Contact Information

Call us at: (614) 722-5389

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

Learn more about Emily Sites

Biography

Emily Sites, MS, CGC, is a Columbus native who has been with our team since 2015. Her specialty focus is Neurofibromatosis, and she is the coordinator of our Neurofibromatosis Clinic.

Research

Publications

                  Koboldt DC, Mihalic Mosher T, Kelly BJ, Sites E, Bartholomew D, Hickey SE, McBride K, Wilson RK, White P. A de novo nonsense mutation in ASXL3 shared by siblings with Bainbridge-Ropers syndrome. Cold Spring Harb Mol Case Stud. 2018 Jun; 4: 

                


                  Waldrop MA, Boue DR, Sites E, Flanigan KM, Shell R. Clinicopathologic Conference: A Newborn With Hypotonia, Cleft Palate, Micrognathia, and Bilateral Club Feet. Pediatr Neurol. 2017 Sep; 74: 11-14.

                


                  Sites ER, Smolarek TA, Martin LJ, Viskochil DH, Stevenson DA, Ullrich NJ, Messiaen LM, Schorry EK. Analysis of copy number variants in 11 pairs of monozygotic twins with neurofibromatosis type 1. Am J Med Genet A. 2017 Mar; 173: 647-653.

                


                  Stuart HM, Roberts NA, Hilton EN, McKenzie EA, Daly SB, Hadfield KD, Rahal JS, Gardiner NJ, Tanley SW, Lewis MA, Sites E, Angle B, Alves C, Lourenço T, Rodrigues M, Calado A, Amado M, Guerreiro N, Serras I, Beetz C, Varga RE, Silay MS, Darlow JM, Dobson MG, Barton DE, Hunziker M, Puri P, Feather SA, Goodship JA, Goodship TH, Lambert HJ, Cordell HJ, UK VUR Study Group., Saggar A, Kinali M, 4C Study Group., Lorenz C, Moeller K, Schaefer F, Bayazit AK, Weber S, Newman WG, Woolf AS. Urinary tract effects of HPSE2 mutations. J Am Soc Nephrol. 2015 Apr; 26: 797-804.

View More Publications

Education

Date of Appointment at Nationwide Children’s Hospital: 08/03/2015

Graduate School

University of Cincinnati

Date Completed: 06/30/2010

Contact Information

Genetic and Genomic Medicine

Call us at: (614) 722-5389

                    700 Children's DriveColumbus, OH 43205 (map)

Contact Information

Call us at: (614) 722-5389

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

Learn more about Emily Sites

Biography

Emily Sites, MS, CGC, is a Columbus native who has been with our team since 2015. Her specialty focus is Neurofibromatosis, and she is the coordinator of our Neurofibromatosis Clinic.

Research

Publications

                  Koboldt DC, Mihalic Mosher T, Kelly BJ, Sites E, Bartholomew D, Hickey SE, McBride K, Wilson RK, White P. A de novo nonsense mutation in ASXL3 shared by siblings with Bainbridge-Ropers syndrome. Cold Spring Harb Mol Case Stud. 2018 Jun; 4: 

                


                  Waldrop MA, Boue DR, Sites E, Flanigan KM, Shell R. Clinicopathologic Conference: A Newborn With Hypotonia, Cleft Palate, Micrognathia, and Bilateral Club Feet. Pediatr Neurol. 2017 Sep; 74: 11-14.

                


                  Sites ER, Smolarek TA, Martin LJ, Viskochil DH, Stevenson DA, Ullrich NJ, Messiaen LM, Schorry EK. Analysis of copy number variants in 11 pairs of monozygotic twins with neurofibromatosis type 1. Am J Med Genet A. 2017 Mar; 173: 647-653.

                


                  Stuart HM, Roberts NA, Hilton EN, McKenzie EA, Daly SB, Hadfield KD, Rahal JS, Gardiner NJ, Tanley SW, Lewis MA, Sites E, Angle B, Alves C, Lourenço T, Rodrigues M, Calado A, Amado M, Guerreiro N, Serras I, Beetz C, Varga RE, Silay MS, Darlow JM, Dobson MG, Barton DE, Hunziker M, Puri P, Feather SA, Goodship JA, Goodship TH, Lambert HJ, Cordell HJ, UK VUR Study Group., Saggar A, Kinali M, 4C Study Group., Lorenz C, Moeller K, Schaefer F, Bayazit AK, Weber S, Newman WG, Woolf AS. Urinary tract effects of HPSE2 mutations. J Am Soc Nephrol. 2015 Apr; 26: 797-804.

