Asset Details
MbrlCatalogueTitleDetail
Do you wish to reserve the book?
Paternal-age-related de novo mutations and risk for five disorders
by
Larsen, Janne T.
, Homsy, Jason
, Seidman, Jonathan G.
, Weiner, Daniel J.
, Taylor, Jacob L.
, Lal, Dennis
, Petersen, Liselotte
, Daly, Mark J.
, Kosmicki, Jack A.
, Morton, Sarah U.
, Robinson, Elise B.
, Bloemendal, Alex
, Mortensen, Preben Bo
, Debost, Jean-Christophe P. G.
, Wigdor, Emilie M.
, Heyne, Henrike O.
, Seidman, Christine E.
, Agerbo, Esben
, McGrath, John J.
, Howrigan, Daniel P.
in
631/208/1516
/ 631/378/2583
/ 692/617/375/366
/ 692/699/476
/ Adult
/ Age
/ Age Factors
/ Autism
/ Autism Spectrum Disorder - epidemiology
/ Autism Spectrum Disorder - genetics
/ Cardiovascular diseases
/ Child
/ Coronary artery disease
/ Denmark - epidemiology
/ Disorders
/ Epidemiology
/ Epilepsy
/ Epilepsy - epidemiology
/ Epilepsy - genetics
/ Female
/ Genetic Testing
/ Health risk assessment
/ Heart Defects, Congenital - epidemiology
/ Heart Defects, Congenital - genetics
/ Heart diseases
/ Humanities and Social Sciences
/ Humans
/ Incidence
/ Intellectual Disability - epidemiology
/ Intellectual Disability - genetics
/ Male
/ Mental disorders
/ Middle Aged
/ Models, Genetic
/ multidisciplinary
/ Mutation
/ Neurodevelopmental disorders
/ Nucleotides
/ Offspring
/ Paternal Age
/ Paternity
/ Polymorphism, Single Nucleotide
/ Prevalence
/ Registries - statistics & numerical data
/ Risk
/ Risk Assessment - methods
/ Schizophrenia
/ Schizophrenia - epidemiology
/ Schizophrenia - genetics
/ Science
/ Science (multidisciplinary)
/ Whole Exome Sequencing
2019
Hey, we have placed the reservation for you!
By the way, why not check out events that you can attend while you pick your title.
You are currently in the queue to collect this book. You will be notified once it is your turn to collect the book.
Oops! Something went wrong.
Looks like we were not able to place the reservation. Kindly try again later.
Are you sure you want to remove the book from the shelf?
Paternal-age-related de novo mutations and risk for five disorders
by
Larsen, Janne T.
, Homsy, Jason
, Seidman, Jonathan G.
, Weiner, Daniel J.
, Taylor, Jacob L.
, Lal, Dennis
, Petersen, Liselotte
, Daly, Mark J.
, Kosmicki, Jack A.
, Morton, Sarah U.
, Robinson, Elise B.
, Bloemendal, Alex
, Mortensen, Preben Bo
, Debost, Jean-Christophe P. G.
, Wigdor, Emilie M.
, Heyne, Henrike O.
, Seidman, Christine E.
, Agerbo, Esben
, McGrath, John J.
, Howrigan, Daniel P.
in
631/208/1516
/ 631/378/2583
/ 692/617/375/366
/ 692/699/476
/ Adult
/ Age
/ Age Factors
/ Autism
/ Autism Spectrum Disorder - epidemiology
/ Autism Spectrum Disorder - genetics
/ Cardiovascular diseases
/ Child
/ Coronary artery disease
/ Denmark - epidemiology
/ Disorders
/ Epidemiology
/ Epilepsy
/ Epilepsy - epidemiology
/ Epilepsy - genetics
/ Female
/ Genetic Testing
/ Health risk assessment
/ Heart Defects, Congenital - epidemiology
/ Heart Defects, Congenital - genetics
/ Heart diseases
/ Humanities and Social Sciences
/ Humans
/ Incidence
/ Intellectual Disability - epidemiology
/ Intellectual Disability - genetics
/ Male
/ Mental disorders
/ Middle Aged
/ Models, Genetic
/ multidisciplinary
/ Mutation
/ Neurodevelopmental disorders
/ Nucleotides
/ Offspring
/ Paternal Age
/ Paternity
/ Polymorphism, Single Nucleotide
/ Prevalence
/ Registries - statistics & numerical data
/ Risk
/ Risk Assessment - methods
/ Schizophrenia
/ Schizophrenia - epidemiology
/ Schizophrenia - genetics
/ Science
/ Science (multidisciplinary)
/ Whole Exome Sequencing
2019
Oops! Something went wrong.
