| Year |
Citation |
Score |
| 2021 |
Robertson CC, Inshaw JRJ, Onengut-Gumuscu S, Chen WM, Santa Cruz DF, Yang H, Cutler AJ, Crouch DJM, Farber E, Bridges SL, Edberg JC, Kimberly RP, Buckner JH, Deloukas P, Divers J, ... ... Concannon P, et al. Fine-mapping, trans-ancestral and genomic analyses identify causal variants, cells, genes and drug targets for type 1 diabetes. Nature Genetics. PMID 34127860 DOI: 10.1038/s41588-021-00880-5 |
0.304 |
|
| 2020 |
Reiner AS, Robson ME, Mellemkjær L, Tischkowitz M, John EM, Lynch CF, Brooks JD, Boice JD, Knight JA, Teraoka SN, Liang X, Woods M, Shen R, Shore RE, Stram DO, ... ... Concannon P, et al. Radiation treatment, ATM, BRCA1/2, and CHEK2*1100delC pathogenic variants, and risk of contralateral breast cancer. Journal of the National Cancer Institute. PMID 32119081 DOI: 10.1093/Jnci/Djaa031 |
0.345 |
|
| 2020 |
Lee S, Liang X, Woods M, Reiner AS, Concannon P, Bernstein L, Lynch CF, Boice JD, Deasy JO, Bernstein JL, Oh JH. Machine learning on genome-wide association studies to predict the risk of radiation-associated contralateral breast cancer in the WECARE Study. Plos One. 15: e0226157. PMID 32106268 DOI: 10.1371/Journal.Pone.0226157 |
0.341 |
|
| 2020 |
Wojcik GL, Korpe P, Marie C, Mentzer AJ, Carstensen T, Mychaleckyj J, Kirkpatrick BD, Rich SS, Concannon P, Faruque ASG, Haque R, Petri WA, Duggal P. Genome-Wide Association Study of Cryptosporidiosis in Infants Implicates . Mbio. 11. PMID 32019797 DOI: 10.1128/Mbio.03343-19 |
0.348 |
|
| 2020 |
Redondo MJ, Concannon P. Genetics of Type 1 Diabetes Comes of Age. Diabetes Care. 43: 16-18. PMID 31862821 DOI: 10.2337/Dci19-0049 |
0.403 |
|
| 2019 |
Yang X, Leslie G, Doroszuk A, Schneider S, Allen J, Decker B, Dunning AM, Redman J, Scarth J, Plaskocinska I, Luccarini C, Shah M, Pooley K, Dorling L, Lee A, ... ... Concannon P, et al. Cancer Risks Associated With Germline Pathogenic Variants: An International Study of 524 Families. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. JCO1901907. PMID 31841383 DOI: 10.1200/Jco.19.01907 |
0.31 |
|
| 2019 |
Ge Y, Paisie TK, Chen S, Concannon P. UBASH3A Regulates the Synthesis and Dynamics of TCR-CD3 Complexes. Journal of Immunology (Baltimore, Md. : 1950). PMID 31659016 DOI: 10.4049/Jimmunol.1801338 |
0.303 |
|
| 2019 |
Onengut-Gumuscu S, Chen WM, Robertson CC, Bonnie JK, Farber E, Zhu Z, Oksenberg JR, Brant SR, Bridges SL, Edberg JC, Kimberly RP, Gregersen PK, Rewers MJ, Steck AK, Black MH, ... ... Concannon P, et al. Type 1 Diabetes Risk in African-Ancestry Participants and Utility of an Ancestry-Specific Genetic Risk Score. Diabetes Care. PMID 30659077 DOI: 10.2337/Dc18-1727 |
0.369 |
|
| 2018 |
Wojcik GL, Marie C, Abhyankar MM, Yoshida N, Watanabe K, Mentzer AJ, Carstensen T, Mychaleckyj J, Kirkpatrick BD, Rich SS, Concannon P, Haque R, Tsokos GC, Petri WA, Duggal P. Genome-Wide Association Study Reveals Genetic Link between Diarrhea-Associated Entamoeba histolytica Infection and Inflammatory Bowel Disease. Mbio. 9. PMID 30228239 DOI: 10.1128/Mbio.01668-18 |
0.35 |
|
| 2018 |
Ge Y, Concannon P. Molecular-genetic characterization of common, noncoding UBASH3A variants associated with type 1 diabetes. European Journal of Human Genetics : Ejhg. PMID 29491471 DOI: 10.1038/S41431-018-0123-5 |
0.444 |
|
| 2017 |
Newman JRB, Conesa A, Mika M, New FN, Onengut-Gumuscu S, Atkinson MA, Rich SS, McIntyre LM, Concannon P. Disease-specific biases in alternative splicing and tissue-specific dysregulation revealed by multitissue profiling of lymphocyte gene expression in type 1 diabetes. Genome Research. PMID 29025893 DOI: 10.1101/Gr.217984.116 |
0.438 |
|
| 2017 |
Reiner AS, Lynch CF, Sisti JS, John EM, Brooks JD, Bernstein L, Knight JA, Hsu L, Concannon P, Mellemkjær L, Tischkowitz M, Haile RW, Shen R, Malone KE, Woods M, et al. Hormone receptor status of a first primary breast cancer predicts contralateral breast cancer risk in the WECARE study population. Breast Cancer Research : Bcr. 19: 83. PMID 28724391 DOI: 10.1186/S13058-017-0874-X |
0.308 |
|
| 2017 |
Bernstein JL, Concannon P. ATM, radiation, and the risk of second primary breast cancer. International Journal of Radiation Biology. 93: 1121-1127. PMID 28627265 DOI: 10.1080/09553002.2017.1344363 |
0.38 |
|
| 2017 |
Ge Y, Paisie TK, Newman JRB, McIntyre LM, Concannon P. UBASH3A Mediates Risk for Type 1 Diabetes through Inhibition of T-Cell Receptor-Induced NF-κB Signaling. Diabetes. PMID 28607106 DOI: 10.2337/Db16-1023 |
0.429 |
|
| 2017 |
Gorman JA, Hundhausen C, Errett JS, Stone AE, Allenspach EJ, Ge Y, Arkatkar T, Clough C, Dai X, Khim S, Pestal K, Liggitt D, Cerosaletti K, Stetson DB, James RG, ... ... Concannon P, et al. The A946T variant of the RNA sensor IFIH1 mediates an interferon program that limits viral infection but increases the risk for autoimmunity. Nature Immunology. PMID 28553952 DOI: 10.1038/Ni.3766 |
0.376 |
|
| 2017 |
Mychaleckyj JC, Havt A, Nayak U, Pinkerton R, Farber E, Concannon P, Lima AA, Guerrant RL. Genome-wide Analysis in Brazilians Reveals Highly Differentiated Native American Genome Regions. Molecular Biology and Evolution. PMID 28100790 DOI: 10.1093/Molbev/Msw249 |
0.356 |
|
| 2016 |
Ram R, Mehta M, Nguyen QT, Larma I, Boehm BO, Pociot F, Concannon P, Morahan G. Systematic Evaluation of Genes and Genetic Variants Associated with Type 1 Diabetes Susceptibility. Journal of Immunology (Baltimore, Md. : 1950). PMID 26912320 DOI: 10.4049/Jimmunol.1502056 |
0.474 |
|
| 2015 |
Ge Y, Onengut-Gumuscu S, Quinlan AR, Mackey AJ, Wright JA, Buckner JH, Habib T, Rich SS, Concannon P. Targeted Deep Sequencing in Multiple-Affected Sibships of European Ancestry Identifies Rare Deleterious Variants in PTPN22 that Confer Risk for Type 1 Diabetes. Diabetes. PMID 26631741 DOI: 10.2337/Db15-0322 |
0.441 |
|
| 2015 |
Arvey A, van der Veeken J, Plitas G, Rich SS, Concannon P, Rudensky AY. Genetic and epigenetic variation in the lineage specification of regulatory T cells. Elife. 4. PMID 26510014 DOI: 10.7554/Elife.07571 |
0.38 |
|
| 2015 |
Lawrenson K, Iversen ES, Tyrer J, Weber RP, Concannon P, Hazelett DJ, Li Q, Marks JR, Berchuck A, Lee JM, Aben KK, Anton-Culver H, Antonenkova N, et al. Common Variants at the CHEK2 Gene Locus and Risk of Epithelial Ovarian Cancer. Carcinogenesis. PMID 26424751 DOI: 10.1093/carcin/bgv138 |
0.3 |
|
| 2015 |
Rich SS, Concannon P. Summary of the Type 1 Diabetes Genetics Consortium Autoantibody Workshop. Diabetes Care. 38: S45-8. PMID 26405072 DOI: 10.2337/Dcs15-2008 |
0.432 |
|
| 2015 |
