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Kristina L. Allen-Brady, Ph.D. - Publications

Affiliations: 
2006 University of Utah, Salt Lake City, UT 
Area:
Genetics, Obstetrics and Gynecology
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41 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Cannon-Albright LA, Stevens J, Teerlink CC, Facelli JC, Allen-Brady K, Welm AL. A Rare Variant in (rs111879470) Is Associated with Predisposition to Recurrent Breast Cancer in an Extended High-Risk Pedigree. Cancers. 15. PMID 38136396 DOI: 10.3390/cancers15245851  0.324
2021 Allen-Brady K, Chua JWF, Cuffolo R, Koch M, Sorrentino F, Cartwright R. Systematic review and meta-analysis of genetic association studies of pelvic organ prolapse. International Urogynecology Journal. PMID 33893823 DOI: 10.1007/s00192-021-04782-2  0.304
2020 Allen-Brady K, Norton PA, Jolyn Hill A, Cannon-Albright LA. Risk of Pelvic Organ Prolapse Treatment Based on Extended Family History. American Journal of Obstetrics and Gynecology. PMID 31954153 DOI: 10.1016/J.Ajog.2019.12.271  0.305
2019 Dodson MW, Allen-Brady K, Brown LM, Elliott CG, Cannon-Albright LA. Chronic Thromboembolic Pulmonary Hypertension Cases Cluster in Families. Chest. 155: 384-390. PMID 30732691 DOI: 10.1016/J.Chest.2018.10.004  0.329
2017 Allen-Brady K, Firszt R, Fang JC, Wong J, Smith KR, Peterson KA. Population-based Familial Aggregation of Eosinophilic Esophagitis Suggests a Genetic Contribution. The Journal of Allergy and Clinical Immunology. PMID 28192145 DOI: 10.1016/J.Jaci.2016.12.979  0.348
2017 Lince SL, Kluivers KB, Cartwright R, Ruiz-Zapata AM, Kerkhof MH, Pecanka J, Kiemeney LA, Vermeulen SH, Goeman JJ, Allen-Brady K, Norton PA, Oosterwijk E, Poelmans G. Exome chip study provides novel insights into the genetics of pelvic organ prolapse European Journal of Obstetrics & Gynecology and Reproductive Biology. 211: 207-207. DOI: 10.1016/J.Ejogrb.2017.01.043  0.311
2015 Morgan TK, Allen-Brady KL, Monson MA, Leclair CM, Sharp HT, Cannon-Albright LA. Familiality analysis of provoked vestibulodynia treated by vestibulectomy supports genetic predisposition. American Journal of Obstetrics and Gynecology. PMID 26627726 DOI: 10.1016/J.Ajog.2015.11.019  0.368
2015 Allen-Brady K, Cannon-Albright LA, Farnham JM, Norton PA. Evidence for pelvic organ prolapse predisposition genes on chromosomes 10 and 17. American Journal of Obstetrics and Gynecology. 212: 771.e1-7. PMID 25557205 DOI: 10.1016/J.Ajog.2014.12.037  0.358
2015 Richter HE, Whitehead N, Arya L, Ridgeway B, Allen-Brady K, Norton P, Sung V, Shepherd JP, Komesu Y, Gaddis N, Fraser MO, Tan-Kim J, Meikle S, Page GP. Genetic contributions to urgency urinary incontinence in women. The Journal of Urology. 193: 2020-7. PMID 25524241 DOI: 10.1016/J.Juro.2014.12.023  0.364
2015 Norton PA, Allen-Brady K, Wu J, Egger M, Cannon-Albright L. Clinical characteristics of women with familial pelvic floor disorders. International Urogynecology Journal. 26: 401-6. PMID 25352072 DOI: 10.1007/S00192-014-2513-8  0.318
2013 Wu JM, Ward RM, Allen-Brady KL, Edwards TL, Norton PA, Hartmann KE, Hauser ER, Velez Edwards DR. Phenotyping clinical disorders: lessons learned from pelvic organ prolapse. American Journal of Obstetrics and Gynecology. 208: 360-5. PMID 23200709 DOI: 10.1016/J.Ajog.2012.11.030  0.347
2012 Teerlink C, Farnham J, Allen-Brady K, Camp NJ, Thomas A, Leachman S, Cannon-Albright L. A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q. Human Genetics. 131: 77-85. PMID 21706340 DOI: 10.1007/S00439-011-1048-Z  0.608
2011 Allen-Brady K, Cannon-Albright L, Farnham JM, Teerlink C, Vierhout ME, Van Kempen LCL, Kluivers KB, Norton PA. Identification of six loci associated with pelvic organ prolapse using genome-wide association analysis Obstetrics and Gynecology. 118: 1345-1353. PMID 22105264 DOI: 10.1097/Aog.0B013E318236F4B5  0.423
