Theodora Jacobson Matthews

Contact Information

Call us at: (614)722-5346

Fax us at: (614)722-5471

      700 Children's DriveColumbus, OH 43205 (map)

Learn more about Theodora Jacobson Matthews

Biography

Theodora (Teddi) Matthews is a laboratory genetic counselor for the Institute for Genomic Medicine Clinical Laboratory which includes both a cytogenetics and molecular genetics laboratory. She serves as a resource for internal and external health care providers regarding genetic testing, including the appropriate use of tests, limitations/accuracy of tests, possible testing outcomes, sample requirements, interpretation of results and follow up for cases with abnormal results. Teddi also assists in case review and report write-up, the development of new laboratory tests, and teaching. Teddi has an appointment as an Adjunct Assistant Professor in the Department of Pediatrics through The Ohio State University School of Medicine and serves as the OSU genetic counseling coordinator and supervisor.

Academic and Clinical Areas

Pathology and Laboratory Medicine

Clinical Pathology Team

Clinical Pathology

Genetic Counselor, Institute for Genomic Medicine Clinical Laboratory

Primary Section

Clinical Pathology

Awards, Honors & Organizations

IMPACT Project Award Recipient, Nationwide Children’s Hospital, 2017 American Board of Genetic Counseling, Board Certification, 2014 Member, American Board of Genetic Counseling, 2014 - Present Ohio Credential #70.000105, Licensed Genetic Counselor, 2013 - Present Member, National Society of Genetic Counselors, 2012 - Present

Research

View My Publications Publications

                  Mathew MT, Antoniou A, Ramesh N, Hu M, Gaither J, Mouhlas D, Hashimoto S, Humphrey M, Matthews T, Hunter JM, Reshmi S, Schultz M, Lee K, Pfau R, Cottrell C, McBride KL, Navin NE, Chaudhari BP, Leung ML. A Decade's Experience in Pediatric Chromosomal Microarray Reveals Distinct Characteristics Across Ordering Specialties. J Mol Diagn. 2022 Jun 16;  

                


                  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: 

                


                  Ilacqua A, Benedict J, Shoben A, Skotko BG, Matthews T, Benson B, Allain DC. Alzheimer's disease development in adults with Down syndrome: Caregivers' perspectives. Am J Med Genet A. 2020 Jan; 182: 104-114.

                


                  Barrie ES, Li Y, Lamb-Thrush D, Hashimoto S, Matthews T, Mouhlas D, Pyatt R, Reshmi SC, Gastier-Foster JM, Pfau R, Astbury C. Pericentromeric regions of homozygosity on the X chromosome: Another likely benign population variant. Eur J Med Genet. 2018 Jul; 61: 416-420.

                


                  Matthews TJ, Allain DC, Matthews AL, Mitchell A, Santoro SL, Cohen L. An assessment of health, social, communication, and daily living skills of adults with Down syndrome. Am J Med Genet A. 2018 Jun; 176: 1389-1397.

                


                  Swaminathan R, Huang Y, Miller K, Pastore M, Hashimoto S, Jacobson T, Mouhlas D, Lin S. Transferring Exome Sequencing Data from Clinical Laboratories to Healthcare Providers: Lessons Learned at a Pediatric Hospital. Front Genet. 2018; 9: 54.

                


                  Santoro SL, Jacobson T, Lemle S, Bartman T. Integrating a Geneticist in a Multidisciplinary Clinic for Down Syndrome Increases Commitment to Genetic Counseling. Pediatr Qual Saf. 2017 Sep-Oct; 2: e039.

