Username

Password

Forgot Password?

Preview

Sign-in free and Explore the Exciting World of BiomedExperts:

Over 1.500.000 Profiles
More than 1.800 Organizations worldwide
State of the Art Network Visualizations

Manage your own Profile
Locate Experts in your Country/Region
Locate Experts in your 1. and 2. Level Network
Connect to Experts Worldwide

NetworkView

Ellen Magenis

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

Research Profile (preview)

Procedures

Disorders

Chemicals & Drugs

DNA

Physiology

Restriction Fragment Length Polymorphism

Phenomena

Nucleic Acid Hybridization

Living Beings

Concepts & Ideas

Pedigree

Anatomy

Sign-in to see full Profile

Network (preview)

Co-Publications
Name
20
Olson, Susan
12
Lawce, Helen
7
Pillers, De-Ann
6
Weleber, Richard
5
Himoe, Eleanor
5
Grandy, David
4
Bagby, Grover
4
Boyd, Luke
4
Mansoor, Atiya
4
Meyers, Deborah
3
Lupski, James
3
Nickel, Robert
3
Civelli, Olivier
3
Bussey, Kimberly
3
Maslen, Cheryl

Sign-in to see all Coauthors

Publications

TOP 3
Dunlap Jennifer B; Magenis R Ellen; Davis Craig; Himoe Eleanor; Mansoor Atiya
Cytogenetic analysis of a primary bone angiosarcoma.
Boudreau Eilis A; Johnson Kyle P; Jackman Angela R; Blancato Jan; Huizing Marjan; Bendavid Claude; Jones Marypat; Chandrasekharappa Settara C; Lewy Alfred J; Smith Ann C M; Magenis R Ellen
Review of disrupted sleep patterns in Smith-Magenis syndrome and normal melatonin secretion in a patient with an atypical interstitial 17p11.2 deletion.
Wettach George R; Boyd Luke J; Lawce Helen J; Magenis R Ellen; Mansoor Atiya
Cytogenetic analysis of a hemosiderotic fibrolipomatous tumor.

Sign-in to see all Publications

Sign in free and see...

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the visualized research activity
of experts around the globe

Sign-in to see more

Geonetwork of Ellen Magenis (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

