KRISTINA LISA ALLEN BRADY portrait
  • Adjunct Associate Professor, Family And Preventive Medicine
  • Research Associate Professor, Internal Medicine
801-585-5333

Presentations

  • International Urogynecology Annual Meeting. "Genomics: How Far Have we Come? Pedictions for the Next Decade". Virtual Meeting. , Presented, 2020.
  • "Genetic epidemiology methods and their application in autism", Utah Department of Health; Maternal, Child Health Epidemiology Network meeting. , , 2009.
  • "Genetic epidemiology methods and their application in autism", Biology Seminar Series, Utah Valley University. , , 2008.
  • “PedGenie: An analysis tool for genetic association testing in extended pedigrees and genealogies of arbitrary size,” Ataxia-Telangiectasia American Society of Human Genetics Satellite Meeting, Salt Lake City, UT. , , 2005.
  • "Exercise and the Hemodialysis Patient", National Kidney Foundation meeting for patients with end stage renal disease; Salt Lake City, UT. , , 1997.
  • “Dialyzed and Revitalized - Exercise for the Dialysis Patient”, University of Utah Dialysis Program annual retreat for dialysis staff; Park City, UT. , , 1996.
  • Significant linkage evidence for interstitial cystitis/painful bladder syndrome on chromosome 3. American Urological Association (AUA) 112th Annual Scientific Meeting, Boston, Massachusetts, May12-16, 2017. , , 2017.
  • Significant evidence of linkage for early onset pelvic organ prolapse on chromosome 11. American Urogynecologic Society, 34th Annual Scientific Meeting, Seattle, Washington, October 2015. , , 2015.
  • Genetic Influence on Risk Factors for Pelvic Organ Prolapse. American Urogynecologic Society, 34th Annual Scientific Meeting, Seattle, Washington, October 2015. , , 2015.
  • Urgency urinary incontinence genome-wide association study. American Urogynecologic Society, 33rd Annual Scientific Meeting, Washington D.C., July 2014. , , 2014.
  • Risk of associated conditions in first-degree relatives of subjects with urological chronic pelvic pain syndrome. American Urogynecologic Society, 32nd Annual Scientific Meeting, Las Vegas, Nevada, October 16-19, 2013. , , 2013.
  • Familial pelvic floor disorder cases are more likely to have a mixed phenotype. American Urogynecologic Society, 32nd Annual Scientific Meeting, Providence, Rhode Island, September 15-17, 2011. , , 2011.
  • Genetic Determinants of Stress Urinary Incontinence in Women. Annual International Continence Society Meeting, Toronto, Canada. , , 2011.
  • Population-based description of familial clustering in overactive bladder (OAB). Society for Urodynamics and Female Urology. (Oral Poster). Phoenix, Arizona, March 1-5, 2011. , , 2011.
  • Significant genome-wide association analysis in pelvic organ prolapse. "Voted best overall presentation" at the American Urogynecologic Society, 31st Annual Meeting, Long Beach, California, September 29-October 2, 2010. , , 2010.
  • Significant Linkage Evidence for a Pelvic Floor Predisposition Gene on Chromosome 9. Voted "Best non-clinical research presentation award" for the 38th Annual International Continence Society Meeting, Egypt, Cairo, October 20-24, 2008. , , 2008.
  • Significant Linkage Evidence for a Pelvic Floor Predisposition Gene on Chromosome 9. Received "Basic Science Award" at the American Urogynecologic Society, 29th Annual Scientific Meeting, Chicago, IL, September 4th-6th, 2008. , , 2008.
  • "Cancer risk at sites other than the breast among relatives of lobular breast cancer probands." Allen-Brady K & Cannon-Albright LA, co-authors. Presented at Building Interdisciplinary Research Careers in Women's Health Conference, University of Utah, Salt Lake City, UT. , , 2007.
  • “Evaluation of an Empirical Association Method in Extended Pedigrees”, National Library of Medicine Training Director’s Meeting, Bethesda, Maryland. , , 2003.
  • “Predictors of functional ability at baseline in the Hemodialysis (HEMO) Study”, American Society of Nephrology, Miami, Florida. , , 1999.
  • Norton P, Allen-Brady K, Cannon-Albright LA. Significant linkage evidence for pelvic organ prolapse on chromosome 10q26 [Oral poster]. Poster session presented at International Continence Society (ICS) Meeting, Beijing China, October 15-19, 2012. Poster, Presented, 2012.
  • Norton P, Allen-Brady K, Cannon-Albright LA. Familiality of lower urinary tract symptom disorders [Oral poster]. Poster session presented at International Continence Society (ICS) Meeting, Beijing, China, October 15-19, 2012. Poster, Presented, 2012.
