Kristy Lee

Contact Information

Call us at: (614) 355-6895

Institute for Genomic Medicine575 Children’s CrossroadColumbus, OH 43215 (map)

Learn more about Kristy Lee

Biography

Kristy Lee, PhD, FACMG, is a clinical laboratory director within the Institute for Genomic Medicine. She received her PhD in Cancer Biology at the University of Arizona, where she studied modulation of the redox environment as a therapeutic strategy to overcome apoptosis resistance in lymphoma. Kristy’s postdoctoral work at the Huntsman Cancer Institute focused on evaluating DNA repair and chromosome instability in Li-Fraumeni syndrome patients to determine cancer risk. She completed her Clinical Molecular Genetics and Cytogenetics fellowships at the University of Wisconsin-Madison/Wisconsin State Lab of Hygiene.

Research

Publications

                  LaHaye S, Fitch JR, Voytovich KJ, Herman AC, Kelly BJ, Lammi GE, Arbesfeld JA, Wijeratne S, Franklin SJ, Schieffer KM, Bir N, McGrath SD, Miller AR, Wetzel A, Miller KE, Bedrosian TA, Leraas K, Varga EA, Lee K, Gupta A, Setty B, Boué DR, Leonard JR, Finlay JL, Abdelbaki MS, Osorio DS, Koo SC, Koboldt DC, Wagner AH, Eisfeld AK, Mrózek K, Magrini V, Cottrell CE, Mardis ER, Wilson RK, White P. Discovery of clinically relevant fusions in pediatric cancer. BMC Genomics. 2021 Dec 4; 22: 872.

                


                  Melas M, Mathew MT, Mori M, Jayaraman V, Wilson SA, Martin C, Jacobson-Kelly AE, Kelly BJ, Magrini V, Mardis ER, Cottrell CE, Lee K. Somatic variation as an incidental finding in the pediatric next-generation sequencing era. Cold Spring Harb Mol Case Stud. 2021 Dec; 7: 

                


                  Lee K, Abraham RS. Next-generation sequencing for inborn errors of immunity. Hum Immunol. 2021 Mar 11;  

                


                  Miller CR, Lee K, Pfau RB, Reshmi SC, Corsmeier DJ, Hashimoto S, Dave-Wala A, Jayaraman V, Koboldt D, Matthews T, Mouhlas D, Stein M, McKinney A, Grossman T, Kelly BJ, White P, Magrini V, Wilson RK, Mardis ER, Cottrell CE. Disease-associated mosaic variation in clinical exome sequencing: a two-year pediatric tertiary care experience. Cold Spring Harb Mol Case Stud. 2020 Jun; 6: 

                


                  Rudd MK, Schleede JB, Williams SR, Lee K, Laffin J, Pasion R, Papenhausen PR. Monosomy X rescue explains discordant NIPT results and leads to uniparental isodisomy. Prenat Diagn. 2018 Aug 29;  

View More Publications

Education

Date of Appointment at Nationwide Children’s Hospital: 07/23/2018

Graduate School

University of Arizona

Date Completed: 05/01/2013

Contact Information

Institute for Genomic Medicine

Call us at: (614) 355-6895

                    575 Children’s CrossroadColumbus, OH 43215 (map)

Contact Information

Call us at: (614) 355-6895

Institute for Genomic Medicine575 Children’s CrossroadColumbus, OH 43215 (map)

Learn more about Kristy Lee

Biography

Kristy Lee, PhD, FACMG, is a clinical laboratory director within the Institute for Genomic Medicine. She received her PhD in Cancer Biology at the University of Arizona, where she studied modulation of the redox environment as a therapeutic strategy to overcome apoptosis resistance in lymphoma. Kristy’s postdoctoral work at the Huntsman Cancer Institute focused on evaluating DNA repair and chromosome instability in Li-Fraumeni syndrome patients to determine cancer risk. She completed her Clinical Molecular Genetics and Cytogenetics fellowships at the University of Wisconsin-Madison/Wisconsin State Lab of Hygiene.

