Pseudoautosomal region (English Wikipedia)

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

refsWebsite

Global rank English rank

17nih.gov

4^th place

10doi.org

2^nd place

4genenames.org

low place

doi.org

Mangs, Helena; Morris BJ (2007). "The Human Pseudoautosomal Region (PAR): Origin, Function and Future". Current Genomics. 8 (2): 129–136. doi:10.2174/138920207780368141. PMC 2435358. PMID 18660847.
Blaschke RJ, Rappold G (2006). "The pseudoautosomal regions, SHOX and disease". Curr Opin Genet Dev. 16 (3): 233–9. doi:10.1016/j.gde.2006.04.004. PMID 16650979.
Helena Mangs A, Morris BJ (April 2007). "The Human Pseudoautosomal Region (PAR): Origin, Function and Future". Curr. Genomics. 8 (2): 129–36. doi:10.2174/138920207780368141. PMC 2435358. PMID 18660847.
Ciccodicola A, D'Esposito M, Esposito T, et al. (February 2000). "Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region". Hum. Mol. Genet. 9 (3): 395–401. doi:10.1093/hmg/9.3.395. PMID 10655549.
Weng S, Stoner SA, Zhang DE (2016). "Sex chromosome loss and the pseudoautosomal region genes in hematological malignancies". Oncotarget. 7 (44): 72356–72372. doi:10.18632/oncotarget.12050. PMC 5342167. PMID 27655702.
Charchar FJ, Svartman M, El-Mogharbel N, et al. (February 2003). "Complex events in the evolution of the human pseudoautosomal region 2 (PAR2)". Genome Res. 13 (2): 281–6. doi:10.1101/gr.390503. PMC 420362. PMID 12566406.
Levy MA, Fernandes AD, Tremblay DC, Seah C, Bérubé NG (2008). "The SWI/SNF protein ATRX co-regulates pseudoautosomal genes that have translocated to autosomes in the mouse genome". BMC Genomics. 9: 468. doi:10.1186/1471-2164-9-468. PMC 2577121. PMID 18842153.
Eichner, E.M. (February 1991). "The mouse Y* chromosome involves a complex rearrangement including interstitial positioning of the Y-pseudoautosomal region". Cytogenetics and Cell Genetics. 57 (4): 221–230. doi:10.1159/000133152. PMID 1743079.
Blaschke RJ, Rappold G (June 2006). "The pseudoautosomal regions, SHOX and disease". Curr. Opin. Genet. Dev. 16 (3): 233–9. doi:10.1016/j.gde.2006.04.004. PMID 16650979.
Benito-Sanz S, Thomas NS, Huber C, et al. (October 2005). "A novel class of Pseudoautosomal region 1 deletions downstream of SHOX is associated with Leri-Weill dyschondrosteosis". Am. J. Hum. Genet. 77 (4): 533–44. doi:10.1086/449313. PMC 1275603. PMID 16175500.

genenames.org

"Pseudoautosomal regions Gene Family". HUGO Gene Nomenclature Committee. Retrieved 2017-05-11.
"Pseudoautosomal region 1 (PAR1) Gene Family". HUGO Gene Nomenclature Committee. Retrieved 2017-05-12.
"Pseudoautosomal region 2 (PAR2) Gene group". HUGO Gene Nomenclature Committee. Retrieved 2019-08-30.
"WASH6P". HUGO Gene Nomenclature Committee. Retrieved 2019-08-30.

