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Reference EntriesFull Text
Raskind, Wendy H
Journal title:American Men & Women of Science : A Biographical Directory of Today’s Leaders in Physical, Biological and Related Sciences: QIU-SAQ, 2022, p.9331-9331
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Raskind, Wendy H
Journal title:American Men & Women of Science : A Biographical Directory of Today’s Leaders in Physical, Biological and Related Sciences: RA-SAU, 2021, p.9300-9300
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ArticlesPeer ReviewedFull Text
Relative burden of large CNVs on a range of neurodevelopmental phenotypes
Author / Creator:Girirajan, Santhosh ; Brkanac, Zoran ; Coe, Bradley P ; Baker, Carl ; Vives, Laura ; Vu, Tiffany H ; Shafer, Neil ; Bernier, Raphael ; Ferrero, Giovanni B ; Silengo, Margherita ; Warren, Stephen T ; Moreno, Carlos S ; Fichera, Marco ; Romano, Corrado ; Raskind, Wendy H ; Eichler, Evan E
Publisher:United States: Public Library of Science
Journal title:PLoS genetics, 2011-11, Vol.7 (11), p.e1002334
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ArticlesPeer ReviewedFull Text
Caspase-8, association with Alzheimer's Disease and functional analysis of rare variants
Author / Creator:Rehker, Jan ; Rodhe, Johanna ; Nesbitt, Ryan R ; Boyle, Evan A ; Martin, Beth K ; Lord, Jenny ; Karaca, Ilker ; Naj, Adam ; Jessen, Frank ; Helisalmi, Seppo ; Soininen, Hilkka ; Hiltunen, Mikko ; Ramirez, Alfredo ; Scherer, Martin ; Farrer, Lindsay A ; Haines, Jonathan L ; Pericak-Vance, Margaret A ; Raskind, Wendy H ; Cruchaga, Carlos ; Schellenberg, Gerard D ; Joseph, Bertrand ; Brkanac, Zoran
Publisher:United States: Public Library of Science
Journal title:PloS one, 2017-10, Vol.12 (10), p.e0185777
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Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech
Author / Creator:Peter, Beate ; Wijsman, Ellen M ; Nato, Jr, Alejandro Q ; Matsushita, Mark M ; Chapman, Kathy L ; Stanaway, Ian B ; Wolff, John ; Oda, Kaori ; Gabo, Virginia B ; Raskind, Wendy H
Publisher:United States: Public Library of Science
Journal title:PloS one, 2016-04, Vol.11 (4), p.e0153864
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ArticlesPeer ReviewedFull Text
Integrative analysis of RUNX1 downstream pathways and target genes
Author / Creator:Michaud, Joëlle ; Simpson, Ken M ; Escher, Robert ; Buchet-Poyau, Karine ; Beissbarth, Tim ; Carmichael, Catherine ; Ritchie, Matthew E ; Schütz, Frédéric ; Cannon, Ping ; Liu, Marjorie ; Shen, Xiaofeng ; Ito, Yoshiaki ; Raskind, Wendy H ; Horwitz, Marshall S ; Osato, Motomi ; Turner, David R ; Speed, Terence P ; Kavallaris, Maria ; Smyth, Gordon K ; Scott, Hamish S
Publisher:England: BioMed Central Ltd
Journal title:BMC genomics, 2008-07, Vol.9 (1), p.363-363, Article 363
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ArticlesPeer ReviewedFull Text
The effect of algorithms on copy number variant detection
Author / Creator:Tsuang, Debby W ; Millard, Steven P ; Ely, Benjamin ; Chi, Peter ; Wang, Kenneth ; Raskind, Wendy H ; Kim, Sulgi ; Brkanac, Zoran ; Yu, Chang-En
Publisher:United States: Public Library of Science
Journal title:PloS one, 2010-12, Vol.5 (12), p.e14456-e14456
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ArticlesPeer ReviewedFull Text
Wenckebach Periodicity at Rest That Normalizes With Tachycardia in a Family With a NKX2.5 Mutation
Author / Creator:Guntheroth, Warren, MD ; Chun, Lani, BS ; Patton, Kristen K., MD ; Matsushita, Mark M., BS ; Page, Richard L., MD ; Raskind, Wendy H., MD, PhD
Publisher:New York, NY: Elsevier Inc
Journal title:The American journal of cardiology, 2012-12, Vol.110 (11), p.1646-1650
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ArticlesPeer ReviewedFull Text
A p53-Dependent Mouse Spindle Checkpoint
Author / Creator:Cross, Shawn M. ; Sanchez, Carissa A. ; Morgan, Catherine A. ; Schimke, Melana K. ; Ramel, Stig ; Idzerda, Rejean L. ; Raskind, Wendy H. ; Reid, Brian J.
Publisher:Washington, DC: American Society for the Advancement of Science
Journal title:Science (American Association for the Advancement of Science), 1995-03, Vol.267 (5202), p.1353-1356
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ArticlesPeer ReviewedFull Text
Defects in lysosomal function and lipid metabolism in human microglia harboring a TREM2 loss of function mutation
Author / Creator:Filipello, Fabia ; You, Shih-Feng ; Mirfakhar, Farzaneh S. ; Mahali, Sidhartha ; Bollman, Bryan ; Acquarone, Mariana ; Korvatska, Olena ; Marsh, Jacob A. ; Sivaraman, Anirudh ; Martinez, Rita ; Cantoni, Claudia ; De Feo, Luca ; Ghezzi, Laura ; Minaya, Miguel A. ; Renganathan, Arun ; Cashikar, Anil G. ; Satoh, Jun-Ichi ; Beatty, Wandy ; Iyer, Abhirami K. ; Cella, Marina ; Raskind, Wendy H. ; Piccio, Laura ; Karch, Celeste M.