Sign-in to see more

All Publications

2009: Dunlap Jennifer B; Magenis R Ellen; Davis Craig; Himoe Eleanor; Mansoor Atiya
Cytogenetic analysis of a primary bone angiosarcoma.
Cancer genetics and cytogenetics 2009;194(1):1-3.
2009: Boudreau Eilis A; Johnson Kyle P; Jackman Angela R; Blancato Jan; Huizing Marjan; Bendavid Claude; Jones Marypat; Chandrasekharappa Settara C; Lewy Alfred J; Smith Ann C M; Magenis R Ellen
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: Wettach George R; Boyd Luke J; Lawce Helen J; Magenis R Ellen; Mansoor Atiya
Cytogenetic analysis of a hemosiderotic fibrolipomatous tumor.
Cancer genetics and cytogenetics 2008;182(2):140-3.
2007: Heerema Nyla A; Raimondi Susana C; Anderson James R; Biegel Jaclyn; Camitta Bruce M; Cooley Linda D; Gaynon Paul S; Hirsch Betsy; Magenis R Ellen; McGavran Loris; Patil Shivanand; Pettenati Mark J; Pullen Jeanette; Rao Kathleen; Roulston Diane; Schneider Nancy R; Shuster Jonathan J; Sanger Warren; Sutcliffe Maxine J; van Tuinen Peter; Watson Michael S; Carroll Andrew J
Specific extra chromosomes occur in a modal number dependent pattern in pediatric acute lymphoblastic leukemia.
Genes, chromosomes & cancer 2007;46(7):684-93.
2006: Smith Cristina A; Magenis R Ellen; Himoe Eleanor; Smith Cheree; Mansoor Atiya
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: Bi Weimin; Saifi G Mustafa; Girirajan Santhosh; Shi Xin; Szomju Barbara; Firth Helen; Magenis R Ellen; Potocki Lorraine; Elsea Sarah H; Lupski James R
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: Williams Charles A; Beaudet Arthur L; Clayton-Smith Jill; Knoll Joan H; Kyllerman Martin; Laan Laura A; Magenis R Ellen; Moncla Ann; Schinzel Albert A; Summers Jane A; Wagstaff Joseph
Angelman syndrome 2005: updated consensus for diagnostic criteria.
American journal of medical genetics. Part A 2006;140(5):413-8.
2006: Magenis R Ellen
Sexual maldevelopment and sex reversal, chromosomal causes.
Journal of the Association of Genetic Technologists 2006;32(3):72-82.
2005: Boyd Luke J; Livingston Joseph S; Brown Michael G; Lawce Helen J; Gilhooly Joseph T; Wildin Robert S; Linck Leesa M; Magenis R Ellen; Pillers De-Ann M
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: Boyd Luke; Brown Michael G; Kelson Stephen; Lawce Helen; Shuttleworth Sarah; Unsworth Nancy; Magenis R Ellen
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: Akkari Yassmine; Lawce Helen; Kelson Stephen; Smith Cheree; Davis Craig; Boyd Luke; Magenis R Ellen; Olson Susan
Y chromosome heterochromatin of differing lengths in two cell populations of the same individual.
Prenatal diagnosis 2005;25(4):304-6.
2005: Smith Ann C M; Magenis R Ellen; Elsea Sarah H
Overview of Smith-Magenis syndrome.
Journal of the Association of Genetic Technologists 2005;31(4):163-7.
2004: Mansoor Atiya; Fidda Nisreen; Himoe Eleanor; Payne Misty; Lawce Helen; Magenis R Ellen
Myxoinflammatory fibroblastic sarcoma with complex supernumerary ring chromosomes composed of chromosome 3 segments.
Cancer genetics and cytogenetics 2004;152(1):61-5.
2003: O'Dwyer M E; Gatter K M; Loriaux M; Druker B J; Olson S B; Magenis R E; Lawce H; Mauro M J; Maziarz R T; Braziel R M
Demonstration of Philadelphia chromosome negative abnormal clones in patients with chronic myelogenous leukemia during major cytogenetic responses induced by imatinib mesylate.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2003;17(3):481-7.
2002: Braziel Rita M; Launder Teresa M; Druker Brian J; Olson Susan B; Magenis R Ellen; Mauro Michael J; Sawyers Charles L; Paquette Ronald L; O'Dwyer Michael E
Hematopathologic and cytogenetic findings in imatinib mesylate-treated chronic myelogenous leukemia patients: 14 months' experience.
Blood 2002;100(2):435-41.
2001: Bussey K J; Lawce H J; Himoe E; Shu X O; Heerema N A; Perlman E J; Olson S B; Magenis R E
