Kristina Lisa Allen-Brady

Kristina Lisa Allen-Brady, PhD, MSPH, MPT

Languages spoken: English

Academic Information

Departments Primary - Internal Medicine

Divisions: Epidemiology , Public Health

Kristina Allen-Brady, PhD, MSPH, MPH, is a Research Assistant Professor at the University of Utah School of Medicine, Division of Genetic Epidemiology. As a genetic epidemiologist, her research interests include pelvic floor disorders, food allergies, autism, cancer, and development of new methods to analyze genetic data.

Allen-Brady has always been interested in research and seeking to understand the underlying causes of chronic diseases. This curiosity has led her to publish her findings in a number of different journals. She reviews frequently for different journals as well as various grant funding agencies.

 Allen-Brady received her PhD, MSPH, and MPT degrees all from the University of Utah. She is currently a member of the American Society of Human Genetics, the International Society of Genetic Epidemiology, a licensed physical therapist in the state of Utah, and serves on the University of Utah Institutional Review Board (IRB).

Education History

Postdoctoral Fellowship University of Utah, Department of Biomedical Informatics
 Postdoctoral Fellow
Postdoctoral Fellowship University of Utah
 Postdoctoral Fellow
Doctoral Training University of Utah
 PhD
Graduate Training University of Utah
 MSPH
Other Training Intermountain Healthcare
Graduate Training University of Utah
 MPT
Other Training Brigham Young University Jerusalem Center
Other Training Cambridge University
Undergraduate University of Utah
 BA

