Contact Information

Call us at: (614) 355-4595

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

Learn more about Melanie Babcock

Biography

Melanie Babcock, PhD, is a Clinical Director within the Institute for Genomics Medicine (IGM) at Nationwide Children’s Hospital. She is a Clinical Assistant Professor in the Department of Pathology at Ohio State University College of Medicine. She is dual-certified by the American Board of Medical Genetics and Genomics in the specialties of Clinical Cytogenetics and Genomics and Molecular Genetics and Genomics. She completed her PhD training at the Albert Einstein College of Medicine in the Department of Molecular Genetics and her fellowship training at the Icahn School of Medicine at Mount Sinai. She then joined Fabric Genomics as a Clinical Genomic Scientist and became a Director of Clinical Interpretation; she was the clinical liaison and managed the caseload for the UK 100,000 Genomes project. Following which, Dr. Babcock served as an Assistant Director then Associate Director at the Magee Genomics Laboratories at UPMC Magee Womens Hospital, where she focused on techniques including aCGH, FISH, and karyotypes to provide clinically relevant information for both constitutional and hematological cancers. During this time, she was also an Assistant Professor for the Department of Obstetrics, Gynecology & Reproductive Sciences at the University of Pittsburgh School of Medicine. Currently at Nationwide Children’s Hospital, her main interests are in the application of cytogenetic and molecular techniques to better understand the genetic etiology of disease in both the constitutional and oncology setting.

Awards, Honors & Organizations

NIH LRP-Pediatric Research, Albert Einstein College of Medicine Diplomate, American Board of Medical Genetics and Genomics, 2019 - Present

Research

Publications

                  Aarabi M, Baumann J, Babcock M, Kessler E, Sebastian J, Madan-Khetarpal S, Hu J, Ou Z, Yatsenko S. Chromosome 2q12.3-q13 copy number variants in patients with neurodevelopmental disorders: genotype-phenotype correlation and new hotspots. Psychiatr Genet. 2022 Oct 1; 32: 171-177.

                


                  100,000 Genomes Project Pilot Investigators, Smedley D, Smith KR, Martin A, Thomas EA, McDonagh EM, Cipriani V, Ellingford JM, Arno G, Tucci A, Vandrovcova J, Chan G, Williams HJ, Ratnaike T, Wei W, Stirrups K, Ibanez K, Moutsianas L, Wielscher M, Need A, Barnes MR, Vestito L, Buchanan J, Wordsworth S, Ashford S, Rehmström K, Li E, Fuller G, Twiss P, Spasic-Boskovic O, Halsall S, Floto RA, Poole K, Wagner A, Mehta SG, Gurnell M, Burrows N, James R, Penkett C, Dewhurst E, Gräf S, Mapeta R, Kasanicki M, Haworth A, Savage H, Babcock M, Reese MG, Bale M, Baple E, Boustred C, Brittain H, de Burca A, Bleda M, Devereau A, Halai D, Haraldsdottir E, Hyder Z, Kasperaviciute D, Patch C, Polychronopoulos D, Matchan A, Sultana R, Ryten M, Tavares ALT, Tregidgo C, Turnbull C, Welland M, Wood S, Snow C, Williams E, Leigh S, Foulger RE, Daugherty LC, Niblock O, Leong IUS, Wright CF, Davies J, Crichton C, Welch J, Woods K, Abulhoul L, Aurora P, Bockenhauer D, Broomfield A, Cleary MA, Lam T, Dattani M, Footitt E, Ganesan V, Grunewald S, Compeyrot-Lacassagne S, Muntoni F, Pilkington C, Quinlivan R, Thapar N, Wallis C, Wedderburn LR, Worth A, Bueser T, Compton C, Deshpande C, Fassihi H, Haque E, Izatt L, Josifova D, Mohammed S, Robert L, Rose S, Ruddy D, Sarkany R, Say G, Shaw AC, Wolejko A, Habib B, Burns G, Hunter S, Grocock RJ, Humphray SJ, Robinson PN, Haendel M, Simpson MA, Banka S, Clayton-Smith J, Douzgou S, Hall G, Thomas HB, O'Keefe RT, Michaelides M, Moore AT, Malka S, Pontikos N, Browning AC, Straub V, Gorman GS, Horvath R, Quinton R, Schaefer AM, Yu-Wai-Man P, Turnbull DM, McFarland R, Taylor RW, O'Connor E, Yip J, Newland K, Morris HR, Polke J, Wood NW, Campbell C, Camps C, Gibson K, Koelling N, Lester T, Németh AH, Palles C, Patel S, Roy NBA, Sen A, Taylor J, Cacheiro P, Jacobsen JO, Seaby EG, Davison V, Chitty L, Douglas A, Naresh K, McMullan D, Ellard S, Temple IK, Mumford AD, Wilson G, Beales P, Bitner-Glindzicz M, Black G, Bradley JR, Brennan P, Burn J, Chinnery PF, Elliott P, Flinter F, Houlden H, Irving M, Newman W, Rahman S, Sayer JA, Taylor JC, Webster AR, Wilkie AOM, Ouwehand WH, Raymond FL, Chisholm J, Hill S, Bentley D, Scott RH, Fowler T, Rendon A, Caulfield M. 100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report. N Engl J Med. 2021 Nov 11; 385: 1868-1880.

                


                  Verdoni A, Hu J, Surti U, Babcock M, Sheehan E, Clemens M, Drewes S, Walsh L, Clark R, Katari S, Sanfilippo J, Saller DN, Rajkovic A, Yatsenko SA. Reproductive outcomes in individuals with chromosomal reciprocal translocations. Genet Med. 2021 Sep; 23: 1753-1760.