Rich SS, Concannon P. Role of Type 1 Diabetes-Associated SNPs on Autoantibody Positivity in the Type 1 Diabetes Genetics Consortium: Overview. Diabetes Care. 38: S1-3. PMID 26405066 DOI: 10.2337/Dcs15-2001 |
0.438 |
|
| 2015 |
Looney BM, Xia CQ, Concannon P, Ostrov DA, Clare-Salzler MJ. Effects of Type 1 Diabetes-Associated IFIH1 Polymorphisms on MDA5 Function and Expression. Current Diabetes Reports. 15: 96. PMID 26385483 DOI: 10.1007/S11892-015-0656-8 |
0.615 |
|
| 2015 |
Kijas AW, Lim YC, Bolderson E, Cerosaletti K, Gatei M, Jakob B, Tobias F, Taucher-Scholz G, Gueven N, Oakley G, Concannon P, Wolvetang E, Khanna KK, Wiesmüller L, Lavin MF. ATM-dependent phosphorylation of MRE11 controls extent of resection during homology directed repair by signalling through Exonuclease 1. Nucleic Acids Research. 43: 8352-67. PMID 26240375 DOI: 10.1093/Nar/Gkv754 |
0.306 |
|
| 2015 |
Brorsson CA, Onengut S, Chen WM, Wenzlau J, Yu L, Baker P, Williams AJ, Bingley PJ, Hutton JC, Eisenbarth GS, Concannon P, Rich SS, Pociot F. Novel association between immune-mediated susceptibility loci and persistent autoantibody positivity in type 1 diabetes. Diabetes. PMID 25829454 DOI: 10.2337/Db14-1730 |
0.379 |
|
| 2015 |
Onengut-Gumuscu S, Chen WM, Burren O, Cooper NJ, Quinlan AR, Mychaleckyj JC, Farber E, Bonnie JK, Szpak M, Schofield E, Achuthan P, Guo H, Fortune MD, Stevens H, Walker NM, ... ... Concannon P, et al. Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers. Nature Genetics. 47: 381-6. PMID 25751624 DOI: 10.1038/Ng.3245 |
0.468 |
|
| 2015 |
Arvey A, Veeken Jvd, Plitas G, Rich SS, Concannon P, Rudensky AY. Author response: Genetic and epigenetic variation in the lineage specification of regulatory T cells Elife. DOI: 10.7554/Elife.07571.029 |
0.31 |
|
| 2014 |
Evangelou M, Smyth DJ, Fortune MD, Burren OS, Walker NM, Guo H, Onengut-Gumuscu S, Chen WM, Concannon P, Rich SS, Todd JA, Wallace C. A method for gene-based pathway analysis using genomewide association study summary statistics reveals nine new type 1 diabetes associations. Genetic Epidemiology. 38: 661-70. PMID 25371288 DOI: 10.1002/Gepi.21853 |
0.401 |
|
| 2014 |
Antoniou AC, Casadei S, Heikkinen T, Barrowdale D, Pylkäs K, Roberts J, Lee A, Subramanian D, De Leeneer K, Fostira F, Tomiak E, Neuhausen SL, Teo ZL, Khan S, Aittomäki K, ... ... Concannon P, et al. Breast-cancer risk in families with mutations in PALB2. The New England Journal of Medicine. 371: 497-506. PMID 25099575 DOI: 10.1097/Ogx.0000000000000118 |
0.318 |
|
| 2014 |
Tomlinson MJ, Pitsillides A, Pickin R, Mika M, Keene KL, Hou X, Mychaleckyj J, Chen WM, Concannon P, Onengut-Gumuscu S. Fine mapping and functional studies of risk variants for type 1 diabetes at chromosome 16p13.13. Diabetes. 63: 4360-8. PMID 25008175 DOI: 10.2337/Db13-1785 |
0.588 |
|
| 2014 |
Fløyel T, Brorsson C, Nielsen LB, Miani M, Bang-Berthelsen CH, Friedrichsen M, Overgaard AJ, Berchtold LA, Wiberg A, Poulsen P, Hansen L, Rosinger S, Boehm BO, Ram R, Nguyen Q, ... ... Concannon P, et al. CTSH regulates β-cell function and disease progression in newly diagnosed type 1 diabetes patients. Proceedings of the National Academy of Sciences of the United States of America. 111: 10305-10. PMID 24982147 DOI: 10.1073/Pnas.1402571111 |
0.379 |
|
| 2014 |
Fernandez CA, Smith C, Yang W, Daté M, Bashford D, Larsen E, Bowman WP, Liu C, Ramsey LB, Chang T, Turner V, Loh ML, Raetz EA, Winick NJ, Hunger SP, ... ... Concannon P, et al. HLA-DRB1*07:01 is associated with a higher risk of asparaginase allergies. Blood. 124: 1266-76. PMID 24970932 DOI: 10.1182/Blood-2014-03-563742 |
0.32 |
|
| 2014 |
Pontikos N, Smyth DJ, Schuilenburg H, Howson JM, Walker NM, Burren OS, Guo H, Onengut-Gumuscu S, Chen WM, Concannon P, Rich SS, Jayaraman J, Jiang W, Traherne JA, Trowsdale J, et al. A hybrid qPCR/SNP array approach allows cost efficient assessment of KIR gene copy numbers in large samples. Bmc Genomics. 15: 274. PMID 24720548 DOI: 10.1186/1471-2164-15-274 |
0.412 |
|
| 2014 |
Martin NT, Nakamura K, Paila U, Woo J, Brown C, Wright JA, Teraoka SN, Haghayegh S, McCurdy D, Schneider M, Hu H, Quinlan AR, Gatti RA, Concannon P. Homozygous mutation of MTPAP causes cellular radiosensitivity and persistent DNA double-strand breaks. Cell Death & Disease. 5: e1130. PMID 24651433 DOI: 10.1038/Cddis.2014.99 |
0.337 |
|
| 2014 |
Madan R, Guo X, Naylor C, Buonomo EL, Mackay D, Noor Z, Concannon P, Scully KW, Pramoonjago P, Kolling GL, Warren CA, Duggal P, Petri WA. Role of leptin-mediated colonic inflammation in defense against Clostridium difficile colitis. Infection and Immunity. 82: 341-9. PMID 24166957 DOI: 10.1128/Iai.00972-13 |
0.302 |
|
| 2013 |
Brooks JD, Teraoka SN, Bernstein L, Mellemkjær L, Malone KE, Lynch CF, Haile RW, Concannon P, Reiner AS, Duggan DJ, Schiermeyer K, Bernstein JL, Figueiredo JC. Common variants in genes coding for chemotherapy metabolizing enzymes, transporters, and targets: a case-control study of contralateral breast cancer risk in the WECARE Study. Cancer Causes & Control : Ccc. 24: 1605-14. PMID 23775025 DOI: 10.1007/S10552-013-0237-6 |
0.333 |
|
| 2013 |
Bernstein JL, Thomas DC, Shore RE, Robson M, Boice JD, Stovall M, Andersson M, Bernstein L, Malone KE, Reiner AS, Lynch CF, Capanu M, Smith SA, Tellhed L, Teraoka SN, ... ... Concannon P, et al. Contralateral breast cancer after radiotherapy among BRCA1 and BRCA2 mutation carriers: a WECARE study report. European Journal of Cancer (Oxford, England : 1990). 49: 2979-85. PMID 23706288 DOI: 10.1016/J.Ejca.2013.04.028 |
0.342 |
|
| 2013 |
Hinks A, Cobb J, Marion MC, Prahalad S, Sudman M, Bowes J, Martin P, Comeau ME, Sajuthi S, Andrews R, Brown M, Chen WM, Concannon P, Deloukas P, Edkins S, et al. Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis. Nature Genetics. 45: 664-9. PMID 23603761 DOI: 10.1038/Ng.2614 |
0.386 |
|
| 2013 |
Faraco J, Lin L, Kornum BR, Kenny EE, Trynka G, Einen M, Rico TJ, Lichtner P, Dauvilliers Y, Arnulf I, Lecendreux M, Javidi S, Geisler P, Mayer G, Pizza F, ... ... Concannon P, et al. ImmunoChip study implicates antigen presentation to T cells in narcolepsy. Plos Genetics. 9: e1003270. PMID 23459209 DOI: 10.1371/Journal.Pgen.1003270 |
0.404 |
|
| 2013 |
Reiner AS, John EM, Brooks JD, Lynch CF, Bernstein L, Mellemkjær L, Malone KE, Knight JA, Capanu M, Teraoka SN, Concannon P, Liang X, Figueiredo JC, Smith SA, Stovall M, et al. Risk of asynchronous contralateral breast cancer in noncarriers of BRCA1 and BRCA2 mutations with a family history of breast cancer: a report from the Women's Environmental Cancer and Radiation Epidemiology Study. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. 31: 433-9. PMID 23269995 DOI: 10.1200/Jco.2012.43.2013 |
