Online Mendelian Inheritance in Man (Simple English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Online Mendelian Inheritance in Man" in Simple English language version.

refsWebsite

Global rank Simple English rank

4^th place

6^th place

4,380^th place

low place

2^nd place

3^rd place

6^th place

4^th place

archive.org (Global: 6^th place; Simple English: 4^th place)

McKusick, VA (1998). Mendelian inheritance in man: a catalog of human genes and genetic disorders. Baltimore, Maryland: Johns Hopkins University Press. ISBN 978-0-8018-5742-3.

doi.org (Global: 2^nd place; Simple English: 3^rd place)

Hamosh A.; Scott A.; Amberger J.; Bocchini C.; McKusick V. (2004). "Online Mendelian Inheritance in Man (OMIM): a knowledgebase of human genes and genetic disorders". Nucleic Acids Research. 33 (Database issue): D514 – D517. doi:10.1093/nar/gki033. PMC 539987. PMID 15608251.
McKusick V.; Amberger J. (1993). "The morbid anatomy of the human genome: chromosomal location of mutations causing disease". Journal of Medical Genetics. 30 (1): 1–26. doi:10.1136/jmg.30.1.1. PMC 1016229. PMID 8423603.
Tolmie J.; et al. (1995). "The Aicardi-Goutières syndrome (familial, early onset encephalopathy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis)". Journal of Medical Genetics. 32 (11): 881–884. doi:10.1136/jmg.32.11.881. PMC 1051740. PMID 8592332.

nih.gov (Global: 4^th place; Simple English: 6^th place)

ncbi.nlm.nih.gov

Hamosh A.; Scott A.; Amberger J.; Bocchini C.; McKusick V. (2004). "Online Mendelian Inheritance in Man (OMIM): a knowledgebase of human genes and genetic disorders". Nucleic Acids Research. 33 (Database issue): D514 – D517. doi:10.1093/nar/gki033. PMC 539987. PMID 15608251.
"National Center for Biotechnology Information". Retrieved 2011-04-20.
McKusick V.; Amberger J. (1993). "The morbid anatomy of the human genome: chromosomal location of mutations causing disease". Journal of Medical Genetics. 30 (1): 1–26. doi:10.1136/jmg.30.1.1. PMC 1016229. PMID 8423603.
Tolmie J.; et al. (1995). "The Aicardi-Goutières syndrome (familial, early onset encephalopathy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis)". Journal of Medical Genetics. 32 (11): 881–884. doi:10.1136/jmg.32.11.881. PMC 1051740. PMID 8592332.

pubmed.ncbi.nlm.nih.gov

Hamosh A.; Scott A.; Amberger J.; Bocchini C.; McKusick V. (2004). "Online Mendelian Inheritance in Man (OMIM): a knowledgebase of human genes and genetic disorders". Nucleic Acids Research. 33 (Database issue): D514 – D517. doi:10.1093/nar/gki033. PMC 539987. PMID 15608251.
McKusick V.; Amberger J. (1993). "The morbid anatomy of the human genome: chromosomal location of mutations causing disease". Journal of Medical Genetics. 30 (1): 1–26. doi:10.1136/jmg.30.1.1. PMC 1016229. PMID 8423603.
Tolmie J.; et al. (1995). "The Aicardi-Goutières syndrome (familial, early onset encephalopathy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis)". Journal of Medical Genetics. 32 (11): 881–884. doi:10.1136/jmg.32.11.881. PMC 1051740. PMID 8592332.

omim.org (Global: 4,380^th place; Simple English: low place)

"OMIM Entry Statistics". Online Mendelian Inheritance in Man. Baltimore, MD: McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University. 2015. Retrieved 23 July 2015.
"OMIM Help". Retrieved 2011-04-20.
"OMIM Help". Retrieved 2011-04-18.