PHF8 (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "PHF8" in English language version.

refsWebsite

Global rank English rank

23nih.gov

4^th place

12doi.org

2^nd place

3semanticscholar.org

11^th place

8^th place

2ensembl.org

1,626^th place

1,007^th place

1harvard.edu

18^th place

17^th place

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

Loenarz C, Schofield CJ (Mar 2008). "Expanding chemical biology of 2-oxoglutarate oxygenases". Nature Chemical Biology. 4 (3): 152–6. doi:10.1038/nchembio0308-152. PMID 18277970.
Loenarz C, Ge W, Coleman ML, Rose NR, Cooper CD, Klose RJ, et al. (Jan 2010). "PHF8, a gene associated with cleft lip/palate and intellectual disability, encodes for an Nepsilon-dimethyl lysine demethylase". Human Molecular Genetics. 19 (2): 217–22. doi:10.1093/hmg/ddp480. PMC 4673897. PMID 19843542.
Boeckel JN, Derlet A, Glaser SF, Luczak A, Lucas T, Heumüller AW, et al. (July 2016). "JMJD8 Regulates Angiogenic Sprouting and Cellular Metabolism by Interacting With Pyruvate Kinase M2 in Endothelial Cells". Arteriosclerosis, Thrombosis, and Vascular Biology. 36 (7): 1425–1433. doi:10.1161/ATVBAHA.116.307695. PMID 27199445.
Siderius LE, Hamel BC, van Bokhoven H, de Jager F, van den Helm B, Kremer H, et al. (Jul 1999). "X-linked mental retardation associated with cleft lip/palate maps to Xp11.3-q21.3". American Journal of Medical Genetics. 85 (3): 216–20. doi:10.1002/(SICI)1096-8628(19990730)85:3<216::AID-AJMG6>3.0.CO;2-X. PMID 10398231.
Abidi F, Miano M, Murray J, Schwartz C (Jul 2007). "A novel mutation in the PHF8 gene is associated with X-linked mental retardation with cleft lip/cleft palate". Clinical Genetics. 72 (1): 19–22. doi:10.1111/j.1399-0004.2007.00817.x. PMC 2570350. PMID 17594395.
Laumonnier F, Holbert S, Ronce N, Faravelli F, Lenzner S, Schwartz CE, et al. (Oct 2005). "Mutations in PHF8 are associated with X linked mental retardation and cleft lip/cleft palate". Journal of Medical Genetics. 42 (10): 780–6. doi:10.1136/jmg.2004.029439. PMC 1735927. PMID 16199551.
Koivisto AM, Ala-Mello S, Lemmelä S, Komu HA, Rautio J, Järvelä I (Aug 2007). "Screening of mutations in the PHF8 gene and identification of a novel mutation in a Finnish family with XLMR and cleft lip/cleft palate". Clinical Genetics. 72 (2): 145–9. doi:10.1111/j.1399-0004.2007.00836.x. PMID 17661819. S2CID 23326755.
Qiao Y, Liu X, Harvard C, Hildebrand MJ, Rajcan-Separovic E, Holden JJ, et al. (Aug 2008). "Autism-associated familial microdeletion of Xp11.22". Clinical Genetics. 74 (2): 134–44. doi:10.1111/j.1399-0004.2008.01028.x. PMID 18498374. S2CID 22008997.
Sobering AK, Bryant LM, Li D, McGaughran J, Maystadt I, Moortgat S, et al. (July 2022). "Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology". HGG Advances. 3 (3) 100102. doi:10.1016/j.xhgg.2022.100102. PMC 9034099. PMID 35469323.
Millicovsky G, Johnston MC (Sep 1981). "Hyperoxia and hypoxia in pregnancy: simple experimental manipulation alters the incidence of cleft lip and palate in CL/Fr mice". Proceedings of the National Academy of Sciences of the United States of America. 78 (9): 5722–3. Bibcode:1981PNAS...78.5722M. doi:10.1073/pnas.78.9.5722. PMC 348841. PMID 6946511.
Shi M, Wehby GL, Murray JC (Mar 2008). "Review on genetic variants and maternal smoking in the etiology of oral clefts and other birth defects". Birth Defects Research. Part C, Embryo Today. 84 (1): 16–29. doi:10.1002/bdrc.20117. PMC 2570345. PMID 18383123.
Hurst JA, Houlston RS, Roberts A, Gould SJ, Tingey WG (Oct 1995). "Transverse limb deficiency, facial clefting and hypoxic renal damage: an association with treatment of maternal hypertension?". Clinical Dysmorphology. 4 (4): 359–63. doi:10.1097/00019605-199510000-00013. PMID 8574428. S2CID 6330050.