Research

Publications

                  LaHaye S, Fitch JR, Voytovich KJ, Herman AC, Kelly BJ, Lammi GE, Arbesfeld JA, Wijeratne S, Franklin SJ, Schieffer KM, Bir N, McGrath SD, Miller AR, Wetzel A, Miller KE, Bedrosian TA, Leraas K, Varga EA, Lee K, Gupta A, Setty B, Boué DR, Leonard JR, Finlay JL, Abdelbaki MS, Osorio DS, Koo SC, Koboldt DC, Wagner AH, Eisfeld AK, Mrózek K, Magrini V, Cottrell CE, Mardis ER, Wilson RK, White P. Discovery of clinically relevant fusions in pediatric cancer. BMC Genomics. 2021 Dec 4; 22: 872.

                


                  Melas M, Mathew MT, Mori M, Jayaraman V, Wilson SA, Martin C, Jacobson-Kelly AE, Kelly BJ, Magrini V, Mardis ER, Cottrell CE, Lee K. Somatic variation as an incidental finding in the pediatric next-generation sequencing era. Cold Spring Harb Mol Case Stud. 2021 Dec; 7: 

                


                  Lee K, Abraham RS. Next-generation sequencing for inborn errors of immunity. Hum Immunol. 2021 Mar 11;  

                


                  Miller CR, Lee K, Pfau RB, Reshmi SC, Corsmeier DJ, Hashimoto S, Dave-Wala A, Jayaraman V, Koboldt D, Matthews T, Mouhlas D, Stein M, McKinney A, Grossman T, Kelly BJ, White P, Magrini V, Wilson RK, Mardis ER, Cottrell CE. Disease-associated mosaic variation in clinical exome sequencing: a two-year pediatric tertiary care experience. Cold Spring Harb Mol Case Stud. 2020 Jun; 6: 

                


                  Rudd MK, Schleede JB, Williams SR, Lee K, Laffin J, Pasion R, Papenhausen PR. Monosomy X rescue explains discordant NIPT results and leads to uniparental isodisomy. Prenat Diagn. 2018 Aug 29;  

View More Publications

Education

Date of Appointment at Nationwide Children’s Hospital: 07/23/2018

Graduate School

University of Arizona

Date Completed: 05/01/2013

Contact Information

Institute for Genomic Medicine

Call us at: (614) 355-6895

                    575 Children’s CrossroadColumbus, OH 43215 (map)

Contact Information

Call us at: (614) 355-6895

Institute for Genomic Medicine575 Children’s CrossroadColumbus, OH 43215 (map)

Learn more about Kristy Lee

Contact Information

• Call us at:
• (614) 355-6895
• Institute for Genomic Medicine575 Children’s CrossroadColumbus, OH 43215 (map)

Learn more about Kristy Lee

Biography

Kristy Lee, PhD, FACMG, is a clinical laboratory director within the Institute for Genomic Medicine. She received her PhD in Cancer Biology at the University of Arizona, where she studied modulation of the redox environment as a therapeutic strategy to overcome apoptosis resistance in lymphoma. Kristy’s postdoctoral work at the Huntsman Cancer Institute focused on evaluating DNA repair and chromosome instability in Li-Fraumeni syndrome patients to determine cancer risk. She completed her Clinical Molecular Genetics and Cytogenetics fellowships at the University of Wisconsin-Madison/Wisconsin State Lab of Hygiene.

Biography

Kristy Lee, PhD, FACMG, is a clinical laboratory director within the Institute for Genomic Medicine. She received her PhD in Cancer Biology at the University of Arizona, where she studied modulation of the redox environment as a therapeutic strategy to overcome apoptosis resistance in lymphoma. Kristy’s postdoctoral work at the Huntsman Cancer Institute focused on evaluating DNA repair and chromosome instability in Li-Fraumeni syndrome patients to determine cancer risk. She completed her Clinical Molecular Genetics and Cytogenetics fellowships at the University of Wisconsin-Madison/Wisconsin State Lab of Hygiene.