  • Allen-Brady K, Cannon-Albright LA, Norton P. Significant linkage evidence for pelvic organ prolapse on chromosome 10q26 [Oral poster]. Poster session presented at American Urogynecologic Society 33rd Annual Scientific Meeting, Chicago, IL, October 3-6, 2012. Poster, Presented, 2012.
  • Allen-Brady K, Norton P, Cannon-Albright LA. Familiality of lower urinary tract symptom disorders [Oral poster]. Poster session presented at American Urogynecologic Society 33rd Annual Scientific Meeting, Chicago, IL, October 3-6, 2012. Poster, Presented, 2012.
  • Norton P, Allen-Brady K, Cannon-Albright LA. Familial pelvic floor disorder cases are more likely to have a mixed phenotype. Poster session presented at International Continence Society (ICS) Annual Scientific Meeting, Glasgow, United Kingdom, August 29 - September 2, 2011. Poster, Presented, 2011.
  • Allen-Brady K, Cannon D, Robison R, McMahon WM, Coon H.. A unified theory of autism revisited: Linkage evidence points to the IL1RAPL1 gene using a high-risk subset of AGRE families. Poster session presented at American Society of fHiman Genetics Meeting, October 20-24, 2009, Honolulu, Hawaii. Poster, Presented, 2009.
  • Cannon D, McMahon WM, Allen-Brady K, Miller J, Robison R, and Coon H.. Chromosome 15 linkage analysis of two repetitive behavior phenotypes in Utah pedigrees with autism spectrum disorders. Poster session presented at American Society of Human Genetics Meeting, Honolulu, Hawaii. Poster, Presented, 2009.

Languages

  • English, Fluent.

Publications

  • Allen-Brady K, Farnham JM, Weiler J, Camp NJ (date unknown). A cautionary note on the appropriateness of using a linkage resource for an association study. Vol. 4 Suppl 1, S89. Accepted, .
  • Piccolo SR, Abo RP, Allen-Brady K, Camp NJ, Knight S, Anderson JL, Horne BD (date unknown). Evaluation of genetic risk scores for lipid levels using genome-wide markers in the Framingham Heart Study. Vol. 3 Suppl 7, S46. Accepted, .
  • Allen-Brady K, Cannon-Albright L, Farnham JM, Teerlink C, Vierhout ME, van Kempen LCL, Kluivers KB, Norton PA (date unknown). Identification of six loci associated with pelvic organ prolapse using genome-wide association analysis. Vol. 118, 1345-1353. Accepted, .
  • Allen-Brady K, Farnham J, Cannon-Albright L (date unknown). Strategies for selection of subjects for sequencing after detection of a linkage peak. Vol. 5 Suppl 9, S77. Accepted, .
  • Allen-Brady K, Camp NJ, Ward JH, Cannon-Albright LA (date unknown). Lobular breast cancer: excess familiality observed in the Utah Population Database. Vol. 117, 655-61. Accepted, .
  • Peterson K, Clayton F, Qeadan F, Gorman D, Robson J, Allen-Brady K, Fang JC (date unknown). Esophageal Eosinophilia Is Common Among Relatives of Eosinophilic Esophagitis Patients. Accepted, .
  • Curtin K, Wong J, Allen-Brady K, Camp NJ (date unknown). PedGenie: meta genetic association testing in mixed family and case-control designs. Vol. 8, 448. Accepted, .
  • Krikov S, Price RC, Allen-Brady K, Cannon-Albright L, Facelli JC (date unknown). Enabling GeneHunter as a grid service: a case study for implementing analytical services for biomedical grids. 1014. Accepted, .
  • Wirostko BM, Curtin K, Ritch R, Thomas S, Allen-Brady K, Smith KR, Hageman GS, Allingham RR (date unknown). Risk for Exfoliation Syndrome in Women With Pelvic Organ Prolapse : A Utah Project on Exfoliation Syndrome (UPEXS) Study. Vol. 134, 1255-1262. Accepted, .
  • Easton DF, Deffenbaugh AM, Pruss D, Frye C, Wenstrup RJ, Allen-Brady K, Tavtigian SV, Monteiro AN, Iversen ES, Couch FJ, Goldgar DE (date unknown). A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genes. Vol. 81, 873-83. Accepted, .
  • Beddhu S, Allen-Brady K, Cheung AK, Horne BD, Bair T, Muhlestein JB, Anderson JL (date unknown). Impact of renal failure on the risk of myocardial infarction and death. Vol. 62, 1776-83. Accepted, .