Selected Publications

Journal Article

  1. Allen-Brady K, Clayton F, Hazel MW, Stevens J, Pyne AL, Pletneva MA, Cessna M, Stubben C, Robson J, Fang J, Peterson KA (2025). Overlap of Genomic and Transcriptomic Genes Identified in Familial Eosinophilic Esophagitis. Gastroenterology. (Read full article)
  2. Allen-Brady K, Verrilli LE, Austin BA, Letourneau JM, Johnstone EB, Welt CK (2024). Turner syndrome: fertility, familial clustering, and cancer risk. Hum Reprod, 40(2), 391-396. (Read full article)
  3. Allen-Brady K, Johnstone EB, Welt CK (2024). Response to Letter to the Editor: Breast Cancer is Increased in Women with Primary Ovarian Insufficiency. J Clin Endocrinol Metab. (Read full article)
  4. Wang V, Walsh J, Zell J, Verrilli LE, Letourneau J, Johnstone EB, Allen-Brady K, Welt CK (2024). Autoimmune Disease is Increased in Women with Primary Ovarian Insufficiency. J Clin Endocrinol Metab. (Read full article)
  5. Pyne AL, Uchida AM, Hazel MW, Pletneva MA, Allen-Brady K, Peterson KA (2024). Differing Epithelial and Immunologic Activation Patterns Following Food Reintroduction Reveal Different Transcriptional Profiles in Active Eosinophilic Esophagitis. Gastroenterology. (Read full article)
  6. Barnard ME, Farland LV, Yan B, Wang J, Trabert B, Doherty JA, Meeks HD, Madsen M, Guinto E, Collin LJ, Maurer KA, Page JM, Kiser AC, Varner MW, Allen-Brady K, Pollack AZ, Peterson KR, Peterson CM, Schliep KC (2024). Endometriosis Typology and Ovarian Cancer Risk. JAMA, 332(6), 482-489. (Read full article)
  7. Allen-Brady K, Moore B, Verrilli LE, Alvord MA, Kern M, Camp N, Kelley K, Letourneau J, Cannon-Albright L, Yandell M, Johnstone EB, Welt CK (2024). Breast Cancer is Increased in Women with Primary Ovarian Insufficiency. J Clin Endocrinol Metab. (Read full article)
  8. Pyne AL, Uchida AM, Hazel MW, Stubben CJ, Chang JW, Bailey DD, Gonsalves N, Allen-Brady K, Peterson KA, Pletneva MA (2024). Effect of benralizumab on histopathology and inflammatory signatures in a clinical cohort of eosinophilic esophagitis. Dis Esophagus. (Read full article)
  9. Teixeira JB, Bortolini MAT, Silva RSP, Batista NC, Costa E Silva CL, Allen-Brady K, Castro RA (2024). The rs2018736 fibulin-5 polymorphism as a determinant for pelvic organ prolapse: a case-control study. Climacteric, 27(3), 321-325. (Read full article)
  10. Tashjian RZ, Jurynec MJ, Christy K, Stevens J, Teerlink CC, Cannon-Albright L, Allen-Brady K (2024). Identification of rare genetic variants for rotator cuff tearing and repair in high-risk pedigrees. JSES Int, 8(4), 815-821. (Read full article)
  11. Leonard ME, Horns JJ, Allen-Brady K, Ozanne EM, Wallace AS, Brooke BS, Supiano MA, Cohan JN (2024). Recurrence of severe diverticulitis is associated with age and birth decade. J Gastrointest Surg, 28(4), 507-512. (Read full article)
  12. Armon C, Cannon-Albright LA, Allen-Brady K, Wolfson S (2024). Chasing shadows: Investigating X chromosome mediation in late-onset Alzheimer's disease. Adv Neurol (Singap), 3(2). (Read full article)
  13. Cannon-Albright LA, Stevens J, Teerlink CC, Facelli JC, Allen-Brady K, Welm AL (2023). A Rare Variant in MDH2 (rs111879470) Is Associated with Predisposition to Recurrent Breast Cancer in an Extended High-Risk Pedigree. Cancers (Basel), 15(24). (Read full article)
  14. Allen-Brady K, Fyer AJ, Weissman M (2023). The multi-generational familial aggregation of interstitial cystitis, other chronic nociplastic pain disorders, depression, and panic disorder. Psychol Med, 53(16), 7847-7856. (Read full article)
  15. Verrilli LE, Allen-Brady K, Johnstone EB, Alvord MA, Welt CK (2023). Family size for women with primary ovarian insufficiency and their relatives. Hum Reprod, 38(10), 1991-1997. (Read full article)
  16. da Silva RSP, Bortolini MAT, Teixeira JB, Batista NC, Fitz FF, Allen-Brady K, Castro RA (2023). Association between the rs1036819 polymorphism of the ZFAT gene and pelvic organ prolapse: a case-control study. Int Urogynecol J, 34(10), 2611-2617. (Read full article)
  17. Schliep KC, Ghabayen L, Shaaban M, Hughes FR, Pollack AZ, Stanford JB, Brady KA, Kiser A, Peterson CM (2023). Examining the co-occurrence of endometriosis and polycystic ovarian syndrome. AJOG Glob Rep, 3(3), 100259. (Read full article)
