Kyle Walsh | Scholars@Duke

Kyle Walsh
Associate Professor of Neurosurgery

Dr. Walsh’s research program focuses on genetic and epigenetic factors contributing to cancer predisposition in children and adults, with a special interest in brain tumors. This research is informed by both epidemiology and anthropological genetics, with computational work stressing statistical methodologies for “gene hunting” (e.g. GWAS, fine-mapping, admixture mapping, whole-genome sequencing). The laboratory engages in functional genomics research, investigating the biological impact of genetic variants linked to cancer risk, with a particular focus on regulation of telomere maintenance in pre-malignant cells.

Current Appointments & Affiliations

Associate Professor of Neurosurgery, Neurosurgery, Neurosurgery 2017
Associate Professor in Population Health Sciences, Population Health Sciences, Basic Science Departments 2018
Associate Professor in Pediatrics, Pediatrics, Children's Health Discovery Institute, Pediatrics 2018
Associate Professor in Pathology, Pathology, Clinical Science Departments 2018
Member of the Duke Cancer Institute, Duke Cancer Institute, Institutes and Centers 2017

Contact Information

571 Research Drive, Msrb-1, Rm 442, Durham, NC 27710
DUMC Box 3050, Durham, NC 27710
kyle.walsh@duke.edu (919) 684-8732

Background
Education, Training, & Certifications
- Ph.D., Yale University School of Medicine 2011
Leadership & Clinical Positions at Duke
- Director, Division of Neuro-epidemiology
  
  Genes and Biology Program Leader, Children's Health and Discovery Institute
Academic Positions Outside Duke
- Assistant Professor of Neurological Surgery, University of California, San Francisco. 2013 - 2017
Research
Selected Grants
- Immune Correlates and Mechanisms of Perinatal Cytomegalovirus Infection and Later Life ALL Development awarded by National Institutes of Health 2019 - 2021
- The role of rare and common variants in genetic predisposition to medulloblastoma awarded by Sontag Foundation 2017 - 2020
- My Childhood Cancer: Survey Series 2018 - 2020
- Genetic Susceptibility to Pediatric Glioma in Individuals and Diverse populations awarded by University of Southern California 2019 - 2020
- Genetic Susceptibility to pediatric Osteosarcoma and Interaction with Measures of Childhood Growth 2017 - 2018
Industry Relationships
- John Wiley & Sons, Inc.
Publications & Artistic Works
Selected Publications
- Academic Articles
  - Zhang, Chenan, Helen M. Hansen, Eleanor C. Semmes, Julio Gonzalez-Maya, Libby Morimoto, Qingyi Wei, William C. Eward, et al. “Common genetic variation and risk of osteosarcoma in a multi-ethnic pediatric and adolescent population..” Bone 130 (January 2020). https://doi.org/10.1016/j.bone.2019.115070.
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  - Muskens, Ivo S., Chenan Zhang, Adam J. de Smith, Jaclyn A. Biegel, Kyle M. Walsh, and Joseph L. Wiemels. “Germline genetic landscape of pediatric central nervous system tumors..” Neuro Oncol 21, no. 11 (November 4, 2019): 1376–88. https://doi.org/10.1093/neuonc/noz108.
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  - Smith, Adam J. de, Kyle M. Walsh, Libby M. Morimoto, Stephen S. Francis, Helen M. Hansen, Soyoung Jeon, Semira Gonseth, et al. “Heritable variation at the chromosome 21 gene ERG is associated with acute lymphoblastic leukemia risk in children with and without Down syndrome..” Leukemia 33, no. 11 (November 2019): 2746–51. https://doi.org/10.1038/s41375-019-0514-9.
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  - Brown, Austin L., Adam J. de Smith, Vincent U. Gant, Wenjian Yang, Michael E. Scheurer, Kyle M. Walsh, Jonathan M. Chernus, et al. “Inherited genetic susceptibility to acute lymphoblastic leukemia in Down syndrome..” Blood 134, no. 15 (October 10, 2019): 1227–37. https://doi.org/10.1182/blood.2018890764.
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  - Smith, Adam J. de, Geneviève Lavoie, Kyle M. Walsh, Sumeet Aujla, Erica Evans, Helen M. Hansen, Ivan Smirnov, et al. “Predisposing germline mutations in high hyperdiploid acute lymphoblastic leukemia in children..” Genes Chromosomes Cancer 58, no. 10 (October 2019): 723–30. https://doi.org/10.1002/gcc.22765.