SNRPN methylation patterns in germ cell tumors as a reflection of primordial germ cell development.
Genes, chromosomes & cancer 2001;32(4):342-52.
2001: Bunzow J R; Sonders M S; Arttamangkul S; Harrison L M; Zhang G; Quigley D I; Darland T; Suchland K L; Pasumamula S; Kennedy J L; Olson S B; Magenis R E; Amara S G; Grandy D K
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: Warden C R; Pillers D A; Rice M J; Wildes J; Livingston J S; Clark B A; Gilhooly J T; Magenis R E
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: Bussey K J; Lawce H J; Himoe E; Shu X O; Suijkerbuijk R F; Olson S B; Magenis R E
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.
2001: Baty B J; Olson S B; Magenis R E; Carey J C
Trisomy 20 mosaicism in two unrelated girls with skin hypopigmentation and normal intellectual development.
American journal of medical genetics 2001;99(3):210-6.
1999: Bussey K J; Lawce H J; Olson S B; Arthur D C; Kalousek D K; Krailo M; Giller R; Heifetz S; Womer R; Magenis R E
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: McMilin K D; Reiss J A; Brown M G; Black M H; Buckmaster D A; Durum C T; Gunter K A; Lawce H J; Berry T L; Lamb O A; Olson C L; Weeks F F; Yoshitomi M J; Jacky P B; Olson S B; Magenis R E
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: Heinrich M C; Hoatlin M E; Zigler A J; Silvey K V; Bakke A C; Keeble W W; Zhi Y; Reifsteck C A; Grompe M; Brown M G; Magenis R E; Olson S B; Bagby G C
DNA cross-linker-induced G2/M arrest in group C Fanconi anemia lymphoblasts reflects normal checkpoint function.
Blood 1998;91(1):275-87.
1997: Elsea S H; Purandare S M; Adell R A; Juyal R C; Davis J G; Finucane B; Magenis R E; Patel P I
Definition of the critical interval for Smith-Magenis syndrome.
Cytogenetics and cell genetics 1997;79(3-4):276-81.
1996: Boudousquie A C; Lawce H J; Sherman R; Olson S; Magenis R E; Corless C L
Complex translocation [7;22] identified in an epithelioid hemangioendothelioma.
Cancer genetics and cytogenetics 1996;92(2):116-21.
1996: Nickel R E; Magenis R E
Neural tube defects and deletions of 22q11.
American journal of medical genetics 1996;66(1):25-7.
1996: Roa B B; Greenberg F; Gunaratne P; Sauer C M; Lubinsky M S; Kozma C; Meck J M; Magenis R E; Shaffer L G; Lupski J R
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: Toth-Fejel S; Olson S; Gunter K; Quan F; Wolford J; Popovich B W; Magenis R E
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: White D M; Pillers D A; Reiss J A; Brown M G; Magenis R E
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: Slovak M L; Traweek S T; Willman C L; Head D R; Kopecky K J; Magenis R E; Appelbaum F R; Forman S J
Trisomy 11: an association with stem/progenitor cell immunophenotype.
British journal of haematology 1995;90(2):266-73.
1995: Quan F; Zonana J; Gunter K; Peterson K L; Magenis R E; Popovich B W
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: Williams C A; Angelman H; Clayton-Smith J; Driscoll D J; Hendrickson J E; Knoll J H; Magenis R E; Schinzel A; Wagstaff J; Whidden E M
Angelman syndrome: consensus for diagnostic criteria. Angelman Syndrome Foundation.
American journal of medical genetics 1995;56(2):237-8.
1995: Toth-Fejel S; Magenis R E; Leff S; Brown M G; Comegys B; Lawce H; Berry T; Kesner D; Webb M J; Olson S
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: Nickel R E; Pillers D A; Merkens M; Magenis R E; Driscoll D A; Emanuel B S; Zonana J
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: Magenis R E; Smith L; Nadeau J H; Johnson K R; Mountjoy K G; Cone R D
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: Segal G M; Magenis R E; Brown M; Keeble W; Smith T D; Heinrich M C; Bagby G C
Repression of Fanconi anemia gene (FACC) expression inhibits growth of hematopoietic progenitor cells.
The Journal of clinical investigation 1994;94(2):846-52.
