Alayne P Meyer

Contact Information

Call us at: (614) 355-3573

Fax us at: (614) 355-5247

Genetic and Genomic Medicine700 Children’s DriveColumbus, 43205 (map)

Learn more about Alayne P. Meyer

Biography

Alayne P. Meyer, MS, CGC, is a licensed and certified genetic counselor that specializes in neuromuscular genetics. Alayne received her master’s degree in Genetic Counseling from The Ohio State University and has been at Nationwide Children’s since 2019. She sees patients with muscular dystrophy, myopathy, neuropathy, motor neuron disease and other neuromuscular conditions.

Academic and Clinical Areas

Genetic and Genomic Medicine

Genetic Counselor

Primary Department

Genetic and Genomic Medicine

Awards, Honors & Organizations

NSGC Research Grant, NSCG Pediatric Special Interest Group, 2021 Member, NSGC Research Special Interest Group, 2021 - Present Member, NSGC Pediatric Special Interest Group, 2021 - Present Member, NSGC Neurogenetics Special interest Group, 2019 - Present Member, Ohio Association of Genetic Counselors, 2019 - Present Member, National Society of Genetic Counselors, 2016 - Present

Research

Publications

                  Forrest ME, Meyer AP, Laureano Figueroa SM, Antonellis A. A missense, loss-of-function YARS1 variant in a patient with proximal-predominant motor neuropathy. Cold Spring Harb Mol Case Stud. 2022 Oct 28;  

                


                  Meyer AP, Forrest ME, Nicolau S, Wiszniewski W, Bland MP, Tsao CY, Antonellis A, Abreu NJ. Pathogenic missense variants altering codon 336 of GARS1 lead to divergent dominant phenotypes. Hum Mutat. 2022 Mar 25;  

                


                  Meyer AP, Roggenbuck J, LoRusso S, Kissel J, Smith RM, Kline D, Arnold WD. Genotype-Phenotype Correlations and Characterization of Medication Use in Inherited Myotonic Disorders. Front Neurol. 2020; 11: 593.

View More Publications

Education

Date of Appointment at Nationwide Children’s Hospital: 06/10/2019

Graduate School

The Ohio State University

Date Completed: 05/05/2019

Undergraduate School

Purdue University

Date Completed: 05/03/2013

Contact Information

Genetic and Genomic Medicine

Call us at: (614) 355-3573

Fax us at: (614) 355-5247

                    700 Children's DriveColumbus,  43205 (map)

Contact Information

Call us at: (614) 355-3573

Fax us at: (614) 355-5247

Genetic and Genomic Medicine700 Children’s DriveColumbus, 43205 (map)

Learn more about Alayne P. Meyer

Biography

Alayne P. Meyer, MS, CGC, is a licensed and certified genetic counselor that specializes in neuromuscular genetics. Alayne received her master’s degree in Genetic Counseling from The Ohio State University and has been at Nationwide Children’s since 2019. She sees patients with muscular dystrophy, myopathy, neuropathy, motor neuron disease and other neuromuscular conditions.

Academic and Clinical Areas

Genetic and Genomic Medicine

Genetic Counselor

Primary Department

Genetic and Genomic Medicine

Awards, Honors & Organizations

NSGC Research Grant, NSCG Pediatric Special Interest Group, 2021 Member, NSGC Research Special Interest Group, 2021 - Present Member, NSGC Pediatric Special Interest Group, 2021 - Present Member, NSGC Neurogenetics Special interest Group, 2019 - Present Member, Ohio Association of Genetic Counselors, 2019 - Present Member, National Society of Genetic Counselors, 2016 - Present

Research

Publications

                  Forrest ME, Meyer AP, Laureano Figueroa SM, Antonellis A. A missense, loss-of-function YARS1 variant in a patient with proximal-predominant motor neuropathy. Cold Spring Harb Mol Case Stud. 2022 Oct 28;  

                


                  Meyer AP, Forrest ME, Nicolau S, Wiszniewski W, Bland MP, Tsao CY, Antonellis A, Abreu NJ. Pathogenic missense variants altering codon 336 of GARS1 lead to divergent dominant phenotypes. Hum Mutat. 2022 Mar 25;  

                


                  Meyer AP, Roggenbuck J, LoRusso S, Kissel J, Smith RM, Kline D, Arnold WD. Genotype-Phenotype Correlations and Characterization of Medication Use in Inherited Myotonic Disorders. Front Neurol. 2020; 11: 593.

