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Patrick Concannon

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.

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TOP 3
Concannon Patrick; Rich Stephen S; Nepom Gerald T
Genetics of type 1A diabetes.
Concannon Patrick; Chen Wei-Min; Julier Cécile; Morahan Grant; Akolkar Beena; Erlich Henry A; Hilner Joan E; Nerup Jørn; Nierras Concepcion; Pociot Flemming; Todd John A; Rich Stephen S;
Genome-wide scan for linkage to type 1 diabetes in 2,496 multiplex families from the Type 1 Diabetes Genetics Consortium.
Vissinga Christine S; Yeo Tiong C; Warren Sarah; Brawley James V; Phillips Jennifer; Cerosaletti Karen; Concannon Patrick
Nuclear export of NBN is required for normal cellular responses to radiation.

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All Publications

2009: Concannon Patrick; Rich Stephen S; Nepom Gerald T
Genetics of type 1A diabetes.
The New England journal of medicine 2009;360(16):1646-54.
2009: Concannon Patrick; Chen Wei-Min; Julier Cécile; Morahan Grant; Akolkar Beena; Erlich Henry A; Hilner Joan E; Nerup Jørn; Nierras Concepcion; Pociot Flemming; Todd John A; Rich Stephen S;
Genome-wide scan for linkage to type 1 diabetes in 2,496 multiplex families from the Type 1 Diabetes Genetics Consortium.
Diabetes 2009;58(4):1018-22.
2009: Vissinga Christine S; Yeo Tiong C; Warren Sarah; Brawley James V; Phillips Jennifer; Cerosaletti Karen; Concannon Patrick
Nuclear export of NBN is required for normal cellular responses to radiation.
Molecular and cellular biology 2009;29(4):1000-6.
2009: Rich Stephen S; Onengut-Gumuscu Suna; Concannon Patrick
Recent progress in the genetics of diabetes.
Hormone research 2009;71 Suppl 1():17-23.
2009: Mitui M; Nahas S A; Du L T; Yang Z; Lai C H; Nakamura K; Arroyo S; Scott S; Purayidom A; Concannon P; Lavin M; Gatti R A
Functional and computational assessment of missense variants in the ataxia-telangiectasia mutated (ATM) gene: mutations with increased cancer risk.
Human mutation 2009;30(1):12-21.
2008: Stiff Tom; Cerosaletti Karen; Concannon Patrick; O'Driscoll Mark; Jeggo Penny A
Replication independent ATR signalling leads to G2/M arrest requiring Nbs1, 53BP1 and MDC1.
Human molecular genetics 2008;17(20):3247-53.
2008: Concannon Patrick; Onengut-Gumuscu Suna; Todd John A; Smyth Deborah J; Pociot Flemming; Bergholdt Regine; Akolkar Beena; Erlich Henry A; Hilner Joan E; Julier Cécile; Morahan Grant; Nerup Jørn; Nierras Concepcion R; Chen Wei-Min; Rich Stephen S;
A human type 1 diabetes susceptibility locus maps to chromosome 21q22.3.
Diabetes 2008;57(10):2858-61.
2008: Concannon Patrick; Haile Robert W; Børresen-Dale Anne-Lise; Rosenstein Barry S; Gatti Richard A; Teraoka Sharon N; Diep T Anh; Jansen Laila; Atencio David P; Langholz Bryan; Capanu Marinela; Liang Xiaolin; Begg Colin B; Thomas Duncan C; Bernstein Leslie; Olsen Jørgen H; Malone Kathleen E; Lynch Charles F; Anton-Culver Hoda; Bernstein Jonine L;
Variants in the ATM gene associated with a reduced risk of contralateral breast cancer.
Cancer research 2008;68(16):6486-91.
2008: Demuth Ilja; Bradshaw Paul S; Lindner Anika; Anders Marco; Heinrich Stefanie; Kallenbach Julia; Schmelz Karin; Digweed Martin; Meyn M Stephen; Concannon Patrick
Endogenous hSNM1B/Apollo interacts with TRF2 and stimulates ATM in response to ionizing radiation.
DNA repair 2008;7(8):1192-201.
2008: Du Liutao; Lai Chih-Hung; Concannon Patrick; Gatti Richard A
Rapid screen for truncating ATM mutations by PTT-ELISA.