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Acta neuropathologica, 2023-06, Vol.145 (6), p.749-772
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ArticlesPeer ReviewedFull Text
Biochemical and imaging surveillance in Li-Fraumeni syndrome
Author / Creator:Raskind, Wendy H ; Hisama, Fuki M ; Bennett, Robin L
Publisher:England: Elsevier Ltd
Journal title:The lancet oncology, 2016-11, Vol.17 (11), p.e472-e472
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ArticlesPeer ReviewedFull Text
Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes
Author / Creator:Chapman, Nicola H. ; Nato, Alejandro Q. ; Bernier, Raphael ; Ankenman, Katy ; Sohi, Harkirat ; Munson, Jeff ; Patowary, Ashok ; Archer, Marilyn ; Blue, Elizabeth M. ; Webb, Sara Jane ; Coon, Hilary ; Raskind, Wendy H. ; Brkanac, Zoran ; Wijsman, Ellen M.
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Human genetics, 2015-10, Vol.134 (10), p.1055-1068
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Family-based exome sequencing and case-control analysis implicate CEP41 as an ASD gene
Author / Creator:Patowary, Ashok ; Won, So Yeon ; Oh, Shin Ji ; Nesbitt, Ryan R ; Archer, Marilyn ; Nickerson, Debbie ; Raskind, Wendy H. ; Bernier, Raphael ; Lee, Ji Eun ; Brkanac, Zoran
Publisher:London: Nature Publishing Group UK
Journal title:Translational psychiatry, 2019-01, Vol.9 (1), p.4-4, Article 4
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ArticlesPeer ReviewedFull Text
Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample
Author / Creator:Peter, Beate ; Raskind, Wendy H ; Matsushita, Mark ; Lisowski, Mark ; Vu, Tiffany ; Berninger, Virginia W ; Wijsman, Ellen M ; Brkanac, Zoran
Publisher:England: Springer US
Journal title:Journal of neurodevelopmental disorders, 2011-03, Vol.3 (1), p.39-49
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ArticlesPeer ReviewedFull Text
Global Processing Speed in Children with Low Reading Ability and in Children and Adults with Typical Reading Ability: Exploratory Factor Analytic Models
Author / Creator:Peter, Beate ; Matsushita, Mark ; Raskind, Wendy H
Publisher:United States: American Speech-Language-Hearing Association (ASHA)
Journal title:Journal of speech, language, and hearing research, 2011-06, Vol.54 (3), p.885-899
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ArticlesPeer ReviewedFull Text
Genome Scan for Spelling Deficits: Effects of Verbal IQ on Models of Transmission and Trait Gene Localization
Author / Creator:Rubenstein, Kevin ; Matsushita, Mark ; Berninger, Virginia W. ; Raskind, Wendy H. ; Wijsman, Ellen M.
Publisher:Boston: Springer US
Journal title:Behavior genetics, 2011-01, Vol.41 (1), p.31-42
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Genome Scan of a Nonword Repetition Phenotype in Families with Dyslexia: Evidence for Multiple Loci
Author / Creator:Brkanac, Zoran ; Chapman, Nicola H. ; Igo, Robert P. ; Matsushita, Mark M. ; Nielsen, Kathleen ; Berninger, Virginia W. ; Wijsman, Ellen M. ; Raskind, Wendy H.
Publisher:Boston: Springer US
Journal title:Behavior genetics, 2008-09, Vol.38 (5), p.462-475
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Pharmacology and genetics of autism: implications for diagnosis and treatment
Author / Creator:Brkanac, Zoran ; Raskind, Wendy H ; King, Bryan H
Publisher:England: Future Medicine Ltd
Journal title:Personalized medicine, 2008-11, Vol.5 (6), p.599-607
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Expression of the Gene Defect in X-Linked Agammaglobulinemia
Author / Creator:Conley, Mary Ellen ; Brown, Persymphonie ; Pickard, Allan R ; Buckley, Rebecca H ; Miller, Debra S ; Raskind, Wendy H ; Singer, Jack W ; Fialkow, Philip J
Publisher:Boston, MA: Massachusetts Medical Society
Journal title:The New England journal of medicine, 1986-08, Vol.315 (9), p.564-567
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Genetic Evaluation and Counseling of Couples with Recurrent Miscarriage: Recommendations of the National Society of Genetic Counselors
Author / Creator:Laurino, Mercy Y. ; Bennett, Robin L. ; Saraiya, Devki S. ; Baumeister, Lisa ; Doyle, Debra Lochner ; Leppig, Kathleen ; Pettersen, Barbara ; Resta, Robert ; Shields, Larry ; Uhrich, Stefanie ; Varga, Elizabeth A. ; Raskind, Wendy H.
Publisher:New York: Kluwer Academic Publishers‐Plenum Publishers
Journal title:Journal of genetic counseling, 2005-06, Vol.14 (3), p.165-181
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Raskind, Wendy H

