About: Genetics, medicine, and the Plain people

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scientific article published on January 2009

Attributes	Values
rdf:type	Item
description	videnskabelig artikel (da) article científic (ca) articolo scientifico (it) artigo científico (pt) bilimsel makale (tr) vedecký článok (sk) vetenskaplig artikel (sv) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) научни чланак (sr) article scientifique (fr) artículu científicu espublizáu en 2009 (ast) наукова стаття, опублікована в січні 2009 (uk) مقالة علمية نشرت في يناير 2009 (ar) scientific article published on January 2009 (en)
publication date	wds:Q37561095-E8446B49-7DF7-41CE-9726-20570847B51E
publication date	2009-01-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q37561095-90843381-8CD7-44DB-A820-8D24E7690B41
language of work or name	English
cites work	wds:Q37561095-232F3CD1-A36A-43CB-8B3A-021C5B819ABF
cites work	Initial sequencing and analysis of the human genome
author name string	wds:Q37561095-88150D6B-C71C-4DE4-B342-A3044A3901E8 wds:Q37561095-EE26F9E2-D4C6-4AC2-BFF0-B454E190F2E0
author name string	Erik G Puffenberger Kevin A Strauss
rdfs:label	Genetics, medicine, and the Plain people (en) Genetics, medicine, and the Plain people (nl) Genetics, medicine, and the Plain people (ast)
skos:prefLabel	Genetics, medicine, and the Plain people (en) Genetics, medicine, and the Plain people (nl) Genetics, medicine, and the Plain people (ast)
name	Genetics, medicine, and the Plain people (en) Genetics, medicine, and the Plain people (nl) Genetics, medicine, and the Plain people (ast)
title	wds:Q37561095-F1B94750-8228-4BF9-AB5E-7C03B27AD597
title	Genetics, medicine, and the Plain people (en)
page(s)	wds:Q37561095-F13FA79B-4070-4F75-BFA1-E0A44BD4F405
page(s)	513-536
instance of	wds:Q37561095-679097c9-b4f6-4931-bad9-f023f905f17b wds:Q37561095-723CF5C4-2662-400D-B825-99F97D70FE4A
instance of	review article scholarly article
PubMed ID	wds:Q37561095-D21608A2-7C7A-4E82-A88A-A57A05207563
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/19630565
PubMed ID	19630565
published in	wds:Q37561095-EF996D13-5E16-4AFC-8E9B-DCE0425E7231
published in	Annual Review of Genomics and Human Genetics
volume	wds:Q37561095-1D82F6BE-AA3A-4C7F-AF4B-09093A1A6F46
volume	10
DOI	wds:Q37561095-86340551-B4C8-4ABC-8F56-A17DD4B869AF
DOI	http://dx.doi.org/10.1146/ANNUREV-GENOM-082908-150040
DOI	10.1146/ANNUREV-GENOM-082908-150040
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q37561095
is cites work of	Genetic mapping and exome sequencing identify variants associated with five novel diseases Mitochondrial respiratory chain disorders in the Old Order Amish population. Human ITCH E3 ubiquitin ligase deficiency causes syndromic multisystem autoimmune disease. Deciphering the fine-structure of tribal admixture in the Bedouin population using genomic data A homozygous missense mutation in HERC2 associated with global developmental delay and autism spectrum disorder Amish revisited: next-generation sequencing studies of psychiatric disorders among the Plain people Genomic view of bipolar disorder revealed by whole genome sequencing in a genetic isolate A population-specific reference panel empowers genetic studies of Anabaptist populations Homozygous frameshift mutation in TMCO1 causes a syndrome with craniofacial dysmorphism, skeletal anomalies, and mental retardation Biochemical and Hematologic Manifestations of Gastric Intrinsic Factor (GIF) Deficiency: A Treatable Cause of B12 Deficiency in the Old Order Mennonite Population of Southwestern Ontario Clinical variability of isovaleric acidemia in a genetically homogeneous population. Classical maple syrup urine disease and brain development: principles of management and formula design Severity of cardiomyopathy associated with adenine nucleotide translocator-1 deficiency correlates with mtDNA haplogroup One community's effort to control genetic disease Genomic diagnostics within a medically underserved population: efficacy and implications Evolutionary genomic dynamics of Peruvians before, during, and after the Inca Empire A population-based study of KCNH7 p.Arg394His and bipolar spectrum disorder Copy number variants encompassing Mendelian disease genes in a large multigenerational family segregating bipolar disorder Primary ciliary dyskinesia-causing mutations in Amish and Mennonite communities From rumors to genetic isolates A homozygous SLITRK6 nonsense mutation is associated with progressive auditory neuropathy in humans. Oral health and medical conditions among Amish children Charting the Y-chromosome ancestry of present-day Argentinean Mennonites The GenomeAsia 100K Project enables genetic discoveries across Asia TNNT1 nemaline myopathy: natural history and therapeutic frontier Health Needs Assessment of Plain Populations in Lancaster County, Pennsylvania. Genomic continuity of Argentinean Mennonites Glutaric acidemia type 1: Treatment and outcome of 168 patients over three decades Development of carrier testing for common inborn errors of metabolism in the Wisconsin Plain population. Genetic pleiotropy between mood disorders, metabolic, and endocrine traits in a multigenerational pedigree Spinal muscular atrophy within Amish and Mennonite populations: Ancestral haplotypes and natural history Rare variants and loci for age-related macular degeneration in the Ohio and Indiana Amish Health Needs Assessment of Five Pennsylvania Plain Populations
is cites work of	wds:Q33921014-BA6C4159-348A-47CB-AD96-C2CEA8372155 wds:Q33591829-D21F7F57-3559-4F10-A109-86A4ED75F212 wds:Q35183110-81FF3C7B-D3DB-4B4D-AFA8-9728EE6C0EA9 wds:Q34306101-8F97CC5B-3D70-41F4-A4A7-A2971E083990 wds:Q36653669-5669D7DE-2E6B-49EE-AE07-6F3C069E2C1C wds:Q37695558-A1D2375A-E469-4E4C-9396-AE819B9B36CD wds:Q60364425-4252E1FC-5213-42D9-B88D-805A9B61BB8A wds:Q34463175-8F47BB7A-AAEE-4866-B234-A9102F3DB2BF wds:Q37399831-93A6CBCE-BA2F-4D38-81AD-DC2D833106F6 wds:Q91698423-CC566AE9-720E-4514-8944-0816EECAFB51 wds:Q37049872-DEA951B8-15AF-4156-9521-6DD738F36D1A wds:Q37697820-7EA7EAA0-5FA5-4FF2-BA1C-4B6A3707E300

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