Mutation research 2008;640(1-2):139-44.
2007: Rieck Mary; Arechiga Adrian; Onengut-Gumuscu Suna; Greenbaum Carla; Concannon Patrick; Buckner Jane H
Genetic variation in PTPN22 corresponds to altered function of T and B lymphocytes.
Journal of immunology (Baltimore, Md. : 1950) 2007;179(7):4704-10.
2006: Onengut-Gumuscu Suna; Buckner Jane H; Concannon Patrick
A haplotype-based analysis of the PTPN22 locus in type 1 diabetes.
Diabetes 2006;55(10):2883-9.
2006: Onengut-Gumuscu Suna; Concannon Patrick
Recent advances in the immunogenetics of human type 1 diabetes.
Current opinion in immunology 2006;18(5):634-8.
2006: Cerosaletti Karen; Wright Jocyndra; Concannon Patrick
Active role for nibrin in the kinetics of atm activation.
Molecular and cellular biology 2006;26(5):1691-9.
2005: Mitui M; Bernatowska E; Pietrucha B; Piotrowska-Jastrzebska J; Eng L; Nahas S; Teraoka S; Sholty G; Purayidom A; Concannon P; Gatti R A
ATM gene founder haplotypes and associated mutations in Polish families with ataxia-telangiectasia.
Annals of human genetics 2005;69(Pt 6):657-64.
2005: Ben-Omran Tawfeg I; Cerosaletti Karen; Concannon Patrick; Weitzman Sheila; Nezarati Marjan M
A patient with mutations in DNA Ligase IV: clinical features and overlap with Nijmegen breakage syndrome.
American journal of medical genetics. Part A 2005;137A(3):283-7.
2005: Kosoy R; Concannon P
Functional variants in SUMO4, TAB2, and NFkappaB and the risk of type 1 diabetes.
Genes and immunity 2005;6(3):231-5.
2005: Onengut-Gumuscu Suna; Concannon Patrick
The genetics of type 1 diabetes: lessons learned and future challenges.
Journal of autoimmunity 2005;25 Suppl():34-9.
2004: Onengut-Gumuscu S; Ewens K G; Spielman R S; Concannon P
A functional polymorphism (1858C/T) in the PTPN22 gene is linked and associated with type I diabetes in multiplex families.
Genes and immunity 2004;5(8):678-80.
2004: Demuth Ilja; Digweed Martin; Concannon Patrick
Human SNM1B is required for normal cellular response to both DNA interstrand crosslink-inducing agents and ionizing radiation.
Oncogene 2004;23(53):8611-8.
2004: Cerosaletti Karen; Concannon Patrick
Independent roles for nibrin and Mre11-Rad50 in the activation and function of Atm.
The Journal of biological chemistry 2004;279(37):38813-9.
2004: O'Driscoll M; Gennery A R; Seidel J; Concannon P; Jeggo P A
An overview of three new disorders associated with genetic instability: LIG4 syndrome, RS-SCID and ATR-Seckel syndrome.
DNA repair 2004;3(8-9):1227-35.
2004: Barratt Bryan J; Payne Felicity; Lowe Chris E; Hermann Robert; Healy Barry C; Harold Denise; Concannon Patrick; Gharani Neda; McCarthy Mark I; Olavesen Mark G; McCormack Rose; Guja Cristian; Ionescu-Tîrgoviste Constantin; Undlien Dag E; Rønningen Kjersti S; Gillespie Kathleen M; Tuomilehto-Wolf Eva; Tuomilehto Jaakko; Bennett Simon T; Clayton David G; Cordell Heather J; Todd John A
Remapping the insulin gene/IDDM2 locus in type 1 diabetes.
Diabetes 2004;53(7):1884-9.
2004: Kosoy R; Yokoi N; Seino S; Concannon P
Polymorphic variation in the CBLB gene in human type 1 diabetes.
Genes and immunity 2004;5(3):232-5.
2004: Morrison V Anne; Onengut-Gumuscu Suna; Concannon Patrick
A functional variant of IRS1 is associated with type 1 diabetes in families from the US and UK.
Molecular genetics and metabolism 2004;81(4):291-4.