Biography

Kristy Lee, PhD, FACMG, is a clinical laboratory director within the Institute for Genomic Medicine. She received her PhD in Cancer Biology at the University of Arizona, where she studied modulation of the redox environment as a therapeutic strategy to overcome apoptosis resistance in lymphoma. Kristy’s postdoctoral work at the Huntsman Cancer Institute focused on evaluating DNA repair and chromosome instability in Li-Fraumeni syndrome patients to determine cancer risk. She completed her Clinical Molecular Genetics and Cytogenetics fellowships at the University of Wisconsin-Madison/Wisconsin State Lab of Hygiene.

Kristy Lee, PhD, FACMG, is a clinical laboratory director within the Institute for Genomic Medicine. She received her PhD in Cancer Biology at the University of Arizona, where she studied modulation of the redox environment as a therapeutic strategy to overcome apoptosis resistance in lymphoma. Kristy’s postdoctoral work at the Huntsman Cancer Institute focused on evaluating DNA repair and chromosome instability in Li-Fraumeni syndrome patients to determine cancer risk. She completed her Clinical Molecular Genetics and Cytogenetics fellowships at the University of Wisconsin-Madison/Wisconsin State Lab of Hygiene.

Kristy Lee, PhD, FACMG, is a clinical laboratory director within the Institute for Genomic Medicine. She received her PhD in Cancer Biology at the University of Arizona, where she studied modulation of the redox environment as a therapeutic strategy to overcome apoptosis resistance in lymphoma. Kristy’s postdoctoral work at the Huntsman Cancer Institute focused on evaluating DNA repair and chromosome instability in Li-Fraumeni syndrome patients to determine cancer risk. She completed her Clinical Molecular Genetics and Cytogenetics fellowships at the University of Wisconsin-Madison/Wisconsin State Lab of Hygiene.

Research

Publications

                  LaHaye S, Fitch JR, Voytovich KJ, Herman AC, Kelly BJ, Lammi GE, Arbesfeld JA, Wijeratne S, Franklin SJ, Schieffer KM, Bir N, McGrath SD, Miller AR, Wetzel A, Miller KE, Bedrosian TA, Leraas K, Varga EA, Lee K, Gupta A, Setty B, Boué DR, Leonard JR, Finlay JL, Abdelbaki MS, Osorio DS, Koo SC, Koboldt DC, Wagner AH, Eisfeld AK, Mrózek K, Magrini V, Cottrell CE, Mardis ER, Wilson RK, White P. Discovery of clinically relevant fusions in pediatric cancer. BMC Genomics. 2021 Dec 4; 22: 872.

                


                  Melas M, Mathew MT, Mori M, Jayaraman V, Wilson SA, Martin C, Jacobson-Kelly AE, Kelly BJ, Magrini V, Mardis ER, Cottrell CE, Lee K. Somatic variation as an incidental finding in the pediatric next-generation sequencing era. Cold Spring Harb Mol Case Stud. 2021 Dec; 7: 

                


                  Lee K, Abraham RS. Next-generation sequencing for inborn errors of immunity. Hum Immunol. 2021 Mar 11;  

                


                  Miller CR, Lee K, Pfau RB, Reshmi SC, Corsmeier DJ, Hashimoto S, Dave-Wala A, Jayaraman V, Koboldt D, Matthews T, Mouhlas D, Stein M, McKinney A, Grossman T, Kelly BJ, White P, Magrini V, Wilson RK, Mardis ER, Cottrell CE. Disease-associated mosaic variation in clinical exome sequencing: a two-year pediatric tertiary care experience. Cold Spring Harb Mol Case Stud. 2020 Jun; 6: 

                


                  Rudd MK, Schleede JB, Williams SR, Lee K, Laffin J, Pasion R, Papenhausen PR. Monosomy X rescue explains discordant NIPT results and leads to uniparental isodisomy. Prenat Diagn. 2018 Aug 29;  

