Rate of de novo mutations and the importance of father's age to disease risk - Wikidata - wikimedia - TriplyDB

Rate of de novo mutations and the importance of father's age to disease risk

Rate of de novo mutations and the importance of father's age to disease risk

http://www.wikidata.org/entity/Q24632353

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Lamarckian evolution explains human brain evolution and psychiatric disorders Effects of increased paternal age on sperm quality, reproductive outcome and associated epigenetic risks to offspring Neuropathology and animal models of autism: genetic and environmental factors Meiotic interstrand DNA damage escapes paternal repair and causes chromosomal aberrations in the zygote by maternal misrepair Male-mediated developmental toxicity Genome sequence of a 45,000-year-old modern human from western Siberia An unbiased resource of novel SNP markers provides a new chronology for the human Y chromosome and reveals a deep phylogenetic structure in Africa ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19 Exome sequencing reveals new causal mutations in children with epileptic encephalopathies An African American paternal lineage adds an extremely ancient root to the human Y chromosome phylogenetic tree De novo mutations in epileptic encephalopathies Estimating the human mutation rate using autozygosity in a founder population The dysconnection hypothesis (2016)The Evolving Diagnostic and Genetic Landscapes of Autism Spectrum Disorder RELN Mutations in Autism Spectrum Disorder Prenatal Neurogenesis in Autism Spectrum Disorders Modulatory effects of α7 nAChRs on the immune system and its relevance for CNS disorders Case report of novel DYRK1A mutations in 2 individuals with syndromic intellectual disability and a review of the literature Mutations and Modeling of the Chromatin Remodeler CHD8 Define an Emerging Autism Etiology Epigenetics and male reproduction: the consequences of paternal lifestyle on fertility, embryo development, and children lifetime health Behavioral phenotypes of genetic mouse models of autism.Human spermatozoa: revelations on the road to conception The developmental transcriptome of the human brain: implications for neurodevelopmental disorders Medical genomics: The intricate path from genetic variant identification to clinical interpretation Breaking bad: The mutagenic effect of DNA repair The presence, role and clinical use of spermatozoal RNAs Cellular levels of 8-oxoguanine in either DNA or the nucleotide pool play pivotal roles in carcinogenesis and survival of cancer cells Life course health care and preemptive approach to non-communicable diseases Clinical genetic testing for male factor infertility: current applications and future directions The effects of advanced paternal age on fertility Developmental mechanisms in the prodrome to psychosis Progress in the genetics of polygenic brain disorders: significant new challenges for neurobiology Somatic mosaicism: implications for disease and transmission genetics Search for missing schizophrenia genes will require a new developmental neurogenomic perspective Background selection 20 years on: the Wilhelmine E. Key 2012 invitational lecture Genomic signatures of selection at linked sites: unifying the disparity among species Spontaneous 8bp Deletion in Nbeal2 Recapitulates the Gray Platelet Syndrome in Mice Germline mutation rates and the long-term phenotypic effects of mutation accumulation in wild-type laboratory mice and mutator mice Reference-free population genomics from next-generation transcriptome data and the vertebrate-invertebrate gap Early Neolithic genomes from the eastern Fertile Crescent

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Rate of de novo mutations and the importance of father's age to disease risk

http://www.wikidata.org/entity/Q24632353

description

2012 nî lūn-bûn

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2012 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի օգոստոսին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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name

Rate of de novo mutations and the importance of father's age to disease risk

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Rate of de novo mutations and the importance of father's age to disease risk

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Rate of de novo mutations and the importance of father's age to disease risk

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Rate of de novo mutations and the importance of father's age to disease risk

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Rate of de novo mutations and the importance of father's age to disease risk

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Rate of de novo mutations and the importance of father's age to disease risk

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Rate of de novo mutations and the importance of father's age to disease risk

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Rate of de novo mutations and the importance of father's age to disease risk

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Rate of de novo mutations and the importance of father's age to disease risk

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Rate of de novo mutations and the importance of father's age to disease risk

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Agnar Helgason

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Asgeir Sigurdsson

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G Bragi Walters

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Hannes Helgason

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Michael L Frigge

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Olafur Th Magnusson

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Sigurjon A Gudjonsson

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P2860

Analysis of genetic inheritance in a family quartet by whole-genome sequencing

Variation in genome-wide mutation rates within and between human families

Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia

Estimate of the mutation rate per nucleotide in humans

Rates and fitness consequences of new mutations in humans

Disruption of the neurexin 1 gene is associated with schizophrenia

Fast and accurate short read alignment with Burrows-Wheeler transform

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

The origins, patterns and implications of human spontaneous mutation

Mutations in BRIP1 confer high risk of ovarian cancer

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10.1038/NATURE11396

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Gudmar Thorleifsson

Unnur Þorsteinsdóttir

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Adalbjorg Jonasdottir

Kári Stefánsson

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2012-08-23T00:00:00Z

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