View More Publications

Education

Date of Appointment at Nationwide Children’s Hospital: 08/03/2015

Graduate School

University of Cincinnati

Date Completed: 06/30/2010

Contact Information

Genetic and Genomic Medicine

Call us at: (614) 722-5389

                    700 Children's DriveColumbus, OH 43205 (map)

Contact Information

Call us at: (614) 722-5389

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

Learn more about Emily Sites

Contact Information

  • Call us at:
  • (614) 722-5389
  • Genetic and Genomic Medicine700 Children’s DriveColumbus, OH 43205 (map)

Learn more about Emily Sites

Biography

Emily Sites, MS, CGC, is a Columbus native who has been with our team since 2015. Her specialty focus is Neurofibromatosis, and she is the coordinator of our Neurofibromatosis Clinic.

Biography

Emily Sites, MS, CGC, is a Columbus native who has been with our team since 2015. Her specialty focus is Neurofibromatosis, and she is the coordinator of our Neurofibromatosis Clinic.

Biography

Emily Sites, MS, CGC, is a Columbus native who has been with our team since 2015. Her specialty focus is Neurofibromatosis, and she is the coordinator of our Neurofibromatosis Clinic.

Emily Sites, MS, CGC, is a Columbus native who has been with our team since 2015. Her specialty focus is Neurofibromatosis, and she is the coordinator of our Neurofibromatosis Clinic.

Emily Sites, MS, CGC, is a Columbus native who has been with our team since 2015. Her specialty focus is Neurofibromatosis, and she is the coordinator of our Neurofibromatosis Clinic.

Research

Publications

                  Koboldt DC, Mihalic Mosher T, Kelly BJ, Sites E, Bartholomew D, Hickey SE, McBride K, Wilson RK, White P. A de novo nonsense mutation in ASXL3 shared by siblings with Bainbridge-Ropers syndrome. Cold Spring Harb Mol Case Stud. 2018 Jun; 4: 

                


                  Waldrop MA, Boue DR, Sites E, Flanigan KM, Shell R. Clinicopathologic Conference: A Newborn With Hypotonia, Cleft Palate, Micrognathia, and Bilateral Club Feet. Pediatr Neurol. 2017 Sep; 74: 11-14.

                


                  Sites ER, Smolarek TA, Martin LJ, Viskochil DH, Stevenson DA, Ullrich NJ, Messiaen LM, Schorry EK. Analysis of copy number variants in 11 pairs of monozygotic twins with neurofibromatosis type 1. Am J Med Genet A. 2017 Mar; 173: 647-653.

                


                  Stuart HM, Roberts NA, Hilton EN, McKenzie EA, Daly SB, Hadfield KD, Rahal JS, Gardiner NJ, Tanley SW, Lewis MA, Sites E, Angle B, Alves C, Lourenço T, Rodrigues M, Calado A, Amado M, Guerreiro N, Serras I, Beetz C, Varga RE, Silay MS, Darlow JM, Dobson MG, Barton DE, Hunziker M, Puri P, Feather SA, Goodship JA, Goodship TH, Lambert HJ, Cordell HJ, UK VUR Study Group., Saggar A, Kinali M, 4C Study Group., Lorenz C, Moeller K, Schaefer F, Bayazit AK, Weber S, Newman WG, Woolf AS. Urinary tract effects of HPSE2 mutations. J Am Soc Nephrol. 2015 Apr; 26: 797-804.

View More Publications

Research

Publications

                  Koboldt DC, Mihalic Mosher T, Kelly BJ, Sites E, Bartholomew D, Hickey SE, McBride K, Wilson RK, White P. A de novo nonsense mutation in ASXL3 shared by siblings with Bainbridge-Ropers syndrome. Cold Spring Harb Mol Case Stud. 2018 Jun; 4: 

                


                  Waldrop MA, Boue DR, Sites E, Flanigan KM, Shell R. Clinicopathologic Conference: A Newborn With Hypotonia, Cleft Palate, Micrognathia, and Bilateral Club Feet. Pediatr Neurol. 2017 Sep; 74: 11-14.

                


                  Sites ER, Smolarek TA, Martin LJ, Viskochil DH, Stevenson DA, Ullrich NJ, Messiaen LM, Schorry EK. Analysis of copy number variants in 11 pairs of monozygotic twins with neurofibromatosis type 1. Am J Med Genet A. 2017 Mar; 173: 647-653.

                


                  Stuart HM, Roberts NA, Hilton EN, McKenzie EA, Daly SB, Hadfield KD, Rahal JS, Gardiner NJ, Tanley SW, Lewis MA, Sites E, Angle B, Alves C, Lourenço T, Rodrigues M, Calado A, Amado M, Guerreiro N, Serras I, Beetz C, Varga RE, Silay MS, Darlow JM, Dobson MG, Barton DE, Hunziker M, Puri P, Feather SA, Goodship JA, Goodship TH, Lambert HJ, Cordell HJ, UK VUR Study Group., Saggar A, Kinali M, 4C Study Group., Lorenz C, Moeller K, Schaefer F, Bayazit AK, Weber S, Newman WG, Woolf AS. Urinary tract effects of HPSE2 mutations. J Am Soc Nephrol. 2015 Apr; 26: 797-804.

