Today is

Department of

Biomedical Informatics

Photo of  Peter White, PhD

Peter White, PhD

Department Chair and Professor

Research Interests

Biomedical Informatics

Education/Credentials
  • Doctoral Degree: Washington University
  • Fellowship: Children’s Hospital of Philadelphia
Contact Information
  • Cincinnati Children's Hospital Medical Center
  • Room 222
  • 3333 Burnet Ave
  • Cincinnati, Ohio 45229
  • Office 513-803-2341
  • Email peter.white@cchmc.org

Peer Reviewed Publications

McDonald Gibson, K; Nesbitt, A; Cao, K; Yu, Z; Denenberg, E; DeChene, E; Guan, Q; Bhoj, E; Zhou, X; Zhang, B; Wu, C; Dubbs, H; Wilkens, A; Medne, L; Bedoukian, E; White, P; Pennington, J; Lou, M; Conlin, L; Monos, D; Sarmady, M; Marsh, E; Zackai, E; Spinner, N; Krantz, I; Deardorff, M; Santani, A 2018. Novel findings with reassessment of exome data Implications for validation testing and interpretation of genomic data Genetics in Medicine, 20 3, 329

Glessner, J; Bick, A; Ito, K; Homsy, J; Rodriguez-Murillo, L; Fromer, M; Mazaika, E; Vardarajan, B; Italia, M; Leipzig, J; DePalma, S; Golhar, R; Sanders, S; Yamrom, B; Ronemus, M; Iossifov, I; Willsey, A; State, M; Kaltman, J; White, P; Shen, Y; Warburton, D; Brueckner, M; Seidman, C; Goldmuntz, E; Gelb, B; Lifton, R; Seidman, J; Hakonarson, H; Chung, W 2014. Increased Frequency of De Novo Copy Number Variants in Congenital Heart Disease by Integrative Analysis of Single Nucleotide Polymorphism Array and Exome Sequence Data Circulation Research, 115 10, 884

Masino, A; Dechene, E; Dulik, M; Wilkens, A; Spinner, N; Krantz, I; Pennington, J; Robinson, P; White, P 2014. Clinical phenotype-based gene prioritization an initial study using semantic similarity and the human phenotype ontology BMC Bioinformatics, 15 1, 248

Pennington, J; Ruth, B; Italia, M; Miller, J; Wrazien, S; Loutrel, J; Crenshaw, E; White, P 2014. Harvest an open platform for developing web-based biomedical data discovery and reporting applications Journal of the American Medical Informatics Association, 21 2, 379

Tarczy-Hornoch, P; Amendola, L; Aronson, S; Garraway, L; Gray, S; Grundmeier, R; Hindorff, L; Jarvik, G; Karavite, D; Lebo, M; Plon, S; Van Allen, E; Weck, K; White, P; Yang, Y 2013. A survey of informatics approaches to whole-exome and whole-genome clinical reporting in the electronic health record Genetics in Medicine, 15 10, 824

Zaidi, S; Choi, M; Wakimoto, H; Ma, L; Jiang, J; Overton, J; Romano-Adesman, A; Bjornson, R; Breitbart, R; Brown, K; Carriero, N; Cheung, Y; Deanfield, J; DePalma, S; Fakhro, K; Glessner, J; Hakonarson, H; Italia, M; Kaltman, J; Kaski, J; Kim, R; Kline, J; Lee, T; Leipzig, J; Lopez, A; Mane, S; Mitchell, L; Newburger, J; Parfenov, M; Pe'er, I; Porter, G; Roberts, A; Sachidanandam, R; Sanders, S; Seiden, H; State, M; Subramanian, S; Tikhonova, I; Wang, W; Warburton, D; White, P; Williams, I; Zhao, H; Seidman, J; Brueckner, M; Chung, W; Gelb, B; Goldmuntz, E; Seidman, C; Lifton, R 2013. De novo mutations in histone-modifying genes in congenital heart disease Nature, 498 7453, 220

Elia, J; Glessner, J; Wang, K; Takahashi, N; Shtir, C; Hadley, D; Sleiman, P; Zhang, H; Kim, C; Robison, R; Lyon, G; Flory, J; Bradfield, J; Imielinski, M; Hou, C; Frackelton, E; Chiavacci, R; Sakurai, T; Rabin, C; Middleton, F; Thomas, K; Garris, M; Mentch, F; Freitag, C; Steinhausen, H; Todorov, A; Reif, A; Rothenberger, A; Franke, B; Mick, E; Roeyers, H; Buitelaar, J; Lesch, K; Banaschewski, T; Ebstein, R; Mulas, F; Oades, R; Sergeant, J; Sonuga-Barke, E; Renner, T; Romanos, M; Romanos, J; Warnke, A; Walitza, S; Meyer, J; Palmason, H; Seitz, C; Loo, S; Smalley, S; Biederman, J; Kent, L; Asherson, P; Anney, R; Gaynor, J; Shaw, P; Devoto, M; White, P; Grant, S; Buxbaum, J; Rapoport, J; Williams, N; Nelson, S; Faraone, S; Hakonarson, H 2012. Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder Nature Genetics, 44 1, 78

Gai, X; Xie, H; Perin, J; Takahashi, N; Murphy, K; Wenocur, A; D'arcy, M; O'Hara, R; Goldmuntz, E; Grice, D; Shaikh, T; Hakonarson, H; Buxbaum, J; Elia, J; White, P 2012. Rare structural variation of synapse and neurotransmission genes in autism Molecular Psychiatry, 17 4, 402

Elia, J; Gai, X; Hakonarson, H; White, P 2011. Structural variations in attention-deficit hyperactivity disorder The Lancet, 377 9763, 377

Elia, J; Gai, X; Xie, H; Perin, J; Geiger, E; Glessner, J; D'arcy, M; deBerardinis, R; Frackelton, E; Kim, C; Lantieri, F; Muganga, B; Wang, L; Takeda, T; Rappaport, E; Grant, S; Berrettini, W; Devoto, M; Shaikh, T; Hakonarson, H; White, P 2010. Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes Molecular Psychiatry, 15 6, 637