  18. Cohan JN, Horns JJ, Ramsay JM, Huang LC, Allen-Brady K (2023). Diverticulitis Familiality: A Statewide Case-Control Study. J Am Coll Surg. (Read full article)
  19. Reddy CA, Allen-Brady K, Uchida AM, Peterson KA, Hoffman AM, Souza RF, Spechler SJ (2023). Achalasia is Strongly Associated with Eosinophilic Esophagitis and Other Allergic Disorders. Clin Gastroenterol Hepatol, 22(1), 34-41.e2. (Read full article)
  20. Cannon-Albright LA, Stevens J, Facelli JC, Teerlink CC, Allen-Brady K, Agarwal N (2023). High-Risk Pedigree Study Identifies LRBA (rs62346982) as a Likely Predisposition Variant for Prostate Cancer. Cancers (Basel), 15(7). (Read full article)
  21. Kluivers KB, Lince SL, Ruiz-Zapata AM, Post WM, Cartwright R, Kerkhof MH, Widomska J, De Witte W, Pecanka J, Kiemeney LA, Vermeulen SH, Goeman JJ, Allen-Brady K, Oosterwijk E, Poelmans G (2023). Molecular Landscape of Pelvic Organ Prolapse Provides Insights into Disease Etiology. Int J Mol Sci, 24(7). (Read full article)
  22. Cannon-Albright LA, Teerlink CC, Stevens J, Facelli JC, Carr SR, Allen-Brady K, Puri S, Bailey-Wilson JE, Musolf AM, Genetic Epidemiology of Lung Cancer Consortium, Akerley W (2023). A rare FGF5 candidate variant (rs112475347) for predisposition to nonsquamous, nonsmall-cell lung cancer. Int J Cancer, 153(2), 364-372. (Read full article)
  23. Cohan JN, Horns JJ, Hanson HA, Allen-Brady K, Kieffer MC, Huang LC, Brooke BS (2022). The Association Between Family History and Diverticulitis Recurrence: A Population-Based Study. Dis Colon Rectum, 66(2), 269-277. (Read full article)
  24. Allen-Brady K, Colletier KJ, Woller S, Eliason K, Uchida AM, Ro G, Newman M, Peterson KA (2022). Eosinophilic Gastritis and Enteritis Are Increased in Families With Eosinophilic Esophagitis. Am J Gastroenterol, 118(2), 263-268. (Read full article)
  25. Verrilli L, Johnstone E, Welt C, Allen-Brady K (2022). Primary ovarian insufficiency has strong familiality: results of a multigenerational genealogical study. Fertil Steril, 119(1), 128-134. (Read full article)
  26. Brockmeyer DL, Cheshier SH, Stevens J, Facelli JC, Rowe K, Heiss JD, Musolf A, Viskochil DH, Allen-Brady KL, Cannon-Albright LA (2022). A likely HOXC4 predisposition variant for Chiari malformations. J Neurosurg, 1-9. (Read full article)
  27. Schliep KC, Farland LV, Pollack AZ, Buck Louis G, Stanford JB, Allen-Brady K, Varner MW, Kah K, Peterson CM (2022). Endometriosis diagnosis, staging and typology and adverse pregnancy outcome history. Paediatr Perinat Epidemiol, 36(6), 771-781. (Read full article)
  28. Allen-Brady KL, Christensen MB, Sandberg AD, Pastuszak AW (2022). Significant familial clustering of Peyronie's disease in close and distant relatives. Andrology, 10(7), 1361-1367. (Read full article)
  29. Verrilli L, Johnstone E, Allen-Brady K, Welt C (2021). Shared genetics between nonobstructive azoospermia and primary ovarian insufficiency. F S Rev, 2(3), 204-213. (Read full article)
  30. Allen-Brady K, Chua JWF, Cuffolo R, Koch M, Sorrentino F, Cartwright R (2021). Systematic review and meta-analysis of genetic association studies of pelvic organ prolapse. Int Urogynecol J. (Read full article)
  31. Peterson K, Clayton F, Qeadan F, Gorman D, Robson J, Allen-Brady K, Fang JC (2020). Esophageal Eosinophilia Is Common Among Relatives of Eosinophilic Esophagitis Patients. Clin Gastroenterol Hepatol, 20(5), e957-e963. (Read full article)
  32. Allen-Brady K, Norton PA, Hill AJ, Rowe K, Cannon-Albright LA (2020). Risk of pelvic organ prolapse treatment based on extended family history. Am J Obstet Gynecol, 223(1), 105.e1-105.e8. (Read full article)
  33. Byun J, Peterson CM, Backonja U, Taylor RN, Stanford JB, Allen-Brady KL, Smith KR, Louis GMB, Schliep KC (2020). Adiposity and Endometriosis Severity and Typology. J Minim Invasive Gynecol, 27(7), 1516-1523. (Read full article)
  34. Robson J, Korgenski K, Parsons K, McClain A, Barbagelata C, Allen-Brady K, Patel R, OGorman M, Peterson K, Guthery S (2019). Sensitivity and Specificity of Administrative Medical Coding for Pediatric Eosinophilic Esophagitis. J Pediatr Gastroenterol Nutr, 69(2), e49-e53. (Read full article)