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  - Xu, Xinyuan, Danwen Qian, Hongliang Liu, Diana Cruz, Sheng Luo, Kyle M. Walsh, James L. Abbruzzese, Xuefeng Zhang, and Qingyi Wei. “Genetic variants in the liver kinase B1-AMP-activated protein kinase pathway genes and pancreatic cancer risk..” Mol Carcinog 58, no. 8 (August 2019): 1338–48. https://doi.org/10.1002/mc.23018.
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  - Feng, Yun, Hongliang Liu, Bensong Duan, Zhensheng Liu, James Abbruzzese, Kyle M. Walsh, Xuefeng Zhang, and Qingyi Wei. “Potential functional variants in SMC2 and TP53 in the AURORA pathway genes and risk of pancreatic cancer..” Carcinogenesis 40, no. 4 (June 10, 2019): 521–28. https://doi.org/10.1093/carcin/bgz029.
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  - Yang, Wenjun, Hongliang Liu, Bensong Duan, Xinyuan Xu, Dennis Carmody, Sheng Luo, Kyle M. Walsh, et al. “Three novel genetic variants in NRF2 signaling pathway genes are associated with pancreatic cancer risk..” Cancer Sci 110, no. 6 (June 2019): 2022–32. https://doi.org/10.1111/cas.14017.
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  - Walsh, Kyle M., and Elizabeth B. Claus. “Diet and risk of glioma: targets for prevention remain elusive..” Neuro Oncol, April 23, 2019. https://doi.org/10.1093/neuonc/noz074.
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  - Takahashi, Hannah, Alex J. Cornish, Amit Sud, Philip J. Law, Linden Disney-Hogg, Lisa Calvocoressi, Lingeng Lu, et al. “Mendelian randomization provides support for obesity as a risk factor for meningioma..” Sci Rep 9, no. 1 (January 22, 2019). https://doi.org/10.1038/s41598-018-36186-6.
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  - Semmes, Eleanor C., Chenan Zhang, and Kyle M. Walsh. “Intermediate phenotypes underlying osteosarcoma risk..” Oncotarget 9, no. 100 (December 21, 2018): 37345–46. https://doi.org/10.18632/oncotarget.26476.
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  - Smith, Adam J. de, Kyle M. Walsh, Stephen S. Francis, Chenan Zhang, Helen M. Hansen, Ivan Smirnov, Libby Morimoto, et al. “BMI1 enhancer polymorphism underlies chromosome 10p12.31 association with childhood acute lymphoblastic leukemia..” Int J Cancer 143, no. 11 (December 1, 2018): 2647–58. https://doi.org/10.1002/ijc.31622.
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  - Claus, Elizabeth B., Alex J. Cornish, Peter Broderick, Joellen M. Schildkraut, Sara E. Dobbins, Amy Holroyd, Lisa Calvocoressi, et al. “Genome-wide association analysis identifies a meningioma risk locus at 11p15.5..” Neuro Oncol 20, no. 11 (October 9, 2018): 1485–93. https://doi.org/10.1093/neuonc/noy077.
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  - Zhang, Chenan, Joseph L. Wiemels, Helen M. Hansen, Julio Gonzalez-Maya, Alyson A. Endicott, Adam J. de Smith, Ivan V. Smirnov, et al. “Two HLA Class II Gene Variants Are Independently Associated with Pediatric Osteosarcoma Risk..” Cancer Epidemiol Biomarkers Prev 27, no. 10 (October 2018): 1151–58. https://doi.org/10.1158/1055-9965.EPI-18-0306.
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  - Zhang, Chenan, Libby M. Morimoto, Adam J. de Smith, Helen M. Hansen, Julio Gonzalez-Maya, Alyson A. Endicott, Ivan V. Smirnov, et al. “Genetic determinants of childhood and adult height associated with osteosarcoma risk..” Cancer 124, no. 18 (September 15, 2018): 3742–52. https://doi.org/10.1002/cncr.31645.