2003: Chun Helen H; Sun Xia; Nahas Shareef A; Teraoka Sharon; Lai Chih Hung; Concannon Patrick; Gatti Richard A
Improved diagnostic testing for ataxia-telangiectasia by immunoblotting of nuclear lysates for ATM protein expression.
Molecular genetics and metabolism 2003;80(4):437-43.
2003: White Robert E; Wade-Martins Richard; Hart Stephen L; Frampton Jon; Huey Bryan; Desai-Mehta Ami; Cerosaletti Karen M; Concannon Patrick; James Michael R
Functional delivery of large genomic DNA to human cells with a peptide-lipid vector.
The journal of gene medicine 2003;5(10):883-92.
2003: Cerosaletti Karen M; Concannon Patrick
Nibrin forkhead-associated domain and breast cancer C-terminal domain are both required for nuclear focus formation and phosphorylation.
The Journal of biological chemistry 2003;278(24):21944-51.
2003: Bakhshi Sameer; Cerosaletti Karen M; Concannon Patrick; Bawle Erawati V; Fontanesi James; Gatti Richard A; Bhambhani Kanta
Medulloblastoma with adverse reaction to radiation therapy in nijmegen breakage syndrome.
Journal of pediatric hematology/oncology : official journal of the American Society of Pediatric Hematology/Oncology 2003;25(3):248-51.
2002: Onengut-Gumuscu Suna; Concannon Patrick
Mapping genes for autoimmunity in humans: type 1 diabetes as a model.
Immunological reviews 2002;190():182-94.
2002: Ewens Kathryn G; Johnson Lindsey N; Wapelhorst Beth; O'Brien Kristin; Gutin Sarah; Morrison V Anne; Street Craig; Gregory Simon G; Spielman Richard S; Concannon Patrick
Linkage and association with type 1 diabetes on chromosome 1q42.
Diabetes 2002;51(11):3318-25.
2002: Cerosaletti Karen M; Morrison V Anne; Sabath Daniel E; Willerford Dennis M; Concannon Patrick
Mutations and molecular variants of the NBS1 gene in non-Hodgkin lymphoma.
Genes, chromosomes & cancer 2002;35(3):282-6.
2002: Brawley James V; Concannon Patrick
Complementarity-determining region 1 sequence requirements drive limited V alpha usage in response to influenza hemagglutinin 307-319 peptide.
Journal of immunology (Baltimore, Md. : 1950) 2002;168(8):3894-901.
2002: Resnick Igor B; Kondratenko Irina; Togoev Oleg; Vasserman Natalia; Shagina Irena; Evgrafov Oleg; Tverskaya Svetlana; Cerosaletti Karen M; Gatti Richard A; Concannon Patrick
Nijmegen breakage syndrome: clinical characteristics and mutation analysis in eight unrelated Russian families.
The Journal of pediatrics 2002;140(3):355-61.
2002: Dahlman Ingrid; Eaves Iain A; Kosoy Roman; Morrison V Anne; Heward Joanne; Gough Stephen C L; Allahabadia Amit; Franklyn Jayne A; Tuomilehto Jaakko; Tuomilehto-Wolf Eva; Cucca Francesco; Guja Cristian; Ionescu-Tirgoviste Constantin; Stevens Helen; Carr Philippa; Nutland Sarah; McKinney Patricia; Shield Julian P; Wang William; Cordell Heather J; Walker Neil; Todd John A; Concannon Patrick
Parameters for reliable results in genetic association studies in common disease.
Nature genetics 2002;30(2):149-50.
2001: Jeggo P A; Concannon P
Immune diversity and genomic stability: opposite goals but similar paths.
Journal of photochemistry and photobiology. B, Biology 2001;65(2-3):88-96.
2001: O'Driscoll M; Cerosaletti K M; Girard P M; Dai Y; Stumm M; Kysela B; Hirsch B; Gennery A; Palmer S E; Seidel J; Gatti R A; Varon R; Oettinger M A; Neitzel H; Jeggo P A; Concannon P
DNA ligase IV mutations identified in patients exhibiting developmental delay and immunodeficiency.
Molecular cell 2001;8(6):1175-85.
2001: Cox N J; Wapelhorst B; Morrison V A; Johnson L; Pinchuk L; Spielman R S; Todd J A; Concannon P
Seven regions of the genome show evidence of linkage to type 1 diabetes in a consensus analysis of 767 multiplex families.