1993: Nickel R E; Pillers D A; Merkens M; Magenis R E; Driscoll D A; Emanuel B S; Zonana J
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: Grandy D K; Allen L J; Zhang Y; Magenis R E; Civelli O
Chromosomal localization of three human D5 dopamine receptor genes.
Genomics 1992;13(4):968-73.
1992: Zhao B; Grandy D K; Hagerup J M; Magenis R E; Smith L; Chauhan B C; Henner W D
The human gene for apurinic/apyrimidinic endonuclease (HAP1): sequence and localization to chromosome 14 band q12.
Nucleic acids research 1992;20(15):4097-8.
1991: Greenberg F; Guzzetta V; Montes de Oca-Luna R; Magenis R E; Smith A C; Richter S F; Kondo I; Dobyns W B; Patel P I; Lupski J R
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: Magenis R E; Maslen C L; Smith L; Allen L; Sakai L Y
Localization of the fibrillin (FBN) gene to chromosome 15, band q21.1.
Genomics 1991;11(2):346-51.
1991: Sharma V; Brown D; Smith L; Magenis R E; Litt M
Dinucleotide repeat polymorphism at the D9S55 locus.
Nucleic acids research 1991;19(14):4023.
1991: Sharma V; Smith L; Allen L; Magenis R E; Litt M
Dinucleotide repeat polymorphism at the D14S43 locus.
Nucleic acids research 1991;19(7):1722.
1991: Sharma V; Allen L; Magenis R E; Litt M
Dinucleotide repeat polymorphism at the D21S172 locus.
Nucleic acids research 1991;19(5):1169.
1991: Sharma V; Allen L; Magenis R E; Litt M
A dinucleotide repeat polymorphism at the D1S116 locus.
Nucleic acids research 1991;19(5):1169.
1991: Weber B; Allen L; Magenis R E; Goodfellow P J; Smith L; Hayden M R
Intrachromosomal location of the telomeric repeat (TTAGGG)n.
Mammalian genome : official journal of the International Mammalian Genome Society 1991;1(4):211-6.
1991: Weber B; Allen L; Magenis R E; Hayden M R
A low-copy repeat located in subtelomeric regions of 14 different human chromosomal termini.
Cytogenetics and cell genetics 1991;57(4):179-83.
1990: Grandy D K; Zhou Q Y; Allen L; Litt R; Magenis R E; Civelli O; Litt M
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: Shohat M; Shohat T; Rimoin D L; Mohandas T; Heckenlively J; Magenis R E; Davidson M B; Korenberg J R
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: Knoll J H; Nicholls R D; Magenis R E; Glatt K; Graham J M; Kaplan L; Lalande M
Angelman syndrome: three molecular classes identified with chromosome 15q11q13-specific DNA markers.
American journal of human genetics 1990;47(1):149-54.
1990: Weber B; Collins C; Robbins C; Magenis R E; Delaney A D; Gray J W; Hayden M R
Characterization and organization of DNA sequences adjacent to the human telomere associated repeat (TTAGGG)n.
Nucleic acids research 1990;18(11):3353-61.
1990: Pillers D A; Weleber R G; Powell B R; Hanna C E; Magenis R E; Buist N R
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: Magenis R E; Toth-Fejel S; Allen L J; Black M; Brown M G; Budden S; Cohen R; Friedman J M; Kalousek D; Zonana J
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: Grandy D K; Litt M; Allen L; Bunzow J R; Marchionni M; Makam H; Reed L; Magenis R E; Civelli O
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: Clark B A; Bissonnette J M; Olson S B; Magenis R E
Pregnancy loss in a small chorionic villus sampling series.
American journal of obstetrics and gynecology 1989;161(2):301-2.
1989: Weleber R G; Pillers D A; Powell B R; Hanna C E; Magenis R E; Buist N R
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: Litt M; Luty J; Kwak M; Allen L; Magenis R E; Mandel G
Localization of a human brain sodium channel gene (SCN2A) to chromosome 2.
Genomics 1989;5(2):204-8.
1989: Knoll J H; Nicholls R D; Magenis R E; Graham J M; Lalande M; Latt S A
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: Natt E; Magenis R E; Zimmer J; Mansouri A; Scherer G
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: Maslen C; Magenis R E; Sheehy R; Litt M