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

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000172943 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000041229 – Ensembl, May 2017

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

ui.adsabs.harvard.edu

Millicovsky G, Johnston MC (Sep 1981). "Hyperoxia and hypoxia in pregnancy: simple experimental manipulation alters the incidence of cleft lip and palate in CL/Fr mice". Proceedings of the National Academy of Sciences of the United States of America. 78 (9): 5722–3. Bibcode:1981PNAS...78.5722M. doi:10.1073/pnas.78.9.5722. PMC 348841. PMID 6946511.

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

pubmed.ncbi.nlm.nih.gov

Loenarz C, Schofield CJ (Mar 2008). "Expanding chemical biology of 2-oxoglutarate oxygenases". Nature Chemical Biology. 4 (3): 152–6. doi:10.1038/nchembio0308-152. PMID 18277970.
Loenarz C, Ge W, Coleman ML, Rose NR, Cooper CD, Klose RJ, et al. (Jan 2010). "PHF8, a gene associated with cleft lip/palate and intellectual disability, encodes for an Nepsilon-dimethyl lysine demethylase". Human Molecular Genetics. 19 (2): 217–22. doi:10.1093/hmg/ddp480. PMC 4673897. PMID 19843542.
Boeckel JN, Derlet A, Glaser SF, Luczak A, Lucas T, Heumüller AW, et al. (July 2016). "JMJD8 Regulates Angiogenic Sprouting and Cellular Metabolism by Interacting With Pyruvate Kinase M2 in Endothelial Cells". Arteriosclerosis, Thrombosis, and Vascular Biology. 36 (7): 1425–1433. doi:10.1161/ATVBAHA.116.307695. PMID 27199445.
Siderius LE, Hamel BC, van Bokhoven H, de Jager F, van den Helm B, Kremer H, et al. (Jul 1999). "X-linked mental retardation associated with cleft lip/palate maps to Xp11.3-q21.3". American Journal of Medical Genetics. 85 (3): 216–20. doi:10.1002/(SICI)1096-8628(19990730)85:3<216::AID-AJMG6>3.0.CO;2-X. PMID 10398231.
Abidi F, Miano M, Murray J, Schwartz C (Jul 2007). "A novel mutation in the PHF8 gene is associated with X-linked mental retardation with cleft lip/cleft palate". Clinical Genetics. 72 (1): 19–22. doi:10.1111/j.1399-0004.2007.00817.x. PMC 2570350. PMID 17594395.
Laumonnier F, Holbert S, Ronce N, Faravelli F, Lenzner S, Schwartz CE, et al. (Oct 2005). "Mutations in PHF8 are associated with X linked mental retardation and cleft lip/cleft palate". Journal of Medical Genetics. 42 (10): 780–6. doi:10.1136/jmg.2004.029439. PMC 1735927. PMID 16199551.
Koivisto AM, Ala-Mello S, Lemmelä S, Komu HA, Rautio J, Järvelä I (Aug 2007). "Screening of mutations in the PHF8 gene and identification of a novel mutation in a Finnish family with XLMR and cleft lip/cleft palate". Clinical Genetics. 72 (2): 145–9. doi:10.1111/j.1399-0004.2007.00836.x. PMID 17661819. S2CID 23326755.
Qiao Y, Liu X, Harvard C, Hildebrand MJ, Rajcan-Separovic E, Holden JJ, et al. (Aug 2008). "Autism-associated familial microdeletion of Xp11.22". Clinical Genetics. 74 (2): 134–44. doi:10.1111/j.1399-0004.2008.01028.x. PMID 18498374. S2CID 22008997.
Sobering AK, Bryant LM, Li D, McGaughran J, Maystadt I, Moortgat S, et al. (July 2022). "Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology". HGG Advances. 3 (3) 100102. doi:10.1016/j.xhgg.2022.100102. PMC 9034099. PMID 35469323.
Millicovsky G, Johnston MC (Sep 1981). "Hyperoxia and hypoxia in pregnancy: simple experimental manipulation alters the incidence of cleft lip and palate in CL/Fr mice". Proceedings of the National Academy of Sciences of the United States of America. 78 (9): 5722–3. Bibcode:1981PNAS...78.5722M. doi:10.1073/pnas.78.9.5722. PMC 348841. PMID 6946511.
Shi M, Wehby GL, Murray JC (Mar 2008). "Review on genetic variants and maternal smoking in the etiology of oral clefts and other birth defects". Birth Defects Research. Part C, Embryo Today. 84 (1): 16–29. doi:10.1002/bdrc.20117. PMC 2570345. PMID 18383123.
Hurst JA, Houlston RS, Roberts A, Gould SJ, Tingey WG (Oct 1995). "Transverse limb deficiency, facial clefting and hypoxic renal damage: an association with treatment of maternal hypertension?". Clinical Dysmorphology. 4 (4): 359–63. doi:10.1097/00019605-199510000-00013. PMID 8574428. S2CID 6330050.