View More Publications

Education

Date of Appointment at Nationwide Children’s Hospital: 06/10/2019

Graduate School

The Ohio State University

Date Completed: 05/05/2019

Undergraduate School

Purdue University

Date Completed: 05/03/2013

Contact Information

Genetic and Genomic Medicine

Call us at: (614) 355-3573

Fax us at: (614) 355-5247

                    700 Children's DriveColumbus,  43205 (map)

Contact Information

Call us at: (614) 355-3573

Fax us at: (614) 355-5247

Genetic and Genomic Medicine700 Children’s DriveColumbus, 43205 (map)

Learn more about Alayne P. Meyer

Contact Information

• Call us at:
• (614) 355-3573
• Fax us at:
• (614) 355-5247
• Genetic and Genomic Medicine700 Children’s DriveColumbus, 43205 (map)

Learn more about Alayne P. Meyer

Biography

Alayne P. Meyer, MS, CGC, is a licensed and certified genetic counselor that specializes in neuromuscular genetics. Alayne received her master’s degree in Genetic Counseling from The Ohio State University and has been at Nationwide Children’s since 2019. She sees patients with muscular dystrophy, myopathy, neuropathy, motor neuron disease and other neuromuscular conditions.

Biography

Alayne P. Meyer, MS, CGC, is a licensed and certified genetic counselor that specializes in neuromuscular genetics. Alayne received her master’s degree in Genetic Counseling from The Ohio State University and has been at Nationwide Children’s since 2019. She sees patients with muscular dystrophy, myopathy, neuropathy, motor neuron disease and other neuromuscular conditions.

Biography

Alayne P. Meyer, MS, CGC, is a licensed and certified genetic counselor that specializes in neuromuscular genetics. Alayne received her master’s degree in Genetic Counseling from The Ohio State University and has been at Nationwide Children’s since 2019. She sees patients with muscular dystrophy, myopathy, neuropathy, motor neuron disease and other neuromuscular conditions.

Alayne P. Meyer, MS, CGC, is a licensed and certified genetic counselor that specializes in neuromuscular genetics. Alayne received her master’s degree in Genetic Counseling from The Ohio State University and has been at Nationwide Children’s since 2019. She sees patients with muscular dystrophy, myopathy, neuropathy, motor neuron disease and other neuromuscular conditions.

Alayne P. Meyer, MS, CGC, is a licensed and certified genetic counselor that specializes in neuromuscular genetics. Alayne received her master’s degree in Genetic Counseling from The Ohio State University and has been at Nationwide Children’s since 2019. She sees patients with muscular dystrophy, myopathy, neuropathy, motor neuron disease and other neuromuscular conditions.

Academic and Clinical Areas

Genetic and Genomic Medicine

Genetic Counselor

Primary Department

Genetic and Genomic Medicine

Academic and Clinical Areas

Genetic and Genomic Medicine

Genetic Counselor

Primary Department

Genetic and Genomic Medicine

Academic and Clinical Areas

Genetic and Genomic Medicine

Genetic Counselor

Primary Department

Genetic and Genomic Medicine

Genetic and Genomic Medicine

Genetic Counselor

Primary Department

Genetic and Genomic Medicine

• Genetic and Genomic Medicine
• Genetic Counselor
• Primary Department
• Genetic and Genomic Medicine

Awards, Honors & Organizations

NSGC Research Grant, NSCG Pediatric Special Interest Group, 2021 Member, NSGC Research Special Interest Group, 2021 - Present Member, NSGC Pediatric Special Interest Group, 2021 - Present Member, NSGC Neurogenetics Special interest Group, 2019 - Present Member, Ohio Association of Genetic Counselors, 2019 - Present Member, National Society of Genetic Counselors, 2016 - Present

Awards, Honors & Organizations

NSGC Research Grant, NSCG Pediatric Special Interest Group, 2021 Member, NSGC Research Special Interest Group, 2021 - Present Member, NSGC Pediatric Special Interest Group, 2021 - Present Member, NSGC Neurogenetics Special interest Group, 2019 - Present Member, Ohio Association of Genetic Counselors, 2019 - Present Member, National Society of Genetic Counselors, 2016 - Present

