Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 20 of 23


Quantifying the Effects of 16p11.2 Copy Number Variants on Brain Structure: A Multisite Genetic-First Study.

Martin-Brevet S, Rodríguez-Herreros B, Nielsen JA, Moreau C, Modenato C, Maillard AM, Pain A, Richetin S, Jønch AE, Qureshi AY, Zürcher NR, Conus P; 16p11.2 European Consortium; Simons Variation in Individuals Project (VIP) Consortium, Chung WK, Sherr EH, Spiro JE, Kherif F, Beckmann JS, Hadjikhani N, Reymond A, Buckner RL, Draganski B, Jacquemont S.

Biol Psychiatry. 2018 Mar 27. pii: S0006-3223(18)31401-X. doi: 10.1016/j.biopsych.2018.02.1176. [Epub ahead of print]


Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities.

D'Angelo D, Lebon S, Chen Q, Martin-Brevet S, Snyder LG, Hippolyte L, Hanson E, Maillard AM, Faucett WA, Macé A, Pain A, Bernier R, Chawner SJ, David A, Andrieux J, Aylward E, Baujat G, Caldeira I, Conus P, Ferrari C, Forzano F, Gérard M, Goin-Kochel RP, Grant E, Hunter JV, Isidor B, Jacquette A, Jønch AE, Keren B, Lacombe D, Le Caignec C, Martin CL, Männik K, Metspalu A, Mignot C, Mukherjee P, Owen MJ, Passeggeri M, Rooryck-Thambo C, Rosenfeld JA, Spence SJ, Steinman KJ, Tjernagel J, Van Haelst M, Shen Y, Draganski B, Sherr EH, Ledbetter DH, van den Bree MB, Beckmann JS, Spiro JE, Reymond A, Jacquemont S, Chung WK; Cardiff University Experiences of Children With Copy Number Variants (ECHO) Study; 16p11.2 European Consortium; Simons Variation in Individuals Project (VIP) Consortium.

JAMA Psychiatry. 2016 Jan;73(1):20-30. doi: 10.1001/jamapsychiatry.2015.2123.


Is there concordance in attitudes and beliefs between parents and scientists about autism spectrum disorder?

Fischbach RL, Harris MJ, Ballan MS, Fischbach GD, Link BG.

Autism. 2016 Apr;20(3):353-63. doi: 10.1177/1362361315585310. Epub 2015 May 26.


The pattern of cortical dysfunction in a mouse model of a schizophrenia-related microdeletion.

Fénelon K, Xu B, Lai CS, Mukai J, Markx S, Stark KL, Hsu PK, Gan WB, Fischbach GD, MacDermott AB, Karayiorgou M, Gogos JA.

J Neurosci. 2013 Sep 11;33(37):14825-39. doi: 10.1523/JNEUROSCI.1611-13.2013.


A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.

Zufferey F, Sherr EH, Beckmann ND, Hanson E, Maillard AM, Hippolyte L, Macé A, Ferrari C, Kutalik Z, Andrieux J, Aylward E, Barker M, Bernier R, Bouquillon S, Conus P, Delobel B, Faucett WA, Goin-Kochel RP, Grant E, Harewood L, Hunter JV, Lebon S, Ledbetter DH, Martin CL, Männik K, Martinet D, Mukherjee P, Ramocki MB, Spence SJ, Steinman KJ, Tjernagel J, Spiro JE, Reymond A, Beckmann JS, Chung WK, Jacquemont S; Simons VIP Consortium; 16p11.2 European Consortium.

J Med Genet. 2012 Oct;49(10):660-8. doi: 10.1136/jmedgenet-2012-101203. Erratum in: J Med Genet. 2014 Jul;51(7):478.


The best of times, the worst of times for psychiatric disease.

Karayiorgou M, Flint J, Gogos JA, Malenka RC; Genetic and Neural Complexity in Psychiatry 2011 Working Group.

Nat Neurosci. 2012 May 25;15(6):811-2. doi: 10.1038/nn.3115. No abstract available.


Simons Variation in Individuals Project (Simons VIP): a genetics-first approach to studying autism spectrum and related neurodevelopmental disorders.

Simons Vip Consortium.

Neuron. 2012 Mar 22;73(6):1063-7. doi: 10.1016/j.neuron.2012.02.014. Epub 2012 Mar 21.


Deficiency of Dgcr8, a gene disrupted by the 22q11.2 microdeletion, results in altered short-term plasticity in the prefrontal cortex.

Fénelon K, Mukai J, Xu B, Hsu PK, Drew LJ, Karayiorgou M, Fischbach GD, Macdermott AB, Gogos JA.

Proc Natl Acad Sci U S A. 2011 Mar 15;108(11):4447-52. doi: 10.1073/pnas.1101219108. Epub 2011 Feb 28.


The Simons Simplex Collection: a resource for identification of autism genetic risk factors.

Fischbach GD, Lord C.

Neuron. 2010 Oct 21;68(2):192-5. doi: 10.1016/j.neuron.2010.10.006.


Rescuing Z+ agrin splicing in Nova null mice restores synapse formation and unmasks a physiologic defect in motor neuron firing.

Ruggiu M, Herbst R, Kim N, Jevsek M, Fak JJ, Mann MA, Fischbach G, Burden SJ, Darnell RB.

Proc Natl Acad Sci U S A. 2009 Mar 3;106(9):3513-8. doi: 10.1073/pnas.0813112106. Epub 2009 Feb 12.


Neuroethicists needed now more than ever.

Fischbach RL, Fischbach GD.

Am J Bioeth. 2008 Jan;8(1):47-8. doi: 10.1080/15265160701828568. No abstract available.


NRG1 and synaptic function in the CNS.

Fischbach GD.

Neuron. 2007 May 24;54(4):495-7.


Neuregulin effect on quantal content dissociated from effect on miniature endplate potential amplitude.

Mann MA, Das S, Zhang J, Wagner M, Fischbach GD.

J Neurophysiol. 2006 Aug;96(2):671-6.


Schizophrenia: signals from the other side.

Fischbach GD.

Nat Med. 2006 Jul;12(7):734-5. No abstract available.


The brain doesn't lie.

Fischbach RL, Fischbach GD.

Am J Bioeth. 2005 Spring;5(2):54-5; discussion W5. No abstract available.


Neuregulin-1 increases the proliferation of neuronal progenitors from embryonic neural stem cells.

Liu Y, Ford BD, Mann MA, Fischbach GD.

Dev Biol. 2005 Jul 15;283(2):437-45.


Stem cells: science, policy, and ethics.

Fischbach GD, Fischbach RL.

J Clin Invest. 2004 Nov;114(10):1364-70.


Neuregulin induces the expression of transcription factors and myosin heavy chains typical of muscle spindles in cultured human muscle.

Jacobson C, Duggan D, Fischbach G.

Proc Natl Acad Sci U S A. 2004 Aug 17;101(33):12218-23. Epub 2004 Aug 9.


Neuregulin-1 suppresses muscarinic receptor expression and acetylcholine-activated muscarinic K+ channels in cardiac myocytes.

Ford BD, Liu Y, Mann MA, Krauss R, Phillips K, Gan L, Fischbach GD.

Biochem Biophys Res Commun. 2003 Aug 15;308(1):23-8.


Supplemental Content

Loading ...
Support Center