Contact Information
Call us at: (614)355-6672
Fax us at: (614) 355-6671
Email David A Greenberg, PhD
Battelle Center for Mathematical MedicineAbigail Wexner Research Institute575 Children’s CrossroadColumbus, OH 43215 (map)
Learn more about David A Greenberg
Biography
David Greenberg, PhD, is a faculty member of the Battelle Center for Mathematical Medicine. Dr. Greenberg's interests focus on the genetics of common disease in general and on the development of methodology for studying common disease genetics in particular. He also has the oldest and one of the largest studies in the genetics of idiopathic generalized epilepsy, with collaborations at more than 15 hospitals across the country. This research has been successful, with the identification of at least five areas of the genome that harbor genes for idiopathic generalized epilepsy, and the identification of two of the loci. His experience in real-world genetics as well as theory emphasizes the importance of understanding the clinical picture of disease in order to define the phenotype that will lead to a successful genetic analysis.Dr. Greenberg has also developed analysis approaches and has been a leading advocate for the use of computer simulation in the study of genetic analysis. He has published extensively in computer simulation and developed the computer simulator used at the 11th and 14th Genetic Analysis Workshops. He has used his experience in genetic simulation to develop a suite of programs used to teach linkage analysis and association analysis to postdocs and students. This approach has been gratifyingly successful, with trainees developing a clear sense of the strengths and weakness of linkage methods and association methods. He has also supervised the development of a genetics data base analysis system with a web-based interface that allows researchers to conduct analysis experiments and vary phenotype definitions.
See David A Greenberg’s Curriculum Vitae (CV)
Academic and Clinical Areas
Battelle Center for Mathematical Medicine
Faculty
Greenberg Lab
Principal Investigator
Neurology
Principal Investigator
Primary Department
Battelle Center for Mathematical Medicine
Research
Lab(s)
Battelle Center for Mathematical Medicine
Greenberg Lab
Publications
Shakeshaft A, Panjwani N, Collingwood A, Crudgington H, Hall A, Andrade DM, Beier CP, Fong CY, Gardella E, Gesche J, Greenberg DA, Hamandi K, Koht J, Lim KS, Møller RS, Ng CC, Orsini A, Rees MI, Rubboli G, Selmer KK, Striano P, Syvertsen M, Thomas RH, Zarubova J, Richardson MP, Strug LJ, Pal DK. Sex-specific disease modifiers in juvenile myoclonic epilepsy. Sci Rep. 2022 Feb 21; 12: 2785.
Brown LA, Hamlett GE, Zhu Y, Wiley JF, Moore TM, DiDomenico GE, Visoki E, Greenberg DM, Gur RC, Gur RE, Barzilay R. Worry about COVID-19 as a predictor of future insomnia. J Sleep Res. 2022 Feb 14; e13564.
Wang M, Greenberg DA, Stewart WCL. In Response: ME2 association analysis in adolescent-onset genetic generalized epilepsy. Epilepsia. 2019 Jul 29;
Simchovitz A, Hanan M, Niederhoffer N, Madrer N, Yayon N, Bennett ER, Greenberg DS, Kadener S, Soreq H. NEAT1 is overexpressed in Parkinson's disease substantia nigra and confers drug-inducible neuroprotection from oxidative stress. FASEB J. 2019 Jul 16; fj201900830R.
Young-Xu Y, Snider JT, van Aalst R, Mahmud SM, Thommes EW, Lee JKH, Greenberg DP, Chit A. Analysis of relative effectiveness of high-dose versus standard-dose influenza vaccines using an instrumental variable method. Vaccine. 2019 Mar 7; 37: 1484-1490.
Wang M, Greenberg DA, Stewart WCL. Replication, reanalysis, and gene expression: ME2 and genetic generalized epilepsy. Epilepsia. 2019 Mar; 60: 539-546.
Pathak S, Miller J, Morris EC, Stewart WCL, Greenberg DA. DNA methylation of the BRD2 promoter is associated with juvenile myoclonic epilepsy in Caucasians. Epilepsia. 2018 May; 59: 1011-1019.
Dagan R, Ben-Shimol S, Simell B, Greenberg D, Porat N, Käyhty H, Givon-Lavi N. A toddler PCV booster dose following 3 infancy priming doses increases circulating serotype-specific IGG levels but does not increase protection against carriage. Vaccine. 2018 May 11; 36: 2774-2782.
Lipner EM, Greenberg DA. The Rise and Fall and Rise of Linkage Analysis as a Technique for Finding and Characterizing Inherited Influences on Disease Expression. Methods Mol Biol. 2018; 1706: 381-397.
Mukhopadhyay N, Noble JA, Govil M, Marazita ML, Greenberg DA. Identifying genetic risk loci for diabetic complications and showing evidence for heterogeneity of type 1 diabetes based on complications risk. PLoS One. 2018; 13: e0192696.