  • Allen-Brady K, Firszt R, Fang JC, Wong J, Smith KR, Peterson KA (date unknown). Population-based familial aggregation of eosinophilic esophagitis suggests a genetic contribution. Vol. 140, 1138-1143. Accepted, .
  • Lee S, Piccolo SR, Allen-Brady K (date unknown). Robust meta-analysis shows that glioma transcriptional subtyping complements traditional approaches. Vol. 37, 317-29. Accepted, .
  • Allen-Brady K, Robison R, Cannon D, Varvil T, Villalobos M, Pingree C, Leppert MF, Miller J, McMahon WM, Coon H (date unknown). Genome-wide linkage in Utah autism pedigrees. Vol. 15, 1006-15. Accepted, .
  • Allen BG, Allen-Brady K, Weeks DL (date unknown). Reduction of XNkx2-10 expression leads to anterior defects and malformation of the embryonic heart. Vol. 123, 719-29. Accepted, .
  • Camp NJ, Farnham JM, Allen-Brady K, Cannon-Albright LA (date unknown). Statistical recombinant mapping in extended high-risk Utah pedigrees narrows the 8q24 prostate cancer locus to 2.0 Mb. Vol. 67, 1456-64. Accepted, .
  • Peterson K, Firszt R, Fang J, Wong J, Smith KR, Allen-Brady K (date unknown). Risk of autoimmunity in EoE and families - A population-based cohort study. Vol. 111, 926-32. Accepted, .
  • Allen-Brady K, Camp NJ (date unknown). Characterization of the linkage disequilibrium structure and identification of tagging-SNPs in five DNA repair genes. Vol. 5, 99. Accepted, .
  • Robson J, Korgenski K, Parsons K, McClain A, Barbagelata C, Allen-Brady K, Patel R, O'Gorman M, Peterson K, Guthery S (date unknown). Sensitivity and Specificity of Administrative Medical Coding for Pediatric Eosinophilic Esophagitis. Vol. 69, e49-e53. Accepted, .
  • Allen-Brady K, Cai G, Cannon D, Robison R, McMahon WM, Coon H, Buxbaum JD (date unknown). No evidence for IL1RAPL1 involvement in selected high-risk autism pedigrees from the AGRE data set. Vol. 4, 293-6. Accepted, .
  • Allen-Brady K, Norton PA, Hill AJ, Rowe K, Cannon-Albright LA (date unknown). Risk of pelvic organ prolapse treatment based on extended family history. Vol. 223, 105.e1-105.e8. Accepted, .
  • Allen-Brady K, Farnham J, Cannon-Albright LA (date unknown). Strategies for selection of subjects for sequencing after detection of a linkage peak. Vol. 5, S77. Accepted, .
  • 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, Dubrowinskaja N, Park-Simon TW, Dörk T, Garcia-Closas M, Figueroa J, Sherman M, Lissowska J, Easton DF, Dunning AM, Rajaraman P, Sigurdson AJ, Doody MM, Linet MS, Pharoah PD, Schmidt MK, Cox A (date unknown). A role for XRCC2 gene polymorphisms in breast cancer risk and survival. Vol. 48, 477-84. Accepted, .
  • Allen-Brady K, Cannon-Albright LA, Neuhausen SL, Camp NJ (date unknown). A role for XRCC4 in age at diagnosis and breast cancer risk. Vol. 15, 1306-10. Accepted, .
  • Kim SH, Lee S, Piccolo SR, Allen-Brady K, Park EJ, Chun JN, Kim TW, Cho NH, Kim IG, So I, Jeon JH (date unknown). Menthol induces cell-cycle arrest in PC-3 cells by down-regulating G2/M genes, including polo-like kinase 1. Vol. 422, 436-41. Accepted, .
  • 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, Pelvic Floor Disorders Network. (date unknown). Genetic contributions to urgency urinary incontinence in women. Vol. 193, 2020-7. Accepted, .
  • Allen-Brady K, Cannon-Albright LA, Farnham JM, Norton PA (date unknown). Evidence for pelvic organ prolapse predisposition genes on chromosomes 10 and 17. Vol. 212, 771.e1-7. Accepted, .
  • 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 (date unknown). A high-density SNP genome-wide linkage scan in a large autism extended pedigree. Vol. 14, 590-600. Accepted, .
  • Allen-Brady K, Farnham JM, Camp NJ, Karlins E, Ostrander EA, Cannon-Albright LA (date unknown). No evidence of BRCA2 mutations in chromosome 13q-linked Utah high-risk prostate cancer pedigrees. Vol. 2, 94. Accepted, .