0.318 |
|
| 2013 |
Fernandez CA, Relling MV, Smith C, Yang W, Larsen EC, Bowman WP, Liu C, Ramsey LB, Chang T, Turner V, Loh ML, Raetz EA, Winick NJ, Hunger SP, Carroll WL, ... ... Concannon P, et al. HLA-DRB1*07:01 Is Associated With Asparaginase Allergies In Children With Acute Lymphoblastic Leukemia Blood. 122: 60-60. DOI: 10.1182/Blood.V122.21.60.60 |
0.336 |
|
| 2012 |
Eyre S, Bowes J, Diogo D, Lee A, Barton A, Martin P, Zhernakova A, Stahl E, Viatte S, McAllister K, Amos CI, Padyukov L, Toes RE, Huizinga TW, Wijmenga C, ... ... Concannon P, et al. High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis. Nature Genetics. 44: 1336-40. PMID 23143596 DOI: 10.1038/Ng.2462 |
0.381 |
|
| 2012 |
Howson JM, Cooper JD, Smyth DJ, Walker NM, Stevens H, She JX, Eisenbarth GS, Rewers M, Todd JA, Akolkar B, Concannon P, Erlich HA, Julier C, Morahan G, Nerup J, et al. Evidence of gene-gene interaction and age-at-diagnosis effects in type 1 diabetes. Diabetes. 61: 3012-7. PMID 22891215 DOI: 10.2337/Db11-1694 |
0.417 |
|
| 2012 |
Cooper JD, Howson JM, Smyth D, Walker NM, Stevens H, Yang JH, She JX, Eisenbarth GS, Rewers M, Todd JA, Akolkar B, Concannon P, Erlich HA, Julier C, Morahan G, et al. Confirmation of novel type 1 diabetes risk loci in families. Diabetologia. 55: 996-1000. PMID 22278338 DOI: 10.1007/S00125-012-2450-3 |
0.404 |
|
| 2012 |
Tischkowitz M, Capanu M, Sabbaghian N, Li L, Liang X, Vallée MP, Tavtigian SV, Concannon P, Foulkes WD, Bernstein L, Bernstein JL, Begg CB. Rare germline mutations in PALB2 and breast cancer risk: a population-based study. Human Mutation. 33: 674-80. PMID 22241545 DOI: 10.1002/Humu.22022 |
0.351 |
|
| 2012 |
Hunt KA, Smyth DJ, Balschun T, Ban M, Mistry V, Ahmad T, Anand V, Barrett JC, Bhaw-Rosun L, Bockett NA, Brand OJ, Brouwer E, Concannon P, Cooper JD, Dias KR, et al. Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry. Nature Genetics. 44: 3-5. PMID 22200769 DOI: 10.1038/Ng.1037 |
0.325 |
|
| 2012 |
Brooks JD, Teraoka SN, Reiner AS, Satagopan JM, Bernstein L, Thomas DC, Capanu M, Stovall M, Smith SA, Wei S, Shore RE, Boice JD, Lynch CF, Mellemkjaer L, Malone KE, ... ... Concannon P, et al. Variants in activators and downstream targets of ATM, radiation exposure, and contralateral breast cancer risk in the WECARE study. Human Mutation. 33: 158-64. PMID 21898661 DOI: 10.1002/Humu.21604 |
0.348 |
|
| 2012 |
Keene KL, Quinlan AR, Hou X, Hall IM, Mychaleckyj JC, Onengut-Gumuscu S, Concannon P. Evidence for two independent associations with type 1 diabetes at the 12q13 locus Genes and Immunity. 13: 66-70. PMID 21850031 DOI: 10.1038/Gene.2011.56 |
0.426 |
|
| 2011 |
Capanu M, Concannon P, Haile RW, Bernstein L, Malone KE, Lynch CF, Liang X, Teraoka SN, Diep AT, Thomas DC, Bernstein JL, Begg CB. Assessment of rare BRCA1 and BRCA2 variants of unknown significance using hierarchical modeling. Genetic Epidemiology. 35: 389-97. PMID 21520273 DOI: 10.1002/Gepi.20587 |
0.376 |
|
| 2011 |
Figueiredo JC, Brooks JD, Conti DV, Poynter JN, Teraoka SN, Malone KE, Bernstein L, Lee WD, Duggan DJ, Siniard A, Concannon P, Capanu M, Lynch CF, Olsen JH, Haile RW, et al. Risk of contralateral breast cancer associated with common variants in BRCA1 and BRCA2: potential modifying effect of BRCA1/BRCA2 mutation carrier status. Breast Cancer Research and Treatment. 127: 819-29. PMID 21161372 DOI: 10.1007/S10549-010-1285-1 |
0.389 |
|
| 2010 |
Saidi A, Li T, Weih F, Concannon P, Wang ZQ. Dual functions of Nbs1 in the repair of DNA breaks and proliferation ensure proper V(D)J recombination and T-cell development. Molecular and Cellular Biology. 30: 5572-81. PMID 20921278 DOI: 10.1128/Mcb.00917-10 |
0.335 |
|
| 2010 |
Noble JA, Valdes AM, Varney MD, Carlson JA, Moonsamy P, Fear AL, Lane JA, Lavant E, Rappner R, Louey A, Concannon P, Mychaleckyj JC, Erlich HA. HLA class I and genetic susceptibility to type 1 diabetes: results from the Type 1 Diabetes Genetics Consortium. Diabetes. 59: 2972-9. PMID 20798335 DOI: 10.2337/Db10-0699 |
0.355 |
|
| 2010 |
Pociot F, Akolkar B, Concannon P, Erlich HA, Julier C, Morahan G, Nierras CR, Todd JA, Rich SS, Nerup J. Genetics of type 1 diabetes: what's next? Diabetes. 59: 1561-71. PMID 20587799 DOI: 10.2337/Db10-0076 |
0.429 |
|
| 2010 |
Malone KE, Begg CB, Haile RW, Borg A, Concannon P, Tellhed L, Xue S, Teraoka S, Bernstein L, Capanu M, Reiner AS, Riedel ER, Thomas DC, Mellemkjaer L, Lynch CF, et al. Population-based study of the risk of second primary contralateral breast cancer associated with carrying a mutation in BRCA1 or BRCA2. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. 28: 2404-10. PMID 20368571 DOI: 10.1200/Jco.2009.24.2495 |
0.323 |
|
| 2010 |
Bernstein JL, Haile RW, Stovall M, Boice JD, Shore RE, Langholz B, Thomas DC, Bernstein L, Lynch CF, Olsen JH, Malone KE, Mellemkjaer L, Borresen-Dale AL, Rosenstein BS, Teraoka SN, ... ... Concannon P, et al. Radiation exposure, the ATM Gene, and contralateral breast cancer in the women's environmental cancer and radiation epidemiology study. Journal of the National Cancer Institute. 102: 475-83. PMID 20305132 DOI: 10.1093/Jnci/Djq055 |
0.314 |
|
| 2010 |
Reding KW, Bernstein JL, Langholz BM, Bernstein L, Haile RW, Begg CB, Lynch CF, Concannon P, Borg A, Teraoka SN, Törngren T, Diep A, Xue S, Bertelsen L, Liang X, et al. Adjuvant systemic therapy for breast cancer in BRCA1/BRCA2 mutation carriers in a population-based study of risk of contralateral breast cancer. Breast Cancer Research and Treatment. 123: 491-8. PMID 20135344 DOI: 10.1007/S10549-010-0769-3 |
0.35 |
|
| 2010 |
Poynter JN, Langholz B, Largent J, Mellemkjaer L, Bernstein L, Malone KE, Lynch CF, Borg A, Concannon P, Teraoka SN, Xue S, Diep AT, Törngren T, Begg CB, Capanu M, et al. Reproductive factors and risk of contralateral breast cancer by BRCA1 and BRCA2 mutation status: results from the WECARE study. Cancer Causes & Control : Ccc. 21: 839-46. PMID 20130978 DOI: 10.1007/S10552-010-9510-0 |
0.315 |
|
| 2010 |
Borg A, Haile RW, Malone KE, Capanu M, Diep A, Törngren T, Teraoka S, Begg CB, Thomas DC, Concannon P, Mellemkjaer L, Bernstein L, Tellhed L, Xue S, Olson ER, et al. Characterization of BRCA1 and BRCA2 deleterious mutations and variants of unknown clinical significance in unilateral and bilateral breast cancer: the WECARE study. Human Mutation. 31: E1200-40. PMID 20104584 DOI: 10.1002/Humu.21202 |