Cheng B, Chatzinoff Y, Szczepanski D, Bing C, Shaikh S, Wyman O, Perry CE, Richardson JA, Burns DK, Evers BM, Greenberg DE, Chopra R. Remote acoustic sensing as a safety mechanism during exposure of metal implants to alternating magnetic fields. PLoS One. 2018; 13: e0197380.
View More Publications
Contact Information
Battelle Center for Mathematical Medicine
Call us at: (614)355-6672
Fax us at: (614) 355-6671
Email David A Greenberg
Abigail Wexner Research Institute575 Children's CrossroadColumbus, OH 43215 (map)
Contact Information
Call us at: (614)355-6672
Fax us at: (614) 355-6671
Email David A Greenberg, PhD
Battelle Center for Mathematical MedicineAbigail Wexner Research Institute575 Children’s CrossroadColumbus, OH 43215 (map)
Learn more about David A Greenberg
Biography
David Greenberg, PhD, is a faculty member of the Battelle Center for Mathematical Medicine. Dr. Greenberg's interests focus on the genetics of common disease in general and on the development of methodology for studying common disease genetics in particular. He also has the oldest and one of the largest studies in the genetics of idiopathic generalized epilepsy, with collaborations at more than 15 hospitals across the country. This research has been successful, with the identification of at least five areas of the genome that harbor genes for idiopathic generalized epilepsy, and the identification of two of the loci. His experience in real-world genetics as well as theory emphasizes the importance of understanding the clinical picture of disease in order to define the phenotype that will lead to a successful genetic analysis.Dr. Greenberg has also developed analysis approaches and has been a leading advocate for the use of computer simulation in the study of genetic analysis. He has published extensively in computer simulation and developed the computer simulator used at the 11th and 14th Genetic Analysis Workshops. He has used his experience in genetic simulation to develop a suite of programs used to teach linkage analysis and association analysis to postdocs and students. This approach has been gratifyingly successful, with trainees developing a clear sense of the strengths and weakness of linkage methods and association methods. He has also supervised the development of a genetics data base analysis system with a web-based interface that allows researchers to conduct analysis experiments and vary phenotype definitions.
See David A Greenberg’s Curriculum Vitae (CV)
Academic and Clinical Areas
Battelle Center for Mathematical Medicine
Faculty
Greenberg Lab
Principal Investigator
Neurology
Principal Investigator
Primary Department
Battelle Center for Mathematical Medicine
Research
Lab(s)
Battelle Center for Mathematical Medicine
Greenberg Lab
Publications
Shakeshaft A, Panjwani N, Collingwood A, Crudgington H, Hall A, Andrade DM, Beier CP, Fong CY, Gardella E, Gesche J, Greenberg DA, Hamandi K, Koht J, Lim KS, Møller RS, Ng CC, Orsini A, Rees MI, Rubboli G, Selmer KK, Striano P, Syvertsen M, Thomas RH, Zarubova J, Richardson MP, Strug LJ, Pal DK. Sex-specific disease modifiers in juvenile myoclonic epilepsy. Sci Rep. 2022 Feb 21; 12: 2785.
Brown LA, Hamlett GE, Zhu Y, Wiley JF, Moore TM, DiDomenico GE, Visoki E, Greenberg DM, Gur RC, Gur RE, Barzilay R. Worry about COVID-19 as a predictor of future insomnia. J Sleep Res. 2022 Feb 14; e13564.
Wang M, Greenberg DA, Stewart WCL. In Response: ME2 association analysis in adolescent-onset genetic generalized epilepsy. Epilepsia. 2019 Jul 29;
Simchovitz A, Hanan M, Niederhoffer N, Madrer N, Yayon N, Bennett ER, Greenberg DS, Kadener S, Soreq H. NEAT1 is overexpressed in Parkinson's disease substantia nigra and confers drug-inducible neuroprotection from oxidative stress. FASEB J. 2019 Jul 16; fj201900830R.
Young-Xu Y, Snider JT, van Aalst R, Mahmud SM, Thommes EW, Lee JKH, Greenberg DP, Chit A. Analysis of relative effectiveness of high-dose versus standard-dose influenza vaccines using an instrumental variable method. Vaccine. 2019 Mar 7; 37: 1484-1490.
Wang M, Greenberg DA, Stewart WCL. Replication, reanalysis, and gene expression: ME2 and genetic generalized epilepsy. Epilepsia. 2019 Mar; 60: 539-546.
Pathak S, Miller J, Morris EC, Stewart WCL, Greenberg DA. DNA methylation of the BRD2 promoter is associated with juvenile myoclonic epilepsy in Caucasians. Epilepsia. 2018 May; 59: 1011-1019.
Dagan R, Ben-Shimol S, Simell B, Greenberg D, Porat N, Käyhty H, Givon-Lavi N. A toddler PCV booster dose following 3 infancy priming doses increases circulating serotype-specific IGG levels but does not increase protection against carriage. Vaccine. 2018 May 11; 36: 2774-2782.
Lipner EM, Greenberg DA. The Rise and Fall and Rise of Linkage Analysis as a Technique for Finding and Characterizing Inherited Influences on Disease Expression. Methods Mol Biol. 2018; 1706: 381-397.
