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Wendy Raskind

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Beate Peter; Le Button; Kathy Chapman; Carol Stoel-Gammon; Wendy H Raskind
Deficits in sequential processing manifest in motor and linguistic tasks in a multigenerational family with childhood apraxia of speech.
Le Button; Beate Peter; Carol Stoel-Gammon; Wendy H Raskind
Associations among measures of sequential processing in motor and linguistics tasks in adults with and without a family history of childhood apraxia of speech: a replication study.
Wendy H Raskind; Todd Richards; Mark M Eckert; Beate Peter; Virginia W Berninger
The genetics of reading disabilities: from phenotypes to candidate genes.

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All Publications

2013: Beate Peter; Le Button; Kathy Chapman; Carol Stoel-Gammon; Wendy H Raskind
Deficits in sequential processing manifest in motor and linguistic tasks in a multigenerational family with childhood apraxia of speech.
Clinical linguistics & phonetics 2013;27(3):163-91.
2013: Le Button; Beate Peter; Carol Stoel-Gammon; Wendy H Raskind
Associations among measures of sequential processing in motor and linguistics tasks in adults with and without a family history of childhood apraxia of speech: a replication study.
Clinical linguistics & phonetics 2013;27(3):192-212.
2012: Wendy H Raskind; Todd Richards; Mark M Eckert; Beate Peter; Virginia W Berninger
The genetics of reading disabilities: from phenotypes to candidate genes.
Frontiers in psychology 2012;3():601.
2011: Santhosh Girirajan; Carlos S Moreno; Wendy H Raskind; Corrado Romano; Neil Shafer; Margherita Silengo; Laura Vives; Tiffany H Vu; Stephen Warren; Carl Baker; Raphael Bernier; Zoran Brkanac; Bradley P Coe; Giovanni B Ferrero; Marco Fichera; Evan E Eichler
Relative burden of large CNVs on a range of neurodevelopmental phenotypes.
PLoS genetics 2011;7(11):e1002334.
2011: O Korvatska; Annette Estes; Jeffrey Munson; Geraldine Dawson; L M Bekris; R Kohen; Chang-En Yu; Gerard D Schellenberg; Wendy H Raskind
Mutations in the TSGA14 gene in families with autism spectrum disorders.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2011;156B(3):303-11.
2011: Beate Peter; Wendy H Raskind; Mark Matsushita; Mark Lisowski; Tiffany Vu; Virginia W Berninger; Ellen M Wijsman; Zoran Brkanac
Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample.
Journal of neurodevelopmental disorders 2011;3(1):39-49.
2011: Kevin Rubenstein; Mark Matsushita; Virginia W Berninger; Wendy H Raskind; Ellen M Wijsman
Genome scan for spelling deficits: effects of verbal IQ on models of transmission and trait gene localization.
Behavior genetics 2011;41(1):31-42.
2010: Dong-Hui Chen; Wendy H Raskind; William W Parson; Joshua A Sonnen; Tiffany Vu; Yunlin Zheng; Mark Matsushita; John Wolff; Hillary Lipe; Thomas D Bird
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 2010;296(1-2):22-9.
2010: Parvoneh Poorkaj-Navas; Wendy H Raskind; James B Leverenz; Mark Matsushita; Cyrus P Zabetian; Ali Samii; Sophia Kim; Nayiry Gazi; John G Nutt; John Wolff; Dora Yearout; J Lynne Greenup; Ellen J Steinbart; Thomas D Bird
A novel X-linked four-repeat tauopathy with Parkinsonism and spasticity.
Movement disorders : official journal of the Movement Disorder Society 2010;25(10):1409-17.
2010: Debby W Tsuang; Steven P Millard; Benjamin Ely; Peter Chi; Kenneth Wang; Wendy H Raskind; Sulgi Kim; Zoran Brkanac; Chang-En Yu
The effect of algorithms on copy number variant detection.
PloS one 2010;5(12):e14456.
2009: Wendy H Raskind; Mark Matsushita; Beate Peter; Jeffrey Biberston; John Wolff; Hillary Lipe; Ruben Burbank; Thomas D Bird
Familial dyskinesia and facial myokymia (FDFM): Follow-up of a large family and linkage to chromosome 3p21-3q21.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2009;150B(4):570-4.