View More Publications

Research

Publications

                  Koboldt DC, Mihalic Mosher T, Kelly BJ, Sites E, Bartholomew D, Hickey SE, McBride K, Wilson RK, White P. A de novo nonsense mutation in ASXL3 shared by siblings with Bainbridge-Ropers syndrome. Cold Spring Harb Mol Case Stud. 2018 Jun; 4: 

                


                  Waldrop MA, Boue DR, Sites E, Flanigan KM, Shell R. Clinicopathologic Conference: A Newborn With Hypotonia, Cleft Palate, Micrognathia, and Bilateral Club Feet. Pediatr Neurol. 2017 Sep; 74: 11-14.

                


                  Sites ER, Smolarek TA, Martin LJ, Viskochil DH, Stevenson DA, Ullrich NJ, Messiaen LM, Schorry EK. Analysis of copy number variants in 11 pairs of monozygotic twins with neurofibromatosis type 1. Am J Med Genet A. 2017 Mar; 173: 647-653.

                


                  Stuart HM, Roberts NA, Hilton EN, McKenzie EA, Daly SB, Hadfield KD, Rahal JS, Gardiner NJ, Tanley SW, Lewis MA, Sites E, Angle B, Alves C, Lourenço T, Rodrigues M, Calado A, Amado M, Guerreiro N, Serras I, Beetz C, Varga RE, Silay MS, Darlow JM, Dobson MG, Barton DE, Hunziker M, Puri P, Feather SA, Goodship JA, Goodship TH, Lambert HJ, Cordell HJ, UK VUR Study Group., Saggar A, Kinali M, 4C Study Group., Lorenz C, Moeller K, Schaefer F, Bayazit AK, Weber S, Newman WG, Woolf AS. Urinary tract effects of HPSE2 mutations. J Am Soc Nephrol. 2015 Apr; 26: 797-804.

View More Publications

Publications

                  Koboldt DC, Mihalic Mosher T, Kelly BJ, Sites E, Bartholomew D, Hickey SE, McBride K, Wilson RK, White P. A de novo nonsense mutation in ASXL3 shared by siblings with Bainbridge-Ropers syndrome. Cold Spring Harb Mol Case Stud. 2018 Jun; 4: 

                


                  Waldrop MA, Boue DR, Sites E, Flanigan KM, Shell R. Clinicopathologic Conference: A Newborn With Hypotonia, Cleft Palate, Micrognathia, and Bilateral Club Feet. Pediatr Neurol. 2017 Sep; 74: 11-14.

                


                  Sites ER, Smolarek TA, Martin LJ, Viskochil DH, Stevenson DA, Ullrich NJ, Messiaen LM, Schorry EK. Analysis of copy number variants in 11 pairs of monozygotic twins with neurofibromatosis type 1. Am J Med Genet A. 2017 Mar; 173: 647-653.

                


                  Stuart HM, Roberts NA, Hilton EN, McKenzie EA, Daly SB, Hadfield KD, Rahal JS, Gardiner NJ, Tanley SW, Lewis MA, Sites E, Angle B, Alves C, Lourenço T, Rodrigues M, Calado A, Amado M, Guerreiro N, Serras I, Beetz C, Varga RE, Silay MS, Darlow JM, Dobson MG, Barton DE, Hunziker M, Puri P, Feather SA, Goodship JA, Goodship TH, Lambert HJ, Cordell HJ, UK VUR Study Group., Saggar A, Kinali M, 4C Study Group., Lorenz C, Moeller K, Schaefer F, Bayazit AK, Weber S, Newman WG, Woolf AS. Urinary tract effects of HPSE2 mutations. J Am Soc Nephrol. 2015 Apr; 26: 797-804.

View More Publications

                  Koboldt DC, Mihalic Mosher T, Kelly BJ, Sites E, Bartholomew D, Hickey SE, McBride K, Wilson RK, White P. A de novo nonsense mutation in ASXL3 shared by siblings with Bainbridge-Ropers syndrome. Cold Spring Harb Mol Case Stud. 2018 Jun; 4: 

                


                  Waldrop MA, Boue DR, Sites E, Flanigan KM, Shell R. Clinicopathologic Conference: A Newborn With Hypotonia, Cleft Palate, Micrognathia, and Bilateral Club Feet. Pediatr Neurol. 2017 Sep; 74: 11-14.