Mukhopadhyay N, Noble JA, Govil M, Marazita ML, Greenberg DA. Identifying genetic risk loci for diabetic complications and showing evidence for heterogeneity of type 1 diabetes based on complications risk. PLoS One. 2018; 13: e0192696.
Cheng B, Chatzinoff Y, Szczepanski D, Bing C, Shaikh S, Wyman O, Perry CE, Richardson JA, Burns DK, Evers BM, Greenberg DE, Chopra R. Remote acoustic sensing as a safety mechanism during exposure of metal implants to alternating magnetic fields. PLoS One. 2018; 13: e0197380.
View More Publications
Contact Information
Battelle Center for Mathematical Medicine
Call us at: (614)355-6672
Fax us at: (614) 355-6671
Email David A Greenberg
Abigail Wexner Research Institute575 Children's CrossroadColumbus, OH 43215 (map)
Contact Information
Call us at: (614)355-6672
Fax us at: (614) 355-6671
Email David A Greenberg, PhD
Battelle Center for Mathematical MedicineAbigail Wexner Research Institute575 Children’s CrossroadColumbus, OH 43215 (map)
Learn more about David A Greenberg
Contact Information
- Call us at:
- (614)355-6672
- Fax us at:
- (614) 355-6671
- Email David A Greenberg, PhD
- Battelle Center for Mathematical MedicineAbigail Wexner Research Institute575 Children’s CrossroadColumbus, OH 43215 (map)
Learn more about David A Greenberg
Biography
David Greenberg, PhD, is a faculty member of the Battelle Center for Mathematical Medicine. Dr. Greenberg's interests focus on the genetics of common disease in general and on the development of methodology for studying common disease genetics in particular. He also has the oldest and one of the largest studies in the genetics of idiopathic generalized epilepsy, with collaborations at more than 15 hospitals across the country. This research has been successful, with the identification of at least five areas of the genome that harbor genes for idiopathic generalized epilepsy, and the identification of two of the loci. His experience in real-world genetics as well as theory emphasizes the importance of understanding the clinical picture of disease in order to define the phenotype that will lead to a successful genetic analysis.Dr. Greenberg has also developed analysis approaches and has been a leading advocate for the use of computer simulation in the study of genetic analysis. He has published extensively in computer simulation and developed the computer simulator used at the 11th and 14th Genetic Analysis Workshops. He has used his experience in genetic simulation to develop a suite of programs used to teach linkage analysis and association analysis to postdocs and students. This approach has been gratifyingly successful, with trainees developing a clear sense of the strengths and weakness of linkage methods and association methods. He has also supervised the development of a genetics data base analysis system with a web-based interface that allows researchers to conduct analysis experiments and vary phenotype definitions.
See David A Greenberg’s Curriculum Vitae (CV)
Biography
David Greenberg, PhD, is a faculty member of the Battelle Center for Mathematical Medicine. Dr. Greenberg's interests focus on the genetics of common disease in general and on the development of methodology for studying common disease genetics in particular. He also has the oldest and one of the largest studies in the genetics of idiopathic generalized epilepsy, with collaborations at more than 15 hospitals across the country. This research has been successful, with the identification of at least five areas of the genome that harbor genes for idiopathic generalized epilepsy, and the identification of two of the loci. His experience in real-world genetics as well as theory emphasizes the importance of understanding the clinical picture of disease in order to define the phenotype that will lead to a successful genetic analysis.Dr. Greenberg has also developed analysis approaches and has been a leading advocate for the use of computer simulation in the study of genetic analysis. He has published extensively in computer simulation and developed the computer simulator used at the 11th and 14th Genetic Analysis Workshops. He has used his experience in genetic simulation to develop a suite of programs used to teach linkage analysis and association analysis to postdocs and students. This approach has been gratifyingly successful, with trainees developing a clear sense of the strengths and weakness of linkage methods and association methods. He has also supervised the development of a genetics data base analysis system with a web-based interface that allows researchers to conduct analysis experiments and vary phenotype definitions.
See David A Greenberg’s Curriculum Vitae (CV)
Biography
David Greenberg, PhD, is a faculty member of the Battelle Center for Mathematical Medicine. Dr. Greenberg's interests focus on the genetics of common disease in general and on the development of methodology for studying common disease genetics in particular. He also has the oldest and one of the largest studies in the genetics of idiopathic generalized epilepsy, with collaborations at more than 15 hospitals across the country. This research has been successful, with the identification of at least five areas of the genome that harbor genes for idiopathic generalized epilepsy, and the identification of two of the loci. His experience in real-world genetics as well as theory emphasizes the importance of understanding the clinical picture of disease in order to define the phenotype that will lead to a successful genetic analysis.Dr. Greenberg has also developed analysis approaches and has been a leading advocate for the use of computer simulation in the study of genetic analysis. He has published extensively in computer simulation and developed the computer simulator used at the 11th and 14th Genetic Analysis Workshops. He has used his experience in genetic simulation to develop a suite of programs used to teach linkage analysis and association analysis to postdocs and students. This approach has been gratifyingly successful, with trainees developing a clear sense of the strengths and weakness of linkage methods and association methods. He has also supervised the development of a genetics data base analysis system with a web-based interface that allows researchers to conduct analysis experiments and vary phenotype definitions.