View More Publications

Research

Publications

                  LaHaye S, Fitch JR, Voytovich KJ, Herman AC, Kelly BJ, Lammi GE, Arbesfeld JA, Wijeratne S, Franklin SJ, Schieffer KM, Bir N, McGrath SD, Miller AR, Wetzel A, Miller KE, Bedrosian TA, Leraas K, Varga EA, Lee K, Gupta A, Setty B, Boué DR, Leonard JR, Finlay JL, Abdelbaki MS, Osorio DS, Koo SC, Koboldt DC, Wagner AH, Eisfeld AK, Mrózek K, Magrini V, Cottrell CE, Mardis ER, Wilson RK, White P. Discovery of clinically relevant fusions in pediatric cancer. BMC Genomics. 2021 Dec 4; 22: 872.

                


                  Melas M, Mathew MT, Mori M, Jayaraman V, Wilson SA, Martin C, Jacobson-Kelly AE, Kelly BJ, Magrini V, Mardis ER, Cottrell CE, Lee K. Somatic variation as an incidental finding in the pediatric next-generation sequencing era. Cold Spring Harb Mol Case Stud. 2021 Dec; 7: 

                


                  Lee K, Abraham RS. Next-generation sequencing for inborn errors of immunity. Hum Immunol. 2021 Mar 11;  

                


                  Miller CR, Lee K, Pfau RB, Reshmi SC, Corsmeier DJ, Hashimoto S, Dave-Wala A, Jayaraman V, Koboldt D, Matthews T, Mouhlas D, Stein M, McKinney A, Grossman T, Kelly BJ, White P, Magrini V, Wilson RK, Mardis ER, Cottrell CE. Disease-associated mosaic variation in clinical exome sequencing: a two-year pediatric tertiary care experience. Cold Spring Harb Mol Case Stud. 2020 Jun; 6: 

                


                  Rudd MK, Schleede JB, Williams SR, Lee K, Laffin J, Pasion R, Papenhausen PR. Monosomy X rescue explains discordant NIPT results and leads to uniparental isodisomy. Prenat Diagn. 2018 Aug 29;  

View More Publications

Research

Publications

                  LaHaye S, Fitch JR, Voytovich KJ, Herman AC, Kelly BJ, Lammi GE, Arbesfeld JA, Wijeratne S, Franklin SJ, Schieffer KM, Bir N, McGrath SD, Miller AR, Wetzel A, Miller KE, Bedrosian TA, Leraas K, Varga EA, Lee K, Gupta A, Setty B, Boué DR, Leonard JR, Finlay JL, Abdelbaki MS, Osorio DS, Koo SC, Koboldt DC, Wagner AH, Eisfeld AK, Mrózek K, Magrini V, Cottrell CE, Mardis ER, Wilson RK, White P. Discovery of clinically relevant fusions in pediatric cancer. BMC Genomics. 2021 Dec 4; 22: 872.

                


                  Melas M, Mathew MT, Mori M, Jayaraman V, Wilson SA, Martin C, Jacobson-Kelly AE, Kelly BJ, Magrini V, Mardis ER, Cottrell CE, Lee K. Somatic variation as an incidental finding in the pediatric next-generation sequencing era. Cold Spring Harb Mol Case Stud. 2021 Dec; 7: 

                


                  Lee K, Abraham RS. Next-generation sequencing for inborn errors of immunity. Hum Immunol. 2021 Mar 11;  

                


                  Miller CR, Lee K, Pfau RB, Reshmi SC, Corsmeier DJ, Hashimoto S, Dave-Wala A, Jayaraman V, Koboldt D, Matthews T, Mouhlas D, Stein M, McKinney A, Grossman T, Kelly BJ, White P, Magrini V, Wilson RK, Mardis ER, Cottrell CE. Disease-associated mosaic variation in clinical exome sequencing: a two-year pediatric tertiary care experience. Cold Spring Harb Mol Case Stud. 2020 Jun; 6: 

                


                  Rudd MK, Schleede JB, Williams SR, Lee K, Laffin J, Pasion R, Papenhausen PR. Monosomy X rescue explains discordant NIPT results and leads to uniparental isodisomy. Prenat Diagn. 2018 Aug 29;  

