Analysis of morphine responses in mice reveals a QTL on Chromosome 7 [version 2; referees: 2 approved] door Wim E. Crusio, Esha Dhawan, Elissa J. Chesler, Anna Delprato

Onderwerpen: “…Neurogenetics…”
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Analysis of morphine responses in mice reveals a QTL on Chromosome 7 [version 1; referees: 2 approved] door Wim E. Crusio, Esha Dhawan, Elissa J. Chesler, Anna Delprato

Onderwerpen: “…Neurogenetics…”
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Investigating rare genetic variants in common migraine door Weir, G

Onderwerpen: “…Neurogenetics…”

Whole brain and regional hyperintense white matter volume and blood pressure: overlap of genetic loci produced by bivariate, whole-genome linkage analyses door Kochunov, P, Glahn, D, Lancaster, J, Winkler, A, Kent, J, Olvera, R, Cole, SA, Dyer, T, Almasy, L, Duggirala, R, Fox, P, Blangero, J

Onderwerpen: “…Neurogenetics…”

Analysis of genetic variability and whole genome linkage of whole-brain, subcortical, and ependymal hyperintense white matter volume door Kochunov, P, Glahn, D, Winkler, A, Duggirala, R, Olvera, R, Cole, S, Dyer, T, Almasy, L, Fox, P, Blangero, J

Onderwerpen: “…Neurogenetics…”

Transcriptomics of cortical gray matter thickness decline during normal aging door Kochunov, P, Charlesworth, J, Winkler, A, Hong, L, Nichols, T, Curran, J, Sprooten, E, Jahanshad, N, Thompson, P, Johnson, M, Kent, J, Landman, B, Mitchell, B, Cole, SA, Dyer, T, Moses, E, Goring, H, Almasy, L, Duggirala, R, Olvera, R, Glahn, D, Blangero, J

Onderwerpen: “…Neurogenetics…”

Cortical thickness or grey matter volume? The importance of selecting the phenotype for imaging genetics studies door Winkler, A, Kochunov, P, Blangero, J, Almasy, L, Zilles, K, Fox, P, Duggirala, R, Glahn, D

Onderwerpen: “…Neurogenetics…”

Genetic analysis of cortical thickness and fractional anisotropy of water diffusion in the brain door Kochunov, P, Glahn, D, Nichols, T, Winkler, A, Hong, E, Holcomb, H, Stein, J, Thompson, P, Curran, J, Carless, M, Olvera, R, Johnson, M, Cole, SA, Kochunov, V, Kent, J, Blangero, J

Onderwerpen: “…Neurogenetics…”

Sensorimotor control of Drosophila copulation door Herbert, MR

Onderwerpen: “…Neurogenetics…”

Computational neurogenetic modeling / door Benuskova, Lubica, 1958-, Kasabov, Nikola K.

Onderwerpen: “…Neurogenetics…”

Leukocyte telomere length and hippocampus volume: a meta-analysis [version 1; referees: 2 approved] door Gustav Nilsonne, Sandra Tamm, Kristoffer N. T. Månsson, Torbjörn Åkerstedt, Mats Lekander

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A proton-inhibited DEG/ENaC ion channel maintains neuronal ionstasis and promotes neuronal survival under stress door Dionysia Petratou, Martha Gjikolaj, Eva Kaulich, William Schafer, Nektarios Tavernarakis

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A novel pseudoderivative-based mutation operator for real-coded adaptive genetic algorithms [v2; ref status: indexed, http://f1000r.es/1td] door Maxinder S Kanwal, Avinash S Ramesh, Lauren A Huang

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ANGDelMut – a web-based tool for predicting and analyzing functional loss mechanisms of amyotrophic lateral sclerosis-associated angiogenin mutations [v3; ref status: indexed, http... door Aditya K Padhi, Suhas V Vasaikar, Bhyravabhotla Jayaram, James Gomes

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ANGDelMut – a web-based tool for predicting and analyzing functional loss mechanisms of amyotrophic lateral sclerosis-associated angiogenin mutations [v2; ref status: indexed, http... door Aditya K Padhi, Suhas V Vasaikar, Bhyravabhotla Jayaram, James Gomes

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GPER1 Signaling Initiates Migration of Female V-SVZ-Derived Cells door Iris Haumann, Muriel Anne Sturm, Max Anstötz, Gabriele M. Rune

Onderwerpen: “…Neurogenetics…”
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The regulation of enteric neuron connectivity by semaphorin 5A is affected by the autism-associated S956G missense mutation door Morgane E. Le Dréan, Catherine Le Berre-Scoul, Vincent Paillé, Martial Caillaud, Thibauld Oullier, Jacques Gonzales, Philippe Hulin, Michel Neunlist, Sophie Talon, Hélène Boudin

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Whole exome sequencing identifies a novel homozygous frameshift mutation in the ASPM gene, which causes microcephaly 5, primary, autosomal recessive [version 1; referees: 2 approve... door Desaraju Suresh Bhargav, N. Sreedevi, N. Swapna, Soumya Vivek, Srinivas Kovvali

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Using computation to enhance diagnosis and therapy: a novel mutation operator for real-coded adaptive genetic algorithms [v1; ref status: indexed, http://f1000r.es/wf] door Maxinder S Kanwal, Avinash S Ramesh, Lauren A Huang

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The role of polycomb repressive complex 2 in postnatal subventricular zone neural stem/progenitor cell self-renewal and multipotency door Chang, EH

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