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Ellen Magenis

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Stephen R Williams; Micheala A Aldred; Vazken M Der Kaloustian; Fahed Halal; Gordon Gowans; D Ross McLeod; Sara Zondag; Helga V Toriello; R Ellen Magenis; Sarah H Elsea
Haploinsufficiency of HDAC4 causes brachydactyly mental retardation syndrome, with brachydactyly type E, developmental delays, and behavioral problems.
Jennifer B Dunlap; R Ellen Magenis; Craig Davis; Eleanor Himoe; Atiya Mansoor
Cytogenetic analysis of a primary bone angiosarcoma.
Eilis A Boudreau; Kyle Patrick Johnson; Angela R Jackman; Jan Blancato; Marjan Huizing; Claude Bendavid; Marypat Jones; Settara C Chandrasekharappa; Alfred J Lewy; Ann C M Smith; R Ellen Magenis
Review of disrupted sleep patterns in Smith-Magenis syndrome and normal melatonin secretion in a patient with an atypical interstitial 17p11.2 deletion.

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2010: Stephen R Williams; Micheala A Aldred; Vazken M Der Kaloustian; Fahed Halal; Gordon Gowans; D Ross McLeod; Sara Zondag; Helga V Toriello; R Ellen Magenis; Sarah H Elsea
Haploinsufficiency of HDAC4 causes brachydactyly mental retardation syndrome, with brachydactyly type E, developmental delays, and behavioral problems.
American journal of human genetics 2010;87(2):219-28.
2009: Jennifer B Dunlap; R Ellen Magenis; Craig Davis; Eleanor Himoe; Atiya Mansoor
Cytogenetic analysis of a primary bone angiosarcoma.
Cancer genetics and cytogenetics 2009;194(1):1-3.
2009: Eilis A Boudreau; Kyle Patrick Johnson; Angela R Jackman; Jan Blancato; Marjan Huizing; Claude Bendavid; Marypat Jones; Settara C Chandrasekharappa; Alfred J Lewy; Ann C M Smith; R Ellen Magenis
Review of disrupted sleep patterns in Smith-Magenis syndrome and normal melatonin secretion in a patient with an atypical interstitial 17p11.2 deletion.
American journal of medical genetics. Part A 2009;149A(7):1382-91.
2008: George R Wettach; Luke Boyd; Helen Lawce; R Ellen Magenis; Atiya Mansoor
Cytogenetic analysis of a hemosiderotic fibrolipomatous tumor.
Cancer genetics and cytogenetics 2008;182(2):140-3.
2007: Nyla A Heerema; Susana C Raimondi; James Robert Anderson; Jaclyn Biegel; Bruce M Camitta; Linda D Cooley; Paul S Gaynon; Betsy Hirsch; R Ellen Magenis; Loris McGavran; Shivanand Patil; Mark J Pettenati; Jeanette Pullen; Kathleen W Rao; Diane Roulston; Nancy R Schneider; Jonathan J Shuster; Warren G Sanger; Maxine J Sutcliffe; Peter van Tuinen; Michael S Watson; Andrew J Carroll
Specific extra chromosomes occur in a modal number dependent pattern in pediatric acute lymphoblastic leukemia.
Genes, chromosomes & cancer 2007;46(7):684-93.
2006: Cristina Smith; R Ellen Magenis; Eleanor Himoe; Cheree Smith; Atiya Mansoor
Chondromyxoid fibroma of the nasal cavity with an interstitial insertion between chromosomes 6 and 19.
Cancer genetics and cytogenetics 2006;171(2):97-100.
2006: Weimin Bi; Gulam Mustafa Saifi; Santhosh Girirajan; Xin Shi; Barbara Szomju; Helen Firth; R Ellen Magenis; Lorraine Potocki; Sarah H Elsea; James R Lupski
RAI1 point mutations, CAG repeat variation, and SNP analysis in non-deletion Smith-Magenis syndrome.
American journal of medical genetics. Part A 2006;140(22):2454-63.
2006: Charles A Williams; Arthur L Beaudet; Jill Clayton-Smith; Joan H Knoll; Martin Kyllerman; Laura A Laan; R Ellen Magenis; Anne Moncla; Albert A Schinzel; Jane A Summers; Joseph Wagstaff
Angelman syndrome 2005: updated consensus for diagnostic criteria.
American journal of medical genetics. Part A 2006;140(5):413-8.
2006: R Ellen Magenis
Sexual maldevelopment and sex reversal, chromosomal causes.
Journal of the Association of Genetic Technologists 2006;32(3):72-82.
2005: Luke Boyd; Joseph S Livingston; Michael G Brown; Helen Lawce; Joseph T Gilhooly; Robert S Wildin; Leesa M Linck; R Ellen Magenis; De-Ann M Pillers
Meiotic exchange event within the stalk region of an inverted chromosome 22 results in a recombinant chromosome with duplication of the distal long arm.
American journal of medical genetics. Part A 2005;138(4):355-60.