See David A Greenberg’s Curriculum Vitae (CV)
David Greenberg, PhD, is a faculty member of the Battelle Center for Mathematical Medicine. Dr. Greenberg's interests focus on the genetics of common disease in general and on the development of methodology for studying common disease genetics in particular. He also has the oldest and one of the largest studies in the genetics of idiopathic generalized epilepsy, with collaborations at more than 15 hospitals across the country. This research has been successful, with the identification of at least five areas of the genome that harbor genes for idiopathic generalized epilepsy, and the identification of two of the loci. His experience in real-world genetics as well as theory emphasizes the importance of understanding the clinical picture of disease in order to define the phenotype that will lead to a successful genetic analysis.Dr. Greenberg has also developed analysis approaches and has been a leading advocate for the use of computer simulation in the study of genetic analysis. He has published extensively in computer simulation and developed the computer simulator used at the 11th and 14th Genetic Analysis Workshops. He has used his experience in genetic simulation to develop a suite of programs used to teach linkage analysis and association analysis to postdocs and students. This approach has been gratifyingly successful, with trainees developing a clear sense of the strengths and weakness of linkage methods and association methods. He has also supervised the development of a genetics data base analysis system with a web-based interface that allows researchers to conduct analysis experiments and vary phenotype definitions.
See David A Greenberg’s Curriculum Vitae (CV)
See David A Greenberg’s Curriculum Vitae (CV)
Academic and Clinical Areas
Battelle Center for Mathematical Medicine
Faculty
Greenberg Lab
Principal Investigator
Neurology
Principal Investigator
Primary Department
Battelle Center for Mathematical Medicine
Academic and Clinical Areas
Battelle Center for Mathematical Medicine
Faculty
Greenberg Lab
Principal Investigator
Neurology
Principal Investigator
Primary Department
Battelle Center for Mathematical Medicine
Academic and Clinical Areas
Battelle Center for Mathematical Medicine
Faculty
Greenberg Lab
Principal Investigator
Neurology
Principal Investigator
Primary Department
Battelle Center for Mathematical Medicine
Battelle Center for Mathematical Medicine
Faculty
Greenberg Lab
Principal Investigator
Neurology
Principal Investigator
Primary Department
Battelle Center for Mathematical Medicine
- Battelle Center for Mathematical Medicine
- Faculty
- Greenberg Lab
- Principal Investigator
- Neurology
- Principal Investigator
- Primary Department
- Battelle Center for Mathematical Medicine
Research
Lab(s)
Battelle Center for Mathematical Medicine
Greenberg Lab
Publications
Shakeshaft A, Panjwani N, Collingwood A, Crudgington H, Hall A, Andrade DM, Beier CP, Fong CY, Gardella E, Gesche J, Greenberg DA, Hamandi K, Koht J, Lim KS, Møller RS, Ng CC, Orsini A, Rees MI, Rubboli G, Selmer KK, Striano P, Syvertsen M, Thomas RH, Zarubova J, Richardson MP, Strug LJ, Pal DK. Sex-specific disease modifiers in juvenile myoclonic epilepsy. Sci Rep. 2022 Feb 21; 12: 2785.
Brown LA, Hamlett GE, Zhu Y, Wiley JF, Moore TM, DiDomenico GE, Visoki E, Greenberg DM, Gur RC, Gur RE, Barzilay R. Worry about COVID-19 as a predictor of future insomnia. J Sleep Res. 2022 Feb 14; e13564.
Wang M, Greenberg DA, Stewart WCL. In Response: ME2 association analysis in adolescent-onset genetic generalized epilepsy. Epilepsia. 2019 Jul 29;
Simchovitz A, Hanan M, Niederhoffer N, Madrer N, Yayon N, Bennett ER, Greenberg DS, Kadener S, Soreq H. NEAT1 is overexpressed in Parkinson's disease substantia nigra and confers drug-inducible neuroprotection from oxidative stress. FASEB J. 2019 Jul 16; fj201900830R.
Young-Xu Y, Snider JT, van Aalst R, Mahmud SM, Thommes EW, Lee JKH, Greenberg DP, Chit A. Analysis of relative effectiveness of high-dose versus standard-dose influenza vaccines using an instrumental variable method. Vaccine. 2019 Mar 7; 37: 1484-1490.
Wang M, Greenberg DA, Stewart WCL. Replication, reanalysis, and gene expression: ME2 and genetic generalized epilepsy. Epilepsia. 2019 Mar; 60: 539-546.
Pathak S, Miller J, Morris EC, Stewart WCL, Greenberg DA. DNA methylation of the BRD2 promoter is associated with juvenile myoclonic epilepsy in Caucasians. Epilepsia. 2018 May; 59: 1011-1019.
