Cowden syndrome (English Wikipedia)

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

refsWebsite

Global rank English rank

17nih.gov

4^th place

14doi.org

2^nd place

9worldcat.org

5^th place

3semanticscholar.org

11^th place

8^th place

doi.org

Mester J, Eng C (January 2015). "Cowden syndrome: recognizing and managing a not-so-rare hereditary cancer syndrome". Journal of Surgical Oncology. 111 (1): 125–30. doi:10.1002/jso.23735. PMID 25132236. S2CID 33056798.
Gosein MA, Narinesingh D, Nixon CA, Goli SR, Maharaj P, Sinanan A (August 2016). "Multi-organ benign and malignant tumors: recognizing Cowden syndrome: a case report and review of the literature". BMC Research Notes. 9: 388. doi:10.1186/s13104-016-2195-z. PMC 4973052. PMID 27488391.
Pilarski R, Burt R, Kohlman W, Pho L, Shannon KM, Swisher E (November 2013). "Cowden syndrome and the PTEN hamartoma tumor syndrome: systematic review and revised diagnostic criteria". Journal of the National Cancer Institute. 105 (21): 1607–16. doi:10.1093/jnci/djt277. PMID 24136893.
Porto AC, Roider E, Ruzicka T (2013). "Cowden Syndrome: report of a case and brief review of literature". Anais Brasileiros de Dermatologia. 88 (6 Suppl 1): 52–5. doi:10.1590/abd1806-4841.20132578. PMC 3876002. PMID 24346879.
Ma, Huiying; Brosens, Lodewijk A. A.; Offerhaus, G. Johan A.; Giardiello, Francis M.; de Leng, Wendy W. J.; Montgomery, Elizabeth A. (January 2018). "Pathology and genetics of hereditary colorectal cancer". Pathology. 50 (1): 49–59. doi:10.1016/j.pathol.2017.09.004. ISSN 1465-3931. PMID 29169633.
Jelsig AM, Qvist N, Brusgaard K, Nielsen CB, Hansen TP, Ousager LB (July 2014). "Hamartomatous polyposis syndromes: a review". Orphanet Journal of Rare Diseases. 9: 101. doi:10.1186/1750-1172-9-101. PMC 4112971. PMID 25022750.
Gustafson S, Zbuk KM, Scacheri C, Eng C (October 2007). "Cowden syndrome". Seminars in Oncology. 34 (5): 428–34. doi:10.1053/j.seminoncol.2007.07.009. PMID 17920899.
Pilarski R (February 2009). "Cowden syndrome: a critical review of the clinical literature". Journal of Genetic Counseling. 18 (1): 13–27. doi:10.1007/s10897-008-9187-7. PMID 18972196. S2CID 5671218.
Yehia, Lamis; Niazi, Farshad; Ni, Ying; Ngeow, Joanne; Sankunny, Madhav; Liu, Zhigang; Wei, Wei; Mester, Jessica; Keri, Ruth; Zhang, Bin; Eng, Charis (5 November 2015). "Germline Heterozygous Variants in SEC23B Are Associated with Cowden Syndrome and Enriched in Apparently Sporadic Thyroid Cancer". Am J Hum Genet. 97 (5): 661–676. doi:10.1016/j.ajhg.2015.10.001. PMC 4667132. PMID 26522472.
Yehia, Lamis; Jindal, Supriya; Komar, Anton; Eng, Charis (15 September 2018). "Non-canonical role of cancer-associated mutant SEC23B in the ribosome biogenesis pathway". Hum Mol Genet. 27 (18): 3154–3164. doi:10.1093/hmg/ddy226. PMC 6121187. PMID 29893852.
LLOYD, KENNETH M. (1963-01-01). "Cowden's Disease". Annals of Internal Medicine. 58 (1): 136–142. doi:10.7326/0003-4819-58-1-136. ISSN 0003-4819. PMID 13931122.
Liaw, Danny; Marsh, Debbie J.; Li, Jing; Dahia, Patricia L. M.; Wang, Steven I.; Zheng, Zimu; Bose, Shikha; Call, Katherine M.; Tsou, Hui C.; Peacoke, Monica; Eng, Charis (May 1997). "Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome". Nature Genetics. 16 (1): 64–67. doi:10.1038/ng0597-64. ISSN 1061-4036. PMID 9140396. S2CID 33101761.

dx.doi.org

LLOYD, KENNETH M. (1963-01-01). "Cowden's Disease". Annals of Internal Medicine. 58 (1): 136–142. doi:10.7326/0003-4819-58-1-136. ISSN 0003-4819. PMID 13931122.
Liaw, Danny; Marsh, Debbie J.; Li, Jing; Dahia, Patricia L. M.; Wang, Steven I.; Zheng, Zimu; Bose, Shikha; Call, Katherine M.; Tsou, Hui C.; Peacoke, Monica; Eng, Charis (May 1997). "Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome". Nature Genetics. 16 (1): 64–67. doi:10.1038/ng0597-64. ISSN 1061-4036. PMID 9140396. S2CID 33101761.