View More Publications

Education

Fellowship

Icahn School of Medicine

Date Completed: 01/05/2016

Graduate School

Albert Einstein College of Medicine

Date Completed: 06/30/2006

Professional Experience

2022 - Present Nationwide Children’s Hospital, Clinical Director Clinical Institute for Genomic Medicine2022 - 2022 Magee Genomics Laboratories, UPMC Magee Womens Hospital, Associate Director2019 - 2022 Magee Genomics Laboratories, UPMC Magee Womens Hospital, Assistant Director

Contact Information

Institute for Genomic Medicine

Call us at: (614) 355-4595

                    575 Children’s CrossroadColumbus, OH 43215 (map)

Contact Information

Call us at: (614) 355-4595

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

Learn more about Melanie Babcock

Biography

Melanie Babcock, PhD, is a Clinical Director within the Institute for Genomics Medicine (IGM) at Nationwide Children’s Hospital. She is a Clinical Assistant Professor in the Department of Pathology at Ohio State University College of Medicine. She is dual-certified by the American Board of Medical Genetics and Genomics in the specialties of Clinical Cytogenetics and Genomics and Molecular Genetics and Genomics. She completed her PhD training at the Albert Einstein College of Medicine in the Department of Molecular Genetics and her fellowship training at the Icahn School of Medicine at Mount Sinai. She then joined Fabric Genomics as a Clinical Genomic Scientist and became a Director of Clinical Interpretation; she was the clinical liaison and managed the caseload for the UK 100,000 Genomes project. Following which, Dr. Babcock served as an Assistant Director then Associate Director at the Magee Genomics Laboratories at UPMC Magee Womens Hospital, where she focused on techniques including aCGH, FISH, and karyotypes to provide clinically relevant information for both constitutional and hematological cancers. During this time, she was also an Assistant Professor for the Department of Obstetrics, Gynecology & Reproductive Sciences at the University of Pittsburgh School of Medicine. Currently at Nationwide Children’s Hospital, her main interests are in the application of cytogenetic and molecular techniques to better understand the genetic etiology of disease in both the constitutional and oncology setting.

Awards, Honors & Organizations

NIH LRP-Pediatric Research, Albert Einstein College of Medicine Diplomate, American Board of Medical Genetics and Genomics, 2019 - Present

Research

Publications

                  Aarabi M, Baumann J, Babcock M, Kessler E, Sebastian J, Madan-Khetarpal S, Hu J, Ou Z, Yatsenko S. Chromosome 2q12.3-q13 copy number variants in patients with neurodevelopmental disorders: genotype-phenotype correlation and new hotspots. Psychiatr Genet. 2022 Oct 1; 32: 171-177.

                


                  100,000 Genomes Project Pilot Investigators, Smedley D, Smith KR, Martin A, Thomas EA, McDonagh EM, Cipriani V, Ellingford JM, Arno G, Tucci A, Vandrovcova J, Chan G, Williams HJ, Ratnaike T, Wei W, Stirrups K, Ibanez K, Moutsianas L, Wielscher M, Need A, Barnes MR, Vestito L, Buchanan J, Wordsworth S, Ashford S, Rehmström K, Li E, Fuller G, Twiss P, Spasic-Boskovic O, Halsall S, Floto RA, Poole K, Wagner A, Mehta SG, Gurnell M, Burrows N, James R, Penkett C, Dewhurst E, Gräf S, Mapeta R, Kasanicki M, Haworth A, Savage H, Babcock M, Reese MG, Bale M, Baple E, Boustred C, Brittain H, de Burca A, Bleda M, Devereau A, Halai D, Haraldsdottir E, Hyder Z, Kasperaviciute D, Patch C, Polychronopoulos D, Matchan A, Sultana R, Ryten M, Tavares ALT, Tregidgo C, Turnbull C, Welland M, Wood S, Snow C, Williams E, Leigh S, Foulger RE, Daugherty LC, Niblock O, Leong IUS, Wright CF, Davies J, Crichton C, Welch J, Woods K, Abulhoul L, Aurora P, Bockenhauer D, Broomfield A, Cleary MA, Lam T, Dattani M, Footitt E, Ganesan V, Grunewald S, Compeyrot-Lacassagne S, Muntoni F, Pilkington C, Quinlivan R, Thapar N, Wallis C, Wedderburn LR, Worth A, Bueser T, Compton C, Deshpande C, Fassihi H, Haque E, Izatt L, Josifova D, Mohammed S, Robert L, Rose S, Ruddy D, Sarkany R, Say G, Shaw AC, Wolejko A, Habib B, Burns G, Hunter S, Grocock RJ, Humphray SJ, Robinson PN, Haendel M, Simpson MA, Banka S, Clayton-Smith J, Douzgou S, Hall G, Thomas HB, O'Keefe RT, Michaelides M, Moore AT, Malka S, Pontikos N, Browning AC, Straub V, Gorman GS, Horvath R, Quinton R, Schaefer AM, Yu-Wai-Man P, Turnbull DM, McFarland R, Taylor RW, O'Connor E, Yip J, Newland K, Morris HR, Polke J, Wood NW, Campbell C, Camps C, Gibson K, Koelling N, Lester T, Németh AH, Palles C, Patel S, Roy NBA, Sen A, Taylor J, Cacheiro P, Jacobsen JO, Seaby EG, Davison V, Chitty L, Douglas A, Naresh K, McMullan D, Ellard S, Temple IK, Mumford AD, Wilson G, Beales P, Bitner-Glindzicz M, Black G, Bradley JR, Brennan P, Burn J, Chinnery PF, Elliott P, Flinter F, Houlden H, Irving M, Newman W, Rahman S, Sayer JA, Taylor JC, Webster AR, Wilkie AOM, Ouwehand WH, Raymond FL, Chisholm J, Hill S, Bentley D, Scott RH, Fowler T, Rendon A, Caulfield M. 100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report. N Engl J Med. 2021 Nov 11; 385: 1868-1880.

                


                  Verdoni A, Hu J, Surti U, Babcock M, Sheehan E, Clemens M, Drewes S, Walsh L, Clark R, Katari S, Sanfilippo J, Saller DN, Rajkovic A, Yatsenko SA. Reproductive outcomes in individuals with chromosomal reciprocal translocations. Genet Med. 2021 Sep; 23: 1753-1760.