Dagan R, Ben-Shimol S, Simell B, Greenberg D, Porat N, Käyhty H, Givon-Lavi N. A toddler PCV booster dose following 3 infancy priming doses increases circulating serotype-specific IGG levels but does not increase protection against carriage. Vaccine. 2018 May 11; 36: 2774-2782.
Lipner EM, Greenberg DA. The Rise and Fall and Rise of Linkage Analysis as a Technique for Finding and Characterizing Inherited Influences on Disease Expression. Methods Mol Biol. 2018; 1706: 381-397.
Mukhopadhyay N, Noble JA, Govil M, Marazita ML, Greenberg DA. Identifying genetic risk loci for diabetic complications and showing evidence for heterogeneity of type 1 diabetes based on complications risk. PLoS One. 2018; 13: e0192696.
Cheng B, Chatzinoff Y, Szczepanski D, Bing C, Shaikh S, Wyman O, Perry CE, Richardson JA, Burns DK, Evers BM, Greenberg DE, Chopra R. Remote acoustic sensing as a safety mechanism during exposure of metal implants to alternating magnetic fields. PLoS One. 2018; 13: e0197380.
View More Publications
Research
Lab(s)
Battelle Center for Mathematical Medicine
Greenberg Lab
Publications
Shakeshaft A, Panjwani N, Collingwood A, Crudgington H, Hall A, Andrade DM, Beier CP, Fong CY, Gardella E, Gesche J, Greenberg DA, Hamandi K, Koht J, Lim KS, Møller RS, Ng CC, Orsini A, Rees MI, Rubboli G, Selmer KK, Striano P, Syvertsen M, Thomas RH, Zarubova J, Richardson MP, Strug LJ, Pal DK. Sex-specific disease modifiers in juvenile myoclonic epilepsy. Sci Rep. 2022 Feb 21; 12: 2785.
Brown LA, Hamlett GE, Zhu Y, Wiley JF, Moore TM, DiDomenico GE, Visoki E, Greenberg DM, Gur RC, Gur RE, Barzilay R. Worry about COVID-19 as a predictor of future insomnia. J Sleep Res. 2022 Feb 14; e13564.
Wang M, Greenberg DA, Stewart WCL. In Response: ME2 association analysis in adolescent-onset genetic generalized epilepsy. Epilepsia. 2019 Jul 29;
Simchovitz A, Hanan M, Niederhoffer N, Madrer N, Yayon N, Bennett ER, Greenberg DS, Kadener S, Soreq H. NEAT1 is overexpressed in Parkinson's disease substantia nigra and confers drug-inducible neuroprotection from oxidative stress. FASEB J. 2019 Jul 16; fj201900830R.
Young-Xu Y, Snider JT, van Aalst R, Mahmud SM, Thommes EW, Lee JKH, Greenberg DP, Chit A. Analysis of relative effectiveness of high-dose versus standard-dose influenza vaccines using an instrumental variable method. Vaccine. 2019 Mar 7; 37: 1484-1490.
Wang M, Greenberg DA, Stewart WCL. Replication, reanalysis, and gene expression: ME2 and genetic generalized epilepsy. Epilepsia. 2019 Mar; 60: 539-546.
Pathak S, Miller J, Morris EC, Stewart WCL, Greenberg DA. DNA methylation of the BRD2 promoter is associated with juvenile myoclonic epilepsy in Caucasians. Epilepsia. 2018 May; 59: 1011-1019.
Dagan R, Ben-Shimol S, Simell B, Greenberg D, Porat N, Käyhty H, Givon-Lavi N. A toddler PCV booster dose following 3 infancy priming doses increases circulating serotype-specific IGG levels but does not increase protection against carriage. Vaccine. 2018 May 11; 36: 2774-2782.
Lipner EM, Greenberg DA. The Rise and Fall and Rise of Linkage Analysis as a Technique for Finding and Characterizing Inherited Influences on Disease Expression. Methods Mol Biol. 2018; 1706: 381-397.
Mukhopadhyay N, Noble JA, Govil M, Marazita ML, Greenberg DA. Identifying genetic risk loci for diabetic complications and showing evidence for heterogeneity of type 1 diabetes based on complications risk. PLoS One. 2018; 13: e0192696.
Cheng B, Chatzinoff Y, Szczepanski D, Bing C, Shaikh S, Wyman O, Perry CE, Richardson JA, Burns DK, Evers BM, Greenberg DE, Chopra R. Remote acoustic sensing as a safety mechanism during exposure of metal implants to alternating magnetic fields. PLoS One. 2018; 13: e0197380.