  35. Dodson MW, Allen-Brady K, Brown LM, Elliott CG, Cannon-Albright LA (2018). Chronic Thromboembolic Pulmonary Hypertension Cases Cluster in Families. Chest, 155(2), 384-390. (Read full article)
  36. Hemmert R, Schliep KC, Willis S, Peterson CM, Louis GB, Allen-Brady K, Simonsen SE, Stanford JB, Byun J, Smith KR (2018). Modifiable life style factors and risk for incident endometriosis. Paediatr Perinat Epidemiol, 33(1), 19-25. (Read full article)
  37. Allen-Brady K, Rowe K, Cessna M, Lenherr S, Norton P (2018). Significant Linkage Evidence for Interstitial Cystitis/Painful Bladder Syndrome on Chromosome 3. J Urol, 199(1), 172-177. (Read full article)
  38. Allen-Brady K, Firszt R, Fang JC, Wong J, Smith KR, Peterson KA (2017). Population-based familial aggregation of eosinophilic esophagitis suggests a genetic contribution. J Allergy Clin Immunol, 140(4), 1138-1143. (Read full article)
  39. Wirostko BM, Curtin K, Ritch R, Thomas S, Allen-Brady K, Smith KR, Hageman GS, Allingham RR (2016). Risk for Exfoliation Syndrome in Women With Pelvic Organ Prolapse : A Utah Project on Exfoliation Syndrome (UPEXS) Study. JAMA Ophthalmol, 134(11), 1255-1262. (Read full article)
  40. Peterson K, Firszt R, Fang J, Wong J, Smith KR, Allen-Brady K (2016). Risk of autoimmunity in EoE and families - A population-based cohort study. Am J Gastroenterol, 111, 926-32.
  41. Peterson K, Firszt R, Fang J, Wong J, Smith KR, Brady KA (2016). Risk of Autoimmunity in EoE and Families: A Population-Based Cohort Study. Am J Gastroenterol, 111(7), 926-32. (Read full article)
  42. Morgan TK, Allen-Brady KL, Monson MA, Leclair CM, Sharp HT, Cannon-Albright LA (2016). Familiality analysis of provoked vestibulodynia treated by vestibulectomy supports genetic predisposition. Am J Obstet Gynecol, 214(5), 609.e1-7. (Read full article)
  43. 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 (2014). Genetic contributions to urgency urinary incontinence in women. J Urol, 193(6), 2020-7. (Read full article)
  44. Allen-Brady K, Cannon-Albright LA, Farnham JM, Norton PA (2014). Evidence for pelvic organ prolapse predisposition genes on chromosomes 10 and 17. Am J Obstet Gynecol, 212(6), 771.e1-7. (Read full article)
  45. Allen-Brady K, Norton PA, Cannon-Albright L (2014). Risk of associated conditions in relatives of subjects with interstitial cystitis. Female Pelvic Med Reconstr Surg, 21(2), 93-8. (Read full article)
  46. Norton PA, Allen-Brady K, Wu J, Egger M, Cannon-Albright L (2014). Clinical characteristics of women with familial pelvic floor disorders. Int Urogynecol J, 26(3), 401-6. (Read full article)
  47. Lee S, Piccolo SR, Allen-Brady K (2014). Robust meta-analysis shows that glioma transcriptional subtyping complements traditional approaches. Cell Oncol (Dordr), 37(5), 317-29. (Read full article)
  48. Wu JM, Ward RM, Allen-Brady KL, Edwards TL, Norton PA, Hartmann KE, Hauser ER, Velez Edwards DR (2013). Phenotyping clinical disorders: lessons learned from pelvic organ prolapse. Am J Obstet Gynecol, 208(5), 360-5. (Read full article)
  49. Norton PA, Allen-Brady K, Cannon-Albright LA (2013). The familiality of pelvic organ prolapse in the Utah Population Database. Int Urogynecol J, 24(3), 413-8. (Read full article)
  50. Kim SH, Lee S, Piccolo SR, Allen-Brady K, Park EJ, Chun JN, Kim TW, Cho NH, Kim IG, So I, Jeon JH (2012). Menthol induces cell-cycle arrest in PC-3 cells by down-regulating G2/M genes, including polo-like kinase 1. Biochem Biophys Res Commun, 422(3), 436-41. (Read full article)
  51. Teerlink C, Farnham J, Allen-Brady K, Camp NJ, Thomas A, Leachman S, Cannon-Albright L (2012). A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q. Hum Genet, 131(1), 77-85. (Read full article)
  52. Allen-Brady K, Cannon-Albright L, Farnham JM, Teerlink C, Vierhout ME, van Kempen LCL, Kluivers KB, Norton PA (2011). Identification of six loci associated with pelvic organ prolapse using genome-wide association analysis. Obstet Gynecol, 118(6), 1345-1353. (Read full article)