  • Morgan TK, Allen-Brady KL, Monson MA, Leclair CM, Sharp HT, Cannon-Albright LA (date unknown). Familiality analysis of provoked vestibulodynia treated by vestibulectomy supports genetic predisposition. Vol. 214, 609.e1-7. Accepted, .
  • Wu JM, Ward RM, Allen-Brady KL, Edwards TL, Norton PA, Hartmann KE, Hauser ER, Velez Edwards DR (date unknown). Phenotyping clinical disorders: lessons learned from pelvic organ prolapse. Vol. 208, 360-5. Accepted, .
  • Allen-Brady K, Norton PA, Farnham JM, Teerlink C, Cannon-Albright LA (date unknown). Significant linkage evidence for a predisposition gene for pelvic floor disorders on chromosome 9q21. Vol. 84, 678-82. Accepted, .
  • 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, Chang-Claude J, Flesch-Janys D, Abbas S, Salazar R, Mannermaa A, Kataja V, Kosma VM, Lindblom A, Margolin S, Heikkinen T, Kämpjärvi K, Aaltonen K, Nevanlinna H, Bogdanova N, Coinac I, Schürmann P, Dörk T, Bartram CR, Schmutzler RK, Tchatchou S, Burwinkel B, Brauch H, Torres D, Hamann U, Justenhoven C, Ribas G, Arias JI, Benitez J, Bojesen SE, Nordestgaard BG, Flyger HL, Peto J, Fletcher O, Johnson N, Dos Santos Silva I, Fasching PA, Beckmann MW, Strick R, Ekici AB, Broeks A, Schmidt MK, van Leeuwen FE, Van't Veer LJ, Southey MC, Hopper JL, Apicella C, Haiman CA, Henderson BE, Le Marchand L, Kolonel LN, Kristensen V, Grenaker Alnaes G, Hunter DJ, Kraft P, Cox DG, Hankinson SE, Seynaeve C, Vreeswijk MP, Tollenaar RA, Devilee P, Chanock S, Lissowska J, Brinton L, Peplonska B, Czene K, Hall P, Li Y, Liu J, Balasubramanian S, Rafii S, Reed MW, Pooley KA, Conroy D, Baynes C, Kang D, Yoo KY, Noh DY, Ahn SH, Shen CY, Wang HC, Yu JC, Wu PE, Anton-Culver H, Ziogoas A, Egan K, Newcomb P, Titus-Ernstoff L, Trentham Dietz A, Sigurdson AJ, Alexander BH, Bhatti P, Allen-Brady K, Cannon-Albright LA, Wong J, Australian Ovarian Cancer Study Group., Chenevix-Trench G, Spurdle AB, Beesley J, Pharoah PD, Easton DF, Garcia-Closas M, Breast Cancer Association Consortium. (date unknown). Five polymorphisms and breast cancer risk: results from the Breast Cancer Association Consortium. Vol. 18, 1610-6. Accepted, .
  • Allen-Brady K, Chua JWF, Cuffolo R, Koch M, Sorrentino F, Cartwright R (date unknown). Systematic review and meta-analysis of genetic association studies of pelvic organ prolapse. Accepted, .
  • Allen-Brady K, Wong J, Camp NJ (date unknown). PedGenie: an analysis approach for genetic association testing in extended pedigrees and genealogies of arbitrary size. Vol. 7, 209. Accepted, .
  • Coon H, Villalobos ME, Robison RJ, Camp NJ, Cannon DS, Allen-Brady K, Miller JS, McMahon WM (date unknown). Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigrees. Vol. 1, 8. Accepted, .
  • Allen-Brady K, Cannon D, Robison R, McMahon WM, Coon H (date unknown). A unified theory of autism revisited: linkage evidence points to chromosome X using a high-risk subset of AGRE families. Vol. 3, 47-52. Accepted, .
  • 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, Camp NJ, Cox A (date unknown). A breast cancer risk haplotype in the caspase-8 gene. Vol. 69, 2724-8. Accepted, .
  • Allen-Brady K (date unknown). Genetic polymorphisms and metastatic breast cancer survival. Vol. 3, 155-8. Accepted, .
  • Brune CW, Korvatska E, Allen-Brady K, Cook EH Jr, Dawson G, Devlin B, Estes A, Hennelly M, Hyman SL, McMahon WM, Munson J, Rodier PM, Schellenberg GD, Stodgell CJ, Coon H (date unknown). Heterogeneous association between engrailed-2 and autism in the CPEA network. Vol. 147B, 187-93. Accepted, .
