University of Washington specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	37	58	6.2K
2	Health Sciences	10	10	885
3	Education	7	7	973
4	Language Studies	6	6	617
5	Arts	4	4	140

Wendy H. Raskind

133

Publications

11.9K

Citations

H-Index

Page 1

	Year	Citations
A p53-Dependent Mouse Spindle Checkpoint Shawn M. Cross, Carissa A. Sanchez, Catherine Morgan, Science Knockout MouseChromatinGenome InstabilityCell Cycle CheckpointsDevelopmental Biology	1995	671
The natural history of hereditary multiple exostoses. Gregory A. Schmale, E U Conrad, Wendy H. Raskind Journal of Bone and Joint Surgery Genetic TestingFamily MembersGeneticsGenetic EpidemiologyPathology	1994	618
Mutation of a Putative Mitochondrial Iron Transporter Gene (ABC7) in X-Linked Sideroblastic Anemia and Ataxia (XLSA/A) Rando Allikmets, Wendy H. Raskind, Amy Hutchinson, Human Molecular Genetics Xlsa/a GeneIron MetabolismGeneticsMolecular BiologyMolecular Genetics	1999	404
Actionable, Pathogenic Incidental Findings in 1,000 Participants’ Exomes Michael O. Dorschner, Laura M. Amendola, Emily H. Turner, The American Journal of Human Genetics Pathogenic Incidental FindingsGenetic EpidemiologyMendelian DisorderPathology	2013	381
Actionable exomic incidental findings in 6503 participants: challenges of variant classification Laura M. Amendola, Michael O. Dorschner, Peggy D. Robertson, Genome Research Genome-wide Association StudyEpidemiologySequencingExome SequencingGenetics	2015	356
Writing problems in developmental dyslexia: Under-recognized and under-treated Virginia W. Berninger, Kathleen Nielsen, Robert D. Abbott, Journal of School Psychology Writing DifficultiesLanguage DevelopmentCognitive DevelopmentDevelopmental Language DisorderDevelopmental Dyslexia	2007	344
Relative Burden of Large CNVs on a Range of Neurodevelopmental Phenotypes Santhosh Girirajan, Zoran Brkanac, Bradley P. Coe, PLoS Genetics NeurogenomicsBrain DevelopmentNeurological DisorderGeneticsGenetic Epidemiology	2011	327
Clonal Development, Stem-Cell Differentiation, and Clinical Remissions in Acute Nonlymphocytic Leukemia Philip J. Fialkow, Jack W. Singer, Wendy H. Raskind, New England Journal of Medicine Hematological MalignancyStem-cell DifferentiationDevelopmental BiologyBone Marrow FailureElderly Patients	1987	311
Missense Mutations in the Regulatory Domain of PKCγ: A New Mechanism for Dominant Nonepisodic Cerebellar Ataxia Dong-Hui Chen, Zoran Brkanac, Christophe L. M. J. Verlinde, The American Journal of Human Genetics Neurodegenerative DiseasesRegulatory DomainMolecular NeuroscienceMissense MutationsGenetic Disorder	2003	238
Loss of heterozygosity involving the APC and MCC genetic loci occurs in the majority of human esophageal cancers. Robert F. Boynton, Patricia L. Blount, Jing Yin, Proceedings of the National Academy of Sciences Chromosome 5QEsophageal CancerGeneticsPathologyMcc Genetic Loci	1992	225

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