Awards, Honors & Organizations

NSGC Research Grant, NSCG Pediatric Special Interest Group, 2021 Member, NSGC Research Special Interest Group, 2021 - Present Member, NSGC Pediatric Special Interest Group, 2021 - Present Member, NSGC Neurogenetics Special interest Group, 2019 - Present Member, Ohio Association of Genetic Counselors, 2019 - Present Member, National Society of Genetic Counselors, 2016 - Present

NSGC Research Grant, NSCG Pediatric Special Interest Group, 2021 Member, NSGC Research Special Interest Group, 2021 - Present Member, NSGC Pediatric Special Interest Group, 2021 - Present Member, NSGC Neurogenetics Special interest Group, 2019 - Present Member, Ohio Association of Genetic Counselors, 2019 - Present Member, National Society of Genetic Counselors, 2016 - Present

• NSGC Research Grant, NSCG Pediatric Special Interest Group, 2021
• Member, NSGC Research Special Interest Group, 2021 - Present
• Member, NSGC Pediatric Special Interest Group, 2021 - Present
• Member, NSGC Neurogenetics Special interest Group, 2019 - Present
• Member, Ohio Association of Genetic Counselors, 2019 - Present
• Member, National Society of Genetic Counselors, 2016 - Present

Research

Publications

                  Forrest ME, Meyer AP, Laureano Figueroa SM, Antonellis A. A missense, loss-of-function YARS1 variant in a patient with proximal-predominant motor neuropathy. Cold Spring Harb Mol Case Stud. 2022 Oct 28;  

                


                  Meyer AP, Forrest ME, Nicolau S, Wiszniewski W, Bland MP, Tsao CY, Antonellis A, Abreu NJ. Pathogenic missense variants altering codon 336 of GARS1 lead to divergent dominant phenotypes. Hum Mutat. 2022 Mar 25;  

                


                  Meyer AP, Roggenbuck J, LoRusso S, Kissel J, Smith RM, Kline D, Arnold WD. Genotype-Phenotype Correlations and Characterization of Medication Use in Inherited Myotonic Disorders. Front Neurol. 2020; 11: 593.

View More Publications

Research

Publications

                  Forrest ME, Meyer AP, Laureano Figueroa SM, Antonellis A. A missense, loss-of-function YARS1 variant in a patient with proximal-predominant motor neuropathy. Cold Spring Harb Mol Case Stud. 2022 Oct 28;  

                


                  Meyer AP, Forrest ME, Nicolau S, Wiszniewski W, Bland MP, Tsao CY, Antonellis A, Abreu NJ. Pathogenic missense variants altering codon 336 of GARS1 lead to divergent dominant phenotypes. Hum Mutat. 2022 Mar 25;  

                


                  Meyer AP, Roggenbuck J, LoRusso S, Kissel J, Smith RM, Kline D, Arnold WD. Genotype-Phenotype Correlations and Characterization of Medication Use in Inherited Myotonic Disorders. Front Neurol. 2020; 11: 593.

View More Publications

Research

Publications

                  Forrest ME, Meyer AP, Laureano Figueroa SM, Antonellis A. A missense, loss-of-function YARS1 variant in a patient with proximal-predominant motor neuropathy. Cold Spring Harb Mol Case Stud. 2022 Oct 28;  

                


                  Meyer AP, Forrest ME, Nicolau S, Wiszniewski W, Bland MP, Tsao CY, Antonellis A, Abreu NJ. Pathogenic missense variants altering codon 336 of GARS1 lead to divergent dominant phenotypes. Hum Mutat. 2022 Mar 25;  

                


                  Meyer AP, Roggenbuck J, LoRusso S, Kissel J, Smith RM, Kline D, Arnold WD. Genotype-Phenotype Correlations and Characterization of Medication Use in Inherited Myotonic Disorders. Front Neurol. 2020; 11: 593.

View More Publications

Publications

                  Forrest ME, Meyer AP, Laureano Figueroa SM, Antonellis A. A missense, loss-of-function YARS1 variant in a patient with proximal-predominant motor neuropathy. Cold Spring Harb Mol Case Stud. 2022 Oct 28;  

                


                  Meyer AP, Forrest ME, Nicolau S, Wiszniewski W, Bland MP, Tsao CY, Antonellis A, Abreu NJ. Pathogenic missense variants altering codon 336 of GARS1 lead to divergent dominant phenotypes. Hum Mutat. 2022 Mar 25;  

                


                  Meyer AP, Roggenbuck J, LoRusso S, Kissel J, Smith RM, Kline D, Arnold WD. Genotype-Phenotype Correlations and Characterization of Medication Use in Inherited Myotonic Disorders. Front Neurol. 2020; 11: 593.