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  - Mancini, Andrew, Ana Xavier-Magalhães, Wendy S. Woods, Kien-Thiet Nguyen, Alexandra M. Amen, Josie L. Hayes, Christof Fellmann, et al. “Disruption of the β1L Isoform of GABP Reverses Glioblastoma Replicative Immortality in a TERT Promoter Mutation-Dependent Manner..” Cancer Cell 34, no. 3 (September 10, 2018): 513-528.e8. https://doi.org/10.1016/j.ccell.2018.08.003.
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  - Wallace, A. D., G. A. Wendt, L. F. Barcellos, A. J. de Smith, K. M. Walsh, C. Metayer, J. F. Costello, J. L. Wiemels, and S. S. Francis. “To ERV is human: A phenotype-wide scan linking polymorphic human endogenous retrovirus-K insertions to complex phenotypes.” Frontiers in Genetics 9, no. AUG (August 14, 2018). https://doi.org/10.3389/fgene.2018.00298.
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  - Ojha, Juhi, Iryna Dyagil, Stuart C. Finch, Robert F. Reiss, Adam J. de Smith, Semira Gonseth, Mi Zhou, et al. “Genomic characterization of chronic lymphocytic leukemia (CLL) in radiation-exposed Chornobyl cleanup workers..” Environ Health 17, no. 1 (May 2, 2018). https://doi.org/10.1186/s12940-018-0387-9.
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  - Hayes, Josie, Yao Yu, Llewellyn E. Jalbert, Tali Mazor, Lindsey E. Jones, Matthew D. Wood, Kyle M. Walsh, et al. “Genomic analysis of the origins and evolution of multicentric diffuse lower-grade gliomas..” Neuro Oncol 20, no. 5 (April 9, 2018): 632–41. https://doi.org/10.1093/neuonc/nox205.
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  - Wiemels, Joseph L., Kyle M. Walsh, Adam J. de Smith, Catherine Metayer, Semira Gonseth, Helen M. Hansen, Stephen S. Francis, et al. “GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24.21..” Nat Commun 9, no. 1 (January 18, 2018). https://doi.org/10.1038/s41467-017-02596-9.
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  - Wallace, Amelia D., Stephen S. Francis, Xiaorong Shao, Adam J. de Smith, Kyle M. Walsh, Roberta Mckean-Cowdin, Xiaomei Ma, et al. “A germ-line deletion of APOBEC3B does not contribute to subtype-specific childhood acute lymphoblastic leukemia etiology..” Haematologica 103, no. 1 (January 2018): e29–31. https://doi.org/10.3324/haematol.2017.179317.
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  - Zhang, Chenan, Adam J. de Smith, Ivan V. Smirnov, John K. Wiencke, Joseph L. Wiemels, John S. Witte, and Kyle M. Walsh. “Non-additive and epistatic effects of HLA polymorphisms contributing to risk of adult glioma..” J Neurooncol 135, no. 2 (November 2017): 237–44. https://doi.org/10.1007/s11060-017-2569-7.
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  - Bazyka, D., S. C. Finch, I. M. Ilienko, O. Lyaskivska, I. Dyagil, N. Trotsiuk, N. Gudzenko, et al. “Buccal mucosa micronuclei counts in relation to exposure to low dose-rate radiation from the Chornobyl nuclear accident and other medical and occupational radiation exposures..” Environ Health 16, no. 1 (June 23, 2017). https://doi.org/10.1186/s12940-017-0273-x.
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  - Endicott, Alyson A., Libby M. Morimoto, Cassie N. Kline, Joseph L. Wiemels, Catherine Metayer, and Kyle M. Walsh. “Perinatal factors associated with clinical presentation of osteosarcoma in children and adolescents..” Pediatr Blood Cancer 64, no. 6 (June 2017). https://doi.org/10.1002/pbc.26349.
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  - Pekmezci, Melike, Terri Rice, Annette M. Molinaro, Kyle M. Walsh, Paul A. Decker, Helen Hansen, Hugues Sicotte, et al. “Adult infiltrating gliomas with WHO 2016 integrated diagnosis: additional prognostic roles of ATRX and TERT..” Acta Neuropathol 133, no. 6 (June 2017): 1001–16. https://doi.org/10.1007/s00401-017-1690-1.
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  - Telomeres Mendelian Randomization Collaboration, George, Philip C. Haycock, Stephen Burgess, Aayah Nounu, Jie Zheng, George N. Okoli, Jack Bowden, et al. “Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study..” Jama Oncol 3, no. 5 (May 1, 2017): 636–51. https://doi.org/10.1001/jamaoncol.2016.5945.