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Raskind, Wendy H

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Relative burden of large CNVs on a range of neurodevelopmental phenotypes

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Caspase-8, association with Alzheimer's Disease and functional analysis of rare variants

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Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech

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Integrative analysis of RUNX1 downstream pathways and target genes

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The effect of algorithms on copy number variant detection

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Wenckebach Periodicity at Rest That Normalizes With Tachycardia in a Family With a NKX2.5 Mutation

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A p53-Dependent Mouse Spindle Checkpoint

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Defects in lysosomal function and lipid metabolism in human microglia harboring a TREM2 loss of function mutation

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Biochemical and imaging surveillance in Li-Fraumeni syndrome

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Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes

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Family-based exome sequencing and case-control analysis implicate CEP41 as an ASD gene

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Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample

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Global Processing Speed in Children with Low Reading Ability and in Children and Adults with Typical Reading Ability: Exploratory Factor Analytic Models

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Genome Scan for Spelling Deficits: Effects of Verbal IQ on Models of Transmission and Trait Gene Localization

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Genome Scan of a Nonword Repetition Phenotype in Families with Dyslexia: Evidence for Multiple Loci

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Pharmacology and genetics of autism: implications for diagnosis and treatment

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Expression of the Gene Defect in X-Linked Agammaglobulinemia

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Genetic Evaluation and Counseling of Couples with Recurrent Miscarriage: Recommendations of the National Society of Genetic Counselors

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