2005: Luke Boyd; Michael G Brown; Stephen Kelson; Helen Lawce; Sarah Shuttleworth; Nancy Unsworth; R Ellen Magenis
Mosaicism of proximal 15q duplication/deletion resulting in Prader-Willi syndrome with normal methylation.
American journal of medical genetics. Part A 2005;138A(2):181-4.
2005: Yassmine Akkari; Helen Lawce; Stephen Kelson; Cheree Smith; Craig Davis; Luke Boyd; R Ellen Magenis; Susan B Olson
Y chromosome heterochromatin of differing lengths in two cell populations of the same individual.
Prenatal diagnosis 2005;25(4):304-6.
2005: Ann C M Smith; R Ellen Magenis; Sarah H Elsea
Overview of Smith-Magenis syndrome.
Journal of the Association of Genetic Technologists 2005;31(4):163-7.
2004: Atiya Mansoor; Nisreen Fidda; Eleanor Himoe; Misty Payne; Helen Lawce; R Ellen Magenis
Myxoinflammatory fibroblastic sarcoma with complex supernumerary ring chromosomes composed of chromosome 3 segments.
Cancer genetics and cytogenetics 2004;152(1):61-5.
2003: Michael O'Dwyer; Ken M Gatter; Marc Loriaux; Brian J Druker; Susan B Olson; R Ellen Magenis; Helen Lawce; Michael J Mauro; Richard T Maziarz; Rita M Braziel
Demonstration of Philadelphia chromosome negative abnormal clones in patients with chronic myelogenous leukemia during major cytogenetic responses induced by imatinib mesylate.
Leukemia 2003;17(3):481-7.
2002: Rita M Braziel; Teresa M Launder; Brian J Druker; Susan B Olson; R Ellen Magenis; Michael J Mauro; Charles L Sawyers; Ronald L Paquette; Michael O'Dwyer
Hematopathologic and cytogenetic findings in imatinib mesylate-treated chronic myelogenous leukemia patients: 14 months' experience.
Blood 2002;100(2):435-41.
2001: Kimberly J Bussey; Helen Lawce; Eleanor Himoe; X O Shu; Nyla A Heerema; Elizabeth J. Perlman; Susan B Olson; R Ellen Magenis
SNRPN methylation patterns in germ cell tumors as a reflection of primordial germ cell development.
Genes, chromosomes & cancer 2001;32(4):342-52.
2001: James R Bunzow; MS Sonders; Seksiri Arttamangkul; L M Harrison; G Zhang; DI Quigley; T Darland; Katherine L Suchland; S Pasumamula; James L Kennedy; Susan B Olson; R Ellen Magenis; Susan Amara; David K Grandy
Amphetamine, 3,4-methylenedioxymethamphetamine, lysergic acid diethylamide, and metabolites of the catecholamine neurotransmitters are agonists of a rat trace amine receptor.
Molecular pharmacology 2001;60(6):1181-8.
2001: Craig R Warden; De-Ann M Pillers; Mary J Rice; J Wildes; J S Livingston; B A Clark; Joseph T Gilhooly; R Ellen Magenis
Interstitial duplication of the short arm of chromosome 1 in a newborn with congenital heart disease and multiple malformations.
American journal of medical genetics 2001;101(2):100-5.
2001: Bonnie Jeanne Baty; Susan B Olson; R Ellen Magenis; John C Carey
Trisomy 20 mosaicism in two unrelated girls with skin hypopigmentation and normal intellectual development.
American journal of medical genetics 2001;99(3):210-6.
2001: Kimberly J Bussey; Helen Lawce; Eleanor Himoe; X O Shu; R F Suijkerbuijk; Susan B Olson; R Ellen Magenis
Chromosomes 1 and 12 abnormalities in pediatric germ cell tumors by interphase fluorescence in situ hybridization.
Cancer genetics and cytogenetics 2001;125(2):112-8.
1999: Kimberly J Bussey; Helen Lawce; Susan B Olson; D C Arthur; D K Kalousek; Mark Krailo; Roger Giller; SA Heifetz; Richard B Womer; R Ellen Magenis
Chromosome abnormalities of eighty-one pediatric germ cell tumors: sex-, age-, site-, and histopathology-related differences--a Children's Cancer Group study.
Genes, chromosomes & cancer 1999;25(2):134-46.
1998: K D McMilin; Jacob A. Reiss; M G Brown; M H Black; D A Buckmaster; C T Durum; K A Gunter; Helen Lawce; T L Berry; O A Lamb; C L Olson; F F Weeks; M J Yoshitomi; P B Jacky; Susan B Olson; R Ellen Magenis
Clinical outcomes of four patients with microdeletion in the long arm of chromosome 2.
American journal of medical genetics 1998;78(1):36-43.