  53. Allen-Brady K, Farnham J, Cannon-Albright L (2011). Strategies for selection of subjects for sequencing after detection of a linkage peak. BMC Proc, 5 Suppl 9, S77. (Read full article)
  54. Allen-Brady K, Cai G, Cannon D, Robison R, McMahon WM, Coon H, Buxbaum JD (2011). No evidence for IL1RAPL1 involvement in selected high-risk autism pedigrees from the AGRE data set. Autism Res, 4(4), 293-6. (Read full article)
  55. 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-Prez JI, Menndez-Rodrguez P, Bentez J, Grundmann M, Dubrowinskaja N, Park-Simon TW, Drk 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 (2011). A role for XRCC2 gene polymorphisms in breast cancer risk and survival. J Med Genet, 48(7), 477-84. (Read full article)
  56. Allen-Brady K, Farnham J, Cannon-Albright LA (2011). Strategies for selection of subjects for sequencing after detection of a linkage peak. BMC Proc, 5(Suppl 9), S77.
  57. Allen-Brady K, Camp NJ (2011). Genetic distance and markers used in linkage mapping. Methods Mol Biol, 713, 43-53. (Read full article)
  58. Krikov S, Price RC, Matney SA, Allen-Brady K, Facelli JC (2010). Enabling GeneHunter as a grid service: a case study for implementing analytical services in biomedical grids. Methods Inf Med, 50(4), 364-71. (Read full article)
  59. Allen-Brady K, Robison R, Cannon D, Varvil T, Villalobos M, Pingree C, Leppert MF, Miller J, McMahon WM, Coon H (2010). Genome-wide linkage in Utah autism pedigrees. Mol Psychiatry, 15(10), 1006-15. (Read full article)
  60. Coon H, Villalobos ME, Robison RJ, Camp NJ, Cannon DS, Allen-Brady K, Miller JS, McMahon WM (2010). Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigrees. Mol Autism, 1(1), 8. (Read full article)
  61. Allen-Brady K, Cannon D, Robison R, McMahon WM, Coon H (2010). A unified theory of autism revisited: linkage evidence points to chromosome X using a high-risk subset of AGRE families. Autism Res, 3(2), 47-52. (Read full article)
  62. Cannon DS, Miller JS, Robison RJ, Villalobos ME, Wahmhoff NK, Allen-Brady K, McMahon WM, Coon H (2010). Genome-wide linkage analyses of two repetitive behavior phenotypes in Utah pedigrees with autism spectrum disorders. Mol Autism, 1(1), 3. (Read full article)
  63. Piccolo SR, Abo RP, Allen-Brady K, Camp NJ, Knight S, Anderson JL, Horne BD (2009). Evaluation of genetic risk scores for lipid levels using genome-wide markers in the Framingham Heart Study. BMC Proc, 3 Suppl 7, S46. (Read full article)
  64. 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 (2009). A high-density SNP genome-wide linkage scan in a large autism extended pedigree. Mol Psychiatry, 14(6), 590-600. (Read full article)
  65. Allen-Brady K, Farnham JM, Camp NJ, Karlins E, Ostrander EA, Cannon-Albright LA (2009). No evidence of BRCA2 mutations in chromosome 13q-linked Utah high-risk prostate cancer pedigrees. BMC Res Notes, 2, 94. (Read full article)
  66. 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, Kmpjrvi K, Aaltonen K, Nevanlinna H, Bogdanova N, Coinac I, Schrmann P, Drk 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, Vant 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 (2009). Five polymorphisms and breast cancer risk: results from the Breast Cancer Association Consortium. Cancer Epidemiol Biomarkers Prev, 18(5), 1610-6. (Read full article)
  67. Allen-Brady K, Norton PA, Farnham JM, Teerlink C, Cannon-Albright LA (2009). Significant linkage evidence for a predisposition gene for pelvic floor disorders on chromosome 9q21. Am J Hum Genet, 84(5), 678-82. (Read full article)
  68. 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 (2009). A breast cancer risk haplotype in the caspase-8 gene. Cancer Res, 69(7), 2724-8. (Read full article)
  69. Krikov S, Price RC, Allen-Brady K, Cannon-Albright L, Facelli JC (2008). Enabling GeneHunter as a grid service: a case study for implementing analytical services for biomedical grids. AMIA Annu Symp Proc, 1014. (Read full article)
  70. 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 (2008). Heterogeneous association between engrailed-2 and autism in the CPEA network. Am J Med Genet B Neuropsychiatr Genet, 147B(2), 187-93. (Read full article)
