De novo and inherited CNVs in MZ twin pairs selected for discordance and concordance on Attention Problems - Wikidata - wikimedia - TriplyDB

De novo and inherited CNVs in MZ twin pairs selected for discordance and concordance on Attention Problems

De novo and inherited CNVs in MZ twin pairs selected for discordance and concordance on Attention Problems

http://www.wikidata.org/entity/Q36253450

about

Comparison of Genomic and Epigenomic Expression in Monozygotic Twins Discordant for Rett Syndrome.The Adult Netherlands Twin Register: twenty-five years of survey and biological data collection De novo copy number variations in cloned dogs from the same nuclear donor Copy number variations burden on miRNA genes reveals layers of complexities involved in the regulation of pathways and phenotypic expression Genome-wide blood DNA methylation alterations at regulatory elements and heterochromatic regions in monozygotic twins discordant for obesity and liver fat.Copy number variation burden on asthma subgenome in normal cohorts identifies susceptibility markers.Heritability in inflammatory bowel disease: from the first twin study to genome-wide association studies Twin Mitochondrial Sequence Analysis Distribution of disease-associated copy number variants across distinct disorders of cognitive development.Twin, association and current "omics" studies.Establishment of the Avera Twin Register in the Midwest USA.Genetics of attention-deficit/hyperactivity disorder: an update.The etiology of autistic traits in preschoolers: a population-based twin study.Attention-Deficit/Hyperactivity Disorder: Focus upon Aberrant N-Methyl-D-Aspartate Receptors Systems.Absence of substantial copy number differences in a pair of monozygotic twins discordant for features of autism spectrum disorder.Whole-Exome Sequencing in Nine Monozygotic Discordant Twins.Twins, tissue, and time: an assessment of SNPs and CNVs.Theoretical framework of population genetics with somatic mutations taken into account: application to copy number variations in humans.Genomic screening of testicular germ cell tumors from monozygotic twins Post-zygotic genomic changes in glutamate and dopamine pathway genes may explain discordance of monozygotic twins for schizophrenia.Copy Number Variants and Exome Sequencing Analysis in Six Pairs of Chinese Monozygotic Twins Discordant for Congenital Heart Disease.Global patterns of large copy number variations in the human genome reveal complexity in chromosome organization.Copy Number Variation Analysis of 100 Twin Pairs Enriched for Neurodevelopmental Disorders.Large Autosomal Copy-Number Differences within Unselected Monozygotic Twin Pairs are Rare.Copy number variation distribution in six monozygotic twin pairs discordant for schizophrenia.CNV Concordance in 1,097 MZ Twin Pairs.Genetic instrumental variable regression: Explaining socioeconomic and health outcomes in nonexperimental data.

P2860

Q30453156-66E2DE0B-9675-46F1-B1D0-141B71E35954 Q30585076-E98F7D11-DEED-464B-B578-FE4D84E19299 Q35061735-C5DDD574-4741-401F-A86C-6652D24F7800 Q35109014-1D323C87-7A27-4C6A-B572-6E8850C70A94 Q35368842-C0CFDE07-BFFD-461E-9C51-592944F7B67C Q35420597-3DDB01D3-DDCA-436E-AFC7-F9028E0BB851 Q35670604-B3638030-E7CB-4FD7-BCC1-AC9F2DC4833B Q37158331-88B8072B-011B-4ED7-A101-C8739C313786 Q37174458-96375805-453A-4934-99A5-8C4BBCE1B80E Q38141076-2FC0666D-8DC6-48D4-B016-FAB3D0813B56 Q38614581-1B492B5C-2B02-4517-9F7A-368F347919E5 Q38664320-06CFB7F2-2E2C-4839-85C3-CD37C112394A Q38681834-F15CCE38-6488-4518-B941-0BD0643EB404 Q38683432-65335668-077F-4B42-88FC-D53AD1668EC5 Q39245818-707DFDBE-E787-4804-B530-383F0EFA6497 Q40197489-0FA07F7E-3266-49CF-B843-B7BED1A3A99D Q41217516-0E97B78A-4016-4526-94C3-DF4EE8805A9F Q41760724-34AD296D-43AE-4869-8E9E-5D5453726FD7 Q41952598-92F7B1C3-D401-474A-8B3D-0DB52AF813BE Q47135953-7A3AB163-EEED-4C37-B2B1-E5862BC85809 Q47138529-BE3B9748-E9C5-4169-BCCF-CBCCE5378A33 Q47377704-E6FDE024-8596-43FC-A14A-03442C8DFF1E Q47747851-920DAD96-4C52-423B-A098-D481F2E43010 Q48380129-405B7423-AA46-4454-8BE3-6CB10F8237C4 Q50658828-6CB865EE-931A-4250-819D-223494536244 Q50978367-03208BC0-C119-4627-813E-EAAF3703381D Q52568652-C6A5E9ED-10A4-46A8-A507-4807FECF76B8