2009: Zoran Brkanac; David Spencer; Jay Shendure; Peggy D Robertson; Mark Matsushita; Tiffany Vu; Thomas D Bird; Maynard V Olson; Wendy H Raskind
IFRD1 is a candidate gene for SMNA on chromosome 7q22-q23.
American journal of human genetics 2009;84(5):692-7.
2008: Zoran Brkanac; Nicola H Chapman; Robert P Igo; Mark M Matsushita; Kathleen Nielsen; Virginia W Berninger; Ellen M Wijsman; Wendy H Raskind
Genome scan of a nonword repetition phenotype in families with dyslexia: evidence for multiple loci.
Behavior genetics 2008;38(5):462-75.
2008: Alona Gad; Mercy Laurino; Kenneth R Maravilla; Mark Matsushita; Wendy H Raskind
Sensorineural deafness, distinctive facial features, and abnormal cranial bones: a new variant of Waardenburg syndrome?
American journal of medical genetics. Part A 2008;146A(14):1880-5.
2007: Zoran Brkanac; Nicola H Chapman; Mark M Matsushita; Lani Chun; Kathleen Nielsen; Elizabeth Cochrane; Virginia W Berninger; Ellen M Wijsman; Wendy H Raskind
Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2007;144B(4):556-60.
2006: Robert P Igo; Nicola H Chapman; Virginia W Berninger; Mark Matsushita; Zoran Brkanac; Joseph H Rothstein; Ted Holzman; Kathleen Nielsen; Wendy H Raskind; Ellen M Wijsman
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 : the official publication of the International Society of Psychiatric Genetics 2006;141B(1):15-27.
2006: Todd L Richards; Elizabeth H Aylward; Katherine M Field; Amie C Grimme; Wendy H Raskind; Anne L Richards; William E Nagy; Mark A Eckert; Christiana Leonard; Robert D Abbott; Virginia W Berninger
Converging evidence for triple word form theory in children with dyslexia.
Developmental neuropsychology 2006;30(1):547-89.
2005: Cyrus Zabetian; Ali Samii; A D Mosley; John W Roberts; Berta C Leis; Dora Yearout; Wendy H Raskind; Alida Griffith
A clinic-based study of the LRRK2 gene in Parkinson disease yields new mutations.
Neurology 2005;65(5):741-4.
2005: Wendy H Raskind; Robert P Igo; Nicola H Chapman; Virginia W Berninger; Jennifer B Thomson; Mark Matsushita; Zoran Brkanac; Ted Holzman; M Brown; Ellen M Wijsman
A genome scan in multigenerational families with dyslexia: Identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiency.
Molecular psychiatry 2005;10(7):699-711.
2005: Mercy Y Laurino; Robin L Bennett; Devki S Saraiya; Lisa Baumeister; Debra Lochner Doyle; Kathleen Leppig; Barbara Pettersen; Robert Resta; Larry Shields; Stefanie Uhrich; Elizabeth A Varga; Wendy H Raskind
Genetic evaluation and counseling of couples with recurrent miscarriage: recommendations of the National Society of Genetic Counselors.
Journal of genetic counseling 2005;14(3):165-81.
2005: Dong-Hui Chen; Patrick J Cimino; Laura P W Ranum; Huda Y Zoghbi; Ichiro Yabe; Lawrence J Schut; Russell L Margolis; Hillary Lipe; A Feleke; Mark Matsushita; John Wolff; C Morgan; D Lau; Magali Fernandez; Hidenao Sasaki; Wendy H Raskind; Thomas D Bird
The clinical and genetic spectrum of spinocerebellar ataxia 14.
Neurology 2005;64(7):1258-60.
2005: Dong-Hui Chen; Mark Matsushita; Shirley Rainier; Brandon Meaney; Lisa Tisch; Abreham Feleke; John Wolff; Hillary Lipe; John K Fink; Thomas D Bird; Wendy H Raskind
Presence of alanine-to-valine substitutions in myofibrillogenesis regulator 1 in paroxysmal nonkinesigenic dyskinesia: confirmation in 2 kindreds.
Archives of neurology 2005;62(4):597-600.