Phage 8-9 defines a cluster of site polymorphisms on chromosome 16q22-q24 [HGM9 no. D16S20]
Nucleic acids research 1988;16(16):8195.
1988: Lawrence H J; Magenis R E; Fast L D; Kamoun M
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: Traweek S T; Riscoe M K; Ferro A J; Braziel R M; Magenis R E; Fitchen J H
Methylthioadenosine phosphorylase deficiency in acute leukemia: pathologic, cytogenetic, and clinical features.
Blood 1988;71(6):1568-73.
1988: Magenis R E
On the origin of chromosome anomaly.
American journal of human genetics 1988;42(4):529-33.
1988: Smith B; Skarecky D; Bengtsson U; Magenis R E; Carpenter N; Wasmuth J J
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: Litt M; Buroker N E; Kondoleon S; Douglass J; Liston D; Sheehy R; Magenis R E
Chromosomal localization of the human proenkephalin and prodynorphin genes.
American journal of human genetics 1988;42(2):327-34.
1988: Magenis R E; Sheehy R R; Brown M G; McDermid H E; White B N; Zonana J; Weleber R
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: Maslen C L; Jones C; Glaser T; Magenis R E; Sheehy R; Kellogg J; Litt M
Seven polymorphic loci mapping to human chromosomal region 11q22-qter.
Genomics 1988;2(1):66-75.
1987: Magenis R E; Brown M G; Lacy D A; Budden S; LaFranchi S
Is Angelman syndrome an alternate result of del(15)(q11q13)?
American journal of medical genetics 1987;28(4):829-38.
1987: Kondoleon S; Vissing H; Luo X Y; Magenis R E; Kellogg J; Litt M
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: Natt E; Westphal E M; Toth-Fejel S E; Magenis R E; Buist N R; Rettenmeier R; Scherer G
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: Lawrence H J; Broudy V C; Magenis R E; Olson S; Tomar D; Barton S; Fitchen J H; Bagby G C
Cytogenetic evidence for involvement of B lymphocytes in acquired idiopathic sideroblastic anemias.
Blood 1987;70(4):1003-5.
1987: Palmer C G; Miles J H; Howard-Peebles P N; Magenis R E; Patil S; Friedman J M
Fetal karyotype following ascertainment of fetal anomalies by ultrasound.
Prenatal diagnosis 1987;7(8):551-5.
1987: Buroker N; Bestwick R; Haight G; Magenis R E; Litt M
A hypervariable repeated sequence on human chromosome 1p36.
Human genetics 1987;77(2):175-81.
1987: Affara N A; Ferguson-Smith M A; Magenis R E; Tolmie J L; Boyd E; Cooke A; Jamieson D; Kwok K; Mitchell M; Snadden L
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: Sheehy R R; Brown M G; Warren R J; Schwartzman M; Magenis R E
Y-derived sequences detected in a 45,X male by in situ hybridization.
American journal of medical genetics 1987;27(4):831-9.
1987: Buroker N E; Bufton L; Surti U; Leppert M; Kumlin E; Sheehy R; Magenis R E; Litt M
A hypervariable region at the D19S11 locus.
Human genetics 1987;76(1):90-5.
1987: Magenis R E; Casanova M; Fellous M; Olson S; Sheehy R
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: Ferguson-Smith M A; Affara N A; Magenis R E
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: Magenis R E; Barton S J
Delineation of human prometaphase paracentromeric regions using sequential GTG- and C-banding.
Cytogenetics and cell genetics 1987;45(3-4):132-40.
1986: Bufton L; Mohandas T K; Magenis R E; Sheehy R; Bestwick R K; Litt M
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: Magenis R E; Gusella J; Weliky K; Olson S; Haight G; Toth-Fejel S; Sheehy R
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: Litt M; Sheehy R; Bruns G A; Magenis R E
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: Magenis R E; Brown M G; Allen L; Reiss J
De novo partial duplication of 17p [dup(17)(p12----p11.2)]: clinical report.
American journal of medical genetics 1986;24(3):415-20.
1986: Bufton L; Bruns G A; Magenis R E; Tomar D; Shaw D; Brook D; Litt M
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: Litt M; Bruns G A; Sheehy R; Magenis R E
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: Olson S B; Magenis R E; Lovrien E W
