Nonsyndromic deafness (English Wikipedia)

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

refsWebsite

Global rank English rank

12doi.org

2^nd place

10nih.gov

4^th place

8worldcat.org

5^th place

5semanticscholar.org

11^th place

8^th place

1medlineplus.gov

1,581^st place

1,299^th place

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

doi.org

Guilford, Parry; Arab, Saida Ben; Blanchard, Stéphane; Levilliers, Jacqueline; Weissenbach, Jean; Belkahia, Ali; Petit, Christine (1994). "A non–syndromic form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q". Nature Genetics. 6 (1): 24–28. doi:10.1038/ng0194-24. ISSN 1061-4036. PMID 8136828. S2CID 19240967.
Kalatzis, V (1998-09-01). "The fundamental and medical impacts of recent progress in research on hereditary hearing loss". Human Molecular Genetics. 7 (10): 1589–1597. doi:10.1093/hmg/7.10.1589. ISSN 1460-2083. PMID 9735380.
Vona, Barbara; Doll, Julia; Hofrichter, Michaela A. H.; Haaf, Thomas (2020-08-01). "Non-syndromic hearing loss: clinical and diagnostic challenges". Medizinische Genetik. 32 (2): 117–129. doi:10.1515/medgen-2020-2022. ISSN 1863-5490. S2CID 222005315.
Funamura, Jamie L. (2017). "Evaluation and management of nonsyndromic congenital hearing loss". Current Opinion in Otolaryngology & Head and Neck Surgery. 25 (5): 385–389. doi:10.1097/moo.0000000000000398. ISSN 1068-9508. PMID 28682819. S2CID 11889662.
Sloan-Heggen, Christina M.; Bierer, Amanda O.; Shearer, A. Eliot; Kolbe, Diana L.; Nishimura, Carla J.; Frees, Kathy L.; Ephraim, Sean S.; Shibata, Seiji B.; Booth, Kevin T.; Campbell, Colleen A.; Ranum, Paul T.; Weaver, Amy E.; Black-Ziegelbein, E. Ann; Wang, Donghong; Azaiez, Hela (2016-03-11). "Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss". Human Genetics. 135 (4): 441–450. doi:10.1007/s00439-016-1648-8. ISSN 0340-6717. PMC 4796320. PMID 26969326.
Vona, Barbara; Doll, Julia; Hofrichter, Michaela A. H.; Haaf, Thomas (2020-08-01). "Non-syndromic hearing loss: clinical and diagnostic challenges". Medizinische Genetik. 32 (2): 117–129. doi:10.1515/medgen-2020-2022. ISSN 1863-5490. S2CID 222005315.
Sommen, Manou; van Camp, Guy; Boudewyns, An (2013). "Genetic and clinical diagnosis in non-syndromic hearing loss". Hearing, Balance and Communication. 11 (3): 138–145. doi:10.3109/21695717.2013.812380. ISSN 2169-5717. S2CID 73090556.
Hone, S.W.; Smith, R.J.H. (2003). "Genetic screening for hearing loss". Clinical Otolaryngology and Allied Sciences. 28 (4): 285–290. doi:10.1046/j.1365-2273.2003.00700.x. ISSN 0307-7772. PMID 12871240.

dx.doi.org

Guilford, Parry; Arab, Saida Ben; Blanchard, Stéphane; Levilliers, Jacqueline; Weissenbach, Jean; Belkahia, Ali; Petit, Christine (1994). "A non–syndromic form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q". Nature Genetics. 6 (1): 24–28. doi:10.1038/ng0194-24. ISSN 1061-4036. PMID 8136828. S2CID 19240967.
Funamura, Jamie L. (2017). "Evaluation and management of nonsyndromic congenital hearing loss". Current Opinion in Otolaryngology & Head and Neck Surgery. 25 (5): 385–389. doi:10.1097/moo.0000000000000398. ISSN 1068-9508. PMID 28682819. S2CID 11889662.
Sommen, Manou; van Camp, Guy; Boudewyns, An (2013). "Genetic and clinical diagnosis in non-syndromic hearing loss". Hearing, Balance and Communication. 11 (3): 138–145. doi:10.3109/21695717.2013.812380. ISSN 2169-5717. S2CID 73090556.
Hone, S.W.; Smith, R.J.H. (2003). "Genetic screening for hearing loss". Clinical Otolaryngology and Allied Sciences. 28 (4): 285–290. doi:10.1046/j.1365-2273.2003.00700.x. ISSN 0307-7772. PMID 12871240.

medlineplus.gov (Global: 1,581^st place; English: 1,299^th place)

Reference, Genetics Home. "nonsyndromic hearing loss". Genetics Home Reference. Retrieved 14 April 2017.