1998: Michael C Heinrich; Maureen Hoatlin; AJ Zigler; KV Silvey; Antony C (Tony) Bakke; Winifred Keeble; Yu Zhi; Carol A Reifsteck; Markus Grompe; M G Brown; R Ellen Magenis; Susan B Olson; Grover C Bagby
DNA cross-linker-induced G2/M arrest in group C Fanconi anemia lymphoblasts reflects normal checkpoint function.
Blood 1998;91(1):275-87.
1997: Sarah H Elsea; Smita M Purandare; R A Adell; RC Juyal; J G Davis; Brenda Finucane; R Ellen Magenis; Pragna I Patel
Definition of the critical interval for Smith-Magenis syndrome.
Cytogenetics and cell genetics 1997;79(3-4):276-81.
1996: Robert E Nickel; R Ellen Magenis
Neural tube defects and deletions of 22q11.
American journal of medical genetics 1996;66(1):25-7.
1996: A C Boudousquie; Helen Lawce; R Sherman; Susan B Olson; R Ellen Magenis; Christopher L Corless
Complex translocation [7;22] identified in an epithelioid hemangioendothelioma.
Cancer genetics and cytogenetics 1996;92(2):116-21.
1996: Benjamin B Roa; F Greenberg; P Gunaratne; C M Sauer; MS Lubinsky; Chahira Kozma; Jeanne M Meck; R Ellen Magenis; Lisa Shaffer; James R Lupski
Duplication of the PMP22 gene in 17p partial trisomy patients with Charcot-Marie-Tooth type-1 neuropathy.
Human genetics 1996;97(5):642-9.
1996: S Toth-Fejel; Susan B Olson; K Gunter; F Quan; J Wolford; B W Popovich; R Ellen Magenis
The impact of imprinting: Prader-Willi syndrome resulting from chromosome translocation, recombination, and nondisjunction.
American journal of human genetics 1996;58(5):1008-16.
1995: D M White; De-Ann M Pillers; Jacob A. Reiss; M G Brown; R Ellen Magenis
Interstitial deletions of the short arm of chromosome 4 in patients with a similar combination of multiple minor anomalies and mental retardation.
American journal of medical genetics 1995;57(4):588-97.
1995: Marilyn L Slovak; ST Traweek; C L Willman; D R Head; K J Kopecky; R Ellen Magenis; F R Appelbaum; Stephen J Forman
Trisomy 11: an association with stem/progenitor cell immunophenotype.
British journal of haematology 1995;90(2):266-73.
1995: F Quan; Jonathan (Jon) Zonana; K Gunter; K L Peterson; R Ellen Magenis; B W Popovich
An atypical case of fragile X syndrome caused by a deletion that includes the FMR1 gene.
American journal of human genetics 1995;56(5):1042-51.
1995: Charles A Williams; H Angelman; Jill Clayton-Smith; Daniel J Driscoll; J E Hendrickson; J H Knoll; R Ellen Magenis; A Schinzel; J Wagstaff; E M Whidden
Angelman syndrome: consensus for diagnostic criteria. Angelman Syndrome Foundation.
American journal of medical genetics 1995;56(2):237-8.
1995: S Toth-Fejel; R Ellen Magenis; S Leff; M G Brown; B Comegys; Helen Lawce; T Berry; D Kesner; M J Webb; Susan B Olson
Prenatal diagnosis of chromosome 15 abnormalities in the Prader-Willi/Angelman syndrome region by traditional and molecular cytogenetics.
American journal of medical genetics 1995;55(4):444-52.
1994: Robert E Nickel; De-Ann M Pillers; Mark J Merkens; R Ellen Magenis; Deborah A Driscoll; B S Emanuel; Jonathan (Jon) Zonana
Velo-cardio-facial syndrome and DiGeorge sequence with meningomyelocele and deletions of the 22q11 region.
American journal of medical genetics 1994;52(4):445-9.
1994: R Ellen Magenis; L Smith; J H Nadeau; K R Johnson; K G Mountjoy; Roger D Cone
Mapping of the ACTH, MSH, and neural (MC3 and MC4) melanocortin receptors in the mouse and human.
Mammalian genome : official journal of the International Mammalian Genome Society 1994;5(8):503-8.
1994: G M Segal; R Ellen Magenis; M Brown; Winifred Keeble; T D Smith; Michael C Heinrich; Grover C Bagby
Repression of Fanconi anemia gene (FACC) expression inhibits growth of hematopoietic progenitor cells.
The Journal of clinical investigation 1994;94(2):846-52.
1993: Robert E Nickel; De-Ann M Pillers; Mark J Merkens; R Ellen Magenis; Deborah A Driscoll; B S Emanuel; Jonathan (Jon) Zonana
Velo-cardio-facial and DiGeorge syndromes with meningomyelocele and deletions of the 22Q11 region.
European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift für Kinderchirurgie 1993;3 Suppl 1():27-8.
1992: B Zhao; David K Grandy; J M Hagerup; R Ellen Magenis; L Smith; B C Chauhan; W D Henner
The human gene for apurinic/apyrimidinic endonuclease (HAP1): sequence and localization to chromosome 14 band q12.