nih.gov

pubmed.ncbi.nlm.nih.gov

Mester J, Eng C (January 2015). "Cowden syndrome: recognizing and managing a not-so-rare hereditary cancer syndrome". Journal of Surgical Oncology. 111 (1): 125–30. doi:10.1002/jso.23735. PMID 25132236. S2CID 33056798.
Gosein MA, Narinesingh D, Nixon CA, Goli SR, Maharaj P, Sinanan A (August 2016). "Multi-organ benign and malignant tumors: recognizing Cowden syndrome: a case report and review of the literature". BMC Research Notes. 9: 388. doi:10.1186/s13104-016-2195-z. PMC 4973052. PMID 27488391.
Pilarski R, Burt R, Kohlman W, Pho L, Shannon KM, Swisher E (November 2013). "Cowden syndrome and the PTEN hamartoma tumor syndrome: systematic review and revised diagnostic criteria". Journal of the National Cancer Institute. 105 (21): 1607–16. doi:10.1093/jnci/djt277. PMID 24136893.
Porto AC, Roider E, Ruzicka T (2013). "Cowden Syndrome: report of a case and brief review of literature". Anais Brasileiros de Dermatologia. 88 (6 Suppl 1): 52–5. doi:10.1590/abd1806-4841.20132578. PMC 3876002. PMID 24346879.
Ma, Huiying; Brosens, Lodewijk A. A.; Offerhaus, G. Johan A.; Giardiello, Francis M.; de Leng, Wendy W. J.; Montgomery, Elizabeth A. (January 2018). "Pathology and genetics of hereditary colorectal cancer". Pathology. 50 (1): 49–59. doi:10.1016/j.pathol.2017.09.004. ISSN 1465-3931. PMID 29169633.
Jelsig AM, Qvist N, Brusgaard K, Nielsen CB, Hansen TP, Ousager LB (July 2014). "Hamartomatous polyposis syndromes: a review". Orphanet Journal of Rare Diseases. 9: 101. doi:10.1186/1750-1172-9-101. PMC 4112971. PMID 25022750.
Gustafson S, Zbuk KM, Scacheri C, Eng C (October 2007). "Cowden syndrome". Seminars in Oncology. 34 (5): 428–34. doi:10.1053/j.seminoncol.2007.07.009. PMID 17920899.
Pilarski R (February 2009). "Cowden syndrome: a critical review of the clinical literature". Journal of Genetic Counseling. 18 (1): 13–27. doi:10.1007/s10897-008-9187-7. PMID 18972196. S2CID 5671218.
Yehia, Lamis; Niazi, Farshad; Ni, Ying; Ngeow, Joanne; Sankunny, Madhav; Liu, Zhigang; Wei, Wei; Mester, Jessica; Keri, Ruth; Zhang, Bin; Eng, Charis (5 November 2015). "Germline Heterozygous Variants in SEC23B Are Associated with Cowden Syndrome and Enriched in Apparently Sporadic Thyroid Cancer". Am J Hum Genet. 97 (5): 661–676. doi:10.1016/j.ajhg.2015.10.001. PMC 4667132. PMID 26522472.
Yehia, Lamis; Jindal, Supriya; Komar, Anton; Eng, Charis (15 September 2018). "Non-canonical role of cancer-associated mutant SEC23B in the ribosome biogenesis pathway". Hum Mol Genet. 27 (18): 3154–3164. doi:10.1093/hmg/ddy226. PMC 6121187. PMID 29893852.
LLOYD, KENNETH M. (1963-01-01). "Cowden's Disease". Annals of Internal Medicine. 58 (1): 136–142. doi:10.7326/0003-4819-58-1-136. ISSN 0003-4819. PMID 13931122.
Liaw, Danny; Marsh, Debbie J.; Li, Jing; Dahia, Patricia L. M.; Wang, Steven I.; Zheng, Zimu; Bose, Shikha; Call, Katherine M.; Tsou, Hui C.; Peacoke, Monica; Eng, Charis (May 1997). "Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome". Nature Genetics. 16 (1): 64–67. doi:10.1038/ng0597-64. ISSN 1061-4036. PMID 9140396. S2CID 33101761.