View More Publications
Research
Lab(s)
Battelle Center for Mathematical Medicine
Greenberg Lab
Publications
Shakeshaft A, Panjwani N, Collingwood A, Crudgington H, Hall A, Andrade DM, Beier CP, Fong CY, Gardella E, Gesche J, Greenberg DA, Hamandi K, Koht J, Lim KS, Møller RS, Ng CC, Orsini A, Rees MI, Rubboli G, Selmer KK, Striano P, Syvertsen M, Thomas RH, Zarubova J, Richardson MP, Strug LJ, Pal DK. Sex-specific disease modifiers in juvenile myoclonic epilepsy. Sci Rep. 2022 Feb 21; 12: 2785.
Brown LA, Hamlett GE, Zhu Y, Wiley JF, Moore TM, DiDomenico GE, Visoki E, Greenberg DM, Gur RC, Gur RE, Barzilay R. Worry about COVID-19 as a predictor of future insomnia. J Sleep Res. 2022 Feb 14; e13564.
Wang M, Greenberg DA, Stewart WCL. In Response: ME2 association analysis in adolescent-onset genetic generalized epilepsy. Epilepsia. 2019 Jul 29;
Simchovitz A, Hanan M, Niederhoffer N, Madrer N, Yayon N, Bennett ER, Greenberg DS, Kadener S, Soreq H. NEAT1 is overexpressed in Parkinson's disease substantia nigra and confers drug-inducible neuroprotection from oxidative stress. FASEB J. 2019 Jul 16; fj201900830R.
Young-Xu Y, Snider JT, van Aalst R, Mahmud SM, Thommes EW, Lee JKH, Greenberg DP, Chit A. Analysis of relative effectiveness of high-dose versus standard-dose influenza vaccines using an instrumental variable method. Vaccine. 2019 Mar 7; 37: 1484-1490.
Wang M, Greenberg DA, Stewart WCL. Replication, reanalysis, and gene expression: ME2 and genetic generalized epilepsy. Epilepsia. 2019 Mar; 60: 539-546.
Pathak S, Miller J, Morris EC, Stewart WCL, Greenberg DA. DNA methylation of the BRD2 promoter is associated with juvenile myoclonic epilepsy in Caucasians. Epilepsia. 2018 May; 59: 1011-1019.
Dagan R, Ben-Shimol S, Simell B, Greenberg D, Porat N, Käyhty H, Givon-Lavi N. A toddler PCV booster dose following 3 infancy priming doses increases circulating serotype-specific IGG levels but does not increase protection against carriage. Vaccine. 2018 May 11; 36: 2774-2782.
Lipner EM, Greenberg DA. The Rise and Fall and Rise of Linkage Analysis as a Technique for Finding and Characterizing Inherited Influences on Disease Expression. Methods Mol Biol. 2018; 1706: 381-397.
Mukhopadhyay N, Noble JA, Govil M, Marazita ML, Greenberg DA. Identifying genetic risk loci for diabetic complications and showing evidence for heterogeneity of type 1 diabetes based on complications risk. PLoS One. 2018; 13: e0192696.
Cheng B, Chatzinoff Y, Szczepanski D, Bing C, Shaikh S, Wyman O, Perry CE, Richardson JA, Burns DK, Evers BM, Greenberg DE, Chopra R. Remote acoustic sensing as a safety mechanism during exposure of metal implants to alternating magnetic fields. PLoS One. 2018; 13: e0197380.
View More Publications
Lab(s)
Battelle Center for Mathematical Medicine
Greenberg Lab
Publications
Shakeshaft A, Panjwani N, Collingwood A, Crudgington H, Hall A, Andrade DM, Beier CP, Fong CY, Gardella E, Gesche J, Greenberg DA, Hamandi K, Koht J, Lim KS, Møller RS, Ng CC, Orsini A, Rees MI, Rubboli G, Selmer KK, Striano P, Syvertsen M, Thomas RH, Zarubova J, Richardson MP, Strug LJ, Pal DK. Sex-specific disease modifiers in juvenile myoclonic epilepsy. Sci Rep. 2022 Feb 21; 12: 2785.
Brown LA, Hamlett GE, Zhu Y, Wiley JF, Moore TM, DiDomenico GE, Visoki E, Greenberg DM, Gur RC, Gur RE, Barzilay R. Worry about COVID-19 as a predictor of future insomnia. J Sleep Res. 2022 Feb 14; e13564.
Wang M, Greenberg DA, Stewart WCL. In Response: ME2 association analysis in adolescent-onset genetic generalized epilepsy. Epilepsia. 2019 Jul 29;
Simchovitz A, Hanan M, Niederhoffer N, Madrer N, Yayon N, Bennett ER, Greenberg DS, Kadener S, Soreq H. NEAT1 is overexpressed in Parkinson's disease substantia nigra and confers drug-inducible neuroprotection from oxidative stress. FASEB J. 2019 Jul 16; fj201900830R.
Young-Xu Y, Snider JT, van Aalst R, Mahmud SM, Thommes EW, Lee JKH, Greenberg DP, Chit A. Analysis of relative effectiveness of high-dose versus standard-dose influenza vaccines using an instrumental variable method. Vaccine. 2019 Mar 7; 37: 1484-1490.