Nucleic acids research 1992;20(15):4097-8.
1992: David K Grandy; L J Allen; Y Zhang; R Ellen Magenis; Olivier Civelli
Chromosomal localization of three human D5 dopamine receptor genes.
Genomics 1992;13(4):968-73.
1991: F Greenberg; V Guzzetta; R Montes de Oca-Luna; R Ellen Magenis; A C Smith; S F Richter; I Kondo; William B Dobyns; Pragna I Patel; James R Lupski
Molecular analysis of the Smith-Magenis syndrome: a possible contiguous-gene syndrome associated with del(17)(p11.2).
American journal of human genetics 1991;49(6):1207-18.
1991: R Ellen Magenis; Cheryl L Maslen; L Smith; L Allen; Lynn Y Sakai
Localization of the fibrillin (FBN) gene to chromosome 15, band q21.1.
Genomics 1991;11(2):346-51.
1991: V Sharma; D Brown; L Smith; R Ellen Magenis; M Litt
Dinucleotide repeat polymorphism at the D9S55 locus.
Nucleic acids research 1991;19(14):4023.
1991: V Sharma; L Smith; L Allen; R Ellen Magenis; M Litt
Dinucleotide repeat polymorphism at the D14S43 locus.
Nucleic acids research 1991;19(7):1722.
1991: V Sharma; L Allen; R Ellen Magenis; M Litt
Dinucleotide repeat polymorphism at the D21S172 locus.
Nucleic acids research 1991;19(5):1169.
1991: V Sharma; L Allen; R Ellen Magenis; M Litt
A dinucleotide repeat polymorphism at the D1S116 locus.
Nucleic acids research 1991;19(5):1169.
1991: B Weber; L Allen; R Ellen Magenis; Paul J Goodfellow; L Smith; Michael R Hayden
Intrachromosomal location of the telomeric repeat (TTAGGG)n.
Mammalian genome : official journal of the International Mammalian Genome Society 1991;1(4):211-6.
1991: B Weber; L Allen; R Ellen Magenis; Michael R Hayden
A low-copy repeat located in subtelomeric regions of 14 different human chromosomal termini.
Cytogenetics and cell genetics 1991;57(4):179-83.
1990: David K Grandy; Q Y Zhou; L Allen; R Litt; R Ellen Magenis; Olivier Civelli; M Litt
A human D1 dopamine receptor gene is located on chromosome 5 at q35.1 and identifies an EcoRI RFLP.
American journal of human genetics 1990;47(5):828-34.
1990: Mordechai Shohat; Tamy Shohat; David L Rimoin; T Mohandas; John R Heckenlively; R Ellen Magenis; M B Davidson; Julie R Korenberg
Rearrangement of chromosome 15 in the region q11.2----q12 in an individual with obesity syndrome and her normal mother.
American journal of medical genetics 1990;37(2):173-7.
1990: JH Knoll; Robert D Nicholls; R Ellen Magenis; K Glatt; J M Graham; L Kaplan; Marc Lalande
Angelman syndrome: three molecular classes identified with chromosome 15q11q13-specific DNA markers.
American journal of human genetics 1990;47(1):149-54.
1990: B Weber; C Collins; C Robbins; R Ellen Magenis; A D Delaney; Joe Gray; Michael R Hayden
Characterization and organization of DNA sequences adjacent to the human telomere associated repeat (TTAGGG)n.
Nucleic acids research 1990;18(11):3353-61.
1990: De-Ann M Pillers; Richard G Weleber; B R Powell; Cheryl E Hanna; R Ellen Magenis; N R Buist
Aland Island eye disease (Forsius-Eriksson ocular albinism) and an Xp21 deletion in a patient with Duchenne muscular dystrophy, glycerol kinase deficiency, and congenital adrenal hypoplasia.
American journal of medical genetics 1990;36(1):23-8.
1990: R Ellen Magenis; S Toth-Fejel; L J Allen; M Black; M G Brown; Sarojini S Budden; R Cohen; Jan M Friedman; D Kalousek; Jonathan (Jon) Zonana
Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: specific regions, extent of deletions, parental origin, and clinical consequences.
American journal of medical genetics 1990;35(3):333-49.
1989: David K Grandy; M Litt; L Allen; James R Bunzow; M Marchionni; H Makam; L Reed; R Ellen Magenis; Olivier Civelli
The human dopamine D2 receptor gene is located on chromosome 11 at q22-q23 and identifies a TaqI RFLP.
American journal of human genetics 1989;45(5):778-85.
1989: B A Clark; John M Bissonnette; Susan B Olson; R Ellen Magenis
Pregnancy loss in a small chorionic villus sampling series.
American journal of obstetrics and gynecology 1989;161(2):301-2.
1989: Richard G Weleber; De-Ann M Pillers; B R Powell; Cheryl E Hanna; R Ellen Magenis; N R Buist
Aland Island eye disease (Forsius-Eriksson syndrome) associated with contiguous deletion syndrome at Xp21. Similarity to incomplete congenital stationary night blindness.