View More Publications

Education

Fellowship

Icahn School of Medicine

Date Completed: 01/05/2016

Graduate School

Albert Einstein College of Medicine

Date Completed: 06/30/2006

Professional Experience

2022 - Present Nationwide Children’s Hospital, Clinical Director Clinical Institute for Genomic Medicine2022 - 2022 Magee Genomics Laboratories, UPMC Magee Womens Hospital, Associate Director2019 - 2022 Magee Genomics Laboratories, UPMC Magee Womens Hospital, Assistant Director

Contact Information

Institute for Genomic Medicine

Call us at: (614) 355-4595

                    575 Children’s CrossroadColumbus, OH 43215 (map)

Contact Information

Call us at: (614) 355-4595

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

Learn more about Melanie Babcock

Contact Information

  • Call us at:
  • (614) 355-4595
  • Institute for Genomic Medicine575 Children’s CrossroadColumbus, OH 43215 (map)

Learn more about Melanie Babcock

Biography

Melanie Babcock, PhD, is a Clinical Director within the Institute for Genomics Medicine (IGM) at Nationwide Children’s Hospital. She is a Clinical Assistant Professor in the Department of Pathology at Ohio State University College of Medicine. She is dual-certified by the American Board of Medical Genetics and Genomics in the specialties of Clinical Cytogenetics and Genomics and Molecular Genetics and Genomics. She completed her PhD training at the Albert Einstein College of Medicine in the Department of Molecular Genetics and her fellowship training at the Icahn School of Medicine at Mount Sinai. She then joined Fabric Genomics as a Clinical Genomic Scientist and became a Director of Clinical Interpretation; she was the clinical liaison and managed the caseload for the UK 100,000 Genomes project. Following which, Dr. Babcock served as an Assistant Director then Associate Director at the Magee Genomics Laboratories at UPMC Magee Womens Hospital, where she focused on techniques including aCGH, FISH, and karyotypes to provide clinically relevant information for both constitutional and hematological cancers. During this time, she was also an Assistant Professor for the Department of Obstetrics, Gynecology & Reproductive Sciences at the University of Pittsburgh School of Medicine. Currently at Nationwide Children’s Hospital, her main interests are in the application of cytogenetic and molecular techniques to better understand the genetic etiology of disease in both the constitutional and oncology setting.

Biography

Melanie Babcock, PhD, is a Clinical Director within the Institute for Genomics Medicine (IGM) at Nationwide Children’s Hospital. She is a Clinical Assistant Professor in the Department of Pathology at Ohio State University College of Medicine. She is dual-certified by the American Board of Medical Genetics and Genomics in the specialties of Clinical Cytogenetics and Genomics and Molecular Genetics and Genomics. She completed her PhD training at the Albert Einstein College of Medicine in the Department of Molecular Genetics and her fellowship training at the Icahn School of Medicine at Mount Sinai. She then joined Fabric Genomics as a Clinical Genomic Scientist and became a Director of Clinical Interpretation; she was the clinical liaison and managed the caseload for the UK 100,000 Genomes project. Following which, Dr. Babcock served as an Assistant Director then Associate Director at the Magee Genomics Laboratories at UPMC Magee Womens Hospital, where she focused on techniques including aCGH, FISH, and karyotypes to provide clinically relevant information for both constitutional and hematological cancers. During this time, she was also an Assistant Professor for the Department of Obstetrics, Gynecology & Reproductive Sciences at the University of Pittsburgh School of Medicine. Currently at Nationwide Children’s Hospital, her main interests are in the application of cytogenetic and molecular techniques to better understand the genetic etiology of disease in both the constitutional and oncology setting.

Biography

Melanie Babcock, PhD, is a Clinical Director within the Institute for Genomics Medicine (IGM) at Nationwide Children’s Hospital. She is a Clinical Assistant Professor in the Department of Pathology at Ohio State University College of Medicine. She is dual-certified by the American Board of Medical Genetics and Genomics in the specialties of Clinical Cytogenetics and Genomics and Molecular Genetics and Genomics. She completed her PhD training at the Albert Einstein College of Medicine in the Department of Molecular Genetics and her fellowship training at the Icahn School of Medicine at Mount Sinai. She then joined Fabric Genomics as a Clinical Genomic Scientist and became a Director of Clinical Interpretation; she was the clinical liaison and managed the caseload for the UK 100,000 Genomes project. Following which, Dr. Babcock served as an Assistant Director then Associate Director at the Magee Genomics Laboratories at UPMC Magee Womens Hospital, where she focused on techniques including aCGH, FISH, and karyotypes to provide clinically relevant information for both constitutional and hematological cancers. During this time, she was also an Assistant Professor for the Department of Obstetrics, Gynecology & Reproductive Sciences at the University of Pittsburgh School of Medicine. Currently at Nationwide Children’s Hospital, her main interests are in the application of cytogenetic and molecular techniques to better understand the genetic etiology of disease in both the constitutional and oncology setting.

Melanie Babcock, PhD, is a Clinical Director within the Institute for Genomics Medicine (IGM) at Nationwide Children’s Hospital. She is a Clinical Assistant Professor in the Department of Pathology at Ohio State University College of Medicine. She is dual-certified by the American Board of Medical Genetics and Genomics in the specialties of Clinical Cytogenetics and Genomics and Molecular Genetics and Genomics. She completed her PhD training at the Albert Einstein College of Medicine in the Department of Molecular Genetics and her fellowship training at the Icahn School of Medicine at Mount Sinai. She then joined Fabric Genomics as a Clinical Genomic Scientist and became a Director of Clinical Interpretation; she was the clinical liaison and managed the caseload for the UK 100,000 Genomes project. Following which, Dr. Babcock served as an Assistant Director then Associate Director at the Magee Genomics Laboratories at UPMC Magee Womens Hospital, where she focused on techniques including aCGH, FISH, and karyotypes to provide clinically relevant information for both constitutional and hematological cancers. During this time, she was also an Assistant Professor for the Department of Obstetrics, Gynecology & Reproductive Sciences at the University of Pittsburgh School of Medicine. Currently at Nationwide Children’s Hospital, her main interests are in the application of cytogenetic and molecular techniques to better understand the genetic etiology of disease in both the constitutional and oncology setting.

