SATB2 (French Wikipedia)

Analysis of information sources in references of the Wikipedia article "SATB2" in French language version.

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dx.doi.org

Kikuno R, Nagase T, Ishikawa K, Hirosawa M, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O «Prediction of the coding sequences of unidentified human genes. XIV. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro». DNA Res., vol. 6, 3, Juny 1999, pàg. 197–205. DOI 10.1093/dnares/6.3.197. PMID 10470851.
Rosenfeld JA, Ballif BC, Lucas A, et al. «Small deletions of SATB2 cause some of the clinical features of the 2q33.1 microdeletion syndrome.». PLoS ONE, vol. 4, 8, 2009, pàg. e6568. DOI 10.1371/journal.pone.0006568. PMID 19668335.
Jugessur A, Shi M, Gjessing HK, et al. «Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia.». PLoS ONE, vol. 5, 7, 2010, pàg. e11493. DOI 10.1371/journal.pone.0011493. PMC 2901336. PMID 20634891.
Beaty TH, Hetmanski JB, Fallin MD, et al. «Analysis of candidate genes on chromosome 2 in oral cleft case-parent trios from three populations.». Hum. Genet., vol. 120, 4, 2006, pàg. 501–18. DOI 10.1007/s00439-006-0235-9. PMID 16953426.
Dixon MJ, Marazita ML, Beaty TH, Murray JC «Cleft lip and palate: understanding genetic and environmental influences». Nat. Rev. Genet., vol. 12, 3, Març 2011, pàg. 167–78. DOI 10.1038/nrg2933. PMC 3086810. PMID 21331089.
FitzPatrick DR, Carr IM, McLaren L, Leek JP, Wightman P, Williamson K, Gautier P, McGill N, Hayward C, Firth H, Markham AF, Fantes JA, Bonthron DT «Identification of SATB2 as the cleft palate gene on 2q32-q33». Hum. Mol. Genet., vol. 12, 19, Octubre 2003, pàg. 2491–501. DOI 10.1093/hmg/ddg248. PMID 12915443.

nih.gov

ncbi.nlm.nih.gov

Kikuno R, Nagase T, Ishikawa K, Hirosawa M, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O «Prediction of the coding sequences of unidentified human genes. XIV. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro». DNA Res., vol. 6, 3, Juny 1999, pàg. 197–205. DOI 10.1093/dnares/6.3.197. PMID 10470851.
«Entrez Gene: SATB homeobox 2».
Rosenfeld JA, Ballif BC, Lucas A, et al. «Small deletions of SATB2 cause some of the clinical features of the 2q33.1 microdeletion syndrome.». PLoS ONE, vol. 4, 8, 2009, pàg. e6568. DOI 10.1371/journal.pone.0006568. PMID 19668335.
Jugessur A, Shi M, Gjessing HK, et al. «Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia.». PLoS ONE, vol. 5, 7, 2010, pàg. e11493. DOI 10.1371/journal.pone.0011493. PMC 2901336. PMID 20634891.
Beaty TH, Hetmanski JB, Fallin MD, et al. «Analysis of candidate genes on chromosome 2 in oral cleft case-parent trios from three populations.». Hum. Genet., vol. 120, 4, 2006, pàg. 501–18. DOI 10.1007/s00439-006-0235-9. PMID 16953426.
Dixon MJ, Marazita ML, Beaty TH, Murray JC «Cleft lip and palate: understanding genetic and environmental influences». Nat. Rev. Genet., vol. 12, 3, Març 2011, pàg. 167–78. DOI 10.1038/nrg2933. PMC 3086810. PMID 21331089.
FitzPatrick DR, Carr IM, McLaren L, Leek JP, Wightman P, Williamson K, Gautier P, McGill N, Hayward C, Firth H, Markham AF, Fantes JA, Bonthron DT «Identification of SATB2 as the cleft palate gene on 2q32-q33». Hum. Mol. Genet., vol. 12, 19, Octubre 2003, pàg. 2491–501. DOI 10.1093/hmg/ddg248. PMID 12915443.