Archives of ophthalmology 1989;107(8):1170-9.
1989: M Litt; J Luty; M Kwak; L Allen; R Ellen Magenis; Gail Mandel
Localization of a human brain sodium channel gene (SCN2A) to chromosome 2.
Genomics 1989;5(2):204-8.
1989: JH Knoll; Robert D Nicholls; R Ellen Magenis; J M Graham; Marc Lalande; S A Latt
Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion.
American journal of medical genetics 1989;32(2):285-90.
1989: E Natt; R Ellen Magenis; J Zimmer; A Mansouri; Gerd Scherer
Regional assignment of the human loci for uvomorulin (UVO) and chymotrypsinogen B (CTRB) with the help of two overlapping deletions on the long arm of chromosome 16.
Cytogenetics and cell genetics 1989;50(2-3):145-8.
1988: Cheryl L Maslen; R Ellen Magenis; R Sheehy; M Litt
Phage 8-9 defines a cluster of site polymorphisms on chromosome 16q22-q24 [HGM9 no. D16S20].
Nucleic acids research 1988;16(16):8195.
1988: H J Lawrence; R Ellen Magenis; L D Fast; M Kamoun
Erythrophagocytic T-cell lymphoma: immunologic and cytogenetic evidence for a clonal malignancy of the CD8-positive T-cell subclass.
Disease markers 1988;6(3):141-50.
1988: ST Traweek; Michael K Riscoe; A J Ferro; Rita M Braziel; R Ellen Magenis; J H Fitchen
Methylthioadenosine phosphorylase deficiency in acute leukemia: pathologic, cytogenetic, and clinical features.
Blood 1988;71(6):1568-73.
1988: R Ellen Magenis
On the origin of chromosome anomaly.
American journal of human genetics 1988;42(4):529-33.
1988: B Smith; Douglas W Skarecky; U Bengtsson; R Ellen Magenis; N Carpenter; JJ Wasmuth
Isolation of DNA markers in the direction of the Huntington disease gene from the G8 locus.
American journal of human genetics 1988;42(2):335-44.
1988: M Litt; N E Buroker; S Kondoleon; J Douglass; D Liston; R Sheehy; R Ellen Magenis
Chromosomal localization of the human proenkephalin and prodynorphin genes.
American journal of human genetics 1988;42(2):327-34.
1988: R Ellen Magenis; R R Sheehy; M G Brown; H E McDermid; Bradley N White; Jonathan (Jon) Zonana; Richard G Weleber
Parental origin of the extra chromosome in the cat eye syndrome: evidence from heteromorphism and in situ hybridization analysis.
American journal of medical genetics 1988;29(1):9-19.
1988: Cheryl L Maslen; C Jones; Thomas M Glaser; R Ellen Magenis; R Sheehy; J Kellogg; M Litt
Seven polymorphic loci mapping to human chromosomal region 11q22-qter.
Genomics 1988;2(1):66-75.
1987: S Kondoleon; Henrik Vissing; X Y Luo; R Ellen Magenis; J Kellogg; M Litt
A hypervariable RFLP on chromosome 17p13 is defined by an arbitrary single copy probe p144-D6 [HGM9 No. D17S34].
Nucleic acids research 1987;15(24):10605.
1987: R Ellen Magenis; M G Brown; D A Lacy; Sarojini S Budden; Stephen H LaFranchi
Is Angelman syndrome an alternate result of del(15)(q11q13)?
American journal of medical genetics 1987;28(4):829-38.
1987: E Natt; E M Westphal; S E Toth-Fejel; R Ellen Magenis; N R Buist; R Rettenmeier; Gerd Scherer
Inherited and de novo deletion of the tyrosine aminotransferase gene locus at 16q22.1----q22.3 in a patient with tyrosinemia type II.
Human genetics 1987;77(4):352-8.
1987: H J Lawrence; V C Broudy; R Ellen Magenis; Susan B Olson; D Tomar; S Barton; J H Fitchen; Grover C Bagby
Cytogenetic evidence for involvement of B lymphocytes in acquired idiopathic sideroblastic anemias.
Blood 1987;70(4):1003-5.
1987: CG Palmer; Judith H Miles; P N Howard-Peebles; R Ellen Magenis; S Patil; J M Friedman
Fetal karyotype following ascertainment of fetal anomalies by ultrasound.
Prenatal diagnosis 1987;7(8):551-5.
1987: N Buroker; R Bestwick; G Haight; R Ellen Magenis; M Litt
A hypervariable repeated sequence on human chromosome 1p36.
Human genetics 1987;77(2):175-81.
1987: N A Affara; M A Ferguson-Smith; R Ellen Magenis; J L Tolmie; E Boyd; A Cooke; D Jamieson; K Kwok; Michael John Mitchell; L Snadden
Mapping the testis determinants by an analysis of Y-specific sequences in males with apparent XX and XO karyotypes and females with XY karyotypes.