Melanie Babcock, PhD, is a Clinical Director within the Institute for Genomics Medicine (IGM) at Nationwide Children’s Hospital. She is a Clinical Assistant Professor in the Department of Pathology at Ohio State University College of Medicine. She is dual-certified by the American Board of Medical Genetics and Genomics in the specialties of Clinical Cytogenetics and Genomics and Molecular Genetics and Genomics. She completed her PhD training at the Albert Einstein College of Medicine in the Department of Molecular Genetics and her fellowship training at the Icahn School of Medicine at Mount Sinai. She then joined Fabric Genomics as a Clinical Genomic Scientist and became a Director of Clinical Interpretation; she was the clinical liaison and managed the caseload for the UK 100,000 Genomes project. Following which, Dr. Babcock served as an Assistant Director then Associate Director at the Magee Genomics Laboratories at UPMC Magee Womens Hospital, where she focused on techniques including aCGH, FISH, and karyotypes to provide clinically relevant information for both constitutional and hematological cancers. During this time, she was also an Assistant Professor for the Department of Obstetrics, Gynecology & Reproductive Sciences at the University of Pittsburgh School of Medicine.

Currently at Nationwide Children’s Hospital, her main interests are in the application of cytogenetic and molecular techniques to better understand the genetic etiology of disease in both the constitutional and oncology setting.

Awards, Honors & Organizations

NIH LRP-Pediatric Research, Albert Einstein College of Medicine Diplomate, American Board of Medical Genetics and Genomics, 2019 - Present

Awards, Honors & Organizations

NIH LRP-Pediatric Research, Albert Einstein College of Medicine Diplomate, American Board of Medical Genetics and Genomics, 2019 - Present

Awards, Honors & Organizations

NIH LRP-Pediatric Research, Albert Einstein College of Medicine Diplomate, American Board of Medical Genetics and Genomics, 2019 - Present

NIH LRP-Pediatric Research, Albert Einstein College of Medicine Diplomate, American Board of Medical Genetics and Genomics, 2019 - Present

  • NIH LRP-Pediatric Research, Albert Einstein College of Medicine
  • Diplomate, American Board of Medical Genetics and Genomics, 2019 - Present

Research

Publications

                  Aarabi M, Baumann J, Babcock M, Kessler E, Sebastian J, Madan-Khetarpal S, Hu J, Ou Z, Yatsenko S. Chromosome 2q12.3-q13 copy number variants in patients with neurodevelopmental disorders: genotype-phenotype correlation and new hotspots. Psychiatr Genet. 2022 Oct 1; 32: 171-177.

                


                  100,000 Genomes Project Pilot Investigators, Smedley D, Smith KR, Martin A, Thomas EA, McDonagh EM, Cipriani V, Ellingford JM, Arno G, Tucci A, Vandrovcova J, Chan G, Williams HJ, Ratnaike T, Wei W, Stirrups K, Ibanez K, Moutsianas L, Wielscher M, Need A, Barnes MR, Vestito L, Buchanan J, Wordsworth S, Ashford S, Rehmström K, Li E, Fuller G, Twiss P, Spasic-Boskovic O, Halsall S, Floto RA, Poole K, Wagner A, Mehta SG, Gurnell M, Burrows N, James R, Penkett C, Dewhurst E, Gräf S, Mapeta R, Kasanicki M, Haworth A, Savage H, Babcock M, Reese MG, Bale M, Baple E, Boustred C, Brittain H, de Burca A, Bleda M, Devereau A, Halai D, Haraldsdottir E, Hyder Z, Kasperaviciute D, Patch C, Polychronopoulos D, Matchan A, Sultana R, Ryten M, Tavares ALT, Tregidgo C, Turnbull C, Welland M, Wood S, Snow C, Williams E, Leigh S, Foulger RE, Daugherty LC, Niblock O, Leong IUS, Wright CF, Davies J, Crichton C, Welch J, Woods K, Abulhoul L, Aurora P, Bockenhauer D, Broomfield A, Cleary MA, Lam T, Dattani M, Footitt E, Ganesan V, Grunewald S, Compeyrot-Lacassagne S, Muntoni F, Pilkington C, Quinlivan R, Thapar N, Wallis C, Wedderburn LR, Worth A, Bueser T, Compton C, Deshpande C, Fassihi H, Haque E, Izatt L, Josifova D, Mohammed S, Robert L, Rose S, Ruddy D, Sarkany R, Say G, Shaw AC, Wolejko A, Habib B, Burns G, Hunter S, Grocock RJ, Humphray SJ, Robinson PN, Haendel M, Simpson MA, Banka S, Clayton-Smith J, Douzgou S, Hall G, Thomas HB, O'Keefe RT, Michaelides M, Moore AT, Malka S, Pontikos N, Browning AC, Straub V, Gorman GS, Horvath R, Quinton R, Schaefer AM, Yu-Wai-Man P, Turnbull DM, McFarland R, Taylor RW, O'Connor E, Yip J, Newland K, Morris HR, Polke J, Wood NW, Campbell C, Camps C, Gibson K, Koelling N, Lester T, Németh AH, Palles C, Patel S, Roy NBA, Sen A, Taylor J, Cacheiro P, Jacobsen JO, Seaby EG, Davison V, Chitty L, Douglas A, Naresh K, McMullan D, Ellard S, Temple IK, Mumford AD, Wilson G, Beales P, Bitner-Glindzicz M, Black G, Bradley JR, Brennan P, Burn J, Chinnery PF, Elliott P, Flinter F, Houlden H, Irving M, Newman W, Rahman S, Sayer JA, Taylor JC, Webster AR, Wilkie AOM, Ouwehand WH, Raymond FL, Chisholm J, Hill S, Bentley D, Scott RH, Fowler T, Rendon A, Caulfield M. 100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report. N Engl J Med. 2021 Nov 11; 385: 1868-1880.