ncbi.nlm.nih.gov

Gosein MA, Narinesingh D, Nixon CA, Goli SR, Maharaj P, Sinanan A (August 2016). "Multi-organ benign and malignant tumors: recognizing Cowden syndrome: a case report and review of the literature". BMC Research Notes. 9: 388. doi:10.1186/s13104-016-2195-z. PMC 4973052. PMID 27488391.
Porto AC, Roider E, Ruzicka T (2013). "Cowden Syndrome: report of a case and brief review of literature". Anais Brasileiros de Dermatologia. 88 (6 Suppl 1): 52–5. doi:10.1590/abd1806-4841.20132578. PMC 3876002. PMID 24346879.
Jelsig AM, Qvist N, Brusgaard K, Nielsen CB, Hansen TP, Ousager LB (July 2014). "Hamartomatous polyposis syndromes: a review". Orphanet Journal of Rare Diseases. 9: 101. doi:10.1186/1750-1172-9-101. PMC 4112971. PMID 25022750.
Yehia, Lamis; Niazi, Farshad; Ni, Ying; Ngeow, Joanne; Sankunny, Madhav; Liu, Zhigang; Wei, Wei; Mester, Jessica; Keri, Ruth; Zhang, Bin; Eng, Charis (5 November 2015). "Germline Heterozygous Variants in SEC23B Are Associated with Cowden Syndrome and Enriched in Apparently Sporadic Thyroid Cancer". Am J Hum Genet. 97 (5): 661–676. doi:10.1016/j.ajhg.2015.10.001. PMC 4667132. PMID 26522472.
Yehia, Lamis; Jindal, Supriya; Komar, Anton; Eng, Charis (15 September 2018). "Non-canonical role of cancer-associated mutant SEC23B in the ribosome biogenesis pathway". Hum Mol Genet. 27 (18): 3154–3164. doi:10.1093/hmg/ddy226. PMC 6121187. PMID 29893852.

semanticscholar.org

api.semanticscholar.org

Mester J, Eng C (January 2015). "Cowden syndrome: recognizing and managing a not-so-rare hereditary cancer syndrome". Journal of Surgical Oncology. 111 (1): 125–30. doi:10.1002/jso.23735. PMID 25132236. S2CID 33056798.
Pilarski R (February 2009). "Cowden syndrome: a critical review of the clinical literature". Journal of Genetic Counseling. 18 (1): 13–27. doi:10.1007/s10897-008-9187-7. PMID 18972196. S2CID 5671218.
Liaw, Danny; Marsh, Debbie J.; Li, Jing; Dahia, Patricia L. M.; Wang, Steven I.; Zheng, Zimu; Bose, Shikha; Call, Katherine M.; Tsou, Hui C.; Peacoke, Monica; Eng, Charis (May 1997). "Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome". Nature Genetics. 16 (1): 64–67. doi:10.1038/ng0597-64. ISSN 1061-4036. PMID 9140396. S2CID 33101761.

worldcat.org

search.worldcat.org

Habif TP (2016). Clinical dermatology : a color guide to diagnosis and therapy (Sixth ed.). St. Louis, Missouri: Elsevier. ISBN 978-0-323-26183-8. OCLC 911266496.
Callen JP (9 May 2016). Dermatological signs of systemic disease (Fifth ed.). Edinburgh: Elsevier. ISBN 978-0-323-35829-3. OCLC 947111367.
Bolognia J, Schaffer JV, Duncan KO, Ko CJ (2014). Dermatology essentials. Oxford: Saunders/Elsevier. ISBN 9781455708413. OCLC 877821912.
Niederhuber JE, Armitage JO, Doroshow JH, Kastan MB, Tepper JE, Abeloff MD. Abeloff's clinical oncology (Fifth ed.). Philadelphia, PA: Elsevier. ISBN 9781455728657. OCLC 857585932.
Ma, Huiying; Brosens, Lodewijk A. A.; Offerhaus, G. Johan A.; Giardiello, Francis M.; de Leng, Wendy W. J.; Montgomery, Elizabeth A. (January 2018). "Pathology and genetics of hereditary colorectal cancer". Pathology. 50 (1): 49–59. doi:10.1016/j.pathol.2017.09.004. ISSN 1465-3931. PMID 29169633.
Kumar V, Abbas AK, Aster JC, Perkins JA (2014). Robbins and Cotran pathologic basis of disease (Ninth ed.). Philadelphia, PA: Elsevier. ISBN 9781455726134. OCLC 879416939.
Turnpenny, Peter D.; Ellard, Sian (2012). Emery's elements of medical genetics (14th ed.). Philadelphia, PA: Elsevier/Churchill Livingstone. ISBN 9780702040436. OCLC 759158627.
LLOYD, KENNETH M. (1963-01-01). "Cowden's Disease". Annals of Internal Medicine. 58 (1): 136–142. doi:10.7326/0003-4819-58-1-136. ISSN 0003-4819. PMID 13931122.
Liaw, Danny; Marsh, Debbie J.; Li, Jing; Dahia, Patricia L. M.; Wang, Steven I.; Zheng, Zimu; Bose, Shikha; Call, Katherine M.; Tsou, Hui C.; Peacoke, Monica; Eng, Charis (May 1997). "Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome". Nature Genetics. 16 (1): 64–67. doi:10.1038/ng0597-64. ISSN 1061-4036. PMID 9140396. S2CID 33101761.