Nucleic acids research 1987;15(18):7325-42.
1987: R R Sheehy; M G Brown; R J Warren; M Schwartzman; R Ellen Magenis
Y-derived sequences detected in a 45,X male by in situ hybridization.
American journal of medical genetics 1987;27(4):831-9.
1987: N E Buroker; L Bufton; U Surti; M Leppert; E Kumlin; R Sheehy; R Ellen Magenis; M Litt
A hypervariable region at the D19S11 locus.
Human genetics 1987;76(1):90-5.
1987: R Ellen Magenis; M Casanova; M Fellous; Susan B Olson; R Sheehy
Further cytologic evidence for Xp-Yp translocation in XX males using in situ hybridization with Y-derived probe.
Human genetics 1987;75(3):228-33.
1987: Malcolm A Ferguson-Smith; Nabeel A Affara; R Ellen Magenis
Ordering of Y-specific sequences by deletion mapping and analysis of X-Y interchange males and females.
Development (Cambridge, England) 1987;101 Suppl():41-50.
1987: R Ellen Magenis; S J Barton
Delineation of human prometaphase paracentromeric regions using sequential GTG- and C-banding.
Cytogenetics and cell genetics 1987;45(3-4):132-40.
1986: L Bufton; T K Mohandas; R Ellen Magenis; R Sheehy; R K Bestwick; M Litt
A highly polymorphic locus on chromosome 16q revealed by a probe from a chromosome-specific cosmid library.
Human genetics 1986;74(4):425-31.
1986: R Ellen Magenis; James Gusella; K Weliky; Susan B Olson; G Haight; S Toth-Fejel; R Sheehy
Huntington disease-linked restriction fragment length polymorphism localized within band p16.1 of chromosome 4 by in situ hybridization.
American journal of human genetics 1986;39(3):383-91.
1986: M Litt; R Sheehy; G A Bruns; R Ellen Magenis
A polymorphic locus on the long arm of chromosome 20 defined by two probes from a single cosmid.
Human genetics 1986;73(4):340-5.
1986: R Ellen Magenis; M G Brown; L Allen; Jacob A. Reiss
De novo partial duplication of 17p [dup(17)(p12----p11.2)]: clinical report.
American journal of medical genetics 1986;24(3):415-20.
1986: L Bufton; G A Bruns; R Ellen Magenis; D Tomar; D Shaw; D Brook; M Litt
Four restriction fragment length polymorphisms revealed by probes from a single cosmid map to chromosome 19.
American journal of human genetics 1986;38(4):447-60.
1986: M Litt; G A Bruns; R Sheehy; R Ellen Magenis
A highly polymorphic locus in human DNA revealed by probes from cosmid 1-5 maps to chromosome 2q35----37.
American journal of human genetics 1986;38(3):288-96.
1986: Susan B Olson; R Ellen Magenis; E W Lovrien
Human chromosome variation: the discriminatory power of Q-band heteromorphism (variant) analysis in distinguishing between individuals, with specific application to cases of questionable paternity.
American journal of human genetics 1986;38(2):235-52.
1986: N E Buroker; R Ellen Magenis; K Weliky; G Bruns; M Litt
Four restriction fragment length polymorphisms revealed by probes from a single cosmid map to human chromosome 12q.
Human genetics 1986;72(1):86-94.
1985: Susan B Olson; R Ellen Magenis; J G Buckmaster; John M Bissonnette
Chorionic villus sampling: first-trimester prenatal diagnosis of partial 10q trisomy in a family with a 4/10 translocation.
American journal of obstetrics and gynecology 1985;153(7):743-4.
1985: R Ellen Magenis; T A Donlon; D R Tomar
Localization of the beta-globin gene to 11p15 by in situ hybridization: utilization of chromosome 11 rearrangements.
Human genetics 1985;69(4):300-3.
1985: Jacob A. Reiss; Richard G Weleber; M G Brown; C D Bangs; E W Lovrien; R Ellen Magenis
Tandem duplication of proximal 22q: a cause of cat-eye syndrome.
American journal of medical genetics 1985;20(1):165-71.
1984: R Ellen Magenis; M L Tochen; K P Holahan; T Carey; L Allen; M G Brown
Turner syndrome resulting from partial deletion of Y chromosome short arm: localization of male determinants.
The Journal of pediatrics 1984;105(6):916-9.
1984: Cynthia J Curry; R Ellen Magenis; M Brown; J T Lanman; J Tsai; P O'Lague; P Goodfellow; T Mohandas; E A Bergner; L J Shapiro
Inherited chondrodysplasia punctata due to a deletion of the terminal short arm of an X chromosome.
The New England journal of medicine 1984;311(16):1010-5.
1984: Richard G Weleber; R Ellen Magenis
The importance of chromosomal studies in ophthalmology.
International ophthalmology clinics 1984;24(1):15-38.