nih.gov

pubmed.ncbi.nlm.nih.gov

Mangs, Helena; Morris BJ (2007). "The Human Pseudoautosomal Region (PAR): Origin, Function and Future". Current Genomics. 8 (2): 129–136. doi:10.2174/138920207780368141. PMC 2435358. PMID 18660847.
Blaschke RJ, Rappold G (2006). "The pseudoautosomal regions, SHOX and disease". Curr Opin Genet Dev. 16 (3): 233–9. doi:10.1016/j.gde.2006.04.004. PMID 16650979.
Helena Mangs A, Morris BJ (April 2007). "The Human Pseudoautosomal Region (PAR): Origin, Function and Future". Curr. Genomics. 8 (2): 129–36. doi:10.2174/138920207780368141. PMC 2435358. PMID 18660847.
Ciccodicola A, D'Esposito M, Esposito T, et al. (February 2000). "Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region". Hum. Mol. Genet. 9 (3): 395–401. doi:10.1093/hmg/9.3.395. PMID 10655549.
Weng S, Stoner SA, Zhang DE (2016). "Sex chromosome loss and the pseudoautosomal region genes in hematological malignancies". Oncotarget. 7 (44): 72356–72372. doi:10.18632/oncotarget.12050. PMC 5342167. PMID 27655702.
Charchar FJ, Svartman M, El-Mogharbel N, et al. (February 2003). "Complex events in the evolution of the human pseudoautosomal region 2 (PAR2)". Genome Res. 13 (2): 281–6. doi:10.1101/gr.390503. PMC 420362. PMID 12566406.
Levy MA, Fernandes AD, Tremblay DC, Seah C, Bérubé NG (2008). "The SWI/SNF protein ATRX co-regulates pseudoautosomal genes that have translocated to autosomes in the mouse genome". BMC Genomics. 9: 468. doi:10.1186/1471-2164-9-468. PMC 2577121. PMID 18842153.
Eichner, E.M. (February 1991). "The mouse Y* chromosome involves a complex rearrangement including interstitial positioning of the Y-pseudoautosomal region". Cytogenetics and Cell Genetics. 57 (4): 221–230. doi:10.1159/000133152. PMID 1743079.
Blaschke RJ, Rappold G (June 2006). "The pseudoautosomal regions, SHOX and disease". Curr. Opin. Genet. Dev. 16 (3): 233–9. doi:10.1016/j.gde.2006.04.004. PMID 16650979.
Benito-Sanz S, Thomas NS, Huber C, et al. (October 2005). "A novel class of Pseudoautosomal region 1 deletions downstream of SHOX is associated with Leri-Weill dyschondrosteosis". Am. J. Hum. Genet. 77 (4): 533–44. doi:10.1086/449313. PMC 1275603. PMID 16175500.

ncbi.nlm.nih.gov

Mangs, Helena; Morris BJ (2007). "The Human Pseudoautosomal Region (PAR): Origin, Function and Future". Current Genomics. 8 (2): 129–136. doi:10.2174/138920207780368141. PMC 2435358. PMID 18660847.
Helena Mangs A, Morris BJ (April 2007). "The Human Pseudoautosomal Region (PAR): Origin, Function and Future". Curr. Genomics. 8 (2): 129–36. doi:10.2174/138920207780368141. PMC 2435358. PMID 18660847.
Genome Reference Consortium (2017-01-06). "Human genome overview GRCh38.p10". Retrieved 2017-05-10.
Weng S, Stoner SA, Zhang DE (2016). "Sex chromosome loss and the pseudoautosomal region genes in hematological malignancies". Oncotarget. 7 (44): 72356–72372. doi:10.18632/oncotarget.12050. PMC 5342167. PMID 27655702.
Charchar FJ, Svartman M, El-Mogharbel N, et al. (February 2003). "Complex events in the evolution of the human pseudoautosomal region 2 (PAR2)". Genome Res. 13 (2): 281–6. doi:10.1101/gr.390503. PMC 420362. PMID 12566406.
Levy MA, Fernandes AD, Tremblay DC, Seah C, Bérubé NG (2008). "The SWI/SNF protein ATRX co-regulates pseudoautosomal genes that have translocated to autosomes in the mouse genome". BMC Genomics. 9: 468. doi:10.1186/1471-2164-9-468. PMC 2577121. PMID 18842153.
Benito-Sanz S, Thomas NS, Huber C, et al. (October 2005). "A novel class of Pseudoautosomal region 1 deletions downstream of SHOX is associated with Leri-Weill dyschondrosteosis". Am. J. Hum. Genet. 77 (4): 533–44. doi:10.1086/449313. PMC 1275603. PMID 16175500.