View More Publications

Education

Date of Appointment at Nationwide Children’s Hospital: 08/05/2013

Graduate School

Case Western Reserve University

Date Completed: 05/19/2013

Undergraduate School

Case Western Reserve University

Date Completed: 05/15/2011

Professional Experience

2015 - Present Nationwide Children’s Hospital, Certified Genetic Counselor in the Cytogenetics and Molecular Genetics Laboratory2013 - 2015 Nationwide Children’s Hospital, Clinical Pediatrics Certified Genetic Counselor

Contact Information

Call us at: (614)722-5346

Fax us at: (614)722-5471

                    700 Children's DriveColumbus, OH 43205 (map)

Contact Information

Call us at: (614)722-5346

Fax us at: (614)722-5471

      700 Children's DriveColumbus, OH 43205 (map)

Learn more about Theodora Jacobson Matthews

Biography

Academic and Clinical Areas

Pathology and Laboratory Medicine

Clinical Pathology Team

Clinical Pathology

Genetic Counselor, Institute for Genomic Medicine Clinical Laboratory

Primary Section

Clinical Pathology

Awards, Honors & Organizations

Research

View My Publications Publications

                  Mathew MT, Antoniou A, Ramesh N, Hu M, Gaither J, Mouhlas D, Hashimoto S, Humphrey M, Matthews T, Hunter JM, Reshmi S, Schultz M, Lee K, Pfau R, Cottrell C, McBride KL, Navin NE, Chaudhari BP, Leung ML. A Decade's Experience in Pediatric Chromosomal Microarray Reveals Distinct Characteristics Across Ordering Specialties. J Mol Diagn. 2022 Jun 16;  

                


                  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: 

                


                  Ilacqua A, Benedict J, Shoben A, Skotko BG, Matthews T, Benson B, Allain DC. Alzheimer's disease development in adults with Down syndrome: Caregivers' perspectives. Am J Med Genet A. 2020 Jan; 182: 104-114.

                


                  Barrie ES, Li Y, Lamb-Thrush D, Hashimoto S, Matthews T, Mouhlas D, Pyatt R, Reshmi SC, Gastier-Foster JM, Pfau R, Astbury C. Pericentromeric regions of homozygosity on the X chromosome: Another likely benign population variant. Eur J Med Genet. 2018 Jul; 61: 416-420.

                


                  Matthews TJ, Allain DC, Matthews AL, Mitchell A, Santoro SL, Cohen L. An assessment of health, social, communication, and daily living skills of adults with Down syndrome. Am J Med Genet A. 2018 Jun; 176: 1389-1397.

                


                  Swaminathan R, Huang Y, Miller K, Pastore M, Hashimoto S, Jacobson T, Mouhlas D, Lin S. Transferring Exome Sequencing Data from Clinical Laboratories to Healthcare Providers: Lessons Learned at a Pediatric Hospital. Front Genet. 2018; 9: 54.

                


                  Santoro SL, Jacobson T, Lemle S, Bartman T. Integrating a Geneticist in a Multidisciplinary Clinic for Down Syndrome Increases Commitment to Genetic Counseling. Pediatr Qual Saf. 2017 Sep-Oct; 2: e039.

View More Publications

Education

Date of Appointment at Nationwide Children’s Hospital: 08/05/2013

Graduate School

Case Western Reserve University

Date Completed: 05/19/2013

Undergraduate School

Case Western Reserve University

Date Completed: 05/15/2011

Professional Experience

Contact Information

Call us at: (614)722-5346

Fax us at: (614)722-5471

                    700 Children's DriveColumbus, OH 43205 (map)

Contact Information

Call us at: (614)722-5346

Fax us at: (614)722-5471

      700 Children's DriveColumbus, OH 43205 (map)

Learn more about Theodora Jacobson Matthews

Contact Information

Call us at:
(614)722-5346
Fax us at:
(614)722-5471
700 Children’s DriveColumbus, OH 43205 (map)