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  - Smith, Adam J. de, Maneet Kaur, Semira Gonseth, Alyson Endicott, Steve Selvin, Luoping Zhang, Ritu Roy, et al. “Correlates of Prenatal and Early-Life Tobacco Smoke Exposure and Frequency of Common Gene Deletions in Childhood Acute Lymphoblastic Leukemia..” Cancer Res 77, no. 7 (April 1, 2017): 1674–83. https://doi.org/10.1158/0008-5472.CAN-16-2571.
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  - Francis, Stephen Starko, Amelia D. Wallace, George A. Wendt, Linlin Li, Fenyong Liu, Lee W. Riley, Scott Kogan, et al. “In utero cytomegalovirus infection and development of childhood acute lymphoblastic leukemia..” Blood 129, no. 12 (March 23, 2017): 1680–84. https://doi.org/10.1182/blood-2016-07-723148.
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  - Ohba, Shigeo, Joydeep Mukherjee, Tor-Christian Johannessen, Andrew Mancini, Tracy T. Chow, Matthew Wood, Lindsey Jones, et al. “Mutant IDH1 Expression Drives TERT Promoter Reactivation as Part of the Cellular Transformation Process..” Cancer Res 76, no. 22 (November 15, 2016): 6680–89. https://doi.org/10.1158/0008-5472.CAN-16-0696.
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  - Smith, Adam J. de, Juhi Ojha, Stephen S. Francis, Erica Sanders, Alyson A. Endicott, Helen M. Hansen, Ivan Smirnov, et al. “Clonal and microclonal mutational heterogeneity in high hyperdiploid acute lymphoblastic leukemia..” Oncotarget 7, no. 45 (November 8, 2016): 72733–45. https://doi.org/10.18632/oncotarget.12238.
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  - Gonseth, Semira, Adam J. de Smith, Ritu Roy, Mi Zhou, Seung-Tae Lee, Xiaorong Shao, Juhi Ohja, et al. “Genetic contribution to variation in DNA methylation at maternal smoking-sensitive loci in exposed neonates..” Epigenetics 11, no. 9 (September 2016): 664–73. https://doi.org/10.1080/15592294.2016.1209614.
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  - Ojha, Juhi, Veryan Codd, Christopher P. Nelson, Nilesh J. Samani, Ivan V. Smirnov, Nils R. Madsen, Helen M. Hansen, et al. “Genetic Variation Associated with Longer Telomere Length Increases Risk of Chronic Lymphocytic Leukemia..” Cancer Epidemiol Biomarkers Prev 25, no. 7 (July 2016): 1043–49. https://doi.org/10.1158/1055-9965.EPI-15-1329.
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  - Walsh, Kyle M., Todd P. Whitehead, Adam J. de Smith, Ivan V. Smirnov, Minsun Park, Alyson A. Endicott, Stephen S. Francis, et al. “Common genetic variants associated with telomere length confer risk for neuroblastoma and other childhood cancers..” Carcinogenesis 37, no. 6 (June 2016): 576–82. https://doi.org/10.1093/carcin/bgw037.
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  - Wiemels, J. L., A. J. de Smith, J. Xiao, S. -. T. Lee, M. O. Muench, M. E. Fomin, M. Zhou, et al. “A functional polymorphism in the CEBPE gene promoter influences acute lymphoblastic leukemia risk through interaction with the hematopoietic transcription factor Ikaros..” Leukemia 30, no. 5 (May 2016): 1194–97. https://doi.org/10.1038/leu.2015.251.
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  - Endicott, Alyson A., Jennie W. Taylor, and Kyle M. Walsh. “Telomere length connects melanoma and glioma predispositions..” Aging (Albany Ny) 8, no. 3 (March 2016): 423–24. https://doi.org/10.18632/aging.100935.
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  - David, Sean P., Ange Wang, Kristopher Kapphahn, Haley Hedlin, Manisha Desai, Michael Henderson, Lingyao Yang, et al. “Gene by Environment Investigation of Incident Lung Cancer Risk in African-Americans..” Ebiomedicine 4 (February 2016): 153–61. https://doi.org/10.1016/j.ebiom.2016.01.002.