                


                  Sites ER, Smolarek TA, Martin LJ, Viskochil DH, Stevenson DA, Ullrich NJ, Messiaen LM, Schorry EK. Analysis of copy number variants in 11 pairs of monozygotic twins with neurofibromatosis type 1. Am J Med Genet A. 2017 Mar; 173: 647-653.

                


                  Stuart HM, Roberts NA, Hilton EN, McKenzie EA, Daly SB, Hadfield KD, Rahal JS, Gardiner NJ, Tanley SW, Lewis MA, Sites E, Angle B, Alves C, Lourenço T, Rodrigues M, Calado A, Amado M, Guerreiro N, Serras I, Beetz C, Varga RE, Silay MS, Darlow JM, Dobson MG, Barton DE, Hunziker M, Puri P, Feather SA, Goodship JA, Goodship TH, Lambert HJ, Cordell HJ, UK VUR Study Group., Saggar A, Kinali M, 4C Study Group., Lorenz C, Moeller K, Schaefer F, Bayazit AK, Weber S, Newman WG, Woolf AS. Urinary tract effects of HPSE2 mutations. J Am Soc Nephrol. 2015 Apr; 26: 797-804.

View More Publications

  • Koboldt DC, Mihalic Mosher T, Kelly BJ, Sites E, Bartholomew D, Hickey SE, McBride K, Wilson RK, White P. A de novo nonsense mutation in ASXL3 shared by siblings with Bainbridge-Ropers syndrome. Cold Spring Harb Mol Case Stud. 2018 Jun; 4:
  • Waldrop MA, Boue DR, Sites E, Flanigan KM, Shell R. Clinicopathologic Conference: A Newborn With Hypotonia, Cleft Palate, Micrognathia, and Bilateral Club Feet. Pediatr Neurol. 2017 Sep; 74: 11-14.
  • Sites ER, Smolarek TA, Martin LJ, Viskochil DH, Stevenson DA, Ullrich NJ, Messiaen LM, Schorry EK. Analysis of copy number variants in 11 pairs of monozygotic twins with neurofibromatosis type 1. Am J Med Genet A. 2017 Mar; 173: 647-653.
  • Stuart HM, Roberts NA, Hilton EN, McKenzie EA, Daly SB, Hadfield KD, Rahal JS, Gardiner NJ, Tanley SW, Lewis MA, Sites E, Angle B, Alves C, Lourenço T, Rodrigues M, Calado A, Amado M, Guerreiro N, Serras I, Beetz C, Varga RE, Silay MS, Darlow JM, Dobson MG, Barton DE, Hunziker M, Puri P, Feather SA, Goodship JA, Goodship TH, Lambert HJ, Cordell HJ, UK VUR Study Group., Saggar A, Kinali M, 4C Study Group., Lorenz C, Moeller K, Schaefer F, Bayazit AK, Weber S, Newman WG, Woolf AS. Urinary tract effects of HPSE2 mutations. J Am Soc Nephrol. 2015 Apr; 26: 797-804.

Education

Date of Appointment at Nationwide Children’s Hospital: 08/03/2015

Graduate School

University of Cincinnati

Date Completed: 06/30/2010

Education

Date of Appointment at Nationwide Children’s Hospital: 08/03/2015

Graduate School

University of Cincinnati

Date Completed: 06/30/2010

Education

Date of Appointment at Nationwide Children’s Hospital: 08/03/2015

Graduate School

University of Cincinnati

Date Completed: 06/30/2010

Date of Appointment at Nationwide Children’s Hospital: 08/03/2015

Graduate School

University of Cincinnati

Date Completed: 06/30/2010

Date of Appointment at Nationwide Children’s Hospital: 08/03/2015

Graduate School

University of Cincinnati

Date Completed: 06/30/2010

Contact Information

Genetic and Genomic Medicine

Call us at: (614) 722-5389

                    700 Children's DriveColumbus, OH 43205 (map)

Contact Information

Genetic and Genomic Medicine

Call us at: (614) 722-5389

                    700 Children's DriveColumbus, OH 43205 (map)

Contact Information

Genetic and Genomic Medicine

Call us at: (614) 722-5389

                    700 Children's DriveColumbus, OH 43205 (map)

Genetic and Genomic Medicine

Call us at: (614) 722-5389

                    700 Children's DriveColumbus, OH 43205 (map)

Call us at: (614) 722-5389

                    700 Children's DriveColumbus, OH 43205 (map)

Call us at: (614) 722-5389

                    700 Children's DriveColumbus, OH 43205 (map)
  • Call us at:
  • (614) 722-5389
  • 700 Children’s DriveColumbus, OH 43205 (map)