Schizencephaly (English Wikipedia)

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

refsWebsite

Global rank English rank

4nih.gov

4^th place

3doi.org

2^nd place

2semanticscholar.org

11^th place

8^th place

1orpha.net

3,537^th place

7,177^th place

1web.archive.org

1^st place

1worldcat.org

5^th place

1radiopaedia.org

4,968^th place

3,180^th place

doi.org

Tietjen, Ian; Bodell, Adria; Apse, Kira; Mendonza, Ashley M.; Chang, Bernard S.; Shaw, Gary M.; Barkovich, A. James; Lammer, Edward J.; Walsh, Christopher A. (15 June 2007). "Comprehensive EMX2 genotyping of a large schizencephaly case series". American Journal of Medical Genetics Part A. 143A (12): 1313–1316. doi:10.1002/ajmg.a.31767. PMID 17506092. S2CID 34724677.
Yoneda, Yuriko; Haginoya, Kazuhiro; Kato, Mitsuhiro; Osaka, Hitoshi; Yokochi, Kenji; Arai, Hiroshi; Kakita, Akiyoshi; Yamamoto, Takamichi; Otsuki, Yoshiro; Shimizu, Shin-ichi; Wada, Takahito; Koyama, Norihisa; Mino, Yoichi; Kondo, Noriko; Takahashi, Satoru; Hirabayashi, Shinichi; Takanashi, Jun-ichi; Okumura, Akihisa; Kumagai, Toshiyuki; Hirai, Satori; Nabetani, Makoto; Saitoh, Shinji; Hattori, Ayako; Yamasaki, Mami; Kumakura, Akira; Sugo, Yoshinobu; Nishiyama, Kiyomi; Miyatake, Satoko; Tsurusaki, Yoshinori; Doi, Hiroshi; Miyake, Noriko; Matsumoto, Naomichi; Saitsu, Hirotomo (January 2013). "Phenotypic Spectrum of Mutations: Porencephaly to Schizencephaly". Annals of Neurology. 73 (1): 48–57. doi:10.1002/ana.23736. PMID 23225343. S2CID 3218598.
Smigiel, Robert; Cabala, Magdalena; Jakubiak, Aleksandra; Kodera, Hirofumi; Sasiadek, Marek J.; Matsumoto, Naomichi; Sasiadek, Maria M.; Saitsu, Hirotomo (2016-04-01). "Novel COL4A1 mutation in an infant with severe dysmorphic syndrome with schizencephaly, periventricular calcifications, and cataract resembling congenital infection". Birth Defects Research Part A: Clinical and Molecular Teratology. 106 (4): 304–307. doi:10.1002/bdra.23488. ISSN 1542-0760. PMID 26879631.

nih.gov

pubmed.ncbi.nlm.nih.gov

Tietjen, Ian; Bodell, Adria; Apse, Kira; Mendonza, Ashley M.; Chang, Bernard S.; Shaw, Gary M.; Barkovich, A. James; Lammer, Edward J.; Walsh, Christopher A. (15 June 2007). "Comprehensive EMX2 genotyping of a large schizencephaly case series". American Journal of Medical Genetics Part A. 143A (12): 1313–1316. doi:10.1002/ajmg.a.31767. PMID 17506092. S2CID 34724677.
Yoneda, Yuriko; Haginoya, Kazuhiro; Kato, Mitsuhiro; Osaka, Hitoshi; Yokochi, Kenji; Arai, Hiroshi; Kakita, Akiyoshi; Yamamoto, Takamichi; Otsuki, Yoshiro; Shimizu, Shin-ichi; Wada, Takahito; Koyama, Norihisa; Mino, Yoichi; Kondo, Noriko; Takahashi, Satoru; Hirabayashi, Shinichi; Takanashi, Jun-ichi; Okumura, Akihisa; Kumagai, Toshiyuki; Hirai, Satori; Nabetani, Makoto; Saitoh, Shinji; Hattori, Ayako; Yamasaki, Mami; Kumakura, Akira; Sugo, Yoshinobu; Nishiyama, Kiyomi; Miyatake, Satoko; Tsurusaki, Yoshinori; Doi, Hiroshi; Miyake, Noriko; Matsumoto, Naomichi; Saitsu, Hirotomo (January 2013). "Phenotypic Spectrum of Mutations: Porencephaly to Schizencephaly". Annals of Neurology. 73 (1): 48–57. doi:10.1002/ana.23736. PMID 23225343. S2CID 3218598.
Smigiel, Robert; Cabala, Magdalena; Jakubiak, Aleksandra; Kodera, Hirofumi; Sasiadek, Marek J.; Matsumoto, Naomichi; Sasiadek, Maria M.; Saitsu, Hirotomo (2016-04-01). "Novel COL4A1 mutation in an infant with severe dysmorphic syndrome with schizencephaly, periventricular calcifications, and cataract resembling congenital infection". Birth Defects Research Part A: Clinical and Molecular Teratology. 106 (4): 304–307. doi:10.1002/bdra.23488. ISSN 1542-0760. PMID 26879631.