Learn more about Theodora Jacobson Matthews

Biography

Academic and Clinical Areas

Pathology and Laboratory Medicine

Clinical Pathology Team

Clinical Pathology

Genetic Counselor, Institute for Genomic Medicine Clinical Laboratory

Primary Section

Clinical Pathology

Academic and Clinical Areas

Pathology and Laboratory Medicine

Clinical Pathology Team

Clinical Pathology

Genetic Counselor, Institute for Genomic Medicine Clinical Laboratory

Primary Section

Clinical Pathology

Academic and Clinical Areas

Pathology and Laboratory Medicine

Clinical Pathology Team

Clinical Pathology

Genetic Counselor, Institute for Genomic Medicine Clinical Laboratory

Primary Section

Clinical Pathology

Pathology and Laboratory Medicine

Clinical Pathology Team

Clinical Pathology

Genetic Counselor, Institute for Genomic Medicine Clinical Laboratory

Primary Section

Clinical Pathology

Pathology and Laboratory Medicine
Clinical Pathology Team
Clinical Pathology
Genetic Counselor, Institute for Genomic Medicine Clinical Laboratory
Primary Section
Clinical Pathology

Awards, Honors & Organizations

IMPACT Project Award Recipient, Nationwide Children’s Hospital, 2017
American Board of Genetic Counseling, Board Certification, 2014
Member, American Board of Genetic Counseling, 2014 - Present
Ohio Credential #70.000105, Licensed Genetic Counselor, 2013 - Present
Member, National Society of Genetic Counselors, 2012 - Present

Research

View My Publications Publications

                  Mathew MT, Antoniou A, Ramesh N, Hu M, Gaither J, Mouhlas D, Hashimoto S, Humphrey M, Matthews T, Hunter JM, Reshmi S, Schultz M, Lee K, Pfau R, Cottrell C, McBride KL, Navin NE, Chaudhari BP, Leung ML. A Decade's Experience in Pediatric Chromosomal Microarray Reveals Distinct Characteristics Across Ordering Specialties. J Mol Diagn. 2022 Jun 16;  

                


                  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: 

                


                  Ilacqua A, Benedict J, Shoben A, Skotko BG, Matthews T, Benson B, Allain DC. Alzheimer's disease development in adults with Down syndrome: Caregivers' perspectives. Am J Med Genet A. 2020 Jan; 182: 104-114.

                


                  Barrie ES, Li Y, Lamb-Thrush D, Hashimoto S, Matthews T, Mouhlas D, Pyatt R, Reshmi SC, Gastier-Foster JM, Pfau R, Astbury C. Pericentromeric regions of homozygosity on the X chromosome: Another likely benign population variant. Eur J Med Genet. 2018 Jul; 61: 416-420.

                


                  Matthews TJ, Allain DC, Matthews AL, Mitchell A, Santoro SL, Cohen L. An assessment of health, social, communication, and daily living skills of adults with Down syndrome. Am J Med Genet A. 2018 Jun; 176: 1389-1397.

                


                  Swaminathan R, Huang Y, Miller K, Pastore M, Hashimoto S, Jacobson T, Mouhlas D, Lin S. Transferring Exome Sequencing Data from Clinical Laboratories to Healthcare Providers: Lessons Learned at a Pediatric Hospital. Front Genet. 2018; 9: 54.

                


                  Santoro SL, Jacobson T, Lemle S, Bartman T. Integrating a Geneticist in a Multidisciplinary Clinic for Down Syndrome Increases Commitment to Genetic Counseling. Pediatr Qual Saf. 2017 Sep-Oct; 2: e039.

View More Publications

Research

View My Publications Publications

                  Mathew MT, Antoniou A, Ramesh N, Hu M, Gaither J, Mouhlas D, Hashimoto S, Humphrey M, Matthews T, Hunter JM, Reshmi S, Schultz M, Lee K, Pfau R, Cottrell C, McBride KL, Navin NE, Chaudhari BP, Leung ML. A Decade's Experience in Pediatric Chromosomal Microarray Reveals Distinct Characteristics Across Ordering Specialties. J Mol Diagn. 2022 Jun 16;  

                


                  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: 

                


                  Ilacqua A, Benedict J, Shoben A, Skotko BG, Matthews T, Benson B, Allain DC. Alzheimer's disease development in adults with Down syndrome: Caregivers' perspectives. Am J Med Genet A. 2020 Jan; 182: 104-114.