                


                  Verdoni A, Hu J, Surti U, Babcock M, Sheehan E, Clemens M, Drewes S, Walsh L, Clark R, Katari S, Sanfilippo J, Saller DN, Rajkovic A, Yatsenko SA. Reproductive outcomes in individuals with chromosomal reciprocal translocations. Genet Med. 2021 Sep; 23: 1753-1760.

View More Publications

Research

Publications

                  Aarabi M, Baumann J, Babcock M, Kessler E, Sebastian J, Madan-Khetarpal S, Hu J, Ou Z, Yatsenko S. Chromosome 2q12.3-q13 copy number variants in patients with neurodevelopmental disorders: genotype-phenotype correlation and new hotspots. Psychiatr Genet. 2022 Oct 1; 32: 171-177.

                


                  100,000 Genomes Project Pilot Investigators, Smedley D, Smith KR, Martin A, Thomas EA, McDonagh EM, Cipriani V, Ellingford JM, Arno G, Tucci A, Vandrovcova J, Chan G, Williams HJ, Ratnaike T, Wei W, Stirrups K, Ibanez K, Moutsianas L, Wielscher M, Need A, Barnes MR, Vestito L, Buchanan J, Wordsworth S, Ashford S, Rehmström K, Li E, Fuller G, Twiss P, Spasic-Boskovic O, Halsall S, Floto RA, Poole K, Wagner A, Mehta SG, Gurnell M, Burrows N, James R, Penkett C, Dewhurst E, Gräf S, Mapeta R, Kasanicki M, Haworth A, Savage H, Babcock M, Reese MG, Bale M, Baple E, Boustred C, Brittain H, de Burca A, Bleda M, Devereau A, Halai D, Haraldsdottir E, Hyder Z, Kasperaviciute D, Patch C, Polychronopoulos D, Matchan A, Sultana R, Ryten M, Tavares ALT, Tregidgo C, Turnbull C, Welland M, Wood S, Snow C, Williams E, Leigh S, Foulger RE, Daugherty LC, Niblock O, Leong IUS, Wright CF, Davies J, Crichton C, Welch J, Woods K, Abulhoul L, Aurora P, Bockenhauer D, Broomfield A, Cleary MA, Lam T, Dattani M, Footitt E, Ganesan V, Grunewald S, Compeyrot-Lacassagne S, Muntoni F, Pilkington C, Quinlivan R, Thapar N, Wallis C, Wedderburn LR, Worth A, Bueser T, Compton C, Deshpande C, Fassihi H, Haque E, Izatt L, Josifova D, Mohammed S, Robert L, Rose S, Ruddy D, Sarkany R, Say G, Shaw AC, Wolejko A, Habib B, Burns G, Hunter S, Grocock RJ, Humphray SJ, Robinson PN, Haendel M, Simpson MA, Banka S, Clayton-Smith J, Douzgou S, Hall G, Thomas HB, O'Keefe RT, Michaelides M, Moore AT, Malka S, Pontikos N, Browning AC, Straub V, Gorman GS, Horvath R, Quinton R, Schaefer AM, Yu-Wai-Man P, Turnbull DM, McFarland R, Taylor RW, O'Connor E, Yip J, Newland K, Morris HR, Polke J, Wood NW, Campbell C, Camps C, Gibson K, Koelling N, Lester T, Németh AH, Palles C, Patel S, Roy NBA, Sen A, Taylor J, Cacheiro P, Jacobsen JO, Seaby EG, Davison V, Chitty L, Douglas A, Naresh K, McMullan D, Ellard S, Temple IK, Mumford AD, Wilson G, Beales P, Bitner-Glindzicz M, Black G, Bradley JR, Brennan P, Burn J, Chinnery PF, Elliott P, Flinter F, Houlden H, Irving M, Newman W, Rahman S, Sayer JA, Taylor JC, Webster AR, Wilkie AOM, Ouwehand WH, Raymond FL, Chisholm J, Hill S, Bentley D, Scott RH, Fowler T, Rendon A, Caulfield M. 100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report. N Engl J Med. 2021 Nov 11; 385: 1868-1880.

                


                  Verdoni A, Hu J, Surti U, Babcock M, Sheehan E, Clemens M, Drewes S, Walsh L, Clark R, Katari S, Sanfilippo J, Saller DN, Rajkovic A, Yatsenko SA. Reproductive outcomes in individuals with chromosomal reciprocal translocations. Genet Med. 2021 Sep; 23: 1753-1760.

View More Publications

Research

Publications

                  Aarabi M, Baumann J, Babcock M, Kessler E, Sebastian J, Madan-Khetarpal S, Hu J, Ou Z, Yatsenko S. Chromosome 2q12.3-q13 copy number variants in patients with neurodevelopmental disorders: genotype-phenotype correlation and new hotspots. Psychiatr Genet. 2022 Oct 1; 32: 171-177.

                