2011 Lin WY, Camp NJ, Cannon-Albright LA, Allen-Brady K, Balasubramanian S, Reed MW, Hopper JL, Apicella C, Giles GG, Southey MC, Milne RL, Arias-Pérez JI, Menéndez-Rodríguez P, Benítez J, Grundmann M, et al. A role for XRCC2 gene polymorphisms in breast cancer risk and survival. Journal of Medical Genetics. 48: 477-84. PMID 21632523 DOI: 10.1136/Jmedgenet-2011-100018  0.586
2011 Allen-Brady K, Cai G, Cannon D, Robison R, McMahon WM, Coon H, Buxbaum JD. No evidence for IL1RAPL1 involvement in selected high-risk autism pedigrees from the AGRE data set. Autism Research : Official Journal of the International Society For Autism Research. 4: 293-6. PMID 21491612 DOI: 10.1002/Aur.195  0.413
2011 Allen-Brady K, Camp NJ. Genetic distance and markers used in linkage mapping. Methods in Molecular Biology (Clifton, N.J.). 713: 43-53. PMID 21153610 DOI: 10.1007/978-1-60327-416-6_4  0.549
2010 Coon H, Villalobos ME, Robison RJ, Camp NJ, Cannon DS, Allen-Brady K, Miller JS, McMahon WM. Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigrees. Molecular Autism. 1: 8. PMID 20678250 DOI: 10.1186/2040-2392-1-8  0.504
2010 Cannon DS, Miller JS, Robison RJ, Villalobos ME, Wahmhoff NK, Allen-Brady K, McMahon WM, Coon H. Genome-wide linkage analyses of two repetitive behavior phenotypes in Utah pedigrees with autism spectrum disorders. Molecular Autism. 1: 3. PMID 20678246 DOI: 10.1186/2040-2392-1-3  0.384
2010 Allen-Brady K, Cannon D, Robison R, McMahon WM, Coon H. A unified theory of autism revisited: Linkage evidence points to chromosome X using a high-risk subset of AGRE families Autism Research. 3: 47-52. PMID 20437600 DOI: 10.1002/Aur.119  0.406
2010 Allen-Brady K, Robison R, Cannon D, Varvil T, Villalobos M, Pingree C, Leppert MF, Miller J, McMahon WM, Coon H. Genome-wide linkage in Utah autism pedigrees. Molecular Psychiatry. 15: 1006-15. PMID 19455147 DOI: 10.1038/Mp.2009.42  0.377
2009 Piccolo SR, Abo RP, Allen-Brady K, Camp NJ, Knight S, Anderson JL, Horne BD. Evaluation of genetic risk scores for lipid levels using genome-wide markers in the Framingham Heart Study. Bmc Proceedings. 3: S46. PMID 20018038 DOI: 10.1186/1753-6561-3-S7-S46  0.7
2009 Allen-Brady K, Farnham JM, Camp NJ, Karlins E, Ostrander EA, Cannon-Albright LA. No evidence of BRCA2 mutations in chromosome 13q-linked Utah high-risk prostate cancer pedigrees. Bmc Research Notes. 2: 94. PMID 19476645 DOI: 10.1186/1756-0500-2-94  0.54
2009 Gaudet MM, Milne RL, Cox A, Camp NJ, Goode EL, Humphreys MK, Dunning AM, Morrison J, Giles GG, Severi G, Baglietto L, English DR, Couch FJ, Olson JE, Wang X, ... ... Allen-Brady K, et al. Five polymorphisms and breast cancer risk: results from the Breast Cancer Association Consortium. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 18: 1610-6. PMID 19423537 DOI: 10.1158/1055-9965.Epi-08-0745  0.608
2009 Allen-Brady K, Norton PA, Farnham JM, Teerlink C, Cannon-Albright LA. Significant Linkage Evidence for a Predisposition Gene for Pelvic Floor Disorders on Chromosome 9q21 American Journal of Human Genetics. 84: 678-682. PMID 19393595 DOI: 10.1016/J.Ajhg.2009.04.002  0.434
2009 Shephard ND, Abo R, Rigas SH, Frank B, Lin WY, Brock IW, Shippen A, Balasubramanian SP, Reed MW, Bartram CR, Meindl A, Schmutzler RK, Engel C, Burwinkel B, Cannon-Albright LA, ... Allen-Brady K, et al. A breast cancer risk haplotype in the caspase-8 gene. Cancer Research. 69: 2724-8. PMID 19318553 DOI: 10.1158/0008-5472.Can-08-4266  0.726
2009 Allen-Brady K, Miller J, Matsunami N, Stevens J, Block H, Farley M, Krasny L, Pingree C, Lainhart J, Leppert M, McMahon WM, Coon H. A high-density SNP genome-wide linkage scan in a large autism extended pedigree. Molecular Psychiatry. 14: 590-600. PMID 18283277 DOI: 10.1038/Mp.2008.14  0.416