View More Publications

Publications

                  LaHaye S, Fitch JR, Voytovich KJ, Herman AC, Kelly BJ, Lammi GE, Arbesfeld JA, Wijeratne S, Franklin SJ, Schieffer KM, Bir N, McGrath SD, Miller AR, Wetzel A, Miller KE, Bedrosian TA, Leraas K, Varga EA, Lee K, Gupta A, Setty B, Boué DR, Leonard JR, Finlay JL, Abdelbaki MS, Osorio DS, Koo SC, Koboldt DC, Wagner AH, Eisfeld AK, Mrózek K, Magrini V, Cottrell CE, Mardis ER, Wilson RK, White P. Discovery of clinically relevant fusions in pediatric cancer. BMC Genomics. 2021 Dec 4; 22: 872.

                


                  Melas M, Mathew MT, Mori M, Jayaraman V, Wilson SA, Martin C, Jacobson-Kelly AE, Kelly BJ, Magrini V, Mardis ER, Cottrell CE, Lee K. Somatic variation as an incidental finding in the pediatric next-generation sequencing era. Cold Spring Harb Mol Case Stud. 2021 Dec; 7: 

                


                  Lee K, Abraham RS. Next-generation sequencing for inborn errors of immunity. Hum Immunol. 2021 Mar 11;  

                


                  Miller CR, Lee K, Pfau RB, Reshmi SC, Corsmeier DJ, Hashimoto S, Dave-Wala A, Jayaraman V, Koboldt D, Matthews T, Mouhlas D, Stein M, McKinney A, Grossman T, Kelly BJ, White P, Magrini V, Wilson RK, Mardis ER, Cottrell CE. Disease-associated mosaic variation in clinical exome sequencing: a two-year pediatric tertiary care experience. Cold Spring Harb Mol Case Stud. 2020 Jun; 6: 

                


                  Rudd MK, Schleede JB, Williams SR, Lee K, Laffin J, Pasion R, Papenhausen PR. Monosomy X rescue explains discordant NIPT results and leads to uniparental isodisomy. Prenat Diagn. 2018 Aug 29;  

View More Publications

                  LaHaye S, Fitch JR, Voytovich KJ, Herman AC, Kelly BJ, Lammi GE, Arbesfeld JA, Wijeratne S, Franklin SJ, Schieffer KM, Bir N, McGrath SD, Miller AR, Wetzel A, Miller KE, Bedrosian TA, Leraas K, Varga EA, Lee K, Gupta A, Setty B, Boué DR, Leonard JR, Finlay JL, Abdelbaki MS, Osorio DS, Koo SC, Koboldt DC, Wagner AH, Eisfeld AK, Mrózek K, Magrini V, Cottrell CE, Mardis ER, Wilson RK, White P. Discovery of clinically relevant fusions in pediatric cancer. BMC Genomics. 2021 Dec 4; 22: 872.

                


                  Melas M, Mathew MT, Mori M, Jayaraman V, Wilson SA, Martin C, Jacobson-Kelly AE, Kelly BJ, Magrini V, Mardis ER, Cottrell CE, Lee K. Somatic variation as an incidental finding in the pediatric next-generation sequencing era. Cold Spring Harb Mol Case Stud. 2021 Dec; 7: 

                


                  Lee K, Abraham RS. Next-generation sequencing for inborn errors of immunity. Hum Immunol. 2021 Mar 11;  

                


                  Miller CR, Lee K, Pfau RB, Reshmi SC, Corsmeier DJ, Hashimoto S, Dave-Wala A, Jayaraman V, Koboldt D, Matthews T, Mouhlas D, Stein M, McKinney A, Grossman T, Kelly BJ, White P, Magrini V, Wilson RK, Mardis ER, Cottrell CE. Disease-associated mosaic variation in clinical exome sequencing: a two-year pediatric tertiary care experience. Cold Spring Harb Mol Case Stud. 2020 Jun; 6: 