                  100,000 Genomes Project Pilot Investigators, Smedley D, Smith KR, Martin A, Thomas EA, McDonagh EM, Cipriani V, Ellingford JM, Arno G, Tucci A, Vandrovcova J, Chan G, Williams HJ, Ratnaike T, Wei W, Stirrups K, Ibanez K, Moutsianas L, Wielscher M, Need A, Barnes MR, Vestito L, Buchanan J, Wordsworth S, Ashford S, Rehmström K, Li E, Fuller G, Twiss P, Spasic-Boskovic O, Halsall S, Floto RA, Poole K, Wagner A, Mehta SG, Gurnell M, Burrows N, James R, Penkett C, Dewhurst E, Gräf S, Mapeta R, Kasanicki M, Haworth A, Savage H, Babcock M, Reese MG, Bale M, Baple E, Boustred C, Brittain H, de Burca A, Bleda M, Devereau A, Halai D, Haraldsdottir E, Hyder Z, Kasperaviciute D, Patch C, Polychronopoulos D, Matchan A, Sultana R, Ryten M, Tavares ALT, Tregidgo C, Turnbull C, Welland M, Wood S, Snow C, Williams E, Leigh S, Foulger RE, Daugherty LC, Niblock O, Leong IUS, Wright CF, Davies J, Crichton C, Welch J, Woods K, Abulhoul L, Aurora P, Bockenhauer D, Broomfield A, Cleary MA, Lam T, Dattani M, Footitt E, Ganesan V, Grunewald S, Compeyrot-Lacassagne S, Muntoni F, Pilkington C, Quinlivan R, Thapar N, Wallis C, Wedderburn LR, Worth A, Bueser T, Compton C, Deshpande C, Fassihi H, Haque E, Izatt L, Josifova D, Mohammed S, Robert L, Rose S, Ruddy D, Sarkany R, Say G, Shaw AC, Wolejko A, Habib B, Burns G, Hunter S, Grocock RJ, Humphray SJ, Robinson PN, Haendel M, Simpson MA, Banka S, Clayton-Smith J, Douzgou S, Hall G, Thomas HB, O'Keefe RT, Michaelides M, Moore AT, Malka S, Pontikos N, Browning AC, Straub V, Gorman GS, Horvath R, Quinton R, Schaefer AM, Yu-Wai-Man P, Turnbull DM, McFarland R, Taylor RW, O'Connor E, Yip J, Newland K, Morris HR, Polke J, Wood NW, Campbell C, Camps C, Gibson K, Koelling N, Lester T, Németh AH, Palles C, Patel S, Roy NBA, Sen A, Taylor J, Cacheiro P, Jacobsen JO, Seaby EG, Davison V, Chitty L, Douglas A, Naresh K, McMullan D, Ellard S, Temple IK, Mumford AD, Wilson G, Beales P, Bitner-Glindzicz M, Black G, Bradley JR, Brennan P, Burn J, Chinnery PF, Elliott P, Flinter F, Houlden H, Irving M, Newman W, Rahman S, Sayer JA, Taylor JC, Webster AR, Wilkie AOM, Ouwehand WH, Raymond FL, Chisholm J, Hill S, Bentley D, Scott RH, Fowler T, Rendon A, Caulfield M. 100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report. N Engl J Med. 2021 Nov 11; 385: 1868-1880.

                


                  Verdoni A, Hu J, Surti U, Babcock M, Sheehan E, Clemens M, Drewes S, Walsh L, Clark R, Katari S, Sanfilippo J, Saller DN, Rajkovic A, Yatsenko SA. Reproductive outcomes in individuals with chromosomal reciprocal translocations. Genet Med. 2021 Sep; 23: 1753-1760.

View More Publications

Publications

                  Aarabi M, Baumann J, Babcock M, Kessler E, Sebastian J, Madan-Khetarpal S, Hu J, Ou Z, Yatsenko S. Chromosome 2q12.3-q13 copy number variants in patients with neurodevelopmental disorders: genotype-phenotype correlation and new hotspots. Psychiatr Genet. 2022 Oct 1; 32: 171-177.

                


                  100,000 Genomes Project Pilot Investigators, Smedley D, Smith KR, Martin A, Thomas EA, McDonagh EM, Cipriani V, Ellingford JM, Arno G, Tucci A, Vandrovcova J, Chan G, Williams HJ, Ratnaike T, Wei W, Stirrups K, Ibanez K, Moutsianas L, Wielscher M, Need A, Barnes MR, Vestito L, Buchanan J, Wordsworth S, Ashford S, Rehmström K, Li E, Fuller G, Twiss P, Spasic-Boskovic O, Halsall S, Floto RA, Poole K, Wagner A, Mehta SG, Gurnell M, Burrows N, James R, Penkett C, Dewhurst E, Gräf S, Mapeta R, Kasanicki M, Haworth A, Savage H, Babcock M, Reese MG, Bale M, Baple E, Boustred C, Brittain H, de Burca A, Bleda M, Devereau A, Halai D, Haraldsdottir E, Hyder Z, Kasperaviciute D, Patch C, Polychronopoulos D, Matchan A, Sultana R, Ryten M, Tavares ALT, Tregidgo C, Turnbull C, Welland M, Wood S, Snow C, Williams E, Leigh S, Foulger RE, Daugherty LC, Niblock O, Leong IUS, Wright CF, Davies J, Crichton C, Welch J, Woods K, Abulhoul L, Aurora P, Bockenhauer D, Broomfield A, Cleary MA, Lam T, Dattani M, Footitt E, Ganesan V, Grunewald S, Compeyrot-Lacassagne S, Muntoni F, Pilkington C, Quinlivan R, Thapar N, Wallis C, Wedderburn LR, Worth A, Bueser T, Compton C, Deshpande C, Fassihi H, Haque E, Izatt L, Josifova D, Mohammed S, Robert L, Rose S, Ruddy D, Sarkany R, Say G, Shaw AC, Wolejko A, Habib B, Burns G, Hunter S, Grocock RJ, Humphray SJ, Robinson PN, Haendel M, Simpson MA, Banka S, Clayton-Smith J, Douzgou S, Hall G, Thomas HB, O'Keefe RT, Michaelides M, Moore AT, Malka S, Pontikos N, Browning AC, Straub V, Gorman GS, Horvath R, Quinton R, Schaefer AM, Yu-Wai-Man P, Turnbull DM, McFarland R, Taylor RW, O'Connor E, Yip J, Newland K, Morris HR, Polke J, Wood NW, Campbell C, Camps C, Gibson K, Koelling N, Lester T, Németh AH, Palles C, Patel S, Roy NBA, Sen A, Taylor J, Cacheiro P, Jacobsen JO, Seaby EG, Davison V, Chitty L, Douglas A, Naresh K, McMullan D, Ellard S, Temple IK, Mumford AD, Wilson G, Beales P, Bitner-Glindzicz M, Black G, Bradley JR, Brennan P, Burn J, Chinnery PF, Elliott P, Flinter F, Houlden H, Irving M, Newman W, Rahman S, Sayer JA, Taylor JC, Webster AR, Wilkie AOM, Ouwehand WH, Raymond FL, Chisholm J, Hill S, Bentley D, Scott RH, Fowler T, Rendon A, Caulfield M. 100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report. N Engl J Med. 2021 Nov 11; 385: 1868-1880.

