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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

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rdf:type	Item
description	artículu científicu (ast) wetenschappelijk artikel (nl) article scientifique publié en 2005 (fr) наукова стаття, опублікована в жовтні 2005 (uk) im Oktober 2005 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q57309365-7A42C3A6-9394-43CF-9B55-D34B6ABFC746
publication date	2005-10-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q57309365-CE792CCB-225D-47BA-B377-5CB7E747CAA7
language of work or name	English
exact match	wds:Q57309365-2997AFA9-298A-41C9-96FC-C9A276BE4911
exact match	https://scigraph.springernature.com/pub.10.1038/ng1005-1015
cites work	wds:Q57309365-119FC127-450F-4985-9696-DAED8A7BC8F7 wds:Q57309365-258D6EE1-EFBC-4317-A18F-C792D4EA7850 wds:Q57309365-3BFD2A30-4567-4755-8EB0-A785F056F293 wds:Q57309365-409AF8E5-2248-4ABA-8F84-032BDF31A502 wds:Q57309365-71AA3DAB-C271-40FF-A57B-3390C3AA8A47 wds:Q57309365-81A62373-5252-41E1-8F39-D664F643E35F wds:Q57309365-95D03028-5DF7-4C55-8D23-ACBB3234AEF3 wds:Q57309365-D8AB23CE-7A1C-4388-9AA2-47785F7C21FA
cites work	Merlin--rapid analysis of dense genetic maps using sparse gene flow trees Construction of multilocus genetic linkage maps in humans A General Model for the Genetic Analysis of Pedigree Data A high-resolution recombination map of the human genome Efficient multipoint linkage analysis through reduction of inheritance space Exact genetic linkage computations for general pedigrees. Allegro, a new computer program for multipoint linkage analysis Rapid multipoint linkage analysis via inheritance vectors in the Elston-Stewart algorithm
author name string	wds:Q57309365-3747897A-332F-47B4-A954-EB3C416CC3D8 wds:Q57309365-397BAEFB-E989-43BE-A9CC-5BB72196ACD1 wds:Q57309365-4F472D84-3751-4833-AD9A-AB5B6C75173A
author name string	Gunnar Gunnarsson Anna Ingolfsdottir Thorvaldur Thorvaldsson
rdfs:label	Allegro version 2 (en) Allegro version 2 (nl)
skos:prefLabel	Allegro version 2 (en) Allegro version 2 (nl)
name	Allegro version 2 (en) Allegro version 2 (nl)
author	wds:Q57309365-7A53CDBA-F0F6-48CA-A98B-A002BA9B6316 wds:Q57309365-F05D4FB4-5862-42C6-89B6-251DBEF4D1B1
author	Augustine Kong Daníel F. Guðbjartsson
title	wds:Q57309365-ECBB8B55-B1E0-4243-90B6-C0785096241D
title	Allegro version 2 (en)
page(s)	wds:Q57309365-5E2B0B5F-0DC0-473E-886F-4B39F725F2B6
page(s)	1015-1016
instance of	wds:Q57309365-2CC87DEF-764E-4103-A522-A2504CC11ED9
instance of	scholarly article
PubMed ID	wds:Q57309365-4375AF80-333A-452E-AD21-8F6CB9FB657D
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/16195711
PubMed ID	16195711
published in	wds:Q57309365-28338E2B-B4CF-4F58-88BE-BAE6989DD958
published in	Nature Genetics
issue	wds:Q57309365-096967E4-C6D6-4B29-85A6-251D8F6ABDD8
volume	wds:Q57309365-7EE1C85D-F88E-491B-AFD4-C88102647B5F
issue	10
volume	37
DOI	wds:Q57309365-E341828F-DE1C-4040-9358-6EF27551A399
DOI	http://dx.doi.org/10.1038/NG1005-1015
DOI	10.1038/NG1005-1015
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57309365
is cites work of	Unlocking the bottleneck in forward genetics using whole-genome sequencing and identity by descent to isolate causative mutations Common variants underlying cognitive ability: further evidence for association between the SNAP-25 gene and cognition using a family-based study in two independent Dutch cohorts Familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) is caused by mutations in Munc18-2 and impaired binding to syntaxin 11 Adaptor protein complex 4 deficiency causes severe autosomal-recessive intellectual disability, progressive spastic paraplegia, shy character, and short stature Homozygosity mapping in 64 Syrian consanguineous families with non-specific intellectual disability reveals 11 novel loci and high heterogeneity Haplotype-association analysis Previously described sequence variant in CDK5RAP2 gene in a Pakistani family with autosomal recessive primary microcephaly Whole-exome sequencing and high throughput genotyping identified KCNJ11 as the thirteenth MODY gene A direct characterization of human mutation based on microsatellites SMOC1 is essential for ocular and limb development in humans and mice Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies Mitochondrial complex III deficiency caused by a homozygous UQCRC2 mutation presenting with neonatal-onset recurrent metabolic decompensation HomozygosityMapper--an interactive approach to homozygosity mapping Impaired epidermal ceramide synthesis causes autosomal recessive congenital ichthyosis and reveals the importance of ceramide acyl chain length A homozygous nonsense mutation in the human desmocollin-3 (DSC3) gene underlies hereditary hypotrichosis and recurrent skin vesicles Mapping of a gene for alopecia with mental retardation syndrome (APMR3) on chromosome 18q11.2-q12.2. A genome-wide study replicates linkage of 3p22-24 to extreme longevity in humans and identifies possible additional loci ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19 SNP HiTLink: a high-throughput linkage analysis system employing dense SNP data A truncating mutation of TRAPPC9 is associated with autosomal-recessive intellectual disability and postnatal microcephaly NEK1 mutations cause short-rib polydactyly syndrome type majewski Mutations in GMPPA cause a glycosylation disorder characterized by intellectual disability and autonomic dysfunction Loss of dermatan-4-sulfotransferase 1 function results in adducted thumb-clubfoot syndrome A homozygous mutation in ADAMTSL4 causes autosomal-recessive isolated ectopia lentis The human pseudoautosomal regions: a review for genetic epidemiologists Germline BAP1 mutations predispose to malignant mesothelioma The first genomewide interaction and locus-heterogeneity linkage scan in bipolar affective disorder: strong evidence of epistatic effects between loci on chromosomes 2q and 6q. HELLP babies link a novel lincRNA to the trophoblast cell cycle Posterior column ataxia with retinitis pigmentosa in a Japanese family with a novel mutation in FLVCR1. Ignoring intermarker linkage disequilibrium induces false-positive evidence of linkage for consanguineous pedigrees when genotype data is missing for any pedigree member The importance of phase information for human genomics A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study. Genome-wide linkage and follow-up association study of postpartum mood symptoms Genetic linkage analysis in the presence of germline mosaicism Haplotyping methods for pedigrees A system for exact and approximate genetic linkage analysis of SNP data in large pedigrees Efficient genome ancestry inference in complex pedigrees with inbreeding

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