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  - Walsh, Kyle M., Veryan Codd, Terri Rice, Christopher P. Nelson, Ivan V. Smirnov, Lucie S. McCoy, Helen M. Hansen, et al. “Longer genotypically-estimated leukocyte telomere length is associated with increased adult glioma risk..” Oncotarget 6, no. 40 (December 15, 2015): 42468–77. https://doi.org/10.18632/oncotarget.6468.
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  - Walsh, Kyle M., Adam J. de Smith, Helen M. Hansen, Ivan V. Smirnov, Semira Gonseth, Alyson A. Endicott, Jianqiao Xiao, et al. “A Heritable Missense Polymorphism in CDKN2A Confers Strong Risk of Childhood Acute Lymphoblastic Leukemia and Is Preferentially Selected during Clonal Evolution..” Cancer Res 75, no. 22 (November 15, 2015): 4884–94. https://doi.org/10.1158/0008-5472.CAN-15-1105.
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  - Walsh, Kyle M., John K. Wiencke, Daniel H. Lachance, Joseph L. Wiemels, Annette M. Molinaro, Jeanette E. Eckel-Passow, Robert B. Jenkins, and Margaret R. Wrensch. “Telomere maintenance and the etiology of adult glioma..” Neuro Oncol 17, no. 11 (November 2015): 1445–52. https://doi.org/10.1093/neuonc/nov082.
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  - Eckel-Passow, Jeanette E., Daniel H. Lachance, Annette M. Molinaro, Kyle M. Walsh, Paul A. Decker, Hugues Sicotte, Melike Pekmezci, et al. “Glioma Groups Based on 1p/19q, IDH, and TERT Promoter Mutations in Tumors..” N Engl J Med 372, no. 26 (June 25, 2015): 2499–2508. https://doi.org/10.1056/NEJMoa1407279.
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  - Bell, Robert J. A., H Tomas Rube, Alex Kreig, Andrew Mancini, Shaun D. Fouse, Raman P. Nagarajan, Serah Choi, et al. “Cancer. The transcription factor GABP selectively binds and activates the mutant TERT promoter in cancer..” Science 348, no. 6238 (May 29, 2015): 1036–39. https://doi.org/10.1126/science.aab0015.
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  - Reis, Gerald F., Melike Pekmezci, Helen M. Hansen, Terri Rice, Roxanne E. Marshall, Annette M. Molinaro, Joanna J. Phillips, et al. “CDKN2A loss is associated with shortened overall survival in lower-grade (World Health Organization Grades II-III) astrocytomas..” J Neuropathol Exp Neurol 74, no. 5 (May 2015): 442–52. https://doi.org/10.1097/NEN.0000000000000188.
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  - Hsu, Ling-I, Anand P. Chokkalingam, Farren B. S. Briggs, Kyle Walsh, Vonda Crouse, Cecilia Fu, Catherine Metayer, Joseph L. Wiemels, Lisa F. Barcellos, and Patricia A. Buffler. “Association of genetic variation in IKZF1, ARID5B, and CEBPE and surrogates for early-life infections with the risk of acute lymphoblastic leukemia in Hispanic children..” Cancer Causes Control 26, no. 4 (April 2015): 609–19. https://doi.org/10.1007/s10552-015-0550-3.
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  - Ostrom, Quinn T., Luc Bauchet, Faith G. Davis, Isabelle Deltour, James L. Fisher, Chelsea Eastman Langer, Melike Pekmezci, et al. “Response to "the epidemiology of glioma in adults: a 'state of the science' review"..” Neuro Oncol 17, no. 4 (April 2015): 624–26. https://doi.org/10.1093/neuonc/nov022.
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  - Rice, T., D. H. Lachance, A. M. Molinaro, J. E. Eckel-Passow, K. M. Walsh, J. Barnholtz-Sloan, Q. T. Ostrom, et al. “Neuro-oncology practice: Understanding inherited genetic risk of adult glioma - A review.” Neuro Oncology Practice 3, no. 1 (March 20, 2015): 1–16. https://doi.org/10.1093/nop/npv026.
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  - Bainbridge, Matthew N., Georgina N. Armstrong, M Monica Gramatges, Alison A. Bertuch, Shalini N. Jhangiani, Harsha Doddapaneni, Lora Lewis, et al. “Germline mutations in shelterin complex genes are associated with familial glioma..” J Natl Cancer Inst 107, no. 1 (January 2015). https://doi.org/10.1093/jnci/dju384.