2004: Nicola H Chapman; Robert P Igo; Jennifer B Thomson; Mark Matsushita; Zoran Brkanac; Ted Holzman; Virginia W Berninger; Ellen M Wijsman; Wendy H Raskind
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 : the official publication of the International Society of Psychiatric Genetics 2004;131B(1):67-75.
2004: Kathleen A Leppig; Virginia P Sybert; Judith L Ross; Christopher Cunniff; Tina Trejo; Wendy H Raskind; Christine M Disteche
Phenotype and X inactivation in 45,X/46,X,r(X) cases.
American journal of medical genetics. Part A 2004;128A(3):276-84.
2004: Ellen M Wijsman; Nancy M Robinson; Kathryn H Ainsworth; Elisabeth A Rosenthal; Ted Holzman; Wendy H Raskind
Familial aggregation patterns in mathematical ability.
Behavior genetics 2004;34(1):51-62.
2003: Ichiro Yabe; Hidenao Sasaki; Dong-Hui Chen; Wendy H Raskind; Thomas D Bird; Isao Yamashita; Shoji Tsuji; Seiji Kikuchi; Kunio Tashiro
Spinocerebellar ataxia type 14 caused by a mutation in protein kinase C gamma.
Archives of neurology 2003;60(12):1749-51.
2003: Nicola H Chapman; Wendy H Raskind; Jennifer B Thomson; Virginia W Berninger; Ellen M Wijsman
Segregation analysis of phenotypic components of learning disabilities. II. Phonological decoding.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2003;121B(1):60-70.
2003: Dong-Hui Chen; Zoran Brkanac; Christophe Verlinde; Xiao-Jian Tan; Laura Bylenok; David Nochlin; Mark Matsushita; Hillary Lipe; John Wolff; Magali Fernandez; Patrick J Cimino; Thomas D Bird; Wendy H Raskind
Missense mutations in the regulatory domain of PKC gamma: a new mechanism for dominant nonepisodic cerebellar ataxia.
American journal of human genetics 2003;72(4):839-49.
2002: Channing Yu; Kathy K Niakan; Mark Matsushita; George Stamatoyannopoulos; Stuart H Orkin; Wendy H Raskind
X-linked thrombocytopenia with thalassemia from a mutation in the amino finger of GATA-1 affecting DNA binding rather than FOG-1 interaction.
Blood 2002;100(6):2040-5.
2002: Zoran Brkanac; Laura Bylenok; Magali Fernandez; Mark Matsushita; Hillary Lipe; John Wolff; David Nochlin; Wendy H Raskind; Thomas D Bird
A new dominant spinocerebellar ataxia linked to chromosome 19q13.4-qter.
Archives of neurology 2002;59(8):1291-5.
2002: Razia Sultana; Chang-En Yu; Jun Yu; Jeffrey Munson; Donghui Chen; Wenhui Hua; Annette Estes; Fanny Cortes; Flora de la Barra; Dongmei Yu; Syed T Haider; Barbara J Trask; Eric Green; Wendy H Raskind; Christine M Disteche; Ellen M Wijsman; Geraldine Dawson; Daniel R Storm; Gerard D Schellenberg; Enrique C Villacres
Identification of a novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins.
Genomics 2002;80(2):129-34.
2002: Chang-En Yu; Geraldine Dawson; Jeffrey Munson; Ian D'Souza; Julie Osterling; Annette Estes; Anne-Louise Leutenegger; Pamela Flodman; Moyra Smith; Wendy H Raskind; M Anne Spence; William M McMahon; Ellen M Wijsman; Gerard D Schellenberg
Presence of large deletions in kindreds with autism.
American journal of human genetics 2002;71(1):100-15.
2002: Li Hsu; Ellen M Wijsman; Virginia W Berninger; Jennifer B Thomson; Wendy H Raskind
Familial aggregation of dyslexia phenotypes. II: paired correlated measures.
American journal of medical genetics 2002;114(4):471-8.
2002: Zoran Brkanac; Magali Fernandez; Mark Matsushita; Hillary Lipe; John Wolff; Thomas D Bird; Wendy H Raskind
Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22-q32.
American journal of medical genetics 2002;114(4):450-7.