American journal of human genetics 2001;69(4):820-30.
2001: Hiel J A; Weemaes C M; van Engelen B G; Smeets D; Ligtenberg M; van Der Burgt I; van Den Heuvel L P; Cerosaletti K M; Gabreëls F J; Concannon P
Nijmegen breakage syndrome in a Dutch patient not resulting from a defect in NBS1.
Journal of medical genetics 2001;38(6):E19.
2001: Argentaro A; Wapelhorst B; Concannon P; Harley V R
Linkage studies of SOX13, the ICA12 autoantigen gene, in families with type 1 diabetes.
Molecular genetics and metabolism 2001;72(4):356-9.
2001: Desai-Mehta A; Cerosaletti K M; Concannon P
Distinct functional domains of nibrin mediate Mre11 binding, focus formation, and nuclear localization.
Molecular and cellular biology 2001;21(6):2184-91.
2000: Yeo T C; Xia D; Hassouneh S; Yang X O; Sabath D E; Sperling K; Gatti R A; Concannon P; Willerford D M
V(D)J rearrangement in Nijmegen breakage syndrome.
Molecular immunology 2000;37(18):1131-9.
2000: Horikawa Y; Oda N; Cox N J; Li X; Orho-Melander M; Hara M; Hinokio Y; Lindner T H; Mashima H; Schwarz P E; del Bosque-Plata L; Horikawa Y; Oda Y; Yoshiuchi I; Colilla S; Polonsky K S; Wei S; Concannon P; Iwasaki N; Schulze J; Baier L J; Bogardus C; Groop L; Boerwinkle E; Hanis C L; Bell G I
Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus.
Nature genetics 2000;26(2):163-75.
2000: Gatei M; Young D; Cerosaletti K M; Desai-Mehta A; Spring K; Kozlov S; Lavin M F; Gatti R A; Concannon P; Khanna K
ATM-dependent phosphorylation of nibrin in response to radiation exposure.
Nature genetics 2000;25(1):115-9.
2000: Cerosaletti K M; Desai-Mehta A; Yeo T C; Kraakman-Van Der Zwet M; Zdzienicka M Z; Concannon P
Retroviral expression of the NBS1 gene in cultured Nijmegen breakage syndrome cells restores normal radiation sensitivity and nuclear focus formation.
Mutagenesis 2000;15(3):281-6.
1999: Vanasse G J; Concannon P; Willerford D M
Regulated genomic instability and neoplasia in the lymphoid lineage.
Blood 1999;94(12):3997-4010.
1999: Brawley J V; Concannon P
Systematic mutagenesis of TCR complementarity-determining region 3 residues: a single conservative substitution dramatically improves response to both multiple HLA-DR alleles and peptide variants.
Journal of immunology (Baltimore, Md. : 1950) 1999;163(9):4946-52.
1999: Udar N S; Xu S; Bay J O; Dandekar S S; Patel N; Chen X; Liang T Y; Uhrhammer N; Klisak I; Shizuya H; Yang H; Samara G; Nelissen J; Sawicki M; Concannon P; Gatti R A
Physical map of the region surrounding the ataxia-telangiectasia gene on human chromosome 11q22-23.
Neuropediatrics 1999;30(4):176-80.
1999: Teraoka S N; Telatar M; Becker-Catania S; Liang T; Onengüt S; Tolun A; Chessa L; Sanal O; Bernatowska E; Gatti R A; Concannon P
Splicing defects in the ataxia-telangiectasia gene, ATM: underlying mutations and consequences.
American journal of human genetics 1999;64(6):1617-31.
1999: Cox N J; Frigge M; Nicolae D L; Concannon P; Hanis C L; Bell G I; Kong A
Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans.
Nature genetics 1999;21(2):213-5.
1999: Vissinga C S; Yeo T C; Woessner J; Massa H F; Wilson R K; Trask B J; Concannon P
Identification, characterization, and mapping of a mouse homolog of the gene mutated in Nijmegen breakage syndrome.
Cytogenetics and cell genetics 1999;87(1-2):80-4.
1998: Concannon P; Gogolin-Ewens K J; Hinds D A; Wapelhorst B; Morrison V A; Stirling B; Mitra M; Farmer J; Williams S R; Cox N J; Bell G I; Risch N; Spielman R S
A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus.