0.343 |
|
| 2010 |
Figueiredo JC, Haile RW, Bernstein L, Malone KE, Largent J, Langholz B, Lynch CF, Bertelsen L, Capanu M, Concannon P, Borg A, Børresen-Dale AL, Diep A, Teraoka S, Torngren T, et al. Oral contraceptives and postmenopausal hormones and risk of contralateral breast cancer among BRCA1 and BRCA2 mutation carriers and noncarriers: the WECARE Study. Breast Cancer Research and Treatment. 120: 175-83. PMID 19597986 DOI: 10.1007/S10549-009-0455-5 |
0.328 |
|
| 2009 |
Julier C, Akolkar B, Concannon P, Morahan G, Nierras C, Pugliese A. The Type I Diabetes Genetics Consortium 'Rapid Response' family-based candidate gene study: strategy, genes selection and main outcome Genes and Immunity. 10. PMID 19956109 DOI: 10.1038/Gene.2009.99 |
0.463 |
|
| 2009 |
Steck AK, Baschal EE, Jasinski JM, Boehm BO, Bottini N, Concannon P, Julier C, Morahan G, Noble JA, Polychronakos C, She JX, Eisenbarth GS. Rs2476601 T allele (R620W) defines high-risk PTPN22 type i diabetes-associated haplotypes with preliminary evidence for an additional protective haplotype Genes and Immunity. 10: S21-S26. PMID 19956096 DOI: 10.1038/Gene.2009.87 |
0.419 |
|
| 2009 |
Rich SS, Akolkar B, Concannon P, Erlich H, Hilner JE, Julier C, Morahan G, Nerup J, Nierras C, Pociot F, Todd JA. Current status and the future for the genetics of type I diabetes. Genes and Immunity. 10: S128-31. PMID 19956094 DOI: 10.1038/Gene.2009.100 |
0.428 |
|
| 2009 |
Rich SS, Akolkar B, Concannon P, Erlich H, Hilner JE, Julier C, Morahan G, Nerup J, Nierras C, Pociot F, Todd JA. Overview of the Type I Diabetes Genetics Consortium. Genes and Immunity. 10: S1-4. PMID 19956093 DOI: 10.1038/Gene.2009.84 |
0.42 |
|
| 2009 |
Barrett JC, Clayton DG, Concannon P, Akolkar B, Cooper JD, Erlich HA, Julier C, Morahan G, Nerup J, Nierras C, Plagnol V, Pociot F, Schuilenburg H, Smyth DJ, Stevens H, et al. Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. Nature Genetics. 41: 703-7. PMID 19430480 DOI: 10.1038/Ng.381 |
0.367 |
|
| 2009 |
Concannon P, Rich SS, Nepom GT. Genetics of type 1A diabetes. The New England Journal of Medicine. 360: 1646-54. PMID 19369670 DOI: 10.1056/Nejmra0808284 |
0.338 |
|
| 2009 |
Rich SS, Onengut-Gumuscu S, Concannon P. Recent progress in the genetics of diabetes. Hormone Research. 71: 17-23. PMID 19153499 DOI: 10.1159/000178031 |
0.37 |
|
| 2009 |
Rich SS, Akolkar B, Concannon P, Erlich H, Hilner J, Julier C, Morahan G, Nerup J, Nierras C, Pociot F, Todd JA. Results of the MHC fine mapping workshop. Diabetes, Obesity and Metabolism. 11: 108-109. PMID 19143823 DOI: 10.1111/J.1463-1326.2008.01011.X |
0.426 |
|
| 2009 |
Concannon P, Chen WM, Julier C, Morahan G, Akolkar B, Erlich HA, Hilner JE, Nerup J, Nierras C, Pociot F, Todd JA, Rich SS. Genome-wide scan for linkage to type 1 diabetes in 2,496 multiplex families from the Type 1 Diabetes Genetics Consortium. Diabetes. 58: 1018-22. PMID 19136655 DOI: 10.2337/Db08-1551 |
0.406 |
|
| 2009 |
Vissinga CS, Yeo TC, Warren S, Brawley JV, Phillips J, Cerosaletti K, Concannon P. Nuclear export of NBN is required for normal cellular responses to radiation Molecular and Cellular Biology. 29: 1000-1006. PMID 19075003 DOI: 10.1128/Mcb.01131-08 |
0.568 |
|
| 2009 |
Mitui M, Nahas SA, Du LT, Yang Z, Lai CH, Nakamura K, Arroyo S, Scott S, Purayidom A, Concannon P, Lavin M, Gatti RA. Functional and computational assessment of missense variants in the ataxia-telangiectasia mutated (ATM) gene: mutations with increased cancer risk. Human Mutation. 30: 12-21. PMID 18634022 DOI: 10.1002/Humu.20805 |
0.379 |
|
| 2008 |
Concannon P, Haile RW, Børresen-Dale AL, Rosenstein BS, Gatti RA, Teraoka SN, Diep TA, Jansen L, Atencio DP, Langholz B, Capanu M, Liang X, Begg CB, Thomas DC, Bernstein L, et al. Variants in the ATM gene associated with a reduced risk of contralateral breast cancer. Cancer Research. 68: 6486-91. PMID 18701470 DOI: 10.1158/0008-5472.Can-08-0134 |
0.369 |
|
| 2008 |
Concannon P, Onengut-Gumuscu S, Todd JA, Smyth DJ, Pociot F, Bergholdt R, Akolkar B, Erlich HA, Hilner JE, Julier C, Morahan G, Nerup J, Nierras CR, Chen WM, Rich SS, et al. A human type 1 diabetes susceptibility locus maps to chromosome 21q22.3. Diabetes. 57: 2858-61. PMID 18647951 DOI: 10.2337/Db08-0753 |
0.397 |
|
| 2008 |
Du L, Lai CH, Concannon P, Gatti RA. Rapid screen for truncating ATM mutations by PTT-ELISA. Mutation Research. 640: 139-44. PMID 18321536 DOI: 10.1016/J.Mrfmmm.2008.01.002 |
0.332 |
|
| 2008 |
Erlich H, Valdes AM, Noble J, Carlson JA, Varney M, Concannon P, Mychaleckyj JC, Todd JA, Bonella P, Fear AL, Lavant E, Louey A, Moonsamy P. HLA DR-DQ Haplotypes and Genotypes and Type 1 Diabetes Risk: Analysis of the Type 1 Diabetes Genetics Consortium Families Diabetes. 57: 1084-1092. PMID 18252895 DOI: 10.2337/Db07-1331 |
0.436 |
|
| 2008 |
Begg CB, Haile RW, Borg A, Malone KE, Concannon P, Thomas DC, Langholz B, Bernstein L, Olsen JH, Lynch CF, Anton-Culver H, Capanu M, Liang X, Hummer AJ, Sima C, et al. Variation of breast cancer risk among BRCA1/2 carriers. Jama. 299: 194-201. PMID 18182601 DOI: 10.1001/Jama.2007.55-A |
0.309 |
|
| 2008 |
Shilling H, Wei S, Gumuscu SO, Concannon P, Buckner J. Sa.33. The PTPN22 1858C/T Functional Polymorphism is Associated with Relapsing Polychondritis Clinical Immunology. 127: S91. DOI: 10.1016/J.Clim.2008.03.254 |
0.327 |
|
| 2007 |
Rieck M, Arechiga A, Onengut-Gumuscu S, Greenbaum C, Concannon P, Buckner JH. Genetic variation in PTPN22 corresponds to altered function of T and B lymphocytes. Journal of Immunology (Baltimore, Md. : 1950). 179: 4704-10. PMID 17878369 DOI: 10.4049/Jimmunol.179.7.4704 |
0.383 |
|
| 2007 |
Steenkiste A, Valdes AM, Feolo M, Hoffman D, Concannon P, Noble J, Schoch G, Hansen J, Helmberg W, Dorman JS, Thomson G, Pugliese A. 14th International HLA and Immunogenetics Workshop: Report on the HLA component of type 1 diabetes Tissue Antigens. 69: 214-225. PMID 17445204 DOI: 10.1111/J.1399-0039.2006.00772.X |
0.372 |
|
| 2006 |
Rich SS, Concannon P, Erlich H, Julier C, Morahan G, Nerup J, Pociot F, Todd JA. The Type 1 Diabetes Genetics Consortium. Annals of the New York Academy of Sciences. 1079: 1-8. PMID 17130525 DOI: 10.1196/Annals.1375.001 |
0.412 |
|
| 2006 |
Onengut-Gumuscu S, Buckner JH, Concannon P. A haplotype-based analysis of the PTPN22 locus in type 1 diabetes Diabetes. 55: 2883-2889. PMID 17003357 DOI: 10.2337/Db06-0225 |
0.434 |
|
| 2006 |