  71. Thomas A, Camp NJ, Farnham JM, Allen-Brady K, Cannon-Albright LA (2008). Shared genomic segment analysis. Mapping disease predisposition genes in extended pedigrees using SNP genotype assays. Ann Hum Genet, 72(Pt 2), 279-87. (Read full article)
  72. 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 (2008). The Value of Large Pedigrees for Chromosome Mapping in the Era of Dense Marker Sets. Int J Med Biol Front, 14(1/2), 9-24.
  73. Curtin K, Wong J, Allen-Brady K, Camp NJ (2007). PedGenie: meta genetic association testing in mixed family and case-control designs. BMC Bioinformatics, 8, 448. (Read full article)
  74. Easton DF, Deffenbaugh AM, Pruss D, Frye C, Wenstrup RJ, Allen-Brady K, Tavtigian SV, Monteiro AN, Iversen ES, Couch FJ, Goldgar DE (2007). A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genes. Am J Hum Genet, 81(5), 873-83. (Read full article)
  75. Camp NJ, Farnham JM, Allen-Brady K, Cannon-Albright LA (2007). Statistical recombinant mapping in extended high-risk Utah pedigrees narrows the 8q24 prostate cancer locus to 2.0 Mb. Prostate, 67(13), 1456-64. (Read full article)
  76. Allen-Brady K (2007). Genetic polymorphisms and metastatic breast cancer survival. Future Oncol, 3(2), 155-8. (Read full article)
  77. 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 (2007). Effect of linkage disequilibrium between markers in linkage and association analyses. Genet Epidemiol, 31 Suppl 1, S139-48. (Read full article)
  78. Allen-Brady K, Horne BD, Malhotra A, Teerlink C, Camp NJ, Thomas A (2007). Analysis of high-density single-nucleotide polymorphism data: three novel methods that control for linkage disequilibrium between markers in a linkage analysis. BMC Proc, 1 Suppl 1, S160. (Read full article)
  79. Curtin K, Wong J, Allen-Brady K, Camp NJ (2007). Meta-genetic association of rheumatoid arthritis and PTPN22 using PedGenie 2.1. BMC Proc, 1 Suppl 1, S12. (Read full article)
  80. Allen BG, Allen-Brady K, Weeks DL (2006). Reduction of XNkx2-10 expression leads to anterior defects and malformation of the embryonic heart. Mech Dev, 123(10), 719-29. (Read full article)
  81. Allen-Brady K, Cannon-Albright LA, Neuhausen SL, Camp NJ (2006). A role for XRCC4 in age at diagnosis and breast cancer risk. Cancer Epidemiol Biomarkers Prev, 15(7), 1306-10. (Read full article)
  82. Allen-Brady K, Wong J, Camp NJ (2006). PedGenie: an analysis approach for genetic association testing in extended pedigrees and genealogies of arbitrary size. BMC Bioinformatics, 7, 209. (Read full article)
  83. Allen-Brady K, Camp NJ, Ward JH, Cannon-Albright LA (2005). Lobular breast cancer: excess familiality observed in the Utah Population Database. Int J Cancer, 117(4), 655-61. (Read full article)
  84. Allen-Brady K, Camp NJ (2005). Characterization of the linkage disequilibrium structure and identification of tagging-SNPs in five DNA repair genes. BMC Cancer, 5, 99. (Read full article)
  85. Allen-Brady K, Farnham JM, Weiler J, Camp NJ (2003). A cautionary note on the appropriateness of using a linkage resource for an association study. BMC Genet, 4 Suppl 1, S89. (Read full article)
  86. Beddhu S, Allen-Brady K, Cheung AK, Horne BD, Bair T, Muhlestein JB, Anderson JL (2002). Impact of renal failure on the risk of myocardial infarction and death. Kidney Int, 62(5), 1776-83. (Read full article)
  87. Allen KL, Miskulin D, Yan G, Dwyer JT, Frydrych A, Leung J, Poole D, Hemodialysis HEMO Study Group (2002). Association of nutritional markers with physical and mental health status in prevalent hemodialysis patients from the HEMO study. J Ren Nutr, 12(3), 160-9. (Read full article)
  88. Allen KL, Miskulin D, Yan G, Dwyer JT, Frydrych A, Leung J, Poole D, and the Hemodialysis HEMO Study Group (2002). Association of nutritional and behavioral markers on the physical and mental health status in prevalent hemodialysis patients from the HEMO Study. J Ren Nutr, 12(3), 160-9.
  89. Allen KL, Gappmaier E (2001). Exercise Habits and Attitudes of Patients Undergoing Hemodialysis. Cardiopulm Phys Ther J, 12(1), 11-16.