                


                  Rudd MK, Schleede JB, Williams SR, Lee K, Laffin J, Pasion R, Papenhausen PR. Monosomy X rescue explains discordant NIPT results and leads to uniparental isodisomy. Prenat Diagn. 2018 Aug 29;  

View More Publications

• LaHaye S, Fitch JR, Voytovich KJ, Herman AC, Kelly BJ, Lammi GE, Arbesfeld JA, Wijeratne S, Franklin SJ, Schieffer KM, Bir N, McGrath SD, Miller AR, Wetzel A, Miller KE, Bedrosian TA, Leraas K, Varga EA, Lee K, Gupta A, Setty B, Boué DR, Leonard JR, Finlay JL, Abdelbaki MS, Osorio DS, Koo SC, Koboldt DC, Wagner AH, Eisfeld AK, Mrózek K, Magrini V, Cottrell CE, Mardis ER, Wilson RK, White P. Discovery of clinically relevant fusions in pediatric cancer. BMC Genomics. 2021 Dec 4; 22: 872.
• Melas M, Mathew MT, Mori M, Jayaraman V, Wilson SA, Martin C, Jacobson-Kelly AE, Kelly BJ, Magrini V, Mardis ER, Cottrell CE, Lee K. Somatic variation as an incidental finding in the pediatric next-generation sequencing era. Cold Spring Harb Mol Case Stud. 2021 Dec; 7:
• Lee K, Abraham RS. Next-generation sequencing for inborn errors of immunity. Hum Immunol. 2021 Mar 11;
• Miller CR, Lee K, Pfau RB, Reshmi SC, Corsmeier DJ, Hashimoto S, Dave-Wala A, Jayaraman V, Koboldt D, Matthews T, Mouhlas D, Stein M, McKinney A, Grossman T, Kelly BJ, White P, Magrini V, Wilson RK, Mardis ER, Cottrell CE. Disease-associated mosaic variation in clinical exome sequencing: a two-year pediatric tertiary care experience. Cold Spring Harb Mol Case Stud. 2020 Jun; 6:
• Rudd MK, Schleede JB, Williams SR, Lee K, Laffin J, Pasion R, Papenhausen PR. Monosomy X rescue explains discordant NIPT results and leads to uniparental isodisomy. Prenat Diagn. 2018 Aug 29;

Education

Date of Appointment at Nationwide Children’s Hospital: 07/23/2018

Graduate School

University of Arizona

Date Completed: 05/01/2013

Education

Date of Appointment at Nationwide Children’s Hospital: 07/23/2018

Graduate School

University of Arizona

Date Completed: 05/01/2013

Education

Date of Appointment at Nationwide Children’s Hospital: 07/23/2018

Graduate School

University of Arizona

Date Completed: 05/01/2013

Date of Appointment at Nationwide Children’s Hospital: 07/23/2018

Graduate School

University of Arizona

Date Completed: 05/01/2013

Date of Appointment at Nationwide Children’s Hospital: 07/23/2018

Graduate School

University of Arizona

Date Completed: 05/01/2013

Contact Information

Institute for Genomic Medicine

Call us at: (614) 355-6895

                    575 Children’s CrossroadColumbus, OH 43215 (map)

Contact Information

Institute for Genomic Medicine

Call us at: (614) 355-6895

                    575 Children’s CrossroadColumbus, OH 43215 (map)

Contact Information

Institute for Genomic Medicine

Call us at: (614) 355-6895

                    575 Children’s CrossroadColumbus, OH 43215 (map)

Institute for Genomic Medicine

Call us at: (614) 355-6895

                    575 Children’s CrossroadColumbus, OH 43215 (map)

Call us at: (614) 355-6895

                    575 Children’s CrossroadColumbus, OH 43215 (map)

Call us at: (614) 355-6895

                    575 Children’s CrossroadColumbus, OH 43215 (map)

• Call us at:
• (614) 355-6895
• 575 Children’s CrossroadColumbus, OH 43215 (map)