Bernstein JL, Teraoka S, Southey MC, Jenkins MA, Andrulis IL, Knight JA, John EM, Lapinski R, Wolitzer AL, Whittemore AS, West D, Seminara D, Olson ER, Spurdle AB, Chenevix-Trench G, ... ... Concannon P, et al. Population-based estimates of breast cancer risks associated with ATM gene variants c.7271T>G and c.1066-6T>G (IVS10-6T>G) from the Breast Cancer Family Registry. Human Mutation. 27: 1122-8. PMID 16958054 DOI: 10.1002/Humu.20415 |
0.359 |
|
| 2006 |
Onengut-Gumuscu S, Concannon P. Recent advances in the immunogenetics of human type 1 diabetes. Current Opinion in Immunology. 18: 634-8. PMID 16884898 DOI: 10.1016/J.Coi.2006.07.013 |
0.413 |
|
| 2006 |
Langholz B, Bernstein JL, Bernstein L, Olsen JH, Børresen-Dale AL, Rosenstein BS, Gatti RA, Concannon P. On the proposed association of the ATM variants 5557G>A and IVS38-8T>C and bilateral breast cancer. International Journal of Cancer. Journal International Du Cancer. 119: 724-5. PMID 16496408 DOI: 10.1002/Ijc.21876 |
0.317 |
|
| 2006 |
Bernstein JL, Teraoka SN, John EM, Andrulis IL, Knight JA, Lapinski R, Olson ER, Wolitzer AL, Seminara D, Whittemore AS, Concannon P. The CHEK2*1100delC allelic variant and risk of breast cancer: Screening results from the breast cancer family registry Cancer Epidemiology Biomarkers and Prevention. 15: 348-352. PMID 16492927 DOI: 10.1158/1055-9965.Epi-05-0557 |
0.343 |
|
| 2006 |
Bernstein J, Bernstein L, Langholz B, Thomas D, Stovall M, Capanu M, Thompson WD, Olson J, Malone K, Lynch C, Anton-Culver H, Shore R, Boice J, Begg C, Wolitzer A, ... ... Concannon P, et al. The Interaction of Radiation, the Atm Gene and Breast Cancer American Journal of Epidemiology. 163: S251-S251. DOI: 10.1093/Aje/163.Suppl_11.S251-A |
0.302 |
|
| 2005 |
Mitui M, Bernatowska E, Pietrucha B, Piotrowska-Jastrzebska J, Eng L, Nahas S, Teraoka S, Sholty G, Purayidom A, Concannon P, Gatti RA. ATM gene founder haplotypes and associated mutations in Polish families with ataxia-telangiectasia. Annals of Human Genetics. 69: 657-64. PMID 16266405 DOI: 10.1111/J.1529-8817.2005.00199.X |
0.378 |
|
| 2005 |
Onengut-Gumuscu S, Concannon P. The genetics of type 1 diabetes: lessons learned and future challenges. Journal of Autoimmunity. 25: 34-9. PMID 16263245 DOI: 10.1016/J.Jaut.2005.09.007 |
0.37 |
|
| 2005 |
Concannon P, Erlich HA, Julier C, Morahan G, Nerup J, Pociot F, Todd JA, Rich SS. Type 1 diabetes: evidence for susceptibility loci from four genome-wide linkage scans in 1,435 multiplex families. Diabetes. 54: 2995-3001. PMID 16186404 DOI: 10.2337/Diabetes.54.10.2995 |
0.4 |
|
| 2005 |
Ben-Omran TI, Cerosaletti K, Concannon P, Weitzman S, Nezarati MM. A patient with mutations in DNA Ligase IV: clinical features and overlap with Nijmegen breakage syndrome. American Journal of Medical Genetics. Part A. 137: 283-7. PMID 16088910 DOI: 10.1002/Ajmg.A.30869 |
0.334 |
|
| 2005 |
Kosoy R, Concannon P. Functional variants in SUMO4, TAB2, and NFkappaB and the risk of type 1 diabetes. Genes and Immunity. 6: 231-235. PMID 15729364 DOI: 10.1038/Sj.Gene.6364174 |
0.717 |
|
| 2005 |
Valdes AM, Wapelhorst B, Concannon P, Erlich HA, Thomson G, Noble JA. Extended DR3-D6S273-HLA-B haplotypes are associated with increased susceptibility to type 1 diabetes in US Caucasians Tissue Antigens. 65: 115-119. PMID 15663750 DOI: 10.1111/J.1399-0039.2005.00348.X |
0.39 |
|
| 2005 |
Gatti R, Concannon P. ATM mutations associated with breast cancer Breast Cancer Research. 7: 1-2. DOI: 10.1186/Bcr1048 |
0.366 |
|
| 2005 |
Thomson G, Valdes AM, Dorman JS, Steenkiste A, Noble JA, Concannon P, Smith AG, John H, Lernmark A, Pugliese A. The HLA component of type 1 diabetes Human Immunology. 66: 64. DOI: 10.1016/J.Humimm.2005.08.122 |
0.322 |
|
| 2004 |
Onengut-Gumuscu S, Ewens KG, Spielman RS, 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. 5: 678-680. PMID 15526003 DOI: 10.1038/Sj.Gene.6364138 |
0.424 |
|
| 2004 |
Demuth I, Digweed M, Concannon P. Human SNM1B is required for normal cellular response to both DNA interstrand crosslink-inducing agents and ionizing radiation. Oncogene. 23: 8611-8. PMID 15467758 DOI: 10.1038/Sj.Onc.1207895 |
0.334 |
|
| 2004 |
O'Driscoll M, Gennery AR, Seidel J, Concannon P, Jeggo PA. An overview of three new disorders associated with genetic instability: LIG4 syndrome, RS-SCID and ATR-Seckel syndrome. Dna Repair. 3: 1227-35. PMID 15279811 DOI: 10.1016/J.Dnarep.2004.03.025 |
0.336 |
|
| 2004 |
Barratt BJ, Payne F, Lowe CE, Hermann R, Healy BC, Harold D, Concannon P, Gharani N, McCarthy MI, Olavesen MG, McCormack R, Guja C, Ionescu-Tîrgovi?te C, Undlien DE, Rønningen KS, et al. Remapping the insulin gene/IDDM2 locus in type 1 diabetes. Diabetes. 53: 1884-9. PMID 15220214 DOI: 10.2337/Diabetes.53.7.1884 |
0.415 |
|
| 2004 |
Bernstein JL, Langholz B, Haile RW, Bernstein L, Thomas DC, Stovall M, Malone KE, Lynch CF, Olsen JH, Anton-Culver H, Shore RE, Boice JD, Berkowitz GS, Gatti RA, Teitelbaum SL, ... ... Concannon P, et al. Study design: evaluating gene-environment interactions in the etiology of breast cancer - the WECARE study. Breast Cancer Research : Bcr. 6: R199-214. PMID 15084244 DOI: 10.1186/Bcr771 |
0.339 |
|
| 2004 |
Morrison VA, Onengut-Gumuscu S, Concannon P. A functional variant of IRS1 is associated with type 1 diabetes in families from the US and UK. Molecular Genetics and Metabolism. 81: 291-4. PMID 15059616 DOI: 10.1016/J.Ymgme.2003.10.018 |
0.417 |
|
| 2004 |
Kosoy R, Yokoi N, Seino S, Concannon P. Polymorphic variation in the CBLB gene in human type 1 diabetes Genes and Immunity. 5: 232-235. PMID 14961073 DOI: 10.1038/Sj.Gene.6364057 |
0.727 |
|
| 2003 |
Chun HH, Sun X, Nahas SA, Teraoka S, Lai CH, Concannon P, Gatti RA. Improved diagnostic testing for ataxia-telangiectasia by immunoblotting of nuclear lysates for ATM protein expression. Molecular Genetics and Metabolism. 80: 437-43. PMID 14654357 DOI: 10.1016/J.Ymgme.2003.09.008 |
0.304 |
|
| 2003 |
Bernstein JL, Bernstein L, Thompson WD, Lynch CF, Malone KE, Teitelbaum SL, Olsen JH, Anton-Culver H, Boice JD, Rosenstein BS, Børresen-Dale AL, Gatti RA, Concannon P, Haile RW. ATM variants 7271T>G and IVS10-6T>G among women with unilateral and bilateral breast cancer. British Journal of Cancer. 89: 1513-6. PMID 14562025 DOI: 10.1038/Sj.Bjc.6601289 |
0.346 |
|
| 2003 |
White RE, Wade-Martins R, Hart SL, Frampton J, Huey B, Desai-Mehta A, Cerosaletti KM, Concannon P, James MR. Functional delivery of large genomic DNA to human cells with a peptide-lipid vector. The Journal of Gene Medicine. 5: 883-92. PMID 14533197 DOI: 10.1002/Jgm.420 |
0.304 |
|
| 2003 |