                


                  Barrie ES, Li Y, Lamb-Thrush D, Hashimoto S, Matthews T, Mouhlas D, Pyatt R, Reshmi SC, Gastier-Foster JM, Pfau R, Astbury C. Pericentromeric regions of homozygosity on the X chromosome: Another likely benign population variant. Eur J Med Genet. 2018 Jul; 61: 416-420.

                


                  Matthews TJ, Allain DC, Matthews AL, Mitchell A, Santoro SL, Cohen L. An assessment of health, social, communication, and daily living skills of adults with Down syndrome. Am J Med Genet A. 2018 Jun; 176: 1389-1397.

                


                  Swaminathan R, Huang Y, Miller K, Pastore M, Hashimoto S, Jacobson T, Mouhlas D, Lin S. Transferring Exome Sequencing Data from Clinical Laboratories to Healthcare Providers: Lessons Learned at a Pediatric Hospital. Front Genet. 2018; 9: 54.

                


                  Santoro SL, Jacobson T, Lemle S, Bartman T. Integrating a Geneticist in a Multidisciplinary Clinic for Down Syndrome Increases Commitment to Genetic Counseling. Pediatr Qual Saf. 2017 Sep-Oct; 2: e039.

View More Publications

Research

View My Publications Publications

                  Mathew MT, Antoniou A, Ramesh N, Hu M, Gaither J, Mouhlas D, Hashimoto S, Humphrey M, Matthews T, Hunter JM, Reshmi S, Schultz M, Lee K, Pfau R, Cottrell C, McBride KL, Navin NE, Chaudhari BP, Leung ML. A Decade's Experience in Pediatric Chromosomal Microarray Reveals Distinct Characteristics Across Ordering Specialties. J Mol Diagn. 2022 Jun 16;  

                


                  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: 

                


                  Ilacqua A, Benedict J, Shoben A, Skotko BG, Matthews T, Benson B, Allain DC. Alzheimer's disease development in adults with Down syndrome: Caregivers' perspectives. Am J Med Genet A. 2020 Jan; 182: 104-114.

                


                  Barrie ES, Li Y, Lamb-Thrush D, Hashimoto S, Matthews T, Mouhlas D, Pyatt R, Reshmi SC, Gastier-Foster JM, Pfau R, Astbury C. Pericentromeric regions of homozygosity on the X chromosome: Another likely benign population variant. Eur J Med Genet. 2018 Jul; 61: 416-420.

                


                  Matthews TJ, Allain DC, Matthews AL, Mitchell A, Santoro SL, Cohen L. An assessment of health, social, communication, and daily living skills of adults with Down syndrome. Am J Med Genet A. 2018 Jun; 176: 1389-1397.

                


                  Swaminathan R, Huang Y, Miller K, Pastore M, Hashimoto S, Jacobson T, Mouhlas D, Lin S. Transferring Exome Sequencing Data from Clinical Laboratories to Healthcare Providers: Lessons Learned at a Pediatric Hospital. Front Genet. 2018; 9: 54.

                


                  Santoro SL, Jacobson T, Lemle S, Bartman T. Integrating a Geneticist in a Multidisciplinary Clinic for Down Syndrome Increases Commitment to Genetic Counseling. Pediatr Qual Saf. 2017 Sep-Oct; 2: e039.

View More Publications

View My Publications Publications

                  Mathew MT, Antoniou A, Ramesh N, Hu M, Gaither J, Mouhlas D, Hashimoto S, Humphrey M, Matthews T, Hunter JM, Reshmi S, Schultz M, Lee K, Pfau R, Cottrell C, McBride KL, Navin NE, Chaudhari BP, Leung ML. A Decade's Experience in Pediatric Chromosomal Microarray Reveals Distinct Characteristics Across Ordering Specialties. J Mol Diagn. 2022 Jun 16;  

                


                  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: 

                


                  Ilacqua A, Benedict J, Shoben A, Skotko BG, Matthews T, Benson B, Allain DC. Alzheimer's disease development in adults with Down syndrome: Caregivers' perspectives. Am J Med Genet A. 2020 Jan; 182: 104-114.