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

pubmed.ncbi.nlm.nih.gov

Guilford, Parry; Arab, Saida Ben; Blanchard, Stéphane; Levilliers, Jacqueline; Weissenbach, Jean; Belkahia, Ali; Petit, Christine (1994). "A non–syndromic form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q". Nature Genetics. 6 (1): 24–28. doi:10.1038/ng0194-24. ISSN 1061-4036. PMID 8136828. S2CID 19240967.
Kalatzis, V (1998-09-01). "The fundamental and medical impacts of recent progress in research on hereditary hearing loss". Human Molecular Genetics. 7 (10): 1589–1597. doi:10.1093/hmg/7.10.1589. ISSN 1460-2083. PMID 9735380.
Usami, S; Nishio, S; Adam, MP; Ardinger, HH; Pagon, RA; Wallace, SE; Bean, LJH; Stephens, K; Amemiya, A (1993). "Nonsyndromic Hearing Loss and Deafness, Mitochondrial". University of Washington, Seattle. PMID 20301595.
Funamura, Jamie L. (2017). "Evaluation and management of nonsyndromic congenital hearing loss". Current Opinion in Otolaryngology & Head and Neck Surgery. 25 (5): 385–389. doi:10.1097/moo.0000000000000398. ISSN 1068-9508. PMID 28682819. S2CID 11889662.
Sloan-Heggen, Christina M.; Bierer, Amanda O.; Shearer, A. Eliot; Kolbe, Diana L.; Nishimura, Carla J.; Frees, Kathy L.; Ephraim, Sean S.; Shibata, Seiji B.; Booth, Kevin T.; Campbell, Colleen A.; Ranum, Paul T.; Weaver, Amy E.; Black-Ziegelbein, E. Ann; Wang, Donghong; Azaiez, Hela (2016-03-11). "Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss". Human Genetics. 135 (4): 441–450. doi:10.1007/s00439-016-1648-8. ISSN 0340-6717. PMC 4796320. PMID 26969326.
Hone, S.W.; Smith, R.J.H. (2003). "Genetic screening for hearing loss". Clinical Otolaryngology and Allied Sciences. 28 (4): 285–290. doi:10.1046/j.1365-2273.2003.00700.x. ISSN 0307-7772. PMID 12871240.
Smith, Richard JH; Jones, Mary-Kayt N. (1993). "Nonsyndromic Hearing Loss and Deafness, DFNB1". GeneReviews. University of Washington, Seattle. PMID 20301449.

ncbi.nlm.nih.gov

Usami, S; Nishio, S; Adam, MP; Ardinger, HH; Pagon, RA; Wallace, SE; Bean, LJH; Stephens, K; Amemiya, A (1993). "Nonsyndromic Hearing Loss and Deafness, Mitochondrial". University of Washington, Seattle. PMID 20301595.
Sloan-Heggen, Christina M.; Bierer, Amanda O.; Shearer, A. Eliot; Kolbe, Diana L.; Nishimura, Carla J.; Frees, Kathy L.; Ephraim, Sean S.; Shibata, Seiji B.; Booth, Kevin T.; Campbell, Colleen A.; Ranum, Paul T.; Weaver, Amy E.; Black-Ziegelbein, E. Ann; Wang, Donghong; Azaiez, Hela (2016-03-11). "Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss". Human Genetics. 135 (4): 441–450. doi:10.1007/s00439-016-1648-8. ISSN 0340-6717. PMC 4796320. PMID 26969326.
Smith, Richard JH; Jones, Mary-Kayt N. (1993). "Nonsyndromic Hearing Loss and Deafness, DFNB1". GeneReviews. University of Washington, Seattle. PMID 20301449.