Cerosaletti KM, Concannon P. Nibrin forkhead-associated domain and breast cancer C-terminal domain are both required for nuclear focus formation and phosphorylation. The Journal of Biological Chemistry. 278: 21944-51. PMID 12679336 DOI: 10.1074/Jbc.M211689200 |
0.316 |
|
| 2003 |
Bernstein JL, Teraoka S, Haile RW, Børresen-Dale AL, Rosenstein BS, Gatti RA, Diep AT, Jansen L, Atencio DP, Olsen JH, Bernstein L, Teitelbaum SL, Thompson WD, Concannon P. Designing and implementing quality control for multi-center screening of mutations in the ATM gene among women with breast cancer. Human Mutation. 21: 542-50. PMID 12673797 DOI: 10.1002/Humu.10206 |
0.33 |
|
| 2002 |
Onengut-Gumuscu S, Concannon P. Mapping genes for autoimmunity in humans: type 1 diabetes as a model. Immunological Reviews. 190: 182-94. PMID 12493015 DOI: 10.1034/J.1600-065X.2002.19014.X |
0.434 |
|
| 2002 |
Rich SS, Concannon P. Challenges and strategies for investigating the genetic complexity of common human diseases. Diabetes. 51: S288-94. PMID 12475765 DOI: 10.2337/Diabetes.51.2007.S288 |
0.44 |
|
| 2002 |
Ewens KG, Johnson LN, Wapelhorst B, O'Brien K, Gutin S, Morrison VA, Street C, Gregory SG, Spielman RS, Concannon P. Linkage and association with type 1 diabetes on chromosome 1q42. Diabetes. 51: 3318-25. PMID 12401725 DOI: 10.2337/Diabetes.51.11.3318 |
0.438 |
|
| 2002 |
Balraj P, Concannon P, Jamal R, Beghini A, Hoe TS, Khoo AS, Volpi L. An unusual mutation in RECQ4 gene leading to Rothmund-Thomson syndrome. Mutation Research. 508: 99-105. PMID 12379465 DOI: 10.1016/S0027-5107(02)00189-6 |
0.329 |
|
| 2002 |
Cerosaletti KM, Morrison VA, Sabath DE, Willerford DM, Concannon P. Mutations and molecular variants of the NBS1 gene in non-Hodgkin lymphoma. Genes, Chromosomes & Cancer. 35: 282-6. PMID 12353271 DOI: 10.1002/Gcc.10114 |
0.407 |
|
| 2002 |
Concannon P. ATM heterozygosity and cancer risk. Nature Genetics. 32: 89-90. PMID 12205473 DOI: 10.1038/Ng0902-89 |
0.319 |
|
| 2002 |
Brawley JV, Concannon P. 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). 168: 3894-901. PMID 11937544 DOI: 10.4049/Jimmunol.168.8.3894 |
0.324 |
|
| 2002 |
Dahlman I, Eaves IA, Kosoy R, Morrison VA, Heward J, Gough SC, Allahabadia A, Franklyn JA, Tuomilehto J, Tuomilehto-Wolf E, Cucca F, Guja C, Ionescu-Tirgoviste C, Stevens H, Carr P, ... ... Concannon P, et al. Parameters for reliable results in genetic association studies in common disease. Nature Genetics. 30: 149-50. PMID 11799396 DOI: 10.1038/Ng825 |
0.69 |
|
| 2001 |
Jeggo PA, Concannon P. Immune diversity and genomic stability: opposite goals but similar paths. Journal of Photochemistry and Photobiology. B, Biology. 65: 88-96. PMID 11809363 DOI: 10.1016/S1011-1344(01)00243-3 |
0.319 |
|
| 2001 |
O'Driscoll M, Cerosaletti KM, Girard PM, Dai Y, Stumm M, Kysela B, Hirsch B, Gennery A, Palmer SE, Seidel J, Gatti RA, Varon R, Oettinger MA, Neitzel H, Jeggo PA, ... Concannon P, et al. DNA ligase IV mutations identified in patients exhibiting developmental delay and immunodeficiency. Molecular Cell. 8: 1175-85. PMID 11779494 DOI: 10.1016/S1097-2765(01)00408-7 |
0.322 |
|
| 2001 |
Cox NJ, Wapelhorst B, Morrison VA, Johnson L, Pinchuk L, Spielman RS, Todd JA, 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. 69: 820-830. PMID 11507694 DOI: 10.1086/323501 |
0.383 |
|
| 2001 |
Teraoka SN, Malone KE, Doody DR, Suter NM, Ostrander EA, Daling JR, Concannon P. Increased frequency of ATM mutations in breast carcinoma patients with early onset disease and positive family history. Cancer. 92: 479-87. PMID 11505391 DOI: 10.1002/1097-0142(20010801)92:3<479::Aid-Cncr1346>3.0.Co;2-G |
0.332 |
|
| 2001 |
Buscemi G, Savio C, Zannini L, Miccichè F, Masnada D, Nakanishi M, Tauchi H, Komatsu K, Mizutani S, Khanna K, Chen P, Concannon P, Chessa L, Delia D. Chk2 activation dependence on Nbs1 after DNA damage. Molecular and Cellular Biology. 21: 5214-22. PMID 11438675 DOI: 10.1128/Mcb.21.15.5214-5222.2001 |
0.323 |
|
| 2001 |
Argentaro A, Wapelhorst B, Concannon P, Harley VR. Linkage studies of SOX13, the ICA12 autoantigen gene, in families with type 1 diabetes. Molecular Genetics and Metabolism. 72: 356-359. PMID 11286511 DOI: 10.1006/Mgme.2000.3136 |
0.435 |
|
| 2001 |
Desai-Mehta A, Cerosaletti KM, Concannon P. Distinct functional domains of nibrin mediate Mre11 binding, focus formation, and nuclear localization. Molecular and Cellular Biology. 21: 2184-2191. PMID 11238951 DOI: 10.1128/Mcb.21.6.2184-2191.2001 |
0.386 |
|
| 2000 |
Yeo TC, Xia D, Hassouneh S, Yang XO, Sabath DE, Sperling K, Gatti RA, Concannon P, Willerford DM. V(D)J rearrangement in Nijmegen breakage syndrome. Molecular Immunology. 37: 1131-1139. PMID 11451418 DOI: 10.1016/S0161-5890(01)00026-8 |
0.341 |
|
| 2000 |
Horikawa Y, Oda N, Cox NJ, Li X, Orho-Melander M, Hara M, Hinokio Y, Lindner TH, Mashima H, Schwarz PEH, Del Bosque-Plata L, Oda Y, Yoshiuchi I, Colilla S, Polonsky KS, ... ... Concannon P, et al. Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus Nature Genetics. 26: 163-175. PMID 11017071 DOI: 10.1038/79876 |
0.411 |
|
| 2000 |
Wilda M, Demuth I, Concannon P, Sperling K, Hameister H. Expression pattern of the Nijmegen breakage syndrome gene, Nbs1, during murine development Human Molecular Genetics. 9: 1739-1744. PMID 10915761 DOI: 10.1093/Hmg/9.12.1739 |
0.333 |
|
| 2000 |
Gatei M, Young D, Cerosaletti KM, Desai-Mehta A, Spring K, Kozlov S, Lavin MF, Gatti RA, Concannon P, Khanna K. ATM-dependent phosphorylation of nibrin in response to radiation exposure. Nature Genetics. 25: 115-9. PMID 10802669 DOI: 10.1038/75508 |
0.375 |
|
| 2000 |
Cerosaletti KM, Desai-Mehta A, Yeo TC, Zwet MKd, Zdzienicka MZ, Concannon P. Retroviral expression of the NBS1 gene in cultured Nijmegen breakage syndrome cells restores normal radiation sensitivity and nuclear focus formation Mutagenesis. 15: 281-286. PMID 10792024 DOI: 10.1093/Mutage/15.3.281 |
0.356 |
|
| 1999 |
Gatti RA, Tward A, Concannon P. Cancer risk in ATM heterozygotes: A model of phenotypic and mechanistic differences between missense and truncating mutations Molecular Genetics and Metabolism. 68: 419-423. PMID 10607471 DOI: 10.1006/Mgme.1999.2942 |
0.35 |
|
| 1999 |
Teraoka SN, Telatar M, Becker-Catania S, Liang T, Onengüt S, Tolun A, Chessa L, Sanal O, Bernatowska E, Gatti RA, Concannon P. Splicing defects in the ataxia-telangiectasia gene, ATM: underlying mutations and consequences. American Journal of Human Genetics. 64: 1617-31. PMID 10330348 DOI: 10.1086/302418 |
0.325 |
|
| 1999 |
Cox NJ, Frigge M, Nicolae DL, Concannon P, Hanis CL, Bell GI, Kong A. Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans Nature Genetics. 21: 213-215. PMID 9988276 DOI: 10.1038/6002 |
