Wendy H. Raskind mainly investigates Genetics, Mutation, Loss of heterozygosity, Cancer research and Immunology. Her work investigates the relationship between Genetics and topics such as Ataxia that intersect with problems in PRKCG Gene. Her work deals with themes such as GATA1 and Central nervous system disease, which intersect with Mutation.
Her Loss of heterozygosity research includes elements of Hereditary multiple exostoses, Molecular biology, Chromosome and Chondrosarcoma. Her biological study spans a wide range of topics, including Carcinogenesis and Restriction fragment length polymorphism. In Immunology, Wendy H. Raskind works on issues like Stem cell, which are connected to Pathogenesis, Somatic cell, Lymphoblast and Immunoglobulin light chain.
Her scientific interests lie mostly in Genetics, Immunology, Missense mutation, Dyslexia and Molecular biology. Her work is connected to Genetic linkage, Locus, Mutation, Gene and Gene mapping, as a part of Genetics. Her research investigates the connection between Immunology and topics such as Stem cell that intersect with issues in Myeloid.
Her Missense mutation research focuses on subjects like Exome sequencing, which are linked to Genotype and Disease. In the field of Dyslexia, her study on Reading disability overlaps with subjects such as Developmental psychology, Cognitive psychology, Spelling and Family genetics. Her work in Molecular biology tackles topics such as Loss of heterozygosity which are related to areas like Cancer research, Chondrosarcoma and Chromosome.
Her primary areas of study are Genetics, Exome sequencing, Missense mutation, ADCY5 and Exome. As part of her studies on Genetics, Wendy H. Raskind often connects relevant subjects like Ataxia. Her Exome sequencing research incorporates elements of Disease, Age of onset, Genotype, Sanger sequencing and Candidate gene.
Wendy H. Raskind studied Missense mutation and Bioinformatics that intersect with Dystonic disorder. Wendy H. Raskind has included themes like Human genetics, Allele frequency and Genomics in her Exome study. Her studies deal with areas such as Molecular biology, Endoplasmic reticulum and Exon as well as Mutation.
Her main research concerns Genetics, Exome sequencing, Exome, Missense mutation and ADCY5. Her Genetics research is multidisciplinary, incorporating perspectives in Dystonia and Speech sound disorder. Her Exome sequencing study also includes
The study incorporates disciplines such as Allele frequency and Genomics in addition to Exome. Her Missense mutation study is concerned with the larger field of Mutation. Her Mutation research includes themes of Molecular biology, Cell biology and Exon.
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A p53-Dependent Mouse Spindle Checkpoint
Shawn M. Cross;Carissa A. Sanchez;Catherine A. Morgan;Melana K. Schimke.
Science (1995)
Mutation of a Putative Mitochondrial Iron Transporter Gene (ABC7) in X-Linked Sideroblastic Anemia and Ataxia (XLSA/A)
Rando Allikmets;Rando Allikmets;Rando Allikmets;Wendy H Raskind;Wendy H Raskind;Wendy H Raskind;Amy Hutchinson;Amy Hutchinson;Amy Hutchinson;Nichole D Schueck;Nichole D Schueck;Nichole D Schueck.
Human Molecular Genetics (1999)
In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms of pathogenesis
Joëlle Michaud;Feng Wu;Motomi Osato;Gregory M. Cottles.
Blood (2002)
Actionable, Pathogenic Incidental Findings in 1,000 Participants’ Exomes
Michael O. Dorschner;Laura M. Amendola;Emily H. Turner;Peggy D. Robertson.
American Journal of Human Genetics (2013)
Clonal development, stem-cell differentiation, and clinical remissions in acute nonlymphocytic leukemia
Philip J. Fialkow;Jack W. Singer;Wendy H. Raskind;John W. Adamson.
The New England Journal of Medicine (1987)
Evidence for a Multistep Pathogenesis of a Myelodysplastic Syndrome
Wendy H. Raskind;Wendy H. Raskind;Nagendra Tirumali;Nagendra Tirumali;Robert Jacobson;Robert Jacobson;Jack Singer;Jack Singer.
Blood (1984)
Actionable exomic incidental findings in 6503 participants: challenges of variant classification
Laura M. Amendola;Michael O. Dorschner;Peggy D. Robertson;Joseph S. Salama.
Genome Research (2015)
Relative Burden of Large CNVs on a Range of Neurodevelopmental Phenotypes
Santhosh Girirajan;Zoran Brkanac;Bradley P. Coe;Carl Baker.
PLOS Genetics (2011)
Writing problems in developmental dyslexia: under-recognized and under-treated.
Virginia W. Berninger;Kathleen H. Nielsen;Robert D. Abbott;Ellen Wijsman.
Journal of School Psychology (2008)
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;Victoria L. Brown.
Proceedings of the National Academy of Sciences of the United States of America (1992)
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