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  - Claus, Elizabeth B., Kyle M. Walsh, John K. Wiencke, Annette M. Molinaro, Joseph L. Wiemels, Joellen M. Schildkraut, Melissa L. Bondy, Mitchel Berger, Robert Jenkins, and Margaret Wrensch. “Survival and low-grade glioma: the emergence of genetic information..” Neurosurg Focus 38, no. 1 (January 2015). https://doi.org/10.3171/2014.10.FOCUS12367.
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  - Osorio, Joseph A., Shawn L. Hervey-Jumper, Kyle M. Walsh, Jennifer L. Clarke, Nicholas A. Butowski, Michael D. Prados, and Mitchel S. Berger. “Familial gliomas: cases in two pairs of brothers..” J Neurooncol 121, no. 1 (January 2015): 135–40. https://doi.org/10.1007/s11060-014-1611-2.
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  - Smith, Adam J. de, Kyle M. Walsh, Helen M. Hansen, Alyson A. Endicott, John K. Wiencke, Catherine Metayer, and Joseph L. Wiemels. “Somatic Mutation Allelic Ratio Test Using ddPCR (SMART-ddPCR): An Accurate Method for Assessment of Preferential Allelic Imbalance in Tumor DNA..” Plos One 10, no. 11 (2015). https://doi.org/10.1371/journal.pone.0143343.
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  - Ostrom, Quinn T., Luc Bauchet, Faith G. Davis, Isabelle Deltour, James L. Fisher, Chelsea Eastman Langer, Melike Pekmezci, et al. “The epidemiology of glioma in adults: a "state of the science" review..” Neuro Oncol 16, no. 7 (July 2014): 896–913. https://doi.org/10.1093/neuonc/nou087.
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  - Walsh, Kyle M., Adam J. de Smith, Tara C. Welch, Ivan Smirnov, Marc J. Cunningham, Xiaomei Ma, Anand P. Chokkalingam, et al. “Genomic ancestry and somatic alterations correlate with age at diagnosis in Hispanic children with B-cell acute lymphoblastic leukemia..” Am J Hematol 89, no. 7 (July 2014): 721–25. https://doi.org/10.1002/ajh.23727.
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  - Walsh, Kyle M., Veryan Codd, Ivan V. Smirnov, Terri Rice, Paul A. Decker, Helen M. Hansen, Thomas Kollmeyer, et al. “Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk..” Nat Genet 46, no. 7 (July 2014): 731–35. https://doi.org/10.1038/ng.3004.
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  - Smith, Adam J. de, Kyle M. Walsh, Martha B. Ladner, Siming Zhang, Carmen Xiao, Franziska Cohen, Theodore B. Moore, et al. “The role of KIR genes and their cognate HLA class I ligands in childhood acute lymphoblastic leukemia..” Blood 123, no. 16 (April 17, 2014): 2497–2503. https://doi.org/10.1182/blood-2013-11-540625.
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  - Walsh, K. M., A. P. Chokkalingam, L. -. I. Hsu, C. Metayer, A. J. de Smith, D. I. Jacobs, G. V. Dahl, et al. “Associations between genome-wide Native American ancestry, known risk alleles and B-cell ALL risk in Hispanic children..” Leukemia 27, no. 12 (December 2013): 2416–19. https://doi.org/10.1038/leu.2013.130.
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  - Walsh, Kyle M., Adam J. de Smith, Anand P. Chokkalingam, Catherine Metayer, William Roberts, Lisa F. Barcellos, Joseph L. Wiemels, and Patricia A. Buffler. “GATA3 risk alleles are associated with ancestral components in Hispanic children with ALL..” Blood 122, no. 19 (November 7, 2013): 3385–87. https://doi.org/10.1182/blood-2013-08-524124.
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  - Walsh, Kyle M., Terri Rice, Paul A. Decker, Matthew L. Kosel, Thomas Kollmeyer, Helen M. Hansen, Shichun Zheng, et al. “Genetic variants in telomerase-related genes are associated with an older age at diagnosis in glioma patients: evidence for distinct pathways of gliomagenesis..” Neuro Oncol 15, no. 8 (August 2013): 1041–47. https://doi.org/10.1093/neuonc/not051.