0.386 |
|
| 1999 |
Vanasse GJ, Concannon P, Willerford DM. Regulated genomic instability and neoplasia in the lymphoid lineage. Blood. 94: 3997-4010. DOI: 10.1182/Blood.V94.12.3997 |
0.347 |
|
| 1998 |
Concannon P, Gogolin-Ewens KJ, Hinds DA, Wapelhorst B, Morrison VA, Stirling B, Mitra M, Farmer J, Williams SR, Cox NJ, Bell GI, Risch N, Spielman RS. A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus. Nature Genetics. 19: 292-6. PMID 9662408 DOI: 10.1038/985 |
0.423 |
|
| 1998 |
Wright JA, Keegan KS, Herendeen DR, Bentley NJ, Carr AM, Hoekstra MF, Concannon P. Protein kinase mutants of human ATR increase sensitivity to UV and ionizing radiation and abrogate cell cycle checkpoint control. Proceedings of the National Academy of Sciences of the United States of America. 95: 7445-50. PMID 9636169 DOI: 10.1073/Pnas.95.13.7445 |
0.314 |
|
| 1998 |
Cerosaletti KM, Lange E, Stringham HM, Weemaes CMR, Smeets D, Sölder B, Belohradsky BH, Taylor AMR, Karnes P, Elliott A, Komatsu K, Gatti RA, 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. 63: 125-134. PMID 9634525 DOI: 10.1086/301927 |
0.363 |
|
| 1998 |
Varon R, Vissinga C, Platzer M, Cerosaletti KM, Chrzanowska KH, Saar K, Beckmann G, Seemanová E, Cooper PR, Nowak NJ, Stumm M, Weemaes CMR, Gatti RA, Wilson RK, Digweed M, ... ... Concannon P, et al. Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome Cell. 93: 467-476. PMID 9590180 DOI: 10.1016/S0092-8674(00)81174-5 |
0.374 |
|
| 1998 |
Telatar M, Teraoka S, Wang Z, Chun HH, Liang T, Castellvi-Bel S, Udar N, Borresen-Dale AL, Chessa L, Bernatowska-Matuszkiewicz E, Porras O, Watanabe M, Junker A, Concannon P, Gatti RA. Ataxia-telangiectasia: identification and detection of founder-effect mutations in the ATM gene in ethnic populations. American Journal of Human Genetics. 62: 86-97. PMID 9443866 DOI: 10.1086/301673 |
0.336 |
|
| 1997 |
Chen X, Yang L, Udar N, Liang T, Uhrhammer N, Xu S, Bay JO, Wang Z, Dandakar S, Chiplunkar S, Klisak I, Telatar M, Yang H, Concannon P, Gatti RA. CAND3: A ubiquitously expressed gene immediately adjacent and in opposite transcriptional orientation to the ATM gene at 1lq23.1. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 8: 129-33. PMID 27518307 DOI: 10.1007/S003359900371 |
0.371 |
|
| 1997 |
Concannon P, Gatti RA. Diversity of ATM gene mutations detected in patients with ataxia- telangiectasia Human Mutation. 10: 100-107. PMID 9259193 DOI: 10.1002/(Sici)1098-1004(1997)10:2<100::Aid-Humu2>3.0.Co;2-O |
0.341 |
|
| 1997 |
Kovats S, Whiteley PE, Concannon P, Rudensky AY, Blum JS. Presentation of abundant endogenous class II DR-restricted antigens by DM-negative B cell lines. European Journal of Immunology. 27: 1014-21. PMID 9130658 DOI: 10.1002/Eji.1830270431 |
0.301 |
|
| 1997 |
Wei S, Charmley P, Concannon P. Organization, polymorphism, and expression of the human T-cell receptor AV1 subfamily. Immunogenetics. 45: 405-12. PMID 9089098 DOI: 10.1007/S002510050222 |
0.391 |
|
| 1997 |
Wei S, Concannon P. Repertoire and organization of human T-cell receptor alpha region variable genes. Genomics. 38: 442-5. PMID 8975726 DOI: 10.1006/Geno.1996.0652 |
0.378 |
|
| 1996 |
Vissinga C, Springmeyer SC, Concannon P. TCR expression and clonality analysis in pulmonary sarcoidosis. Human Immunology. 48: 98-106. PMID 8824578 DOI: 10.1016/0198-8859(96)00078-X |
0.313 |
|
| 1996 |
Yamagata K, Takeda J, Menzel S, Chen X, Eng S, Lim LR, Concannon P, Hanis CL, Spielman RS, Cox NJ, Bell GI. Searching for NIDDM susceptibility genes: Studies of genes with triplet repeats expressed in skeletal muscle Diabetologia. 39: 725-730. PMID 8781769 DOI: 10.1007/Bf00418545 |
0.405 |
|
| 1996 |
Wapelhorst B, Bell GI, Risch N, Spielman RS, Concannon P. Linkage and association studies in insulin-dependent diabetes with a new dinucleotide repeat polymorphism at the GAD65 locus. Autoimmunity. 21: 127-30. PMID 8679901 DOI: 10.3109/08916939508993360 |
0.456 |
|
| 1996 |
Hanis CL, Boerwinkle E, Chakraborty R, Ellsworth DL, Concannon P, Stirling B, Morrison VA, Wapelhorst B, Spielman RS, Gogolin-Ewens KJ, Shephard JM, Williams SR, Risch N, Hinds D, Iwasaki N, et al. A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2 Nature Genetics. 13: 161-166. PMID 8640221 DOI: 10.1038/Ng0696-161 |
0.409 |
|
| 1996 |
Gambino V, Menzel S, Trabb JB, Xiang KS, Lindner T, Louït A, Chen E, Mereu LE, Furuta H, Iwasaki N, Kawamura M, Omori Y, Rietzsch H, Schulze J, Schröder HE, ... Concannon P, et al. 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. 45: 291-294. PMID 8593932 DOI: 10.2337/Diab.45.3.291 |
0.413 |
|
| 1995 |
Stirling B, Cox NJ, Bell GI, Hanis CL, Spielman RS, Concannon P. Linkage studies in NIDDM with markers near the sulphonylurea receptor gene Diabetologia. 38: 1479-1481. PMID 8786023 DOI: 10.1007/Bf00400610 |
0.413 |
|
| 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 β-Chain Gene Complex Genomics. 29: 760-765. PMID 8575771 DOI: 10.1006/Geno.1995.9940 |
0.545 |
|
| 1995 |
Wei S, Concannon P. Identification of a novel human T-cell receptor V beta subfamily by genomic cloning. Human Immunology. 41: 201-6. PMID 7868375 DOI: 10.1016/0198-8859(94)90037-X |
0.389 |
|
| 1995 |
Charmley P, Keretan E, Snyder K, Clark EA, Concannon P. Relative size and evolution of the germline repertoire of T-cell receptor β-chain gene segments in nonhuman primates Genomics. 25: 150-156. PMID 7774912 DOI: 10.1016/0888-7543(95)80120-B |
0.38 |
|
| 1995 |
Tsaur ML, Menzel S, Lai FP, Espinosa R, Concannon P, Spielman RS, Hanis CL, Cox NJ, Le Beau MM, German MS. 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. 44: 592-6. PMID 7729621 DOI: 10.2337/Diab.44.5.592 |
0.336 |
|
| 1995 |
Charmley P, Concannon P. PCR-based genotyping and haplotype analysis of human TCRBV gene segment polymorphisms Immunogenetics. 42: 254-261. PMID 7672819 DOI: 10.1007/Bf00176442 |
0.438 |
|
| 1995 |
Rowe RE, Wapelhorst B, Bell GI, Risch N, Spielman RS, Concannon P. Linkage and association between insulin-dependent diabetes mellitus (IDDM) susceptibility and markers near the glucokinase gene on chromosome 7. Nature Genetics. 10: 240-2. PMID 7663523 DOI: 10.1038/Ng0695-240 |
0.413 |
|
| 1995 |
Charmley P, Nepom BS, 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. 756: 444-446. PMID 7645870 DOI: 10.1111/J.1749-6632.1995.Tb44558.X |
0.372 |
|
| 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. 756: 307-9. PMID 7645847 DOI: 10.1111/J.1749-6632.1995.Tb44528.X |
0.387 |
|
| 1995 |