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: Buroker N E; Magenis R E; Weliky K; Bruns G; Litt M
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: Olson S B; Magenis R E; Buckmaster J G; Bissonnette J M
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: Reiss J A; Weleber R G; Brown M G; Bangs C D; Lovrien E W; Magenis R E
Tandem duplication of proximal 22q: a cause of cat-eye syndrome.
American journal of medical genetics 1985;20(1):165-71.
1985: Magenis R E; Donlon T A; Tomar D R
Localization of the beta-globin gene to 11p15 by in situ hybridization: utilization of chromosome 11 rearrangements.
Human genetics 1985;69(4):300-3.
1984: Magenis R E; Tochen M L; Holahan K P; Carey T; Allen L; Brown M G
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: Curry C J; Magenis R E; Brown M; Lanman J T; Tsai J; O'Lague P; Goodfellow P; Mohandas T; Bergner E A; Shapiro L J
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: Weleber R G; Magenis R E
The importance of chromosomal studies in ophthalmology.
International ophthalmology clinics 1984;24(1):15-38.
1983: Donlon T A; Litt M; Newcom S R; Magenis R E
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: Frydman M; Magenis R E; Mohandas T K; Kaback M M
Chromosome Abnormalities in infants with prune belly anomaly: association with trisomy 18.
American journal of medical genetics 1983;15(1):145-8.
1983: Olson S B; Magenis R E; Rowe S I; Lovrien E W
Chromosome heteromorphism analysis in cases of disputed paternity.
American journal of medical genetics 1983;15(1):47-55.
1983: Donlon T A; Magenis R E
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: Bufton L; Magenis R E; Lovrien E W
Alpha-1-antitrypsin protease inhibitor (Pi) phenotypes in Down's syndrome patients and their parents.
Clinical genetics 1982;21(1):14-8.
1982: Harris D J; Begleiter M L; Chamberlin J; Hankins L; Magenis R E
Parental trisomy 21 mosaicism.
American journal of human genetics 1982;34(1):125-33.
1982: Zonana J; Brown M G; Magenis R E
Distal 19q duplication.
Human genetics 1982;60(3):267-70.
1982: Magenis R E; Webb M J; McKean R S; Tomar D; Allen L J; Kammer H; Van Dyke D L; Lovrien E
Translocation(X;Y)(p22.33;p11.2) in XX males: etiology of male phenotype.
Human genetics 1982;62(3):271-6.
1981: Anderson R L; Bagby G C; Richert-Boe K; Magenis R E; Koler R D
Therapy-related preleukemic syndrome.
Cancer 1981;47(7):1867-71.
1981: Donlon T A; Magenis R E
Structural organization of the heterochromatic region of human chromosome 9.
Chromosoma 1981;84(3):353-63.
1980: Stubbs E G; Magenis R E
HLA and autism.
Journal of autism and developmental disorders 1980;10(1):15-9.
1980: Chamberlin J; Magenis R E
Parental origin of de novo chromosome rearrangements.
Human genetics 1980;53(3):343-7.
1979: Reiss J A; Brenes P M; Chamberlin J; Magenis R E; Lovrien E W
The 8p- syndrome.
Human genetics 1979;47(2):135-40.
1978: Magenis R E; Reiss J; Bigley R; Chamberlin J; Lovrien E
Exclusion of glutathione reductase from 8pter leads to 8p22 and localization to 8p21.
Cytogenetics and cell genetics 1978;22(1-6):446-8.
1978: Magenis R E; Chamberlin J; Overton K; Lovrien E
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: Magenis R E; Donlon T; Parks M; Rivas M L; Lovrien E W
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: Lovrien E W; Magenis R E; Rivas M L; Lamvik N; Rowe S; Wood J; Hemmerling J
Serum cholinesterase (E2) linkage analysis: possible evidence for localization to chromosome 16.
Cytogenetics and cell genetics 1978;22(1-6):324-6.
1978: Lovrien E W; Magenis R E; Rivas M L; Goodnight S; Moreland R; Rowe S
Linkage study of antithrombin III.
Cytogenetics and cell genetics 1978;22(1-6):319-23.
1978: Prescott G H; Rivas M L; Shanbeck L; Macfarlane D W; Wyandt H E; Breg W R; Lubs H A; Magenis R E; Summitt R L; Palmer C G; Hecht F; Kimberling W; Clow D