Nature genetics 1998;19(3):292-6.
1998: Cerosaletti K M; Lange E; Stringham H M; Weemaes C M; Smeets D; Sölder B; Belohradsky B H; Taylor A M; Karnes P; Elliott A; Komatsu K; Gatti R A; Boehnke M; Concannon P
Fine localization of the Nijmegen breakage syndrome gene to 8q21: evidence for a common founder haplotype.
American journal of human genetics 1998;63(1):125-34.
1998: Varon R; Vissinga C; Platzer M; Cerosaletti K M; Chrzanowska K H; Saar K; Beckmann G; Seemanová E; Cooper P R; Nowak N J; Stumm M; Weemaes C M; Gatti R A; Wilson R K; Digweed M; Rosenthal A; Sperling K; Concannon P; Reis A
Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome.
Cell 1998;93(3):467-76.
1998: Telatar M; Teraoka S; Wang Z; Chun H H; Liang T; Castellvi-Bel S; Udar N; Borresen-Dale A L; Chessa L; Bernatowska-Matuszkiewicz E; Porras O; Watanabe M; Junker A; Concannon P; Gatti R A
Ataxia-telangiectasia: identification and detection of founder-effect mutations in the ATM gene in ethnic populations.
American journal of human genetics 1998;62(1):86-97.
1997: Chen X; Yang L; Udar N; Liang T; Uhrhammer N; Xu S; Bay J O; Wang Z; Dandakar S; Chiplunkar S; Klisak I; Telatar M; Yang H; Concannon P; Gatti R A
CAND3: a ubiquitously expressed gene immediately adjacent and in opposite transcriptional orientation to the ATM gene at 11q23.1.
Mammalian genome : official journal of the International Mammalian Genome Society 1997;8(2):129-33.
1997: Concannon P; Gatti R A
Diversity of ATM gene mutations detected in patients with ataxia-telangiectasia.
Human mutation 1997;10(2):100-7.
1997: Wei S; Charmley P; Concannon P
Organization, polymorphism, and expression of the human T-cell receptor AV1 subfamily.
Immunogenetics 1997;45(6):405-12.
1996: Wei S; Concannon P
Repertoire and organization of human T-cell receptor alpha region variable genes.
Genomics 1996;38(3):442-5.
1996: Wright J; Teraoka S; Onengut S; Tolun A; Gatti R A; Ochs H D; Concannon P
A high frequency of distinct ATM gene mutations in ataxia-telangiectasia.
American journal of human genetics 1996;59(4):839-46.
1996: Telatar M; Wang Z; Udar N; Liang T; Bernatowska-Matuszkiewicz E; Lavin M; Shiloh Y; Concannon P; Good R A; Gatti R A
Ataxia-telangiectasia: mutations in ATM cDNA detected by protein-truncation screening.
American journal of human genetics 1996;59(1):40-4.
1996: Vissinga C; Springmeyer S C; Concannon P
TCR expression and clonality analysis in pulmonary sarcoidosis.
Human immunology 1996;48(1-2):98-106.
1996: Yamagata K; Takeda J; Menzel S; Chen X; Eng S; Lim L R; Concannon P; Hanis C L; Spielman R S; Cox N J; Bell G I
Searching for NIDDM susceptibility genes: studies of genes with triplet repeats expressed in skeletal muscle.
Diabetologia 1996;39(6):725-30.
1996: Hanis C L; Boerwinkle E; Chakraborty R; Ellsworth D L; Concannon P; Stirling B; Morrison V A; Wapelhorst B; Spielman R S; Gogolin-Ewens K J; Shepard J M; Williams S R; Risch N; Hinds D; Iwasaki N; Ogata M; Omori Y; Petzold C; Rietzch H; Schröder H E; Schulze J; Cox N J; Menzel S; Boriraj V V; Chen X; Lim L R; Lindner T; Mereu L E; Wang Y Q; Xiang K; Yamagata K; Yang Y; Bell G I
A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2.
Nature genetics 1996;13(2):161-6.
1996: Brawley J V; Concannon P
Modulation of promiscuous T cell receptor recognition by mutagenesis of CDR2 residues.
The Journal of experimental medicine 1996;183(5):2043-51.