Wang M, Greenberg DA, Stewart WCL. Replication, reanalysis, and gene expression: ME2 and genetic generalized epilepsy. Epilepsia. 2019 Mar; 60: 539-546.
Pathak S, Miller J, Morris EC, Stewart WCL, Greenberg DA. DNA methylation of the BRD2 promoter is associated with juvenile myoclonic epilepsy in Caucasians. Epilepsia. 2018 May; 59: 1011-1019.
Dagan R, Ben-Shimol S, Simell B, Greenberg D, Porat N, Käyhty H, Givon-Lavi N. A toddler PCV booster dose following 3 infancy priming doses increases circulating serotype-specific IGG levels but does not increase protection against carriage. Vaccine. 2018 May 11; 36: 2774-2782.
Lipner EM, Greenberg DA. The Rise and Fall and Rise of Linkage Analysis as a Technique for Finding and Characterizing Inherited Influences on Disease Expression. Methods Mol Biol. 2018; 1706: 381-397.
Mukhopadhyay N, Noble JA, Govil M, Marazita ML, Greenberg DA. Identifying genetic risk loci for diabetic complications and showing evidence for heterogeneity of type 1 diabetes based on complications risk. PLoS One. 2018; 13: e0192696.
Cheng B, Chatzinoff Y, Szczepanski D, Bing C, Shaikh S, Wyman O, Perry CE, Richardson JA, Burns DK, Evers BM, Greenberg DE, Chopra R. Remote acoustic sensing as a safety mechanism during exposure of metal implants to alternating magnetic fields. PLoS One. 2018; 13: e0197380.
View More Publications
Lab(s)
Battelle Center for Mathematical Medicine
Greenberg Lab
Shakeshaft A, Panjwani N, Collingwood A, Crudgington H, Hall A, Andrade DM, Beier CP, Fong CY, Gardella E, Gesche J, Greenberg DA, Hamandi K, Koht J, Lim KS, Møller RS, Ng CC, Orsini A, Rees MI, Rubboli G, Selmer KK, Striano P, Syvertsen M, Thomas RH, Zarubova J, Richardson MP, Strug LJ, Pal DK. Sex-specific disease modifiers in juvenile myoclonic epilepsy. Sci Rep. 2022 Feb 21; 12: 2785.
Brown LA, Hamlett GE, Zhu Y, Wiley JF, Moore TM, DiDomenico GE, Visoki E, Greenberg DM, Gur RC, Gur RE, Barzilay R. Worry about COVID-19 as a predictor of future insomnia. J Sleep Res. 2022 Feb 14; e13564.
Wang M, Greenberg DA, Stewart WCL. In Response: ME2 association analysis in adolescent-onset genetic generalized epilepsy. Epilepsia. 2019 Jul 29;
Simchovitz A, Hanan M, Niederhoffer N, Madrer N, Yayon N, Bennett ER, Greenberg DS, Kadener S, Soreq H. NEAT1 is overexpressed in Parkinson's disease substantia nigra and confers drug-inducible neuroprotection from oxidative stress. FASEB J. 2019 Jul 16; fj201900830R.
Young-Xu Y, Snider JT, van Aalst R, Mahmud SM, Thommes EW, Lee JKH, Greenberg DP, Chit A. Analysis of relative effectiveness of high-dose versus standard-dose influenza vaccines using an instrumental variable method. Vaccine. 2019 Mar 7; 37: 1484-1490.
Wang M, Greenberg DA, Stewart WCL. Replication, reanalysis, and gene expression: ME2 and genetic generalized epilepsy. Epilepsia. 2019 Mar; 60: 539-546.
Pathak S, Miller J, Morris EC, Stewart WCL, Greenberg DA. DNA methylation of the BRD2 promoter is associated with juvenile myoclonic epilepsy in Caucasians. Epilepsia. 2018 May; 59: 1011-1019.
Dagan R, Ben-Shimol S, Simell B, Greenberg D, Porat N, Käyhty H, Givon-Lavi N. A toddler PCV booster dose following 3 infancy priming doses increases circulating serotype-specific IGG levels but does not increase protection against carriage. Vaccine. 2018 May 11; 36: 2774-2782.
Lipner EM, Greenberg DA. The Rise and Fall and Rise of Linkage Analysis as a Technique for Finding and Characterizing Inherited Influences on Disease Expression. Methods Mol Biol. 2018; 1706: 381-397.
Mukhopadhyay N, Noble JA, Govil M, Marazita ML, Greenberg DA. Identifying genetic risk loci for diabetic complications and showing evidence for heterogeneity of type 1 diabetes based on complications risk. PLoS One. 2018; 13: e0192696.
Cheng B, Chatzinoff Y, Szczepanski D, Bing C, Shaikh S, Wyman O, Perry CE, Richardson JA, Burns DK, Evers BM, Greenberg DE, Chopra R. Remote acoustic sensing as a safety mechanism during exposure of metal implants to alternating magnetic fields. PLoS One. 2018; 13: e0197380.