P2860

De novo and inherited CNVs in MZ twin pairs selected for discordance and concordance on Attention Problems

http://www.wikidata.org/entity/Q36253450

description

2012 nî lūn-bûn

@nan

2012年の論文

@ja

2012年論文

@yue

2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

@wuu

2012年论文

@zh

2012年论文

@zh-cn

name

De novo and inherited CNVs in ...... cordance on Attention Problems

@ast

De novo and inherited CNVs in ...... cordance on Attention Problems

@en

type

label

De novo and inherited CNVs in ...... cordance on Attention Problems

@ast

De novo and inherited CNVs in ...... cordance on Attention Problems

@en

prefLabel

De novo and inherited CNVs in ...... cordance on Attention Problems

@ast

De novo and inherited CNVs in ...... cordance on Attention Problems

@en

P1433

Q36253450-2E8E213F-F2A1-480B-B0F9-A3C5ED888D13

P1476

Q36253450-A8E1BA4D-8CF2-47DB-B860-9B7EFC5E7D93

P2093

Q36253450-1E2AF3BE-5EB3-48C0-A512-978861FCCA47

Q36253450-56029549-D8E0-4ABD-8FCB-C149387E199F

Q36253450-6E084DEA-E9FD-4914-BCD3-55083D1FA4A0

Q36253450-6FFC024D-B1B9-4497-BD70-05DFBF74EF7B

Q36253450-B4C18C30-1686-4C9A-A762-61EA0E697737

Q36253450-BD0C87D3-706A-4699-AFC4-99D0A0544A1D

Q36253450-DBAD62ED-D5DC-4FC1-BBB5-86DDE5A86D43

Q36253450-DC6130F9-FD90-40DB-8976-83FEC543B293

Q36253450-DC7E5D09-D11B-4879-8726-5623D2CB5A1C

P2860

Q36253450-07E938DE-2F03-4541-B639-3E56C9215C63

Q36253450-0CEAEB03-51EA-49B4-8F0E-F707D392FF55

Q36253450-0FA8FF74-FA18-4ECE-8E6C-B26AB81E93DC

Q36253450-125DFC6E-3423-47A1-BCBD-88A02DE2EED0

Q36253450-233632FC-BEA4-4579-8D24-333B8649C88D

Q36253450-2AEC0504-051D-4BA5-96FF-20279090282A

Q36253450-2B84E4B7-A8AE-4B31-8C8B-5D9FDD22E464

Q36253450-2CBA337E-02A0-49FA-9B0E-F889B78B80BB

Q36253450-2D5FB50D-1F15-4FAF-A2BE-069F8141804A

Q36253450-2E58B60E-C07C-41E2-9BC9-CC9674C7377A

P2888

Q36253450-3AD4A7B6-5E12-495D-9E7F-21AE7A73D3D4

P304

Q36253450-FE58BE42-892D-4CCB-B5A0-E1DD7EB1F86D

P31

Q36253450-73BEDA71-82BB-46F6-BD02-5FFB817C3E26

P356

Q36253450-436BF524-9D37-4037-B5E7-F8033A441CC2

P433

Q36253450-C14D9596-8CB8-4A6A-BF4C-F4739B338026

P478

Q36253450-25979F80-329E-49B0-9E73-7C83C88D3F19

P50

Q36253450-03529330-A796-407B-AD0E-5C9D892B1100

Q36253450-18C64812-A731-4AF4-A085-379343301710

Q36253450-8DAAB5A3-E12D-442C-89A7-E47EB4739C4B

Q36253450-C247F20F-2BF2-4B93-BB63-9DF429B50BCA

Q36253450-E32A14AF-E1F2-4FBF-9457-9625B05D4ECB

P577

Q36253450-BE5F4E75-14DD-4F9B-AF72-AF9A49BF8102

P5875

Q36253450-5149936B-D505-430B-A641-10E939C3F38C

P6179

Q36253450-4E79AD55-E220-4A1C-855F-265A54324CF3

P698

Q36253450-8DC9713D-2F41-47C8-A4C3-A789F93FC35F

P921

Q36253450-FF24A85F-11E0-4670-98C4-8B75DD8BD54B

P932

Q36253450-6005BD05-E97E-45D0-BCBA-C92A2AB454EC

P356

P1433

European Journal of Human Genetics

P1476

De novo and inherited CNVs in ...... cordance on Attention Problems

@en

P2093

Abdel Abdellaoui

http://www.w3.org/2001/XMLSchema#string

Erik A Ehli

http://www.w3.org/2001/XMLSchema#string

Gareth E Davies

http://www.w3.org/2001/XMLSchema#string

Mathijs Kattenberg

http://www.w3.org/2001/XMLSchema#string

Paul Scheet

http://www.w3.org/2001/XMLSchema#string

Robert R Althoff

http://www.w3.org/2001/XMLSchema#string

Toos van Beijsterveldt

http://www.w3.org/2001/XMLSchema#string

Xiangjun Xiao

http://www.w3.org/2001/XMLSchema#string

Yueshan Hu

http://www.w3.org/2001/XMLSchema#string

P2860

Mapping and sequencing of structural variation from eight human genomes

Copy-number variations associated with neuropsychiatric conditions

Fatty acid metabolism in neurodevelopmental disorder: a new perspective on associations between attention-deficit/hyperactivity disorder, dyslexia, dyspraxia and the autistic spectrum

DUX4, a candidate gene of facioscapulohumeral muscular dystrophy, encodes a transcriptional activator of PITX1

The DUX4 gene at the FSHD1A locus encodes a pro-apoptotic protein

Extensive normal copy number variation of a beta-defensin antimicrobial-gene cluster.

Paired-end mapping reveals extensive structural variation in the human genome

Global variation in copy number in the human genome

PLINK: a tool set for whole-genome association and population-based linkage analyses

A 4q35.2 subtelomeric deletion identified in a screen of patients with co-morbid psychiatric illness and mental retardation

P2888

P304

1037-1043

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1038/EJHG.2012.49

http://www.w3.org/2001/XMLSchema#string

P433

10

http://www.w3.org/2001/XMLSchema#string

P478

20

http://www.w3.org/2001/XMLSchema#string

P50

Jouke-Jan Hottenga

James J Hudziak

P577

2012-04-11T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

223972469

http://www.w3.org/2001/XMLSchema#string

P6179

1022442596

http://www.w3.org/2001/XMLSchema#string

P698

22490988

http://www.w3.org/2001/XMLSchema#string

P921

P932

3449078

http://www.w3.org/2001/XMLSchema#string