View More Publications

                  Forrest ME, Meyer AP, Laureano Figueroa SM, Antonellis A. A missense, loss-of-function YARS1 variant in a patient with proximal-predominant motor neuropathy. Cold Spring Harb Mol Case Stud. 2022 Oct 28;  

                


                  Meyer AP, Forrest ME, Nicolau S, Wiszniewski W, Bland MP, Tsao CY, Antonellis A, Abreu NJ. Pathogenic missense variants altering codon 336 of GARS1 lead to divergent dominant phenotypes. Hum Mutat. 2022 Mar 25;  

                


                  Meyer AP, Roggenbuck J, LoRusso S, Kissel J, Smith RM, Kline D, Arnold WD. Genotype-Phenotype Correlations and Characterization of Medication Use in Inherited Myotonic Disorders. Front Neurol. 2020; 11: 593.

View More Publications

• Forrest ME, Meyer AP, Laureano Figueroa SM, Antonellis A. A missense, loss-of-function YARS1 variant in a patient with proximal-predominant motor neuropathy. Cold Spring Harb Mol Case Stud. 2022 Oct 28;
• Meyer AP, Forrest ME, Nicolau S, Wiszniewski W, Bland MP, Tsao CY, Antonellis A, Abreu NJ. Pathogenic missense variants altering codon 336 of GARS1 lead to divergent dominant phenotypes. Hum Mutat. 2022 Mar 25;
• Meyer AP, Roggenbuck J, LoRusso S, Kissel J, Smith RM, Kline D, Arnold WD. Genotype-Phenotype Correlations and Characterization of Medication Use in Inherited Myotonic Disorders. Front Neurol. 2020; 11: 593.

Education

Date of Appointment at Nationwide Children’s Hospital: 06/10/2019

Graduate School

The Ohio State University

Date Completed: 05/05/2019

Undergraduate School

Purdue University

Date Completed: 05/03/2013

Education

Date of Appointment at Nationwide Children’s Hospital: 06/10/2019

Graduate School

The Ohio State University

Date Completed: 05/05/2019

Undergraduate School

Purdue University

Date Completed: 05/03/2013

Education

Date of Appointment at Nationwide Children’s Hospital: 06/10/2019

Graduate School

The Ohio State University

Date Completed: 05/05/2019

Undergraduate School

Purdue University

Date Completed: 05/03/2013

Date of Appointment at Nationwide Children’s Hospital: 06/10/2019

Graduate School

The Ohio State University

Date Completed: 05/05/2019

Undergraduate School

Purdue University

Date Completed: 05/03/2013

Date of Appointment at Nationwide Children’s Hospital: 06/10/2019

Graduate School

The Ohio State University

Date Completed: 05/05/2019

Undergraduate School

Purdue University

Date Completed: 05/03/2013

Contact Information

Genetic and Genomic Medicine

Call us at: (614) 355-3573

Fax us at: (614) 355-5247

                    700 Children's DriveColumbus,  43205 (map)

Contact Information

Genetic and Genomic Medicine

Call us at: (614) 355-3573

Fax us at: (614) 355-5247

                    700 Children's DriveColumbus,  43205 (map)

Contact Information

Genetic and Genomic Medicine

Call us at: (614) 355-3573

Fax us at: (614) 355-5247

                    700 Children's DriveColumbus,  43205 (map)

Genetic and Genomic Medicine

Call us at: (614) 355-3573

Fax us at: (614) 355-5247

                    700 Children's DriveColumbus,  43205 (map)

Call us at: (614) 355-3573

Fax us at: (614) 355-5247

                    700 Children's DriveColumbus,  43205 (map)

Call us at: (614) 355-3573

Fax us at: (614) 355-5247

                    700 Children's DriveColumbus,  43205 (map)

• Call us at:
• (614) 355-3573
• Fax us at:
• (614) 355-5247
• 700 Children’s DriveColumbus, 43205 (map)