1983: T A Donlon; M Litt; S R Newcom; R Ellen Magenis
Localization of the restriction fragment length polymorphism D14S1 (pAW-101) to chromosome 14q32.1 leads to 32.2 by in situ hybridization.
American journal of human genetics 1983;35(6):1097-106.
1983: M Frydman; R Ellen Magenis; T K Mohandas; M M Kaback
Chromosome Abnormalities in infants with prune belly anomaly: association with trisomy 18.
American journal of medical genetics 1983;15(1):145-8.
1983: Susan B Olson; R Ellen Magenis; S I Rowe; E W Lovrien
Chromosome heteromorphism analysis in cases of disputed paternity.
American journal of medical genetics 1983;15(1):47-55.
1983: T A Donlon; R Ellen Magenis
Methyl green is a substitute for distamycin A in the formation of distamycin A/DAPI C-bands.
Human genetics 1983;65(2):144-6.
1982: Jonathan (Jon) Zonana; M G Brown; R Ellen Magenis
Distal 19q duplication.
Human genetics 1982;60(3):267-70.
1982: R Ellen Magenis; M J Webb; R S McKean; D Tomar; L J Allen; H Kammer; Daniel L Van Dyke; E Lovrien
Translocation(X;Y)(p22.33;p11.2) in XX males: etiology of male phenotype.
Human genetics 1982;62(3):271-6.
1982: L Bufton; R Ellen Magenis; E W Lovrien
Alpha-1-antitrypsin protease inhibitor (Pi) phenotypes in Down's syndrome patients and their parents.
Clinical genetics 1982;21(1):14-8.
1982: D J Harris; M L Begleiter; J Chamberlin; L Hankins; R Ellen Magenis
Parental trisomy 21 mosaicism.
American journal of human genetics 1982;34(1):125-33.
1981: R L Anderson; Grover C Bagby; K Richert-Boe; R Ellen Magenis; R D Koler
Therapy-related preleukemic syndrome.
Cancer 1981;47(7):1867-71.
1981: T A Donlon; R Ellen Magenis
Structural organization of the heterochromatic region of human chromosome 9.
Chromosoma 1981;84(3):353-63.
1980: E G Stubbs; R Ellen Magenis
HLA and autism.
Journal of autism and developmental disorders 1980;10(1):15-9.
1980: J Chamberlin; R Ellen Magenis
Parental origin of de novo chromosome rearrangements.
Human genetics 1980;53(3):343-7.
1979: Jacob A. Reiss; P M Brenes; J Chamberlin; R Ellen Magenis; E W Lovrien
The 8p- syndrome.
Human genetics 1979;47(2):135-40.
1978: R Ellen Magenis; Jacob A. Reiss; R Bigley; J Chamberlin; E Lovrien
Exclusion of glutathione reductase from 8pter leads to 8p22 and localization to 8p21.
Cytogenetics and cell genetics 1978;22(1-6):446-8.
1978: R Ellen Magenis; J Chamberlin; K Overton; E Lovrien
Linkage relationships of HLA and a familial chromosome 6 inversion (pter leads to p23::q23 leads to qter): lack of dose effect in duplication-deficient offspring.
Cytogenetics and cell genetics 1978;22(1-6):418-20.
1978: R Ellen Magenis; T Donlon; M Parks; M L Rivas; E W Lovrien
Linkage relationships of dominant antithrombin III deficiency and the heterochromatic region of chromosome 1.
Cytogenetics and cell genetics 1978;22(1-6):327-9.
1978: E W Lovrien; R Ellen Magenis; M L Rivas; N Lamvik; S Rowe; J Wood; J Hemmerling
Serum cholinesterase (E2) linkage analysis: possible evidence for localization to chromosome 16.
Cytogenetics and cell genetics 1978;22(1-6):324-6.
1978: E W Lovrien; R Ellen Magenis; M L Rivas; S Goodnight; R Moreland; S Rowe
Linkage study of antithrombin III.
Cytogenetics and cell genetics 1978;22(1-6):319-23.
1978: G H Prescott; M L Rivas; L Shanbeck; D W Macfarlane; H E Wyandt; W R Breg; H A Lubs; R Ellen Magenis; R L Summitt; C G Palmer; F Hecht; W Kimberling; D Clow
The Interregional Cytogenetic Register System (ICRS).
Birth defects original article series 1978;14(6C):269-79.
1977: R Ellen Magenis; K M Overton; J Chamberlin; T Brady; E Lovrien
Parental origin of the extra chromosome in Down's syndrome.
Human genetics 1977;37(1):7-16.
1976: G Higginson; D D Weaver; R Ellen Magenis; G H Prescott; C Haag; D J Hepburn
Interstitial deletion of the long arm of chromosome no. 7 (7q-) in an infant with multiple anomalies.
Clinical genetics 1976;10(5):307-12.
1976: R Ellen Magenis; H E Wyandt; K M Overton; J Macfarlane
Parental origin of a ring 13 chromosome in a female with multiple anomalies.