2002: Joäelle Michaud; Feng Wu; Motomi Osato; Gregory M Cottles; Masatoshi Yanagida; Norio Asou; Shigesada Katsuya; Yoshiaki Ito; Kathleen F Benson; Wendy H Raskind; Colette Rossier; Stylianos E Antonarakis; Sara J Israels; Archibald McNicol; Harvey Weiss; Marshall Horwitz; Hamish Scott
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.
Blood 2002;99(4):1364-72.
2001: Magali Fernandez; Wendy H Raskind; Mark Matsushita; John Wolff; Hillary Lipe; Thomas D Bird
Hereditary benign chorea: clinical and genetic features of a distinct disease.
Neurology 2001;57(1):106-10.
2001: Magali Fernandez; Wendy H Raskind; John Wolff; Mark Matsushita; E Yuen; WD Graf; Hillary Lipe; Thomas D Bird
Familial dyskinesia and facial myokymia (FDFM): a novel movement disorder.
Annals of neurology 2001;49(4):486-92.
2000: Wendy H Raskind; Li Hsu; Virginia W Berninger; Jennifer B Thomson; Ellen M Wijsman
Familial aggregation of dyslexia phenotypes.
Behavior genetics 2000;30(5):385-96.
2000: Ellen M Wijsman; D Peterson; Anne-Louise Leutenegger; Jennifer B Thomson; Katrina Goddard; Li Hsu; Virginia W Berninger; Wendy H Raskind
Segregation analysis of phenotypic components of learning disabilities. I. Nonword memory and digit span.
American journal of human genetics 2000;67(3):631-46.
2000: Karen J Woodward; K Kirtland; Stephen R Dlouhy; Wendy H Raskind; Thomas D Bird; Sue Malcolm; D Abeliovich
X inactivation phenotype in carriers of Pelizaeus-Merzbacher disease: skewed in carriers of a duplication and random in carriers of point mutations.
European journal of human genetics : EJHG 2000;8(6):449-54.
2000: Wendy H Raskind; Kathy K Niakan; J Wolff; Mark Matsushita; T Vaughan; George Stamatoyannopoulos; C Watanabe; J Rios; Hans D Ochs
Mapping of a syndrome of X-linked thrombocytopenia with Thalassemia to band Xp11-12: further evidence of genetic heterogeneity of X-linked thrombocytopenia.
Blood 2000;95(7):2262-8.
1999: James Y Garbern; Franca Cambi; Richard Alan Lewis; chris hall; Anders A F Sima; G Kraft; Jean-Michel Vallat; E P Bosch; ME Hodes; Stephen R Dlouhy; Wendy H Raskind; Thomas D Bird; Wendy B Macklin; John Kamholz
Peripheral neuropathy caused by proteolipid protein gene mutations.
Annals of the New York Academy of Sciences 1999;883():351-65.
1999: Howard A Chansky; Thomas E Trumble; Ernest U Conrad; J F Wolff; L W Murray; Wendy H Raskind
Evidence for a polyclonal etiology of palmar fibromatosis.
The Journal of hand surgery 1999;24(2):339-44.
1998: Kathleen F Benson; Marshall Horwitz; John Wolff; Kathryn Friend; E Thompson; S White; Robert I Richards; Wendy H Raskind; Thomas D Bird
CAG repeat expansion in autosomal dominant familial spastic paraparesis: novel expansion in a subset of patients.
Human molecular genetics 1998;7(11):1779-86.
1998: Howard A Chansky; J R Robbins; S Cha; Wendy H Raskind; Ernest U Conrad; Linda J Sandell
Expression of cartilage extracellular matrix and potential regulatory genes in a new human chondrosarcoma cell line.
Journal of orthopaedic research : official publication of the Orthopaedic Research Society 1998;16(5):521-30.
1998: Wendy H Raskind; L Steinmann; V Najfeld
Clonal development of myeloproliferative disorders: clues to hematopoietic differentiation and multistep pathogenesis of cancer.
Leukemia 1998;12(2):108-16.
1998: Wim Wuyts; Wim Van Hul; K De Boulle; Jan Hendrickx; Egbert Bakker; Filip Vanhoenacker; F Mollica; H J Lüdecke; B S Sayli; U E Pazzaglia; Geert R Mortier; B Hamel; Ernest U Conrad; M Matsushita; Wendy H Raskind; Patrick J Willems
Mutations in the EXT1 and EXT2 genes in hereditary multiple exostoses.