                


                  Verdoni A, Hu J, Surti U, Babcock M, Sheehan E, Clemens M, Drewes S, Walsh L, Clark R, Katari S, Sanfilippo J, Saller DN, Rajkovic A, Yatsenko SA. Reproductive outcomes in individuals with chromosomal reciprocal translocations. Genet Med. 2021 Sep; 23: 1753-1760.

View More Publications

                  Aarabi M, Baumann J, Babcock M, Kessler E, Sebastian J, Madan-Khetarpal S, Hu J, Ou Z, Yatsenko S. Chromosome 2q12.3-q13 copy number variants in patients with neurodevelopmental disorders: genotype-phenotype correlation and new hotspots. Psychiatr Genet. 2022 Oct 1; 32: 171-177.

                


                  100,000 Genomes Project Pilot Investigators, Smedley D, Smith KR, Martin A, Thomas EA, McDonagh EM, Cipriani V, Ellingford JM, Arno G, Tucci A, Vandrovcova J, Chan G, Williams HJ, Ratnaike T, Wei W, Stirrups K, Ibanez K, Moutsianas L, Wielscher M, Need A, Barnes MR, Vestito L, Buchanan J, Wordsworth S, Ashford S, Rehmström K, Li E, Fuller G, Twiss P, Spasic-Boskovic O, Halsall S, Floto RA, Poole K, Wagner A, Mehta SG, Gurnell M, Burrows N, James R, Penkett C, Dewhurst E, Gräf S, Mapeta R, Kasanicki M, Haworth A, Savage H, Babcock M, Reese MG, Bale M, Baple E, Boustred C, Brittain H, de Burca A, Bleda M, Devereau A, Halai D, Haraldsdottir E, Hyder Z, Kasperaviciute D, Patch C, Polychronopoulos D, Matchan A, Sultana R, Ryten M, Tavares ALT, Tregidgo C, Turnbull C, Welland M, Wood S, Snow C, Williams E, Leigh S, Foulger RE, Daugherty LC, Niblock O, Leong IUS, Wright CF, Davies J, Crichton C, Welch J, Woods K, Abulhoul L, Aurora P, Bockenhauer D, Broomfield A, Cleary MA, Lam T, Dattani M, Footitt E, Ganesan V, Grunewald S, Compeyrot-Lacassagne S, Muntoni F, Pilkington C, Quinlivan R, Thapar N, Wallis C, Wedderburn LR, Worth A, Bueser T, Compton C, Deshpande C, Fassihi H, Haque E, Izatt L, Josifova D, Mohammed S, Robert L, Rose S, Ruddy D, Sarkany R, Say G, Shaw AC, Wolejko A, Habib B, Burns G, Hunter S, Grocock RJ, Humphray SJ, Robinson PN, Haendel M, Simpson MA, Banka S, Clayton-Smith J, Douzgou S, Hall G, Thomas HB, O'Keefe RT, Michaelides M, Moore AT, Malka S, Pontikos N, Browning AC, Straub V, Gorman GS, Horvath R, Quinton R, Schaefer AM, Yu-Wai-Man P, Turnbull DM, McFarland R, Taylor RW, O'Connor E, Yip J, Newland K, Morris HR, Polke J, Wood NW, Campbell C, Camps C, Gibson K, Koelling N, Lester T, Németh AH, Palles C, Patel S, Roy NBA, Sen A, Taylor J, Cacheiro P, Jacobsen JO, Seaby EG, Davison V, Chitty L, Douglas A, Naresh K, McMullan D, Ellard S, Temple IK, Mumford AD, Wilson G, Beales P, Bitner-Glindzicz M, Black G, Bradley JR, Brennan P, Burn J, Chinnery PF, Elliott P, Flinter F, Houlden H, Irving M, Newman W, Rahman S, Sayer JA, Taylor JC, Webster AR, Wilkie AOM, Ouwehand WH, Raymond FL, Chisholm J, Hill S, Bentley D, Scott RH, Fowler T, Rendon A, Caulfield M. 100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report. N Engl J Med. 2021 Nov 11; 385: 1868-1880.

                


                  Verdoni A, Hu J, Surti U, Babcock M, Sheehan E, Clemens M, Drewes S, Walsh L, Clark R, Katari S, Sanfilippo J, Saller DN, Rajkovic A, Yatsenko SA. Reproductive outcomes in individuals with chromosomal reciprocal translocations. Genet Med. 2021 Sep; 23: 1753-1760.