Human genetics 1976;33(2):181-6.
1976: K M Overton; R Ellen Magenis; T Brady; J Chamberlin; M Parks
Cytogenetic darkroom magic: now you see them, now you don't.
American journal of human genetics 1976;28(4):417-9.
1976: H E Wyandt; F Hecht; R Ellen Magenis; D G Wysham; G Prescott
9p trisomy identified by Giemsa-11.
Human genetics 1976;31(3):355-8.
1976: M L Rivas; P M Conneally; E W Lovrien; R Ellen Magenis; A D Merritt; Deborah A Meyers; C G Palmer; M Parks; L Wang; P L Yu
The linkage and mapping relationships of 1qh.
Birth defects original article series 1976;12(7):347-50.
1976: Deborah A Meyers; P M Conneally; E W Lovrien; R Ellen Magenis; A D Merritt; J A Norton; C G Palmer; M L Rivas; L Wang; P L Yu
Linkage group I: the simultaneous estimation of recombination and interference.
Birth defects original article series 1976;12(7):335-9.
1976: R Ellen Magenis; R D Koler; E Lovrien; R H Bigley; M C DuVal; K M Overton
Further evidence for the assignment of the red cell acid phosphatase gene (ACP1) to the short arm of chromosome 2 from gene dosage effect.
Birth defects original article series 1976;12(7):326-7.
1976: M L Rivas; P M Conneally; E W Lovrien; R Ellen Magenis; A D Merritt; Deborah A Meyers; C G Palmer; M Parks; L Wang; P L Yu
The linkage and mapping relationships of 1 qh.
Cytogenetics and cell genetics 1976;16(1-5):347-50.
1976: Deborah A Meyers; P M Conneally; E W Lovrien; R Ellen Magenis; A D Merritt; J A Norton; C G Palmer; M L Rivas; L Wang; P L Yu
Linkage group I: the simultaneous estimation of recombination and interference.
Cytogenetics and cell genetics 1976;16(1-5):335-9.
1976: R Ellen Magenis; R D Koler; E Lovrien; R H Bigley; M C DuVal; K M Overton
Further evidence for the assignment of the red cell acid phosphatase gene (ACP1) to the short arm of chromosome 2 from gene dosage effect.
Cytogenetics and cell genetics 1976;16(1-5):326-7.
1975: R Ellen Magenis; R D Koler; E Lovrien; R H Bigley; M C DuVal; K M Overton
Gene dosage: evidence for assignment of erythrocyte acid phosphatase locus to chromosome 2.
Proceedings of the National Academy of Sciences of the United States of America 1975;72(11):4526-30.
1975: R Ellen Magenis; K Overton; H Wyandt; T Bergstrom; F Hecht; E Lovrien
Exclusion gene mapping utilizing patients with chromosome imbalance: the HL-A system as a prototype.
Humangenetik 1975;27(2):91-109.
1974: H E Wyandt; R F Vlietinck; R Ellen Magenis; F Hecht
Colored reverse-banding of human chromosomes with acridine orange following alkaline-formalin treatment: densitometric validation and applications.
Humangenetik 1974;23(2):119-30.
1973: F Hecht; R Ellen Magenis; B K McCaw
Clinical cytogenetics. Dawn breaks on a new era.
American journal of diseases of children (1960) 1973;125(3):319-21.
1972: R Ellen Magenis; K M Overton; Jacob A. Reiss; J P Macfarlane; F Hecht
Partial trisomy 15.
Lancet 1972;2(7791):1365-6.
1972: R Ellen Magenis; S Armendares; F Hecht; Richard G Weleber; K Overton
Identification by fluorescence of two G rings: (46,XY,21r) G deletion syndrome I and (46, XX, 22r) G deletion syndrome II.
Annales de génétique 1972;15(4):265.
1972: Jacob A. Reiss; H E Wyandt; R Ellen Magenis; E W Lovrien; F Hecht
Mosaicism with translocation: autoradiographic and fluorescent studies of an inherited reciprocal translocation t(2q+;14q-).
Journal of medical genetics 1972;9(3):280-6.
1972: G H Prescott; R Ellen Magenis; N R Buist
Amniocentesis for antenatal diagnosis of genetic disorders.
Postgraduate medicine 1972;51(3):212-7.
1971: F Hecht; B Tolby; R Ellen Magenis; W J Kimberling; H Wyandt; E W Lovrien
Chromosomal localization of the heterochromatic region 16qh(.76) linked to alpha-haptoglobin in man.
Nature 1971;233(5320):480.
1970: R Ellen Magenis; F Hecht; E W Lovrien
Heritable fragile site on chromosome 16: probable localization of haptoglobin locus in man.
Science (New York, N.Y.) 1970;170(3953):85-7.
1968: R Ellen Magenis; F Hecht; S Milham
Trisomy 13 (D1) syndrome: studies on parental age, sex ratio, and survival.
The Journal of pediatrics 1968;73(2):222-8.