American journal of human genetics 1998;62(2):346-54.
1998: Wendy H Raskind; Ernest U Conrad; Mark Matsushita; Ellen M Wijsman; D E Wells; N Chapman; Linda J Sandell; M Wagner; J Houck
Evaluation of locus heterogeneity and EXT1 mutations in 34 families with hereditary multiple exostoses.
Human mutation 1998;11(3):231-9.
1998: Wendy H Raskind; T Bolin; John Wolff; John K Fink; Mark Matsushita; M Litt; Hillary Lipe; Thomas D Bird
Further localization of a gene for paroxysmal dystonic choreoathetosis to a 5-cM region on chromosome 2q34.
Human genetics 1998;102(1):93-7.
1997: Marshall Horwitz; Kathleen F Benson; Feng-Qian Li; John Wolff; M F Leppert; Lynne Hobson; Marie Mangelsdorf; S Yu; DR Hewett; Robert I Richards; Wendy H Raskind
Genetic heterogeneity in familial acute myelogenous leukemia: evidence for a second locus at chromosome 16q21-23.2.
American journal of human genetics 1997;61(4):873-81.
1997: James Y Garbern; Franca Cambi; X M Tang; Anders A F Sima; Jean-Michel Vallat; E P Bosch; Richard Alan Lewis; chris hall; J Sohi; G Kraft; KL Chen; I Joshi; D G Leonard; W Johnson; Wendy H Raskind; Stephen R Dlouhy; VM Pratt; ME Hodes; Thomas D Bird; John Kamholz
Proteolipid protein is necessary in peripheral as well as central myelin.
Neuron 1997;19(1):205-18.
1997: Wendy H Raskind; Margaret Pericak-Vance; F Lennon; John Wolff; Hillary Lipe; Thomas D Bird
Familial spastic paraparesis: evaluation of locus heterogeneity, anticipation, and haplotype mapping of the SPG4 locus on the short arm of chromosome 2.
American journal of medical genetics 1997;74(1):26-36.
1996: Wendy H Raskind; Ernest U Conrad; M Matsushita
Frequent loss of heterozygosity for markers on chromosome arm 10q in chondrosarcomas.
Genes, chromosomes & cancer 1996;16(2):138-43.
1995: Wim Wuyts; S Ramlakhan; Wim Van Hul; Jacqueline T Hecht; Ans M W van den Ouweland; Wendy H Raskind; F C Hofstede; Edwin Reyniers; Dan E Wells; Bert B A de Vries
Refinement of the multiple exostoses locus (EXT2) to a 3-cM interval on chromosome 11.
American journal of human genetics 1995;57(2):382-7.
1995: Wendy H Raskind; Ernest U Conrad; H Chansky; M Matsushita
Loss of heterozygosity in chondrosarcomas for markers linked to hereditary multiple exostoses loci on chromosomes 8 and 11.
American journal of human genetics 1995;56(5):1132-9.
1995: S M Cross; Carissa A Sanchez; C A Morgan; M K Schimke; S Ramel; Rejean L Idzerda; Wendy H Raskind; Brian J Reid
A p53-dependent mouse spindle checkpoint.
Science (New York, N.Y.) 1995;267(5202):1353-6.
1994: G A Schmale; Ernest U Conrad; Wendy H Raskind
The natural history of hereditary multiple exostoses.
The Journal of bone and joint surgery. American volume 1994;76(7):986-92.
1993: Wendy H Raskind; A M Ferraris; Vesna Najfeld; R J Jacobson; J W Moohr; P J Fialkow
Further evidence for the existence of a clonal Ph-negative stage in some cases of Ph-positive chronic myelocytic leukemia.
Leukemia 1993;7(8):1163-7.
1993: A Cook; Wendy H Raskind; S Blanton; Richard M Pauli; R G Gregg; Clair A Francomano; E Puffenberger; E U Conrad; G Schmale; Gerard D Schellenberg
Genetic heterogeneity in families with hereditary multiple exostoses.
American journal of human genetics 1993;53(1):71-9.