  • Allen-Brady K, Norton PA, Cannon-Albright L (date unknown). Risk of associated conditions in relatives of subjects with interstitial cystitis. Vol. 21, 93-8. Accepted, .
  • Norton PA, Allen-Brady K, Wu J, Egger M, Cannon-Albright L (date unknown). Clinical characteristics of women with familial pelvic floor disorders. Vol. 26, 401-6. Accepted, .
  • Norton PA, Allen-Brady K, Cannon-Albright LA (date unknown). The familiality of pelvic organ prolapse in the Utah Population Database. Vol. 24, 413-8. Accepted, .
  • Thomas A, Camp NJ, Farnham JM, Allen-Brady K, Cannon-Albright LA (date unknown). Shared genomic segment analysis. Mapping disease predisposition genes in extended pedigrees using SNP genotype assays. Vol. 72, 279-87. Accepted, .
  • Cannon DS, Miller JS, Robison RJ, Villalobos ME, Wahmhoff NK, Allen-Brady K, McMahon WM, Coon H (date unknown). Genome-wide linkage analyses of two repetitive behavior phenotypes in Utah pedigrees with autism spectrum disorders. Vol. 1, 3. Accepted, .
  • Dodson MW, Allen-Brady K, Brown LM, Elliott CG, Cannon-Albright LA (date unknown). Chronic Thromboembolic Pulmonary Hypertension Cases Cluster in Families. Vol. 155, 384-390. Accepted, .
  • Byun J, Peterson CM, Backonja U, Taylor RN, Stanford JB, Allen-Brady KL, Smith KR, Louis GMB, Schliep KC (date unknown). Adiposity and Endometriosis Severity and Typology. Vol. 27, 1516-1523. Accepted, .
  • Hemmert R, Schliep KC, Willis S, Peterson CM, Louis GB, Allen-Brady K, Simonsen SE, Stanford JB, Byun J, Smith KR (date unknown). Modifiable life style factors and risk for incident endometriosis. Vol. 33, 19-25. Accepted, .
  • Allen-Brady K, Rowe K, Cessna M, Lenherr S, Norton P (date unknown). Significant Linkage Evidence for Interstitial Cystitis/Painful Bladder Syndrome on Chromosome 3. Vol. 199, 172-177. Accepted, .
  • Teerlink C, Farnham J, Allen-Brady K, Camp NJ, Thomas A, Leachman S, Cannon-Albright L (date unknown). A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q. Vol. 131, 77-85. Accepted, .
  • Krikov S, Price RC, Matney SA, Allen-Brady K, Facelli JC (date unknown). Enabling GeneHunter as a grid service: a case study for implementing analytical services in biomedical grids. Vol. 50, 364-71. Accepted, .
  • Allen-Brady K, Camp NJ (date unknown). Genetic distance and markers used in linkage mapping. Vol. 713, 43-53. Accepted, .
  • 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 (date unknown). The Value of Large Pedigrees for Chromosome Mapping in the Era of Dense Marker Sets. Vol. 14, 9-24. Accepted, .
  • Allen-Brady K, Horne BD, Malhotra A, Teerlink C, Camp NJ, Thomas A (date unknown). Analysis of high-density single-nucleotide polymorphism data: three novel methods that control for linkage disequilibrium between markers in a linkage analysis. Vol. 1 Suppl 1, S160. Accepted, .
  • Curtin K, Wong J, Allen-Brady K, Camp NJ (date unknown). Meta-genetic association of rheumatoid arthritis and PTPN22 using PedGenie 2.1. Vol. 1 Suppl 1, S12. Accepted, .
  • 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 (date unknown). Effect of linkage disequilibrium between markers in linkage and association analyses. Vol. 31 Suppl 1, S139-48. Accepted, .
  • Allen KL, Miskulin D, Yan G, Dwyer JT, Frydrych A, Leung J, Poole D, and the Hemodialysis (HEMO) Study Group (date unknown). Association of nutritional and behavioral markers on the physical and mental health status in prevalent hemodialysis patients from the HEMO Study. Vol. 12, 160-9. Accepted, .
  • Allen KL,Gappmaier E (date unknown). Exercise Habits and Attitudes of Patients Undergoing Hemodialysis. Vol. 12, 11-16. Accepted, .
  • May Maestas M, Perry KD, Smith K, Firszt R, Allen-Brady K, Robson J, Joy E, Peterson K (date unknown). Food impactions in Eosinophilic esophagitis and acute exposures to fine particulate pollution. (pp. 2529-2530). Vol. 74. Accepted, .