While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Paternal-age-related de novo mutations and risk for five disorders
by
Larsen, Janne T.
, Homsy, Jason
, Seidman, Jonathan G.
, Weiner, Daniel J.
, Taylor, Jacob L.
, Lal, Dennis
, Petersen, Liselotte
, Daly, Mark J.
, Kosmicki, Jack A.
, Morton, Sarah U.
, Robinson, Elise B.
, Bloemendal, Alex
, Mortensen, Preben Bo
, Debost, Jean-Christophe P. G.
, Wigdor, Emilie M.
, Heyne, Henrike O.
, Seidman, Christine E.
, Agerbo, Esben
, McGrath, John J.
, Howrigan, Daniel P.
in
631/208/1516
/ 631/378/2583
/ 692/617/375/366
/ 692/699/476
/ Adult
/ Age
/ Age Factors
/ Autism
/ Autism Spectrum Disorder - epidemiology
/ Autism Spectrum Disorder - genetics
/ Cardiovascular diseases
/ Child
/ Coronary artery disease
/ Denmark - epidemiology
/ Disorders
/ Epidemiology
/ Epilepsy
/ Epilepsy - epidemiology
/ Epilepsy - genetics
/ Female
/ Genetic Testing
/ Health risk assessment
/ Heart Defects, Congenital - epidemiology
/ Heart Defects, Congenital - genetics
/ Heart diseases
/ Humanities and Social Sciences
/ Humans
/ Incidence
/ Intellectual Disability - epidemiology
/ Intellectual Disability - genetics
/ Male
/ Mental disorders
/ Middle Aged
/ Models, Genetic
/ multidisciplinary
/ Mutation
/ Neurodevelopmental disorders
/ Nucleotides
/ Offspring
/ Paternal Age
/ Paternity
/ Polymorphism, Single Nucleotide
/ Prevalence
/ Registries - statistics & numerical data
/ Risk
/ Risk Assessment - methods
/ Schizophrenia
/ Schizophrenia - epidemiology
/ Schizophrenia - genetics
/ Science
/ Science (multidisciplinary)
/ Whole Exome Sequencing
2019
Please be aware that the book you have requested cannot be checked out. If you would like to checkout this book, you can reserve another copy
We have requested the book for you!
Your request is successful and it will be processed during the Library working hours. Please check the status of your request in My Requests.
Oops! Something went wrong.
Looks like we were not able to place your request. Kindly try again later.
Paternal-age-related de novo mutations and risk for five disorders
Journal Article
Paternal-age-related de novo mutations and risk for five disorders
2019
Request Book From Autostore
and Choose the Collection Method
Overview
There are established associations between advanced paternal age and offspring risk for psychiatric and developmental disorders. These are commonly attributed to genetic mutations, especially de novo single nucleotide variants (dnSNVs), that accumulate with increasing paternal age. However, the actual magnitude of risk from such mutations in the male germline is unknown. Quantifying this risk would clarify the clinical significance of delayed paternity. Using parent-child trio whole-exome-sequencing data, we estimate the relationship between paternal-age-related dnSNVs and risk for five disorders: autism spectrum disorder (ASD), congenital heart disease, neurodevelopmental disorders with epilepsy, intellectual disability and schizophrenia (SCZ). Using Danish registry data, we investigate whether epidemiologic associations between each disorder and older fatherhood are consistent with the estimated role of dnSNVs. We find that paternal-age-related dnSNVs confer a small amount of risk for these disorders. For ASD and SCZ, epidemiologic associations with delayed paternity reflect factors that may not increase with age.
Advanced paternal age associates with increased risk for psychiatric and developmental disorders in offspring. Here, Taylor et al. utilize parent-child trio exome sequencing data sets to estimate the contribution of paternal age-related de novo mutations to multiple disorders, including heart disease and schizophrenia.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
Subject
/ Adult
/ Age
/ Autism
/ Autism Spectrum Disorder - epidemiology
/ Autism Spectrum Disorder - genetics
/ Child
/ Epilepsy
/ Female
/ Heart Defects, Congenital - epidemiology
/ Heart Defects, Congenital - genetics
/ Humanities and Social Sciences
/ Humans
/ Intellectual Disability - epidemiology
/ Intellectual Disability - genetics
/ Male
/ Mutation
/ Neurodevelopmental disorders
/ Polymorphism, Single Nucleotide
/ Registries - statistics & numerical data
/ Risk
/ Schizophrenia - epidemiology
/ Science
This website uses cookies to ensure you get the best experience on our website.