The Interregional Cytogenetic Register System (ICRS).
Birth defects original article series 1978;14(6C):269-79.
1977: Magenis R E; Overton K M; Chamberlin J; Brady T; Lovrien E
Parental origin of the extra chromosome in Down's syndrome.
Human genetics 1977;37(1):7-16.
1976: Higginson G; Weaver D D; Magenis R E; Prescott G H; Haag C; Hepburn D J
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: Magenis R E; Wyandt H E; Overton K M; Macfarlane J
Parental origin of a ring 13 chromosome in a female with multiple anomalies.
Human genetics 1976;33(2):181-6.
1976: Overton K M; Magenis R E; Brady T; Chamberlin J; Parks M
Cytogenetic darkroom magic: now you see them, now you don't.
American journal of human genetics 1976;28(4):417-9.
1976: Wyandt H E; Hecht F; Magenis R E; Wysham D G; Prescott G
9p trisomy identified by Giemsa-11.
Human genetics 1976;31(3):355-8.
1976: Rivas M L; Conneally P M; Lovrien E W; Magenis R E; Merritt A D; Meyers D A; Palmer C G; Parks M; Wang L; Yu P L
The linkage and mapping relationships of 1qh.
Birth defects original article series 1976;12(7):347-50.
1976: Meyers D A; Conneally P M; Lovrien E W; Magenis R E; Merritt A D; Norton J A; Palmer C G; Rivas M L; Wang L; Yu P L
Linkage group I: the simultaneous estimation of recombination and interference.
Birth defects original article series 1976;12(7):335-9.
1976: Magenis R E; Koler R D; Lovrien E; Bigley R H; DuVal M C; Overton K M
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: Rivas M L; Conneally P M; Lovrien E W; Magenis R E; Merritt A D; Meyers D A; Palmer C G; Parks M; Wang L; Yu P L
The linkage and mapping relationships of 1 qh.
Cytogenetics and cell genetics 1976;16(1-5):347-50.
1976: Meyers D A; Conneally P M; Lovrien E W; Magenis R E; Merritt A D; Norton J A; Palmer C G; Rivas M L; Wang L; Yu P L
Linkage group I: the simultaneous estimation of recombination and interference.
Cytogenetics and cell genetics 1976;16(1-5):335-9.
1976: Magenis R E; Koler R D; Lovrien E; Bigley R H; DuVal M C; Overton K M
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: Magenis R E; Koler R D; Lovrien E; Bigley R H; DuVal M C; Overton K M
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: Magenis R E; Overton K; Wyandt H; Bergstrom T; Hecht F; Lovrien E
Exclusion gene mapping utilizing patients with chromosome imbalance: the HL-A system as a prototype.
Humangenetik 1975;27(2):91-109.
1974: Wyandt H E; Vlietinck R F; Magenis R E; Hecht F
Colored reverse-banding of human chromosomes with acridine orange following alkaline-formalin treatment: densitometric validation and applications.
Humangenetik 1974;23(2):119-30.
1973: Hecht F; Magenis R E; McCaw B K
Clinical cytogenetics. Dawn breaks on a new era.
American journal of diseases of children (1960) 1973;125(3):319-21.
1972: Magenis R E; Armendares S; Hecht F; Weleber R G; Overton K
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: Magenis R E; Overton K M; Reiss J A; Macfarlane J P; Hecht F
Partial trisomy 15.
Lancet 1972;2(7791):1365-6.
1972: Reiss J A; Wyandt H E; Magenis R E; Lovrien E W; Hecht F
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: Prescott G H; Magenis R E; Buist N R
Amniocentesis for antenatal diagnosis of genetic disorders.
Postgraduate medicine 1972;51(3):212-7.
1971: Hecht F; Tolby B; Magenis R E; Kimberling W J; Wyandt H; Lovrien E W
Chromosomal localization of the heterochromatic region 16qh(.76) linked to alpha-haptoglobin in man.
Nature 1971;233(5320):480.
1970: Magenis R E; Hecht F; Lovrien E W
Heritable fragile site on chromosome 16: probable localization of haptoglobin locus in man.
Science (New York, N.Y.) 1970;170(953):85-7.
1968: Magenis R E; Hecht F; Milham S
Trisomy 13 (D1) syndrome: studies on parental age, sex ratio, and survival.
The Journal of pediatrics 1968;73(2):222-8.

Sign-in to see more