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  - Walsh, Kyle M., Adam J. de Smith, Anand P. Chokkalingam, Catherine Metayer, Gary V. Dahl, Ling-i Hsu, Lisa F. Barcellos, Joseph L. Wiemels, and Patricia A. Buffler. “Novel childhood ALL susceptibility locus BMI1-PIP4K2A is specifically associated with the hyperdiploid subtype..” Blood 121, no. 23 (June 6, 2013): 4808–9. https://doi.org/10.1182/blood-2013-04-495390.
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  - Rice, Terri, Shichun Zheng, Paul A. Decker, Kyle M. Walsh, Paige Bracci, Yuanyuan Xiao, Lucie S. McCoy, et al. “Inherited variant on chromosome 11q23 increases susceptibility to IDH-mutated but not IDH-normal gliomas regardless of grade or histology..” Neuro Oncol 15, no. 5 (May 2013): 535–41. https://doi.org/10.1093/neuonc/nos324.
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  - Walsh, Kyle M., Erik Anderson, Helen M. Hansen, Paul A. Decker, Matt L. Kosel, Thomas Kollmeyer, Terri Rice, et al. “Analysis of 60 reported glioma risk SNPs replicates published GWAS findings but fails to replicate associations from published candidate-gene studies..” Genet Epidemiol 37, no. 2 (February 2013): 222–28. https://doi.org/10.1002/gepi.21707.
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  - Walsh, Kyle M., Ivan P. Gorlov, Helen M. Hansen, Xifeng Wu, Margaret R. Spitz, Huifeng Zhang, Emily Y. Lu, et al. “Fine-mapping of the 5p15.33, 6p22.1-p21.31, and 15q25.1 regions identifies functional and histology-specific lung cancer susceptibility loci in African-Americans..” Cancer Epidemiol Biomarkers Prev 22, no. 2 (February 2013): 251–60. https://doi.org/10.1158/1055-9965.EPI-12-1007-T.
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  - Jacobs, D. I., K. M. Walsh, M. Wrensch, J. Wiencke, R. Jenkins, R. S. Houlston, M. Bondy, et al. “Leveraging ethnic group incidence variation to investigate genetic susceptibility to glioma: A novel candidate SNP approach.” Frontiers in Genetics 3, no. OCT (December 1, 2012). https://doi.org/10.3389/fgene.2012.00203.
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  - Walsh, Kyle M., Christopher I. Amos, Angela S. Wenzlaff, Ivan P. Gorlov, Jennette D. Sison, Xifeng Wu, Margaret R. Spitz, et al. “Association study of nicotinic acetylcholine receptor genes identifies a novel lung cancer susceptibility locus near CHRNA1 in African-Americans..” Oncotarget 3, no. 11 (November 2012): 1428–38. https://doi.org/10.18632/oncotarget.746.
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  - DeWan, Andrew T., Kathryn Brigham Egan, Karen Hellenbrand, Keli Sorrentino, Nicole Pizzoferrato, Kyle M. Walsh, and Michael B. Bracken. “Whole-exome sequencing of a pedigree segregating asthma..” Bmc Med Genet 13 (October 9, 2012). https://doi.org/10.1186/1471-2350-13-95.
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  - Jenkins, Robert B., Yuanyuan Xiao, Hugues Sicotte, Paul A. Decker, Thomas M. Kollmeyer, Helen M. Hansen, Matthew L. Kosel, et al. “A low-frequency variant at 8q24.21 is strongly associated with risk of oligodendroglial tumors and astrocytomas with IDH1 or IDH2 mutation..” Nat Genet 44, no. 10 (October 2012): 1122–25. https://doi.org/10.1038/ng.2388.
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  - Kochar, Rabina, Kyle M. Walsh, Anil Jain, Steven J. Spalding, and Philip J. Hashkes. “Decreased use of non-steroidal anti-inflammatory drugs for the treatment of juvenile idiopathic arthritis in the era of modern aggressive treatment..” Rheumatol Int 32, no. 10 (October 2012): 3055–60. https://doi.org/10.1007/s00296-011-2084-7.
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  - Bracci, Paige M., Jennette Sison, Helen Hansen, Kyle M. Walsh, Charles P. Quesenberry, Dan J. Raz, Margaret Wrensch, and John K. Wiencke. “Cigarette smoking associated with lung adenocarcinoma in situ in a large case-control study (SFBALCS)..” J Thorac Oncol 7, no. 9 (September 2012): 1352–60. https://doi.org/10.1097/JTO.0b013e31825aba47.
