CDK13 (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "CDK13" in English language version.

refsWebsite

Global rank English rank

7nih.gov

4^th place

2ensembl.org

1,626^th place

1,007^th place

2harvard.edu

18^th place

17^th place

2doi.org

2^nd place

1handle.net

102^nd place

76^th place

1bbc.co.uk

8^th place

10^th place

bbc.co.uk (Global: 8^th place; English: 10^th place)

Walsh F (2017-01-25). "Child gene study identifies new developmental disorders". BBC News. Retrieved 2017-01-27.

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

Lapidot-Lifson Y, Patinkin D, Prody CA, Ehrlich G, Seidman S, Ben-Aziz R, et al. (January 1992). "Cloning and antisense oligodeoxynucleotide inhibition of a human homolog of cdc2 required in hematopoiesis". Proceedings of the National Academy of Sciences of the United States of America. 89 (2): 579–583. Bibcode:1992PNAS...89..579L. doi:10.1073/pnas.89.2.579. PMC 48282. PMID 1731328.
Deciphering Developmental Disorders Study (February 2017). "Prevalence and architecture of de novo mutations in developmental disorders". Nature. 542 (7642): 433–438. Bibcode:2017Natur.542..433M. doi:10.1038/nature21062. hdl:20.500.11820/a89badba-7288-4be1-b3c5-a9b9e61d920d. PMC 6016744. PMID 28135719.{{cite journal}}: CS1 maint: overridden setting (link)

ensembl.org (Global: 1,626^th place; English: 1,007^th place)

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000065883 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000041297 – Ensembl, May 2017

handle.net (Global: 102^nd place; English: 76^th place)

hdl.handle.net

Deciphering Developmental Disorders Study (February 2017). "Prevalence and architecture of de novo mutations in developmental disorders". Nature. 542 (7642): 433–438. Bibcode:2017Natur.542..433M. doi:10.1038/nature21062. hdl:20.500.11820/a89badba-7288-4be1-b3c5-a9b9e61d920d. PMC 6016744. PMID 28135719.{{cite journal}}: CS1 maint: overridden setting (link)

harvard.edu (Global: 18^th place; English: 17^th place)

ui.adsabs.harvard.edu

Lapidot-Lifson Y, Patinkin D, Prody CA, Ehrlich G, Seidman S, Ben-Aziz R, et al. (January 1992). "Cloning and antisense oligodeoxynucleotide inhibition of a human homolog of cdc2 required in hematopoiesis". Proceedings of the National Academy of Sciences of the United States of America. 89 (2): 579–583. Bibcode:1992PNAS...89..579L. doi:10.1073/pnas.89.2.579. PMC 48282. PMID 1731328.
Deciphering Developmental Disorders Study (February 2017). "Prevalence and architecture of de novo mutations in developmental disorders". Nature. 542 (7642): 433–438. Bibcode:2017Natur.542..433M. doi:10.1038/nature21062. hdl:20.500.11820/a89badba-7288-4be1-b3c5-a9b9e61d920d. PMC 6016744. PMID 28135719.{{cite journal}}: CS1 maint: overridden setting (link)

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

ncbi.nlm.nih.gov

"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
Lapidot-Lifson Y, Patinkin D, Prody CA, Ehrlich G, Seidman S, Ben-Aziz R, et al. (January 1992). "Cloning and antisense oligodeoxynucleotide inhibition of a human homolog of cdc2 required in hematopoiesis". Proceedings of the National Academy of Sciences of the United States of America. 89 (2): 579–583. Bibcode:1992PNAS...89..579L. doi:10.1073/pnas.89.2.579. PMC 48282. PMID 1731328.
"Entrez Gene: CDC2L5 cell division cycle 2-like 5 (cholinesterase-related cell division controller)".
Deciphering Developmental Disorders Study (February 2017). "Prevalence and architecture of de novo mutations in developmental disorders". Nature. 542 (7642): 433–438. Bibcode:2017Natur.542..433M. doi:10.1038/nature21062. hdl:20.500.11820/a89badba-7288-4be1-b3c5-a9b9e61d920d. PMC 6016744. PMID 28135719.{{cite journal}}: CS1 maint: overridden setting (link)

pubmed.ncbi.nlm.nih.gov

Lapidot-Lifson Y, Patinkin D, Prody CA, Ehrlich G, Seidman S, Ben-Aziz R, et al. (January 1992). "Cloning and antisense oligodeoxynucleotide inhibition of a human homolog of cdc2 required in hematopoiesis". Proceedings of the National Academy of Sciences of the United States of America. 89 (2): 579–583. Bibcode:1992PNAS...89..579L. doi:10.1073/pnas.89.2.579. PMC 48282. PMID 1731328.
Deciphering Developmental Disorders Study (February 2017). "Prevalence and architecture of de novo mutations in developmental disorders". Nature. 542 (7642): 433–438. Bibcode:2017Natur.542..433M. doi:10.1038/nature21062. hdl:20.500.11820/a89badba-7288-4be1-b3c5-a9b9e61d920d. PMC 6016744. PMID 28135719.{{cite journal}}: CS1 maint: overridden setting (link)

CDK13 (English Wikipedia)

bbc.co.uk (Global: 8th place; English: 10th place)

doi.org (Global: 2nd place; English: 2nd place)

ensembl.org (Global: 1,626th place; English: 1,007th place)