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Cathy L Barr

Showing results (51-60 of 67) with videos related to

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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 18, 2008
G72/G30 (DAOA) and juvenile-onset mood disordersLissette Gomez, Karen Wigg, Yu Feng, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 28, 2008
Genome scan in sibling pairs with juvenile-onset mood disorders: Evidence for linkage to 13q and XqKaren Wigg, Yu Feng, Lissette Gomez, et al.
Psychoneuroendocrinology|June 16, 2010
No association between oxytocin or prolactin gene variants and childhood-onset mood disordersJohn S Strauss, Natalie L Freeman, Sajid A Shaikh, et al.
Frontiers in Neuroscience|October 7, 2016
Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome EtiologyJohn Alexander, Hera Potamianou, Jinchuan Xing, et al.
Molecular Cell|October 13, 2015
EGFR Mutation Promotes Glioblastoma through Epigenome and Transcription Factor Network RemodelingFeng Liu, Gary C Hon, Genaro R Villa, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 8, 2023
Integrated analysis of single-cell chromatin state and transcriptome identified common vulnerability despite glioblastoma heterogeneityRamya Raviram, Anugraha Raman, Sebastian Preissl, et al.
American Journal of Human Genetics|January 21, 2004
Joint analysis of the DRD5 marker concludes association with attention-deficit/hyperactivity disorder confined to the predominantly inattentive and combined subtypesNaomi Lowe, Aiveen Kirley, Ziarih Hawi, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
Distinct patterns of <i>de novo</i> coding variants contribute to Tourette Syndrome etiologyLingyu Zhan, Dongmei Yu, Franjo Ivankovic, et al.
Child Development|February 13, 2023
Language and reading impairments are associated with increased prevalence of non-right-handednessFilippo Abbondanza, Philip S Dale, Carol A Wang, et al.
Neuron|June 23, 2017
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette SyndromeAlden Y Huang, Dongmei Yu, Lea K Davis, et al.
Pageof 7

Showing results (51-60 of 67) with videos related to

Sort By:
Pageof 7
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 18, 2008
G72/G30 (DAOA) and juvenile-onset mood disordersLissette Gomez, Karen Wigg, Yu Feng, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 28, 2008
Genome scan in sibling pairs with juvenile-onset mood disorders: Evidence for linkage to 13q and XqKaren Wigg, Yu Feng, Lissette Gomez, et al.
Psychoneuroendocrinology|June 16, 2010
No association between oxytocin or prolactin gene variants and childhood-onset mood disordersJohn S Strauss, Natalie L Freeman, Sajid A Shaikh, et al.
Frontiers in Neuroscience|October 7, 2016
Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome EtiologyJohn Alexander, Hera Potamianou, Jinchuan Xing, et al.
Molecular Cell|October 13, 2015
EGFR Mutation Promotes Glioblastoma through Epigenome and Transcription Factor Network RemodelingFeng Liu, Gary C Hon, Genaro R Villa, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 8, 2023
Integrated analysis of single-cell chromatin state and transcriptome identified common vulnerability despite glioblastoma heterogeneityRamya Raviram, Anugraha Raman, Sebastian Preissl, et al.
American Journal of Human Genetics|January 21, 2004
Joint analysis of the DRD5 marker concludes association with attention-deficit/hyperactivity disorder confined to the predominantly inattentive and combined subtypesNaomi Lowe, Aiveen Kirley, Ziarih Hawi, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
Distinct patterns of <i>de novo</i> coding variants contribute to Tourette Syndrome etiologyLingyu Zhan, Dongmei Yu, Franjo Ivankovic, et al.
Child Development|February 13, 2023
Language and reading impairments are associated with increased prevalence of non-right-handednessFilippo Abbondanza, Philip S Dale, Carol A Wang, et al.
Neuron|June 23, 2017
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette SyndromeAlden Y Huang, Dongmei Yu, Lea K Davis, et al.
Pageof 7