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  - Zhao, L., E. W. Triche, K. M. Walsh, M. B. Bracken, A. F. Saftlas, J. Hoh, and A. T. Dewan. “Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients.” Bmc Pregnancy and Childbirth 12 (June 29, 2012). https://doi.org/10.1186/1471-2393-12-61.
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  - Claus, Elizabeth B., Kyle M. Walsh, Lisa Calvocoressi, Melissa L. Bondy, Joellen M. Schildkraut, Margaret Wrensch, and Joseph L. Wiemels. “Cigarette smoking and risk of meningioma: the effect of gender..” Cancer Epidemiol Biomarkers Prev 21, no. 6 (June 2012): 943–50. https://doi.org/10.1158/1055-9965.EPI-11-1059.
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  - Sebastiani, Paola, Nadia Solovieff, Andrew T. Dewan, Kyle M. Walsh, Annibale Puca, Stephen W. Hartley, Efthymia Melista, et al. “Genetic signatures of exceptional longevity in humans..” Plos One 7, no. 1 (2012). https://doi.org/10.1371/journal.pone.0029848.
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  - Wu, Chengqing, Kyle M. Walsh, Andrew T. DeWan, Josephine Hoh, and Zuoheng Wang. “Disease risk prediction with rare and common variants.” Bmc Proceedings 5, no. S9 (December 2011). https://doi.org/10.1186/1753-6561-5-s9-s61.
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  - Walsh, Kyle M., and Michael B. Bracken. “Copy number variation in the dosage-sensitive 16p11.2 interval accounts for only a small proportion of autism incidence: a systematic review and meta-analysis..” Genet Med 13, no. 5 (May 2011): 377–84. https://doi.org/10.1097/GIM.0b013e3182076c0c.
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  - Walsh, Kyle M., Murim Choi, Kjell Oberg, Matthew H. Kulke, James C. Yao, Chengqing Wu, Magdalena Jurkiewicz, et al. “A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum..” Endocr Relat Cancer 18, no. 1 (February 2011): 171–80. https://doi.org/10.1677/ERC-10-0248.
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  - Murk, William, Kyle Walsh, Ling-I Hsu, Linlu Zhao, Michael B. Bracken, and Andrew T. Dewan. “Attempted replication of 50 reported asthma risk genes identifies a SNP in RAD50 as associated with childhood atopic asthma..” Hum Hered 71, no. 2 (2011): 97–105. https://doi.org/10.1159/000319536.
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  - Walsh, Kyle M., Michael B. Bracken, William K. Murk, Josephine Hoh, and Andrew T. Dewan. “Association between reduced copy-number at T-cell receptor gamma (TCRgamma) and childhood allergic asthma: A possible role for somatic mosaicism..” Mutat Res 690, no. 1–2 (August 7, 2010): 89–94. https://doi.org/10.1016/j.mrfmmm.2010.05.005.
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  - Clendenning, Mark, Mark E. Baze, Shuying Sun, Kyle Walsh, Sandya Liyanarachchi, Dan Fix, Victoria Schunemann, et al. “Origins and prevalence of the American Founder Mutation of MSH2..” Cancer Res 68, no. 7 (April 1, 2008): 2145–53. https://doi.org/10.1158/0008-5472.CAN-07-6599.
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- Book Sections
  - Walsh, K. M., and M. R. Wrensch. “Epidemiology of Brain Tumors.” In Youmans and Winn Neurological Surgery. Elsevier, 2016.
  - Walsh, K. M., H. Ohgaki, and M. R. Wrensch. “Epidemiology.” In Gliomas, edited by M. S. Berger and M. Weller, 134:3–18. Elsevier, 2016.
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  - Walsh, K. M., E. B. Claus, and M. R. Wrensch. “Epidemiology.” In Neuro-Oncology: The Essentials, edited by M. Berstein and M. S. Berger. Thieme, 2014.
  - Walsh, K. M., M. S. Berger, and M. R. Wrensch. “Central Nervous System Tumors.” In Clinical Genomics: Practical Applications for Adult Patient Care, edited by M. F. Murray, M. W. Babyatsky, and M. A. Giovanni, 1:187–92. McGraw Hill Professional, 2013.

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