249 related articles for article (PubMed ID: 31661684)
1. A Novel Pathogenic Variant in the CABP2 Gene Causes Severe Nonsyndromic Hearing Loss in a Consanguineous Iranian Family.
Koohiyan M; Noori-Daloii MR; Hashemzadeh-Chaleshtori M; Salehi M; Abtahi H; Tabatabaiefar MA
Audiol Neurootol; 2019; 24(5):258-263. PubMed ID: 31661684
[TBL] [Abstract][Full Text] [Related]
2. Whole exome sequencing identifies novel compound heterozygous pathogenic variants in the MYO15A gene leading to autosomal recessive non-syndromic hearing loss.
Sarmadi A; Nasrniya S; Narrei S; Nouri Z; Abtahi H; Tabatabaiefar MA
Mol Biol Rep; 2020 Jul; 47(7):5355-5364. PubMed ID: 32623615
[TBL] [Abstract][Full Text] [Related]
3. Identification and Clinical Implications of a Novel MYO15A Variant in a Consanguineous Iranian Family by Targeted Exome Sequencing.
Zarepour N; Koohiyan M; Taghipour-Sheshdeh A; Nemati-Zargaran F; Saki N; Mohammadi-Asl J; Tabatabaiefar MA; Hashemzadeh-Chaleshtori M
Audiol Neurootol; 2019; 24(1):25-31. PubMed ID: 30943474
[TBL] [Abstract][Full Text] [Related]
4. A novel pathogenic variant in the LRTOMT gene causes autosomal recessive non-syndromic hearing loss in an Iranian family.
Sarmadi A; Nasrniya S; Soleimani Farsani M; Narrei S; Nouri Z; Sepehrnejad M; Nilforoush MH; Abtahi H; Tabatabaiefar MA
BMC Med Genet; 2020 Jun; 21(1):127. PubMed ID: 32517708
[TBL] [Abstract][Full Text] [Related]
5. Next-generation sequencing reveals a novel pathological mutation in the TMC1 gene causing autosomal recessive non-syndromic hearing loss in an Iranian kindred.
Sadeghian L; Tabatabaiefar MA; Fattahi N; Pourreza MR; Tahmasebi P; Alavi Z; Hashemzadeh Chaleshtori M
Int J Pediatr Otorhinolaryngol; 2019 Sep; 124():99-105. PubMed ID: 31176026
[TBL] [Abstract][Full Text] [Related]
6. A novel missense variant in ESRRB gene causing autosomal recessive non-syndromic hearing loss: in silico analysis of a case.
Ghasemnejad T; Shekari Khaniani M; Nouri Nojadeh J; Mansoori Derakhshan S
BMC Med Genomics; 2022 Feb; 15(1):18. PubMed ID: 35101039
[TBL] [Abstract][Full Text] [Related]
7. A Novel Cadherin 23 Variant for Hereditary Hearing Loss Reveals Additional Support for a DFNB12 Nonsyndromic Phenotype of CDH23.
Koohiyan M; Hashemzadeh-Chaleshtori M; Salehi M; Abtahi H; Noori-Daloii MR; Tabatabaiefar MA
Audiol Neurootol; 2020; 25(5):258-262. PubMed ID: 32485727
[TBL] [Abstract][Full Text] [Related]
8. Novel mutations in MYTH4-FERM domains of myosin 15 are associated with autosomal recessive nonsyndromic hearing loss.
Mehregan H; Mohseni M; Jalalvand K; Arzhangi S; Nikzat N; Banihashemi S; Kahrizi K; Najmabadi H
Int J Pediatr Otorhinolaryngol; 2019 Feb; 117():115-126. PubMed ID: 30579064
[TBL] [Abstract][Full Text] [Related]
9. Whole-Exome Sequencing Identifies a Recurrent Small In-Frame Deletion in MYO15A Causing Autosomal Recessive Nonsyndromic Hearing Loss in 3 Iranian Pedigrees.