1996: Gambino V; Menzel S; Trabb J B; Xiang K S; Lindner T; Louït A; Chen E; Mereu L E; Furuta H; Iwasaki N; Kawamura M; Omori Y; Rietzsch H; Schulze J; Schröder H E; Concannon P; Hanis C L; Spielman R S; Yamagata K; Cox N J; Bell G I
An approach for identifying simple sequence repeat DNA polymorphisms near cloned cDNAs and genes. Linkage studies of the islet amyloid polypeptide/amylin and liver glycogen synthase genes and NIDDM.
Diabetes 1996;45(3):291-4.
1995: Stirling B; Cox N J; Bell G I; Hanis C L; Spielman R S; Concannon P
Linkage studies in NIDDM with markers near the sulphonylurea receptor gene.
Diabetologia 1995;38(12):1479-81.
1995: Charmley P; Concannon P; Hood L; Rowen L
Frequency and polymorphism of simple sequence repeats in a contiguous 685-kb DNA sequence containing the human T-cell receptor beta-chain gene complex.
Genomics 1995;29(3):760-5.
1995: Stirling B; Cox N J; Bell G I; Hanis C L; Spielman R S; Concannon P
Identification of microsatellite markers near the human ob gene and linkage studies in NIDDM-affected sib pairs.
Diabetes 1995;44(8):999-1001.
1995: Vissinga C S; Wei S; Posnett D N; Concannon P
Frequency of human V beta 3+ cells correlates with polymorphism in recombination signal sequences.
Annals of the New York Academy of Sciences 1995;756():90-3.
1995: Charmley P; Nepom B S; Concannon P
Use of a polymorphic dinucleotide repeat DNA marker in a T-cell receptor V beta gene to identify a distinct subset of pauciarticular-onset juvenile rheumatoid arthritis patients.
Annals of the New York Academy of Sciences 1995;756():444-6.
1995: Vissinga C S; Springmeyer S C; Concannon P
T-cell receptor repertoire in pulmonary sarcoidosis.
Annals of the New York Academy of Sciences 1995;756():441-3.
1995: Wei S; Charmley P; Concannon P
DNA sequence and polymorphism analysis of a region of the T-cell receptor beta locus thought to contain a susceptibility gene for multiple sclerosis.
Annals of the New York Academy of Sciences 1995;756():307-9.
1995: Concannon P; Robinson M A
Human T-cell receptor gene nomenclature.
Annals of the New York Academy of Sciences 1995;756():124-9.
1995: Lange E; Borresen A L; Chen X; Chessa L; Chiplunkar S; Concannon P; Dandekar S; Gerken S; Lange K; Liang T
Localization of an ataxia-telangiectasia gene to an approximately 500-kb interval on chromosome 11q23.1: linkage analysis of 176 families by an international consortium.
American journal of human genetics 1995;57(1):112-9.
1995: Rowe R E; Wapelhorst B; Bell G I; Risch N; Spielman R S; Concannon P
Linkage and association between insulin-dependent diabetes mellitus (IDDM) susceptibility and markers near the glucokinase gene on chromosome 7.
Nature genetics 1995;10(2):240-2.
1995: Tsaur M L; Menzel S; Lai F P; Espinosa R; Concannon P; Spielman R S; Hanis C L; Cox N J; Le Beau M M; German M S
Isolation of a cDNA clone encoding a KATP channel-like protein expressed in insulin-secreting cells, localization of the human gene to chromosome band 21q22.1, and linkage studies with NIDDM.
Diabetes 1995;44(5):592-6.
1995: Wei S; Charmley P; Birchfield R I; Concannon P
Human T-cell receptor V beta gene polymorphism and multiple sclerosis.
American journal of human genetics 1995;56(4):963-9.
1995: Charmley P; Keretan E; Snyder K; Clark E A; Concannon P
Relative size and evolution of the germline repertoire of T-cell receptor beta-chain gene segments in nonhuman primates.
Genomics 1995;25(1):150-6.
1995: Wapelhorst B; Bell G I; Risch N; Spielman R S; Concannon P
Linkage and association studies in insulin-dependent diabetes with a new dinucleotide repeat polymorphism at the GAD65 locus.
Autoimmunity 1995;21(2):127-30.
1995: Charmley P; Concannon P
PCR-based genotyping and haplotype analysis of human TCRBV gene segment polymorphisms.