ninds.nih.gov

"NINDS Schizencephaly Information Page". National Institute of Neurological Disorders and Stroke. NIH. Archived from the original on 2013-09-11. Retrieved 2013-09-11.

orpha.net

"Schizencephaly". Orphanet. Retrieved 4 November 2014.

radiopaedia.org

Skandhan, Avni; Gaillard, Frank. "Schizencephaly". Radiopedia. Retrieved 4 November 2014.

semanticscholar.org

api.semanticscholar.org

Tietjen, Ian; Bodell, Adria; Apse, Kira; Mendonza, Ashley M.; Chang, Bernard S.; Shaw, Gary M.; Barkovich, A. James; Lammer, Edward J.; Walsh, Christopher A. (15 June 2007). "Comprehensive EMX2 genotyping of a large schizencephaly case series". American Journal of Medical Genetics Part A. 143A (12): 1313–1316. doi:10.1002/ajmg.a.31767. PMID 17506092. S2CID 34724677.
Yoneda, Yuriko; Haginoya, Kazuhiro; Kato, Mitsuhiro; Osaka, Hitoshi; Yokochi, Kenji; Arai, Hiroshi; Kakita, Akiyoshi; Yamamoto, Takamichi; Otsuki, Yoshiro; Shimizu, Shin-ichi; Wada, Takahito; Koyama, Norihisa; Mino, Yoichi; Kondo, Noriko; Takahashi, Satoru; Hirabayashi, Shinichi; Takanashi, Jun-ichi; Okumura, Akihisa; Kumagai, Toshiyuki; Hirai, Satori; Nabetani, Makoto; Saitoh, Shinji; Hattori, Ayako; Yamasaki, Mami; Kumakura, Akira; Sugo, Yoshinobu; Nishiyama, Kiyomi; Miyatake, Satoko; Tsurusaki, Yoshinori; Doi, Hiroshi; Miyake, Noriko; Matsumoto, Naomichi; Saitsu, Hirotomo (January 2013). "Phenotypic Spectrum of Mutations: Porencephaly to Schizencephaly". Annals of Neurology. 73 (1): 48–57. doi:10.1002/ana.23736. PMID 23225343. S2CID 3218598.

web.archive.org

"NINDS Schizencephaly Information Page". National Institute of Neurological Disorders and Stroke. NIH. Archived from the original on 2013-09-11. Retrieved 2013-09-11.

worldcat.org

Smigiel, Robert; Cabala, Magdalena; Jakubiak, Aleksandra; Kodera, Hirofumi; Sasiadek, Marek J.; Matsumoto, Naomichi; Sasiadek, Maria M.; Saitsu, Hirotomo (2016-04-01). "Novel COL4A1 mutation in an infant with severe dysmorphic syndrome with schizencephaly, periventricular calcifications, and cataract resembling congenital infection". Birth Defects Research Part A: Clinical and Molecular Teratology. 106 (4): 304–307. doi:10.1002/bdra.23488. ISSN 1542-0760. PMID 26879631.