Nasrniya S; Miar P; Narrei S; Sepehrnejad M; Nilforoush MH; Abtahi H; Tabatabaiefar MA
Lab Med; 2022 Mar; 53(2):111-122. PubMed ID: 34388253
[TBL] [Abstract][Full Text] [Related]
10. Identification and clinical implications of a novel pathogenic variant in the
Koohiyan M
Intractable Rare Dis Res; 2020 Feb; 9(1):30-34. PubMed ID: 32201672
[TBL] [Abstract][Full Text] [Related]
11. A Novel Pathologic Variant in OTOF in an Iranian Family Segregating Hereditary Hearing Loss.
Tabatabaiefar MA; Pourreza MR; Tahmasebi P; Saki N; Hashemzadeh Chaleshtori M; Salehi R; Mohammadi-Asl J
Otolaryngol Head Neck Surg; 2018 Jun; 158(6):1084-1092. PubMed ID: 29484972
[TBL] [Abstract][Full Text] [Related]
12. A novel TECTA mutation causes ARNSHL.
Asgharzade S; Tabatabaiefar MA; Modarressi MH; Ghahremani MH; Reiisi S; Tahmasebi P; Abdollahnejad F; Chaleshtori MH
Int J Pediatr Otorhinolaryngol; 2017 Jan; 92():88-93. PubMed ID: 28012541
[TBL] [Abstract][Full Text] [Related]
13. Novel homozygous variants in the TMC1 and CDH23 genes cause autosomal recessive nonsyndromic hearing loss.
Zardadi S; Razmara E; Asgaritarghi G; Jafarinia E; Bitarafan F; Rayat S; Almadani N; Morovvati S; Garshasbi M
Mol Genet Genomic Med; 2020 Dec; 8(12):e1550. PubMed ID: 33205915
[TBL] [Abstract][Full Text] [Related]
14. A novel pathogenic variant in the MARVELD2 gene causes autosomal recessive non-syndromic hearing loss in an Iranian family.
Taghipour-Sheshdeh A; Nemati-Zargaran F; Zarepour N; Tahmasebi P; Saki N; Tabatabaiefar MA; Mohammadi-Asl J; Hashemzadeh-Chaleshtori M
Genomics; 2019 Jul; 111(4):840-848. PubMed ID: 29752989
[TBL] [Abstract][Full Text] [Related]
15. A novel missense mutation in GIPC3 causes sensorineural hearing loss in an Iranian family revealed by targeted next-generation sequencing.
Asgharzade S; Tabatabaiefar MA; Mohammadi-Asl J; Chaleshtori MH
Int J Pediatr Otorhinolaryngol; 2018 May; 108():8-11. PubMed ID: 29605370
[TBL] [Abstract][Full Text] [Related]
16. A novel
Li Q; Liang P; Wang S; Li W; Wang J; Yang Y; An X; Chen J; Zha D
Mol Med Rep; 2021 Jun; 23(6):. PubMed ID: 33846771
[TBL] [Abstract][Full Text] [Related]
17. Whole-exome sequencing efficiently detects rare mutations in autosomal recessive nonsyndromic hearing loss.
Diaz-Horta O; Duman D; Foster J; Sırmacı A; Gonzalez M; Mahdieh N; Fotouhi N; Bonyadi M; Cengiz FB; Menendez I; Ulloa RH; Edwards YJ; Züchner S; Blanton S; Tekin M
PLoS One; 2012; 7(11):e50628. PubMed ID: 23226338
[TBL] [Abstract][Full Text] [Related]
18. Recurrent de novo WFS1 pathogenic variants in Chinese sporadic patients with nonsyndromic sensorineural hearing loss.
Guan J; Wang H; Lan L; Wu Y; Chen G; Zhao C; Wang D; Wang Q
Mol Genet Genomic Med; 2020 Aug; 8(8):e1367. PubMed ID: 32567228
[TBL] [Abstract][Full Text] [Related]
19. Identification of novel variants in Iranian consanguineous pedigrees with nonsyndromic hearing loss by next-generation sequencing.
Bitarafan F; Seyedena SY; Mahmoudi M; Garshasbi M
J Clin Lab Anal; 2020 Dec; 34(12):e23544. PubMed ID: 32864763
[TBL] [Abstract][Full Text] [Related]
20. Novel MYO15A variants are associated with hearing loss in the two Iranian pedigrees.
Khatami S; Askari M; Bahreini F; Hashemzadeh-Chaleshtori M; Hematian S; Asgharzade S
BMC Med Genet; 2020 Nov; 21(1):226. PubMed ID: 33208113
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
