D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Genetics D-index 64 Citations 12,764 149 World Ranking 2015 National Ranking 917

Overview

What is she best known for?

The fields of study she is best known for:

  • Gene
  • Mutation
  • Genetics

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 most cited work include:

  • A p53-Dependent Mouse Spindle Checkpoint (603 citations)
  • Mutation of a Putative Mitochondrial Iron Transporter Gene (ABC7) in X-Linked Sideroblastic Anemia and Ataxia (XLSA/A) (343 citations)
  • 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 (311 citations)

What are the main themes of her work throughout her whole career to date?

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.

She most often published in these fields:

  • Genetics (57.98%)
  • Immunology (16.49%)
  • Missense mutation (20.74%)

What were the highlights of her more recent work (between 2011-2021)?

  • Genetics (57.98%)
  • Exome sequencing (13.30%)
  • Missense mutation (20.74%)

In recent papers she was focusing on the following fields of study:

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.

Between 2011 and 2021, her most popular works were:

  • Actionable, Pathogenic Incidental Findings in 1,000 Participants’ Exomes (303 citations)
  • Actionable exomic incidental findings in 6503 participants: challenges of variant classification (233 citations)
  • Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine (126 citations)

In her most recent research, the most cited papers focused on:

  • Gene
  • Mutation
  • Genetics

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

  • Genotype which is related to area like Apolipoprotein E,
  • Disease and related Immunology and TREM2.

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.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

A p53-Dependent Mouse Spindle Checkpoint

Shawn M. Cross;Carissa A. Sanchez;Catherine A. Morgan;Melana K. Schimke.
Science (1995)

947 Citations

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)

524 Citations

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)

488 Citations

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)

391 Citations

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)

366 Citations

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)

366 Citations

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)

333 Citations

Relative Burden of Large CNVs on a Range of Neurodevelopmental Phenotypes

Santhosh Girirajan;Zoran Brkanac;Bradley P. Coe;Carl Baker.
PLOS Genetics (2011)

330 Citations

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)

317 Citations

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)

279 Citations

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