World Journal of Clinical Cases - Baishideng Publishing Group

Advanced Search

BPG is committed to discovery and dissemination of knowledge

JOURNAL HOME

Homepage

Online Submission

Number of total visits: 3490638

Number of visits today: 2317

Number of downloads: 2674673

MEMBERSHIP

BPG JOURNALS

Cited by in F6Publishing

For:	Razmara E, Azimi H, Bitaraf A, Daneshmand MA, Galehdari M, Dokhanchi M, Esmaeilzadeh-Gharehdaghi E, Garshasbi M. Whole-exome sequencing identified a novel variant in an Iranian patient affected by pycnodysostosis. Mol Genet Genomic Med 2020;8:e1118. [PMID: 31944631 DOI: 10.1002/mgg3.1118] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]

For:

Razmara E, Azimi H, Bitaraf A, Daneshmand MA, Galehdari M, Dokhanchi M, Esmaeilzadeh-Gharehdaghi E, Garshasbi M. Whole-exome sequencing identified a novel variant in an Iranian patient affected by pycnodysostosis. Mol Genet Genomic Med 2020;8:e1118. [PMID: 31944631 DOI: 10.1002/mgg3.1118] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]

Number	Citing Articles
1	Aryan H, Razmara E, Farhud D, Zarif-Yeganeh M, Zokaei S, Hassani SA, Ashrafi MR, Garshasbi M, Tavasoli AR. Novel imaging and clinical phenotypes of CONDSIAS disorder caused by a homozygous frameshift variant of ADPRHL2: a case report. BMC Neurol 2020;20:291. [PMID: 32746785 DOI: 10.1186/s12883-020-01873-3] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 2.5] [Reference Citation Analysis]
2	Al-Araimi M, Al-Hosni A, Maimani AA. A First-Case Report of Pycnodysostosis in an Omani Boy. J Pediatr Genet 2022;11:42-6. [PMID: 35186389 DOI: 10.1055/s-0040-1714364] [Reference Citation Analysis]
3	Razmara E, Azimi H, Bitaraf A, Daneshmand MA, Galehdari M, Dokhanchi M, Esmaeilzadeh-Gharehdaghi E, Garshasbi M. Whole-exome sequencing identified a novel variant in an Iranian patient affected by pycnodysostosis. Mol Genet Genomic Med 2020;8:e1118. [PMID: 31944631 DOI: 10.1002/mgg3.1118] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
4	Soleimanipour F, Razmara E, Rahbarizadeh F, Fallahi E, Khodaeian M, Tavasoli AR, Garshasbi M. A novel missense variant in the LMNB2 gene causes progressive myoclonus epilepsy. Acta Neurol Belg 2022;122:659-67. [PMID: 33783721 DOI: 10.1007/s13760-021-01650-0] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 4.0] [Reference Citation Analysis]