Immunogenetics 1995;42(4):254-61.
1994: Gatti R A; Lange E; Rotman G; Chen X; Uhrhammer N; Liang T; Chiplunkar S; Yang L; Udar N; Dandekar S; Sheikhavandi S; Wang Z; Yang H M; Polikow J; Elashoff M; Teletar M; Sanal O; Chessa L; McConville C; Taylor M; Shiloh Y; Porras O; Borresen A L; Wegner R D; Curry C; Gerken S; Lange K; Concannon P
Genetic haplotyping of ataxia-telangiectasia families localizes the major gene to an approximately 850 kb region on chromosome 11q23.1.
International journal of radiation biology 1994;66(6 Suppl):S57-62.
1994: Wei S; Concannon P
Identification of a novel human T-cell receptor V beta subfamily by genomic cloning.
Human immunology 1994;41(3):201-6.
1994: Telatar M; Concannon P; Tolun A
Dinucleotide repeat polymorphism at 11q23.
Human genetics 1994;94(1):109.
1994: Charmley P; Nepom B S; Concannon P
HLA and T cell receptor beta-chain DNA polymorphisms identify a distinct subset of patients with pauciarticular-onset juvenile rheumatoid arthritis.
Arthritis and rheumatism 1994;37(5):695-701.
1994: Posnett D N; Vissinga C S; Pambuccian C; Wei S; Robinson M A; Kostyu D; Concannon P
Level of human TCRBV3S1 (V beta 3) expression correlates with allelic polymorphism in the spacer region of the recombination signal sequence.
The Journal of experimental medicine 1994;179(5):1707-11.
1994: Telatar M; Concannon P; Tolun A
Dinucleotide repeat polymorphism at the NCAM locus.
Human molecular genetics 1994;3(5):842.
1994: Uhrhammer N; Concannon P; Huo Y; Nakamura Y; Gatti R A
A pulsed-field gel electrophoresis map in the ataxia-telangiectasia region of chromosome 11q22.3.
Genomics 1994;20(2):278-80.
1994: Vissinga C S; Charmley P; Concannon P
Influence of coding region polymorphism on the peripheral expression of a human TCR V beta gene.
Journal of immunology (Baltimore, Md. : 1950) 1994;152(3):1222-7.
1994: Wei S; Charmley P; Robinson M A; Concannon P
The extent of the human germline T-cell receptor V beta gene segment repertoire.
Immunogenetics 1994;40(1):27-36.
1994: Charmley P; Nelson J L; Hansen J A; Branchaud A; Barrington R A; Templin D; Boyer G; Lanier A P; Concannon P
T-cell receptor polymorphisms in Tlingit Indians with rheumatoid arthritis.
Autoimmunity 1994;19(4):247-51.
1993: Snoke K; Alexander J; Franco A; Smith L; Brawley J V; Concannon P; Grey H M; Sette A; Wentworth P
The inhibition of different T cell lines specific for the same antigen with TCR antagonist peptides.
Journal of immunology (Baltimore, Md. : 1950) 1993;151(12):6815-21.
1993: Ostrov D; Krieger J; Sidney J; Sette A; Concannon P
T cell receptor antagonism mediated by interaction between T cell receptor junctional residues and peptide antigen analogues.
Journal of immunology (Baltimore, Md. : 1950) 1993;150(10):4277-83.
1993: Charmley P; Concannon P
Polymorphism and phylogeny of dinucleotide repeats in human T-cell receptor Vb6 genes.
Immunogenetics 1993;38(2):92-7.
1993: Charmley P; Wei S; Concannon P
Polymorphisms in the Tcrb-V2 gene segments localize the Tcrb orphon genes to human chromosome 9p21.
Immunogenetics 1993;38(4):283-6.
1992: Malhotra U; Spielman R; Concannon P
Variability in T cell receptor V beta gene usage in human peripheral blood lymphocytes. Studies of identical twins, siblings, and insulin-dependent diabetes mellitus patients.
Journal of immunology (Baltimore, Md. : 1950) 1992;149(5):1802-8.
1992: Sanal O; Lange E; Telatar M; Sobel E; Salazar-Novak J; Ersoy F; Morrison A; Concannon P; Tolun A; Gatti R A
Ataxia-telangiectasia: linkage analysis of chromosome 11q22-23 markers in Turkish families.