1993: C S Higano; Wendy H Raskind; jack w singer
Use of interferon alfa-2a to treat hematologic relapse of chronic myelogenous leukemia after bone marrow transplantation.
Acta haematologica 1993;89 Suppl 1():8-14.
1992: C S Higano; Wendy H Raskind; jack w singer
Use of alpha interferon for the treatment of relapse of chronic myelogenous leukemia in chronic phase after allogeneic bone marrow transplantation.
Blood 1992;80(6):1437-42.
1992: Wendy H Raskind; John Wolff; Leonard D Hudson; Thomas D Bird
RFLP detected by a genomic probe from the human X-linked proteolipid protein gene, PLP.
Human molecular genetics 1992;1(4):288.
1992: Wendy H Raskind; Thomas H Norwood; Douglas S Levine; Roger C Haggitt; Peter S Rabinovitch; Brian J Reid
Persistent clonal areas and clonal expansion in Barrett's esophagus.
Cancer research 1992;52(10):2946-50.
1991: Wendy H Raskind; C A Williams; Leonard D Hudson; Thomas D Bird
Complete deletion of the proteolipid protein gene (PLP) in a family with X-linked Pelizaeus-Merzbacher disease.
American journal of human genetics 1991;49(6):1355-60.
1991: R F Boynton; Y Huang; P L Blount; Brian J Reid; Wendy H Raskind; Roger C Haggitt; C Newkirk; James Resau; Jing Yin; T McDaniel; Meltzer Stephen J.
Frequent loss of heterozygosity at the retinoblastoma locus in human esophageal cancers.
Cancer research 1991;51(20):5766-9.
1991: P L Blount; S Ramel; Wendy H Raskind; Roger C Haggitt; Carissa A Sanchez; P J Dean; Peter S Rabinovitch; Brian J Reid
17p allelic deletions and p53 protein overexpression in Barrett's adenocarcinoma.
Cancer research 1991;51(20):5482-6.
1991: Wendy H Raskind; Ellen M Wijsman; R A Pagon; Timothy C Cox; M J Bawden; Brian K May; Thomas D Bird
X-linked sideroblastic anemia and ataxia: linkage to phosphoglycerate kinase at Xq13.
American journal of human genetics 1991;48(2):335-41.
1988: Wendy H Raskind; J W Singer; C A Morgan; P J Fialkow
Host origin of marrow stromal cells obtained from marrow transplant recipients and transformed in vitro by simian virus-40.
Experimental hematology 1988;16(10):827-30.
1988: J W Singer; Irwin D Bernstein; P C Davis; T R Walters; Wendy H Raskind; P J Fialkow
The effect of long-term marrow culture on the origin of colony-forming cells in acute myeloblastic leukemia: studies of two patients heterozygous for glucose-6-phosphate dehydrogenase.
Leukemia 1988;2(3):148-52.
1987: P J Fialkow; J W Singer; Wendy H Raskind; J W Adamson; R J Jacobson; Irwin D Bernstein; L W Dow; Vesna Najfeld; R Veith
Clonal development, stem-cell differentiation, and clinical remissions in acute nonlymphocytic leukemia.
The New England journal of medicine 1987;317(8):468-73.
1987: Irwin D Bernstein; J W Singer; Robert G Andrews; A Keating; Jerry S Powell; B H Bjornson; J Cuttner; Vesna Najfeld; G Reaman; Wendy H Raskind
Treatment of acute myeloid leukemia cells in vitro with a monoclonal antibody recognizing a myeloid differentiation antigen allows normal progenitor cells to be expressed.
The Journal of clinical investigation 1987;79(4):1153-9.
1987: Wendy H Raskind; P J Fialkow
The use of cell markers in the study of human hematopoietic neoplasia.
Advances in cancer research 1987;49():127-67.
1985: A M Ferraris; Wendy H Raskind; B H Bjornson; R J Jacobson; J W Singer; P J Fialkow
Heterogeneity of B cell involvement in acute nonlymphocytic leukemia.
Blood 1985;66(2):342-4.
1984: R J Jacobson; M J Temple; J W Singer; Wendy H Raskind; Jerry S Powell; P J Fialkow
A clonal complete remission in a patient with acute nonlymphocytic leukemia originating in a multipotent stem cell.
The New England journal of medicine 1984;310(23):1513-7.