View More Publications

  • Aarabi M, Baumann J, Babcock M, Kessler E, Sebastian J, Madan-Khetarpal S, Hu J, Ou Z, Yatsenko S. Chromosome 2q12.3-q13 copy number variants in patients with neurodevelopmental disorders: genotype-phenotype correlation and new hotspots. Psychiatr Genet. 2022 Oct 1; 32: 171-177.
  • 100,000 Genomes Project Pilot Investigators, Smedley D, Smith KR, Martin A, Thomas EA, McDonagh EM, Cipriani V, Ellingford JM, Arno G, Tucci A, Vandrovcova J, Chan G, Williams HJ, Ratnaike T, Wei W, Stirrups K, Ibanez K, Moutsianas L, Wielscher M, Need A, Barnes MR, Vestito L, Buchanan J, Wordsworth S, Ashford S, Rehmström K, Li E, Fuller G, Twiss P, Spasic-Boskovic O, Halsall S, Floto RA, Poole K, Wagner A, Mehta SG, Gurnell M, Burrows N, James R, Penkett C, Dewhurst E, Gräf S, Mapeta R, Kasanicki M, Haworth A, Savage H, Babcock M, Reese MG, Bale M, Baple E, Boustred C, Brittain H, de Burca A, Bleda M, Devereau A, Halai D, Haraldsdottir E, Hyder Z, Kasperaviciute D, Patch C, Polychronopoulos D, Matchan A, Sultana R, Ryten M, Tavares ALT, Tregidgo C, Turnbull C, Welland M, Wood S, Snow C, Williams E, Leigh S, Foulger RE, Daugherty LC, Niblock O, Leong IUS, Wright CF, Davies J, Crichton C, Welch J, Woods K, Abulhoul L, Aurora P, Bockenhauer D, Broomfield A, Cleary MA, Lam T, Dattani M, Footitt E, Ganesan V, Grunewald S, Compeyrot-Lacassagne S, Muntoni F, Pilkington C, Quinlivan R, Thapar N, Wallis C, Wedderburn LR, Worth A, Bueser T, Compton C, Deshpande C, Fassihi H, Haque E, Izatt L, Josifova D, Mohammed S, Robert L, Rose S, Ruddy D, Sarkany R, Say G, Shaw AC, Wolejko A, Habib B, Burns G, Hunter S, Grocock RJ, Humphray SJ, Robinson PN, Haendel M, Simpson MA, Banka S, Clayton-Smith J, Douzgou S, Hall G, Thomas HB, O’Keefe RT, Michaelides M, Moore AT, Malka S, Pontikos N, Browning AC, Straub V, Gorman GS, Horvath R, Quinton R, Schaefer AM, Yu-Wai-Man P, Turnbull DM, McFarland R, Taylor RW, O’Connor E, Yip J, Newland K, Morris HR, Polke J, Wood NW, Campbell C, Camps C, Gibson K, Koelling N, Lester T, Németh AH, Palles C, Patel S, Roy NBA, Sen A, Taylor J, Cacheiro P, Jacobsen JO, Seaby EG, Davison V, Chitty L, Douglas A, Naresh K, McMullan D, Ellard S, Temple IK, Mumford AD, Wilson G, Beales P, Bitner-Glindzicz M, Black G, Bradley JR, Brennan P, Burn J, Chinnery PF, Elliott P, Flinter F, Houlden H, Irving M, Newman W, Rahman S, Sayer JA, Taylor JC, Webster AR, Wilkie AOM, Ouwehand WH, Raymond FL, Chisholm J, Hill S, Bentley D, Scott RH, Fowler T, Rendon A, Caulfield M. 100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care - Preliminary Report. N Engl J Med. 2021 Nov 11; 385: 1868-1880.
  • Verdoni A, Hu J, Surti U, Babcock M, Sheehan E, Clemens M, Drewes S, Walsh L, Clark R, Katari S, Sanfilippo J, Saller DN, Rajkovic A, Yatsenko SA. Reproductive outcomes in individuals with chromosomal reciprocal translocations. Genet Med. 2021 Sep; 23: 1753-1760.

Education

Fellowship

Icahn School of Medicine

Date Completed: 01/05/2016

Graduate School

Albert Einstein College of Medicine

Date Completed: 06/30/2006

Education

Fellowship

Icahn School of Medicine

Date Completed: 01/05/2016

Graduate School

Albert Einstein College of Medicine

Date Completed: 06/30/2006

Education

Fellowship

Icahn School of Medicine

Date Completed: 01/05/2016

Graduate School

Albert Einstein College of Medicine

Date Completed: 06/30/2006

Fellowship

Icahn School of Medicine

Date Completed: 01/05/2016

Graduate School

Albert Einstein College of Medicine

Date Completed: 06/30/2006

Fellowship

Icahn School of Medicine

Date Completed: 01/05/2016

Graduate School

Albert Einstein College of Medicine

Date Completed: 06/30/2006

Professional Experience

2022 - Present Nationwide Children’s Hospital, Clinical Director Clinical Institute for Genomic Medicine2022 - 2022 Magee Genomics Laboratories, UPMC Magee Womens Hospital, Associate Director2019 - 2022 Magee Genomics Laboratories, UPMC Magee Womens Hospital, Assistant Director

Professional Experience

2022 - Present Nationwide Children’s Hospital, Clinical Director Clinical Institute for Genomic Medicine2022 - 2022 Magee Genomics Laboratories, UPMC Magee Womens Hospital, Associate Director2019 - 2022 Magee Genomics Laboratories, UPMC Magee Womens Hospital, Assistant Director

Professional Experience

2022 - Present Nationwide Children’s Hospital, Clinical Director Clinical Institute for Genomic Medicine2022 - 2022 Magee Genomics Laboratories, UPMC Magee Womens Hospital, Associate Director2019 - 2022 Magee Genomics Laboratories, UPMC Magee Womens Hospital, Assistant Director

2022 - Present Nationwide Children’s Hospital, Clinical Director Clinical Institute for Genomic Medicine2022 - 2022 Magee Genomics Laboratories, UPMC Magee Womens Hospital, Associate Director2019 - 2022 Magee Genomics Laboratories, UPMC Magee Womens Hospital, Assistant Director

2022 - Present Nationwide Children’s Hospital, Clinical Director Clinical Institute for Genomic Medicine

Contact Information

Institute for Genomic Medicine

Call us at: (614) 355-4595

                    575 Children’s CrossroadColumbus, OH 43215 (map)

Contact Information

Institute for Genomic Medicine

Call us at: (614) 355-4595

                    575 Children’s CrossroadColumbus, OH 43215 (map)

Contact Information

Institute for Genomic Medicine

Call us at: (614) 355-4595

                    575 Children’s CrossroadColumbus, OH 43215 (map)

Institute for Genomic Medicine

Call us at: (614) 355-4595

                    575 Children’s CrossroadColumbus, OH 43215 (map)

Call us at: (614) 355-4595

                    575 Children’s CrossroadColumbus, OH 43215 (map)

Call us at: (614) 355-4595

                    575 Children’s CrossroadColumbus, OH 43215 (map)
  • Call us at:
  • (614) 355-4595
  • 575 Children’s CrossroadColumbus, OH 43215 (map)