The FASEB journal : official publication of the Federation of American Societies for Experimental Biology 1992;6(10):2848-52.
1992: Funkhouser S W; Concannon P; Charmley P; Vredevoe D L; Hood L
Differences in T cell receptor restriction fragment length polymorphisms in patients with rheumatoid arthritis.
Arthritis and rheumatism 1992;35(4):465-71.
1992: Malhotra U; Concannon P
T cell receptor beta gene polymorphism and rheumatoid arthritis.
Autoimmunity 1992;12(2):75-7.
1991: Foroud T; Wei S; Ziv Y; Sobel E; Lange E; Chao A; Goradia T; Huo Y; Tolun A; Chessa L; Charmley P; Sanal O; Salman N; Julier C; Concannon P; McConville C; Taylor A M; Shiloh Y; Lange S K; Gatti R A
Localization of an ataxia-telangiectasia locus to a 3-cM interval on chromosome 11q23: linkage analysis of 111 families by an international consortium.
American journal of human genetics 1991;49(6):1263-79.
1991: Wright J A; Hood L; Concannon P
Human T-cell receptor V alpha gene polymorphism.
Human immunology 1991;32(4):277-83.
1990: Sanal O; Wei S; Foroud T; Malhotra U; Concannon P; Charmley P; Salser W; Lange K; Gatti R A
Further mapping of an ataxia-telangiectasia locus to the chromosome 11q23 region.
American journal of human genetics 1990;47(5):860-6.
1990: Charmley P; Chao A; Concannon P; Hood L; Gatti R A
Haplotyping the human T-cell receptor beta-chain gene complex by use of restriction fragment length polymorphisms.
Proceedings of the National Academy of Sciences of the United States of America 1990;87(12):4823-7.
1990: Charmley P; Concannon P; Gatti R A
T-cell receptor beta-chain DNA polymorphism frequencies in healthy HLA-DR homozygotes.
Tissue antigens 1990;35(4):157-64.
1990: Concannon P; Malhotra U; Charmley P; Reynolds J; Lange K; Gatti R A
The ataxia-telangiectasia gene (ATA) on chromosome II is distinct from the ETS-1 gene.
American journal of human genetics 1990;46(4):789-94.
1990: Charmley P; Foroud T; Wei S; Concannon P; Weeks D E; Lange K; Gatti R A
A primary linkage map of the human chromosome 11q22-23 region.
Genomics 1990;6(2):316-23.
1990: Malhotra U; Concannon P
An anonymous marker [HGM provisional #D11S415] maps to human chromosome 11 near the catalase (CAT) gene.
Nucleic acids research 1990;18(2):386.
1989: Milner E C; Lotshaw C L; Willems van Dijk K; Charmley P; Concannon P; Schroeder H W
Isolation and mapping of a polymorphic DNA sequence pH30 on chromosome 4[HGM provisional no. D4S139]
Nucleic acids research 1989;17(10):4002.
1989: Naeim F; Jensen L; Susi E; Yam P; Gatti R; Salser W; Concannon P
Use of deoxyribonucleic acid probes in the identification of cell origin and detection of cellular contamination in human lymphoblastoid cell lines.
Laboratory investigation; a journal of technical methods and pathology 1989;60(3):347-52.
1989: Malhotra U; Concannon P
Human T-cell receptor CD3-delta (CD3D)/MspI DNA polymorphism.
Nucleic acids research 1989;17(6):2373.
1989: Charmley P; Wei S; Sanal O; Malhotra U; Concannon P; Terhorst C; Gatti R A
Human T-cell receptor CD3-gamma (CD3G)/MspI DNA polymorphism.
Nucleic acids research 1989;17(6):2372.
1988: Gatti R A; Berkel I; Boder E; Braedt G; Charmley P; Concannon P; Ersoy F; Foroud T; Jaspers N G; Lange K
Localization of an ataxia-telangiectasia gene to chromosome 11q22-23.
Nature 1988;336(6199):577-80.
1986: Chou C C; Gatti R A; Fuller M L; Concannon P; Wong A; Chada S; Davis R C; Salser W A
Structure and expression of ferritin genes in a human promyelocytic cell line that differentiates in vitro.
Molecular and cellular biology 1986;6(2):566-73.

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