                


                  Barrie ES, Li Y, Lamb-Thrush D, Hashimoto S, Matthews T, Mouhlas D, Pyatt R, Reshmi SC, Gastier-Foster JM, Pfau R, Astbury C. Pericentromeric regions of homozygosity on the X chromosome: Another likely benign population variant. Eur J Med Genet. 2018 Jul; 61: 416-420.

                


                  Matthews TJ, Allain DC, Matthews AL, Mitchell A, Santoro SL, Cohen L. An assessment of health, social, communication, and daily living skills of adults with Down syndrome. Am J Med Genet A. 2018 Jun; 176: 1389-1397.

                


                  Swaminathan R, Huang Y, Miller K, Pastore M, Hashimoto S, Jacobson T, Mouhlas D, Lin S. Transferring Exome Sequencing Data from Clinical Laboratories to Healthcare Providers: Lessons Learned at a Pediatric Hospital. Front Genet. 2018; 9: 54.

                


                  Santoro SL, Jacobson T, Lemle S, Bartman T. Integrating a Geneticist in a Multidisciplinary Clinic for Down Syndrome Increases Commitment to Genetic Counseling. Pediatr Qual Saf. 2017 Sep-Oct; 2: e039.

View More Publications

View My Publications

                  Mathew MT, Antoniou A, Ramesh N, Hu M, Gaither J, Mouhlas D, Hashimoto S, Humphrey M, Matthews T, Hunter JM, Reshmi S, Schultz M, Lee K, Pfau R, Cottrell C, McBride KL, Navin NE, Chaudhari BP, Leung ML. A Decade's Experience in Pediatric Chromosomal Microarray Reveals Distinct Characteristics Across Ordering Specialties. J Mol Diagn. 2022 Jun 16;  

                


                  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: 

                


                  Ilacqua A, Benedict J, Shoben A, Skotko BG, Matthews T, Benson B, Allain DC. Alzheimer's disease development in adults with Down syndrome: Caregivers' perspectives. Am J Med Genet A. 2020 Jan; 182: 104-114.

                


                  Barrie ES, Li Y, Lamb-Thrush D, Hashimoto S, Matthews T, Mouhlas D, Pyatt R, Reshmi SC, Gastier-Foster JM, Pfau R, Astbury C. Pericentromeric regions of homozygosity on the X chromosome: Another likely benign population variant. Eur J Med Genet. 2018 Jul; 61: 416-420.

                


                  Matthews TJ, Allain DC, Matthews AL, Mitchell A, Santoro SL, Cohen L. An assessment of health, social, communication, and daily living skills of adults with Down syndrome. Am J Med Genet A. 2018 Jun; 176: 1389-1397.

                


                  Swaminathan R, Huang Y, Miller K, Pastore M, Hashimoto S, Jacobson T, Mouhlas D, Lin S. Transferring Exome Sequencing Data from Clinical Laboratories to Healthcare Providers: Lessons Learned at a Pediatric Hospital. Front Genet. 2018; 9: 54.

                


                  Santoro SL, Jacobson T, Lemle S, Bartman T. Integrating a Geneticist in a Multidisciplinary Clinic for Down Syndrome Increases Commitment to Genetic Counseling. Pediatr Qual Saf. 2017 Sep-Oct; 2: e039.