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Lab(s)
Battelle Center for Mathematical Medicine
Greenberg Lab
Battelle Center for Mathematical Medicine
Greenberg Lab
Shakeshaft A, Panjwani N, Collingwood A, Crudgington H, Hall A, Andrade DM, Beier CP, Fong CY, Gardella E, Gesche J, Greenberg DA, Hamandi K, Koht J, Lim KS, Møller RS, Ng CC, Orsini A, Rees MI, Rubboli G, Selmer KK, Striano P, Syvertsen M, Thomas RH, Zarubova J, Richardson MP, Strug LJ, Pal DK. Sex-specific disease modifiers in juvenile myoclonic epilepsy. Sci Rep. 2022 Feb 21; 12: 2785.
Brown LA, Hamlett GE, Zhu Y, Wiley JF, Moore TM, DiDomenico GE, Visoki E, Greenberg DM, Gur RC, Gur RE, Barzilay R. Worry about COVID-19 as a predictor of future insomnia. J Sleep Res. 2022 Feb 14; e13564.
Wang M, Greenberg DA, Stewart WCL. In Response: ME2 association analysis in adolescent-onset genetic generalized epilepsy. Epilepsia. 2019 Jul 29;
Simchovitz A, Hanan M, Niederhoffer N, Madrer N, Yayon N, Bennett ER, Greenberg DS, Kadener S, Soreq H. NEAT1 is overexpressed in Parkinson’s disease substantia nigra and confers drug-inducible neuroprotection from oxidative stress. FASEB J. 2019 Jul 16; fj201900830R.
Young-Xu Y, Snider JT, van Aalst R, Mahmud SM, Thommes EW, Lee JKH, Greenberg DP, Chit A. Analysis of relative effectiveness of high-dose versus standard-dose influenza vaccines using an instrumental variable method. Vaccine. 2019 Mar 7; 37: 1484-1490.
Wang M, Greenberg DA, Stewart WCL. Replication, reanalysis, and gene expression: ME2 and genetic generalized epilepsy. Epilepsia. 2019 Mar; 60: 539-546.
Pathak S, Miller J, Morris EC, Stewart WCL, Greenberg DA. DNA methylation of the BRD2 promoter is associated with juvenile myoclonic epilepsy in Caucasians. Epilepsia. 2018 May; 59: 1011-1019.
Dagan R, Ben-Shimol S, Simell B, Greenberg D, Porat N, Käyhty H, Givon-Lavi N. A toddler PCV booster dose following 3 infancy priming doses increases circulating serotype-specific IGG levels but does not increase protection against carriage. Vaccine. 2018 May 11; 36: 2774-2782.
Lipner EM, Greenberg DA. The Rise and Fall and Rise of Linkage Analysis as a Technique for Finding and Characterizing Inherited Influences on Disease Expression. Methods Mol Biol. 2018; 1706: 381-397.
Mukhopadhyay N, Noble JA, Govil M, Marazita ML, Greenberg DA. Identifying genetic risk loci for diabetic complications and showing evidence for heterogeneity of type 1 diabetes based on complications risk. PLoS One. 2018; 13: e0192696.
Cheng B, Chatzinoff Y, Szczepanski D, Bing C, Shaikh S, Wyman O, Perry CE, Richardson JA, Burns DK, Evers BM, Greenberg DE, Chopra R. Remote acoustic sensing as a safety mechanism during exposure of metal implants to alternating magnetic fields. PLoS One. 2018; 13: e0197380.
Contact Information
Battelle Center for Mathematical Medicine
Call us at: (614)355-6672
Fax us at: (614) 355-6671
Email David A Greenberg
Abigail Wexner Research Institute575 Children's CrossroadColumbus, OH 43215 (map)
Contact Information
Battelle Center for Mathematical Medicine
Call us at: (614)355-6672
Fax us at: (614) 355-6671
Email David A Greenberg
Abigail Wexner Research Institute575 Children's CrossroadColumbus, OH 43215 (map)
Contact Information
Battelle Center for Mathematical Medicine
Call us at: (614)355-6672
Fax us at: (614) 355-6671
Email David A Greenberg
Abigail Wexner Research Institute575 Children's CrossroadColumbus, OH 43215 (map)
Battelle Center for Mathematical Medicine
Call us at: (614)355-6672
Fax us at: (614) 355-6671
Email David A Greenberg
Abigail Wexner Research Institute575 Children's CrossroadColumbus, OH 43215 (map)
Call us at: (614)355-6672
Fax us at: (614) 355-6671
Email David A Greenberg
Abigail Wexner Research Institute575 Children's CrossroadColumbus, OH 43215 (map)
Call us at: (614)355-6672
Fax us at: (614) 355-6671
Email David A Greenberg
Abigail Wexner Research Institute575 Children's CrossroadColumbus, OH 43215 (map)
- Call us at:
- (614)355-6672
- Fax us at:
- (614) 355-6671
- Email David A Greenberg
- Abigail Wexner Research Institute575 Children’s CrossroadColumbus, OH 43215 (map)