Review

  1. Yu J, Varella Pereira GM, Allen-Brady K, Cuffolo R, Siddharth A, Koch M, Chua JWF, Sorrentino F, Dytko O, Ng KY, Violette P, Khullar V, Wang ZT, Cartwright R (2023). Genetic polymorphisms associated with urinary tract infection in children and adults: a systematic review and meta-analysis. [Review]. Am J Obstet Gynecol. (Read full article)
  2. Davies M, Jurynec MJ, Gomez-Alvarado F, Hu D, Feeley SE, Allen-Brady K, Tashjian RZ, Feeley BT (2022). Current cellular and molecular biology techniques for the orthopedic surgeon-scientist. [Review]. J Shoulder Elbow Surg, 32(1), e11-e22. (Read full article)
  3. Allen-Brady K, Bortolini MAT, Damaser MS (2022). Mouse Knockout Models for Pelvic Organ Prolapse: a Systematic Review. [Review]. Int Urogynecol J, 33(7), 1765-1788. (Read full article)
  4. Deprest JA, Cartwright R, Dietz HP, Brito LGO, Koch M, Allen-Brady K, Manonai J, Weintraub AY, Chua JWF, Cuffolo R, Sorrentino F, Cattani L, Decoene J, Page AS, Weeg N, Varella Pereira GM, Mori da Cunha de Carvalho MGMC, Mackova K, Hympanova LH, Moalli P, Shynlova O, Alperin M, Bortolini MAT (2022). International Urogynecological Consultation (IUC): pathophysiology of pelvic organ prolapse (POP). [Review]. Int Urogynecol J, 33(7), 1699-1710. (Read full article)

Editorial

  1. Guo Q, Allen-Brady K, Olszewska M (2024). Editorial: Women in applied genetic epidemiology. Front Genet, 15, 1508169. (Read full article)

Letter

  1. Spechler SJ, Reddy CA, Allen-Brady K, Uchida AM, Peterson KA, Hoffman AM, Souza RF (2023). Reply. [Letter to the editor]. Clin Gastroenterol Hepatol. (Read full article)
  2. May Maestas M, Perry KD, Smith K, Firszt R, Allen-Brady K, Robson J, Joy E, Peterson K (2019). Food impactions in Eosinophilic esophagitis and acute exposures to fine particulate pollution. [Letter to the editor]. Allergy, 74(12), 2529-2530. (Read full article)