Concannon P, Robinson MA. Human T-cell receptor gene nomenclature Annals of the New York Academy of Sciences. 756: 124-129. PMID 7645818 DOI: 10.1111/J.1749-6632.1995.Tb44497.X |
0.328 |
|
| 1995 |
Stirling B, Cox NJ, Bell GI, Hanis CL, Spielman RS, Concannon P. Identification of microsatellite markers near the human ob gene and linkage studies in NIDDM-affected sib pairs Diabetes. 44: 999-1001. PMID 7622007 DOI: 10.2337/Diab.44.8.999 |
0.417 |
|
| 1994 |
Wei S, Charmley P, Robinson MA, Concannon P. The extent of the human germline T-cell receptor V beta gene segment repertoire Immunogenetics. 40: 27-36. PMID 8206523 DOI: 10.1007/Bf00163961 |
0.368 |
|
| 1994 |
Charmley P, Nepom BS, Concannon P. HLA and T cell receptor β-chain DNA polymorphisms identify a distinct subset of patients with pauciarticular-onset juvenile rheumatoid arthritis Arthritis & Rheumatism. 37: 695-701. PMID 8185696 DOI: 10.1002/Art.1780370513 |
0.328 |
|
| 1994 |
Posnett DN, Vissinga CS, Pambuccian C, Wei S, Robinson MA, 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. Journal of Experimental Medicine. 179: 1707-1711. PMID 8163948 DOI: 10.1084/Jem.179.5.1707 |
0.415 |
|
| 1994 |
Telatar M, Concannon P, Tolun A. Dinucleotide repeat polymorphism at the NCAM locus. Human Molecular Genetics. 3: 842-842. PMID 8081382 DOI: 10.1093/Hmg/3.5.842 |
0.351 |
|
| 1994 |
Telatar M, Concannon P, Tolun A. Dinucleotide repeat polymorphism at 11q23 Human Genetics. 94: 109-109. PMID 8034289 DOI: 10.1007/Bf02272856 |
0.36 |
|
| 1993 |
Charmley P, Concannon P. Polymorphism and phylogeny of dinucleotide repeats in human T-cell receptor Vb6 genes Immunogenetics. 38: 92-97. PMID 8482584 DOI: 10.1007/Bf00190896 |
0.429 |
|
| 1993 |
Charmley P, Wei S, Concannon P. Polymorphisms in the Tcrb-V2 gene segments localize the Tcrb orphon genes to human chromosome 9p21. Immunogenetics. 38: 283-6. PMID 8319978 DOI: 10.1007/Bf00188805 |
0.346 |
|
| 1992 |
Malhotra U, Concannon P. T Cell Receptor β Gene Polymorphism and Rheumatoid Arthritis Autoimmunity. 12: 75-77. PMID 1352153 DOI: 10.3109/08916939209150312 |
0.342 |
|
| 1992 |
Funkhouser SW, Concannon P, Charmley P, Vredevoe DL, Hood L. Differences in T cell receptor restriction fragment length polymorphisms in patients with rheumatoid arthritis Arthritis and Rheumatism. 35: 465-471. PMID 1348938 DOI: 10.1002/Art.1780350417 |
0.512 |
|
| 1991 |
Nepom BS, Malhotra U, Schwarz DA, Nettles JW, Schaller JG, Concannon P. HLA and T cell receptor polymorphisms in pauciarticular-onset juvenile rheumatoid arthritis. Arthritis & Rheumatism. 34: 1260-1267. PMID 1930315 DOI: 10.1002/Art.1780341009 |
0.391 |
|
| 1991 |
Wright JA, Hood L, Concannon P. Human T-cell receptor V alpha gene polymorphism. Human Immunology. 32: 277-83. PMID 1686027 DOI: 10.1016/0198-8859(91)90091-M |
0.414 |
|
| 1991 |
Charmley P, Beall SS, Concannon P, Hood L, Gatti RA. Further localization of a multiple sclerosis susceptibility gene on chromosome 7q using a new T cell receptor beta-chain DNA polymorphism Journal of Neuroimmunology. 32: 231-240. PMID 1674514 DOI: 10.1016/0165-5728(91)90193-B |
0.359 |
|
| 1990 |
Charmley P, Concannon P, Gatti RA. T-cell receptor β-chain DNA polymorphism frequencies in healthy HLA-DR homozygotes Tissue Antigens. 35: 157-164. PMID 2371713 DOI: 10.1111/J.1399-0039.1990.Tb01773.X |
0.35 |
|
| 1990 |
Charmley P, Foroud T, Wei S, Concannon P, Weeks DE, Lange K, Gatti RA. A primary linkage map of the human chromosome 11q22-23 region Genomics. 6: 316-323. PMID 2307473 DOI: 10.1016/0888-7543(90)90572-C |
0.341 |
|
| 1990 |
Charmley P, Chao A, Concannon P, Hood L, Gatti RA. Haplotyping the human T-cell receptor β-chain gene complex by use of restriction fragment length polymorphisms Proceedings of the National Academy of Sciences of the United States of America. 87: 4823-4827. PMID 1972281 DOI: 10.1073/Pnas.87.12.4823 |
0.327 |
|
| 1990 |
Malhotra U, Concannon P. An anonymous marker [HGM provisional #D11S415] maps to human chromosome 11 near the catalase (CAT) gene. Nucleic Acids Research. 18: 386-386. PMID 1970166 DOI: 10.1093/Nar/18.2.386 |
0.309 |
|
| 1989 |
Gatti RA, Berkel I, Boder E, Braedt G, Charmley P, Concannon P, Ersoy F, Foroud T, Jaspers NG, Lange K. Localization of an ataxia-telangiectasia gene to chromosome 11q22-23. Nature. 336: 577-80. PMID 3200306 DOI: 10.1038/336577A0 |
0.397 |
|
| 1989 |
Freimark B, Pickering L, Concannon P, Fox R. Nucleotide sequence of a uniquely expressed human T cell receptor β chain variable region gene (Vβ) in siogren's syndrome Nucleic Acids Research. 17: 455. PMID 2911483 DOI: 10.1093/Nar/17.1.455 |
0.338 |
|
| 1989 |
Beall SS, Concannon P, Charmley P, McFarland HF, Gatti RA, Hood LE, McFarlin DE, Biddison WE. The germline repertoire of T cell receptor beta-chain genes in patients with chronic progressive multiple sclerosis. Journal of Neuroimmunology. 21: 59-66. PMID 2562801 DOI: 10.1016/0165-5728(89)90159-8 |
0.318 |
|
| 1989 |
Malhotra U, Concannon P. Human T-cell receptor CD3-δ (CD3D) / MspI DNA polymorphism Nucleic Acids Research. 17: 2373-2373. PMID 2468134 DOI: 10.1093/Nar/17.6.2373 |
0.322 |
|
| 1989 |
Charmley P, Wei S, Sanal O, Malhotra U, Concannon P, Terhorst C, Gatti RA. Human T-cell receptor cd3-γ (CD3G) / MspI DNA polymorphism Nucleic Acids Research. 17: 2372. PMID 2468133 DOI: 10.1093/Nar/17.6.2372 |
0.322 |
|
| 1989 |
Fox RI, Freimark BD, Servenius B, Shun-le C, Concannon P. Genetic polymorphisms and DNA sequences of T-cell antigen receptors and histocompatible antigen genes in primary Sjogren's syndrome Journal of Autoimmunity. 2: 600-601. DOI: 10.1016/0896-8411(89)90234-5 |
0.385 |
|
| 1988 |
Wilson RK, Lai E, Concannon P, Barth RK, Hood LE. Structure, organization and polymorphism of murine and human T-cell receptor alpha and beta chain gene families. Immunological Reviews. 101: 149-72. PMID 2965094 DOI: 10.1111/J.1600-065X.1988.Tb00736.X |
0.332 |
|
| 1986 |
Klein MH, Concannon P, Everett M, Kim LDH, Hunkapiller T, Hood L. Diversity and structure of human T-cell receptor alpha-chain variable region genes Proceedings of the National Academy of Sciences of the United States of America. 83: 6598-6602. PMID 3502713 DOI: 10.1073/Pnas.84.19.6884 |
0.461 |
|
| 1986 |
Concannon P, Lai E, Klein M, Siu S, Strauss E, Pickering L, Kung P, Gatti R, Hood L. Human T-cell receptor genes: organization, diversity, and polymorphism. Cold Spring Harbor Symposia On Quantitative Biology. 51: 785-795. PMID 3472761 DOI: 10.1101/Sqb.1986.051.01.091 |
0.446 |
|
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