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.
"Entrez Gene: PHF8 PHD finger protein 8".
Loenarz C, Ge W, Coleman ML, Rose NR, Cooper CD, Klose RJ, et al. (Jan 2010). "PHF8, a gene associated with cleft lip/palate and intellectual disability, encodes for an Nepsilon-dimethyl lysine demethylase". Human Molecular Genetics. 19 (2): 217–22. doi:10.1093/hmg/ddp480. PMC 4673897. PMID 19843542.
"OMIM: Siderius X-linked mental retardation syndrome". Retrieved 2009-10-21.^{[dead link]}
"OMIM: PHD finger protein 8; PHF8". Retrieved 2009-10-21.^{[dead link]}
Abidi F, Miano M, Murray J, Schwartz C (Jul 2007). "A novel mutation in the PHF8 gene is associated with X-linked mental retardation with cleft lip/cleft palate". Clinical Genetics. 72 (1): 19–22. doi:10.1111/j.1399-0004.2007.00817.x. PMC 2570350. PMID 17594395.
Laumonnier F, Holbert S, Ronce N, Faravelli F, Lenzner S, Schwartz CE, et al. (Oct 2005). "Mutations in PHF8 are associated with X linked mental retardation and cleft lip/cleft palate". Journal of Medical Genetics. 42 (10): 780–6. doi:10.1136/jmg.2004.029439. PMC 1735927. PMID 16199551.
Sobering AK, Bryant LM, Li D, McGaughran J, Maystadt I, Moortgat S, et al. (July 2022). "Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology". HGG Advances. 3 (3) 100102. doi:10.1016/j.xhgg.2022.100102. PMC 9034099. PMID 35469323.
Millicovsky G, Johnston MC (Sep 1981). "Hyperoxia and hypoxia in pregnancy: simple experimental manipulation alters the incidence of cleft lip and palate in CL/Fr mice". Proceedings of the National Academy of Sciences of the United States of America. 78 (9): 5722–3. Bibcode:1981PNAS...78.5722M. doi:10.1073/pnas.78.9.5722. PMC 348841. PMID 6946511.
Shi M, Wehby GL, Murray JC (Mar 2008). "Review on genetic variants and maternal smoking in the etiology of oral clefts and other birth defects". Birth Defects Research. Part C, Embryo Today. 84 (1): 16–29. doi:10.1002/bdrc.20117. PMC 2570345. PMID 18383123.

semanticscholar.org (Global: 11^th place; English: 8^th place)

api.semanticscholar.org

Koivisto AM, Ala-Mello S, Lemmelä S, Komu HA, Rautio J, Järvelä I (Aug 2007). "Screening of mutations in the PHF8 gene and identification of a novel mutation in a Finnish family with XLMR and cleft lip/cleft palate". Clinical Genetics. 72 (2): 145–9. doi:10.1111/j.1399-0004.2007.00836.x. PMID 17661819. S2CID 23326755.
Qiao Y, Liu X, Harvard C, Hildebrand MJ, Rajcan-Separovic E, Holden JJ, et al. (Aug 2008). "Autism-associated familial microdeletion of Xp11.22". Clinical Genetics. 74 (2): 134–44. doi:10.1111/j.1399-0004.2008.01028.x. PMID 18498374. S2CID 22008997.
Hurst JA, Houlston RS, Roberts A, Gould SJ, Tingey WG (Oct 1995). "Transverse limb deficiency, facial clefting and hypoxic renal damage: an association with treatment of maternal hypertension?". Clinical Dysmorphology. 4 (4): 359–63. doi:10.1097/00019605-199510000-00013. PMID 8574428. S2CID 6330050.

PHF8 (English Wikipedia)

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

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