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

api.semanticscholar.org

Guilford, Parry; Arab, Saida Ben; Blanchard, Stéphane; Levilliers, Jacqueline; Weissenbach, Jean; Belkahia, Ali; Petit, Christine (1994). "A non–syndromic form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q". Nature Genetics. 6 (1): 24–28. doi:10.1038/ng0194-24. ISSN 1061-4036. PMID 8136828. S2CID 19240967.
Vona, Barbara; Doll, Julia; Hofrichter, Michaela A. H.; Haaf, Thomas (2020-08-01). "Non-syndromic hearing loss: clinical and diagnostic challenges". Medizinische Genetik. 32 (2): 117–129. doi:10.1515/medgen-2020-2022. ISSN 1863-5490. S2CID 222005315.
Funamura, Jamie L. (2017). "Evaluation and management of nonsyndromic congenital hearing loss". Current Opinion in Otolaryngology & Head and Neck Surgery. 25 (5): 385–389. doi:10.1097/moo.0000000000000398. ISSN 1068-9508. PMID 28682819. S2CID 11889662.
Vona, Barbara; Doll, Julia; Hofrichter, Michaela A. H.; Haaf, Thomas (2020-08-01). "Non-syndromic hearing loss: clinical and diagnostic challenges". Medizinische Genetik. 32 (2): 117–129. doi:10.1515/medgen-2020-2022. ISSN 1863-5490. S2CID 222005315.
Sommen, Manou; van Camp, Guy; Boudewyns, An (2013). "Genetic and clinical diagnosis in non-syndromic hearing loss". Hearing, Balance and Communication. 11 (3): 138–145. doi:10.3109/21695717.2013.812380. ISSN 2169-5717. S2CID 73090556.

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

search.worldcat.org

Guilford, Parry; Arab, Saida Ben; Blanchard, Stéphane; Levilliers, Jacqueline; Weissenbach, Jean; Belkahia, Ali; Petit, Christine (1994). "A non–syndromic form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q". Nature Genetics. 6 (1): 24–28. doi:10.1038/ng0194-24. ISSN 1061-4036. PMID 8136828. S2CID 19240967.
Kalatzis, V (1998-09-01). "The fundamental and medical impacts of recent progress in research on hereditary hearing loss". Human Molecular Genetics. 7 (10): 1589–1597. doi:10.1093/hmg/7.10.1589. ISSN 1460-2083. PMID 9735380.
Vona, Barbara; Doll, Julia; Hofrichter, Michaela A. H.; Haaf, Thomas (2020-08-01). "Non-syndromic hearing loss: clinical and diagnostic challenges". Medizinische Genetik. 32 (2): 117–129. doi:10.1515/medgen-2020-2022. ISSN 1863-5490. S2CID 222005315.
Funamura, Jamie L. (2017). "Evaluation and management of nonsyndromic congenital hearing loss". Current Opinion in Otolaryngology & Head and Neck Surgery. 25 (5): 385–389. doi:10.1097/moo.0000000000000398. ISSN 1068-9508. PMID 28682819. S2CID 11889662.
Sloan-Heggen, Christina M.; Bierer, Amanda O.; Shearer, A. Eliot; Kolbe, Diana L.; Nishimura, Carla J.; Frees, Kathy L.; Ephraim, Sean S.; Shibata, Seiji B.; Booth, Kevin T.; Campbell, Colleen A.; Ranum, Paul T.; Weaver, Amy E.; Black-Ziegelbein, E. Ann; Wang, Donghong; Azaiez, Hela (2016-03-11). "Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss". Human Genetics. 135 (4): 441–450. doi:10.1007/s00439-016-1648-8. ISSN 0340-6717. PMC 4796320. PMID 26969326.
Vona, Barbara; Doll, Julia; Hofrichter, Michaela A. H.; Haaf, Thomas (2020-08-01). "Non-syndromic hearing loss: clinical and diagnostic challenges". Medizinische Genetik. 32 (2): 117–129. doi:10.1515/medgen-2020-2022. ISSN 1863-5490. S2CID 222005315.
Sommen, Manou; van Camp, Guy; Boudewyns, An (2013). "Genetic and clinical diagnosis in non-syndromic hearing loss". Hearing, Balance and Communication. 11 (3): 138–145. doi:10.3109/21695717.2013.812380. ISSN 2169-5717. S2CID 73090556.
Hone, S.W.; Smith, R.J.H. (2003). "Genetic screening for hearing loss". Clinical Otolaryngology and Allied Sciences. 28 (4): 285–290. doi:10.1046/j.1365-2273.2003.00700.x. ISSN 0307-7772. PMID 12871240.