Thyroid dyshormonogenesis (English Wikipedia)

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

refsWebsite

Global rank English rank

5nih.gov

4^th place

3doi.org

2^nd place

2worldcat.org

5^th place

2orpha.net

3,537^th place

7,177^th place

1eje-online.org

low place

1indianpediatrics.net

low place

1nature.com

234^th place

397^th place

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

Avbelj M, Tahirovic H, Debeljak M, et al. (May 2007). "High prevalence of thyroid peroxidase gene mutations in patients with thyroid dyshormonogenesis". Eur. J. Endocrinol. 156 (5): 511–9. doi:10.1530/EJE-07-0037. PMID 17468186.
Grasberger, Helmut; Refetoff, Samuel (August 2011). "Genetic causes of congenital hypothyroidism due to dyshormonogenesis". Current Opinion in Pediatrics. 23 (4): 421–428. doi:10.1097/MOP.0b013e32834726a4. ISSN 1040-8703. PMC 3263319. PMID 21543982.
Sheffield, Val C.; Kraiem, Zaki; Beck, John C.; Nishimura, Darryl; Stone, Edwin M.; Salameh, Muhamad; Sadeh, Orit; Glaser, Benjamin (April 1996). "Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification". Nature Genetics. 12 (4): 424–426. doi:10.1038/ng0496-424. ISSN 1546-1718. PMID 8630498.

eje-online.org (Global: low place; English: low place)

Avbelj M, Tahirovic H, Debeljak M, et al. (May 2007). "High prevalence of thyroid peroxidase gene mutations in patients with thyroid dyshormonogenesis". Eur. J. Endocrinol. 156 (5): 511–9. doi:10.1530/EJE-07-0037. PMID 17468186.

indianpediatrics.net (Global: low place; English: low place)

Kumar PG, Anand SS, Sood V, Kotwal N (December 2005). "Thyroid dyshormonogenesis" (PDF). Indian Pediatr. 42 (12): 1233–5. PMID 16424561.

nature.com (Global: 234^th place; English: 397^th place)

Sheffield, Val C.; Kraiem, Zaki; Beck, John C.; Nishimura, Darryl; Stone, Edwin M.; Salameh, Muhamad; Sadeh, Orit; Glaser, Benjamin (April 1996). "Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification". Nature Genetics. 12 (4): 424–426. doi:10.1038/ng0496-424. ISSN 1546-1718. PMID 8630498.

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

pubmed.ncbi.nlm.nih.gov

Avbelj M, Tahirovic H, Debeljak M, et al. (May 2007). "High prevalence of thyroid peroxidase gene mutations in patients with thyroid dyshormonogenesis". Eur. J. Endocrinol. 156 (5): 511–9. doi:10.1530/EJE-07-0037. PMID 17468186.
Kumar PG, Anand SS, Sood V, Kotwal N (December 2005). "Thyroid dyshormonogenesis" (PDF). Indian Pediatr. 42 (12): 1233–5. PMID 16424561.
Grasberger, Helmut; Refetoff, Samuel (August 2011). "Genetic causes of congenital hypothyroidism due to dyshormonogenesis". Current Opinion in Pediatrics. 23 (4): 421–428. doi:10.1097/MOP.0b013e32834726a4. ISSN 1040-8703. PMC 3263319. PMID 21543982.
Sheffield, Val C.; Kraiem, Zaki; Beck, John C.; Nishimura, Darryl; Stone, Edwin M.; Salameh, Muhamad; Sadeh, Orit; Glaser, Benjamin (April 1996). "Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification". Nature Genetics. 12 (4): 424–426. doi:10.1038/ng0496-424. ISSN 1546-1718. PMID 8630498.

ncbi.nlm.nih.gov

Grasberger, Helmut; Refetoff, Samuel (August 2011). "Genetic causes of congenital hypothyroidism due to dyshormonogenesis". Current Opinion in Pediatrics. 23 (4): 421–428. doi:10.1097/MOP.0b013e32834726a4. ISSN 1040-8703. PMC 3263319. PMID 21543982.

orpha.net (Global: 3,537^th place; English: 7,177^th place)

"Orphanet: Clinical signs and symptoms". www.orpha.net. Retrieved 2025-02-26.
"Orphanet: Familial thyroid dyshormonogenesis". www.orpha.net. Retrieved 2025-02-26.

worldcat.org (Global: 5^th place; English: 5^th place)

search.worldcat.org

Grasberger, Helmut; Refetoff, Samuel (August 2011). "Genetic causes of congenital hypothyroidism due to dyshormonogenesis". Current Opinion in Pediatrics. 23 (4): 421–428. doi:10.1097/MOP.0b013e32834726a4. ISSN 1040-8703. PMC 3263319. PMID 21543982.
Sheffield, Val C.; Kraiem, Zaki; Beck, John C.; Nishimura, Darryl; Stone, Edwin M.; Salameh, Muhamad; Sadeh, Orit; Glaser, Benjamin (April 1996). "Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification". Nature Genetics. 12 (4): 424–426. doi:10.1038/ng0496-424. ISSN 1546-1718. PMID 8630498.

Thyroid dyshormonogenesis (English Wikipedia)

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