2008 Thomas A, Camp NJ, Farnham JM, Allen-brady K, Cannon-albright LA. Shared genomic segment analysis. Mapping disease predisposition genes in extended pedigrees using SNP genotype assays Annals of Human Genetics. 72: 279-287. PMID 18093282 DOI: 10.1111/J.1469-1809.2007.00406.X  0.615
2008 Brune CW, Korvatska E, Allen-Brady K, Cook EH, Dawson G, Devlin B, Estes A, Hennelly M, Hyman SL, McMahon WM, Munson J, Rodier PM, Schellenberg GD, Stodgell CJ, Coon H. Heterogeneous association between engrailed-2 and autism in the CPEA network. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 187-93. PMID 17948868 DOI: 10.1002/Ajmg.B.30585  0.388
2007 Allen-Brady K, Horne BD, Malhotra A, Teerlink C, Camp NJ, Thomas A. Analysis of high-density single-nucleotide polymorphism data: three novel methods that control for linkage disequilibrium between markers in a linkage analysis. Bmc Proceedings. 1: S160. PMID 18466506 DOI: 10.1186/1753-6561-1-S1-S160  0.662
2007 Curtin K, Wong J, Allen-Brady K, Camp NJ. Meta-genetic association of rheumatoid arthritis and PTPN22 using PedGenie 2.1. Bmc Proceedings. 1: S12. PMID 18466461 DOI: 10.1186/1753-6561-1-S1-S12  0.625
2007 Dupuis J, Albers K, Allen-Brady K, Cho K, Elston RC, Kappen HJ, Tang H, Thomas A, Thomson G, Tsung E, Yang Q, Zhang W, Zhao K, Zheng G, Ziegler JT. Effect of linkage disequilibrium between markers in linkage and association analyses. Genetic Epidemiology. 31: S139-48. PMID 18046770 DOI: 10.1002/Gepi.20291  0.334
2007 Curtin K, Wong J, Allen-Brady K, Camp NJ. PedGenie: meta genetic association testing in mixed family and case-control designs. Bmc Bioinformatics. 8: 448. PMID 18005446 DOI: 10.1186/1471-2105-8-448  0.576
2007 Easton DF, Deffenbaugh AM, Pruss D, Frye C, Wenstrup RJ, Allen-Brady K, Tavtigian SV, Monteiro AN, Iversen ES, Couch FJ, Goldgar DE. A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genes. American Journal of Human Genetics. 81: 873-83. PMID 17924331 DOI: 10.1086/521032  0.443
2007 Camp NJ, Farnham JM, Allen-Brady K, Cannon-Albright LA. Statistical recombinant mapping in extended high-risk Utah pedigrees narrows the 8q24 prostate cancer locus to 2.0 Mb. The Prostate. 67: 1456-64. PMID 17654497 DOI: 10.1002/Pros.20631  0.586
2007 Allen-Brady K. Genetic polymorphisms and metastatic breast cancer survival. Future Oncology (London, England). 3: 155-8. PMID 17381415 DOI: 10.2217/14796694.3.2.155  0.415
2006 Allen-Brady K, Cannon-Albright LA, Neuhausen SL, Camp NJ. A role for XRCC4 in age at diagnosis and breast cancer risk. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 15: 1306-10. PMID 16835328 DOI: 10.1158/1055-9965.Epi-05-0959  0.612
2006 Allen-Brady K, Wong J, Camp NJ. PedGenie: an analysis approach for genetic association testing in extended pedigrees and genealogies of arbitrary size. Bmc Bioinformatics. 7: 209. PMID 16620382 DOI: 10.1186/1471-2105-7-209  0.631
2005 Allen-Brady K, Camp NJ. Characterization of the linkage disequilibrium structure and identification of tagging-SNPs in five DNA repair genes. Bmc Cancer. 5: 99. PMID 16091150 DOI: 10.1186/1471-2407-5-99  0.629
2005 Allen-Brady K, Camp NJ, Ward JH, Cannon-Albright LA. Lobular breast cancer: excess familiality observed in the Utah Population Database. International Journal of Cancer. 117: 655-61. PMID 15929077 DOI: 10.1002/Ijc.21236  0.603
2003 Allen-Brady K, Farnham JM, Weiler J, Camp NJ. A cautionary note on the appropriateness of using a linkage resource for an association study. Bmc Genetics. 4: S89. PMID 14975157 DOI: 10.1186/1471-2156-4-S1-S89  0.602
2002 Beddhu S, Allen-Brady K, Cheung AK, Horne BD, Bair T, Muhlestein JB, Anderson JL. Impact of renal failure on the risk of myocardial infarction and death. Kidney International. 62: 1776-83. PMID 12371979 DOI: 10.1046/J.1523-1755.2002.00629.X  0.435
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