View More Publications

Mathew MT, Antoniou A, Ramesh N, Hu M, Gaither J, Mouhlas D, Hashimoto S, Humphrey M, Matthews T, Hunter JM, Reshmi S, Schultz M, Lee K, Pfau R, Cottrell C, McBride KL, Navin NE, Chaudhari BP, Leung ML. A Decade’s Experience in Pediatric Chromosomal Microarray Reveals Distinct Characteristics Across Ordering Specialties. J Mol Diagn. 2022 Jun 16;
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:
Ilacqua A, Benedict J, Shoben A, Skotko BG, Matthews T, Benson B, Allain DC. Alzheimer’s disease development in adults with Down syndrome: Caregivers’ perspectives. Am J Med Genet A. 2020 Jan; 182: 104-114.
Barrie ES, Li Y, Lamb-Thrush D, Hashimoto S, Matthews T, Mouhlas D, Pyatt R, Reshmi SC, Gastier-Foster JM, Pfau R, Astbury C. Pericentromeric regions of homozygosity on the X chromosome: Another likely benign population variant. Eur J Med Genet. 2018 Jul; 61: 416-420.
Matthews TJ, Allain DC, Matthews AL, Mitchell A, Santoro SL, Cohen L. An assessment of health, social, communication, and daily living skills of adults with Down syndrome. Am J Med Genet A. 2018 Jun; 176: 1389-1397.
Swaminathan R, Huang Y, Miller K, Pastore M, Hashimoto S, Jacobson T, Mouhlas D, Lin S. Transferring Exome Sequencing Data from Clinical Laboratories to Healthcare Providers: Lessons Learned at a Pediatric Hospital. Front Genet. 2018; 9: 54.
Santoro SL, Jacobson T, Lemle S, Bartman T. Integrating a Geneticist in a Multidisciplinary Clinic for Down Syndrome Increases Commitment to Genetic Counseling. Pediatr Qual Saf. 2017 Sep-Oct; 2: e039.

Education

Date of Appointment at Nationwide Children’s Hospital: 08/05/2013

Graduate School

Case Western Reserve University

Date Completed: 05/19/2013

Undergraduate School

Case Western Reserve University

Date Completed: 05/15/2011

Education

Date of Appointment at Nationwide Children’s Hospital: 08/05/2013

Graduate School

Case Western Reserve University

Date Completed: 05/19/2013

Undergraduate School

Case Western Reserve University

Date Completed: 05/15/2011

Education

Date of Appointment at Nationwide Children’s Hospital: 08/05/2013

Graduate School

Case Western Reserve University

Date Completed: 05/19/2013

Undergraduate School

Case Western Reserve University

Date Completed: 05/15/2011

Date of Appointment at Nationwide Children’s Hospital: 08/05/2013

Graduate School

Case Western Reserve University

Date Completed: 05/19/2013

Undergraduate School

Case Western Reserve University

Date Completed: 05/15/2011

Date of Appointment at Nationwide Children’s Hospital: 08/05/2013

Graduate School

Case Western Reserve University

Date Completed: 05/19/2013

Undergraduate School

Case Western Reserve University

Date Completed: 05/15/2011

Professional Experience

2015 - Present Nationwide Children’s Hospital, Certified Genetic Counselor in the Cytogenetics and Molecular Genetics Laboratory

Contact Information

Call us at: (614)722-5346

Fax us at: (614)722-5471

                    700 Children's DriveColumbus, OH 43205 (map)

Contact Information

Call us at: (614)722-5346

Fax us at: (614)722-5471

                    700 Children's DriveColumbus, OH 43205 (map)

Contact Information

Call us at: (614)722-5346

Fax us at: (614)722-5471

                    700 Children's DriveColumbus, OH 43205 (map)

Call us at: (614)722-5346

Fax us at: (614)722-5471

                    700 Children's DriveColumbus, OH 43205 (map)

Call us at: (614)722-5346

Fax us at: (614)722-5471

                    700 Children's DriveColumbus, OH 43205 (map)

Call us at: (614)722-5346

Fax us at: (614)722-5471

                    700 Children's DriveColumbus, OH 43205 (map)

Contact Information#

Contact Information