Literature DB >> 10802643

OMIM passes the 1,000-disease-gene mark.

S E Antonarakis, V A McKusick.   

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Year:  2000        PMID: 10802643     DOI: 10.1038/75497

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


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  16 in total

Review 1.  Online medical genetics resources: a US perspective.

Authors:  R A Pagon; L Pinsky; C C Beahler
Journal:  BMJ       Date:  2001-04-28

2.  The Ensembl genome database project.

Authors:  T Hubbard; D Barker; E Birney; G Cameron; Y Chen; L Clark; T Cox; J Cuff; V Curwen; T Down; R Durbin; E Eyras; J Gilbert; M Hammond; L Huminiecki; A Kasprzyk; H Lehvaslaiho; P Lijnzaad; C Melsopp; E Mongin; R Pettett; M Pocock; S Potter; A Rust; E Schmidt; S Searle; G Slater; J Smith; W Spooner; A Stabenau; J Stalker; E Stupka; A Ureta-Vidal; I Vastrik; M Clamp
Journal:  Nucleic Acids Res       Date:  2002-01-01       Impact factor: 16.971

3.  Structural characterization of the human proteome.

Authors:  Arne Müller; Robert M MacCallum; Michael J E Sternberg
Journal:  Genome Res       Date:  2002-11       Impact factor: 9.043

Review 4.  Computational tools for prioritizing candidate genes: boosting disease gene discovery.

Authors:  Yves Moreau; Léon-Charles Tranchevent
Journal:  Nat Rev Genet       Date:  2012-07-03       Impact factor: 53.242

5.  Systems pharmacology of arrhythmias.

Authors:  Seth I Berger; Avi Ma'ayan; Ravi Iyengar
Journal:  Sci Signal       Date:  2010-04-20       Impact factor: 8.192

Review 6.  Genetic screening: A primer for primary care.

Authors:  Anne Andermann; Ingeborg Blancquaert
Journal:  Can Fam Physician       Date:  2010-04       Impact factor: 3.275

Review 7.  Does hereditary metabolic disease modulate senescence and ageing?

Authors:  C R Scriver
Journal:  J Inherit Metab Dis       Date:  2002-05       Impact factor: 4.982

8.  Exploiting CpG hypermutability to identify phenotypically significant variation within human protein-coding genes.

Authors:  Hua Ying; Gavin Huttley
Journal:  Genome Biol Evol       Date:  2011-03-11       Impact factor: 3.416

9.  The search for allelic variants that cause monogenic disorders or predispose to common, complex polygenic phenotypes.

Authors:  S E Antonarakis
Journal:  Dialogues Clin Neurosci       Date:  2001-03       Impact factor: 5.986

10.  Viewing Victor McKusick's legacy through the lens of his bibliography.

Authors:  Sonja A Rasmussen; Ariel Pomputius; Joanna S Amberger; Ada Hamosh
Journal:  Am J Med Genet A       Date:  2021-06-23       Impact factor: 2.802

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