Salehi N - Search Results

1

A novel missense variant in PNLDC1 associated with nonobstructive azoospermia.

Rahimian M, Askari M, Salehi N, Jaafarinia M, Forouzanfar M, Almadani N, Riccio A, Totonchi M. Rahimian M, et al. Among authors: salehi n. J Genet. 2024;103:28. J Genet. 2024. PMID: 39223739 Free article.

2

Biallelic variant in cyclin B3 is associated with failure of maternal meiosis II and recurrent digynic triploidy.

Fatemi N, Salehi N, Pignata L, Palumbo P, Cubellis MV, Ramazanali F, Ray P, Varkiani M, Reyhani-Sabet F, Biglari A, Sparago A, Acurzio B, Palumbo O, Carella M, Riccio A, Totonchi M. Fatemi N, et al. Among authors: salehi n. J Med Genet. 2021 Nov;58(11):783-788. doi: 10.1136/jmedgenet-2020-106909. Epub 2020 Sep 16. J Med Genet. 2021. PMID: 32938693 Free PMC article.

3

Novel STAG3 variant associated with primary ovarian insufficiency and non-obstructive azoospermia in an Iranian consanguineous family.

Akbari A, Zoha Tabatabaei S, Salehi N, Padidar K, Almadani N, Ali Sadighi Gilani M, Mashayekhi M, Motevaseli E, Totonchi M. Akbari A, et al. Among authors: salehi n. Gene. 2022 May 5;821:146281. doi: 10.1016/j.gene.2022.146281. Epub 2022 Feb 14. Gene. 2022. PMID: 35176428

4

A novel missense variant in CDK5RAP2 associated with non-obstructive azoospermia.

Rahimian M, Askari M, Salehi N, Riccio A, Jaafarinia M, Almadani N, Totonchi M. Rahimian M, et al. Among authors: salehi n. Taiwan J Obstet Gynecol. 2023 Nov;62(6):830-837. doi: 10.1016/j.tjog.2023.03.015. Taiwan J Obstet Gynecol. 2023. PMID: 38008501 Free article.

5

The construction of a testis transcriptional cell atlas from embryo to adult reveals various somatic cells and their molecular roles.

Salehi N, Totonchi M. Salehi N, et al. J Transl Med. 2023 Nov 27;21(1):859. doi: 10.1186/s12967-023-04722-2. J Transl Med. 2023. PMID: 38012716 Free PMC article.

6

Rare missense variant in MSH4 associated with primary gonadal failure in both 46, XX and 46, XY individuals.

Akbari A, Padidar K, Salehi N, Mashayekhi M, Almadani N, Sadighi Gilani MA, Bashambou A, McElreavey K, Totonchi M. Akbari A, et al. Among authors: salehi n. Hum Reprod. 2021 Mar 18;36(4):1134-1145. doi: 10.1093/humrep/deaa362. Hum Reprod. 2021. PMID: 33448284

7

Integration and gene co-expression network analysis of scRNA-seq transcriptomes reveal heterogeneity and key functional genes in human spermatogenesis.

Salehi N, Karimi-Jafari MH, Totonchi M, Amiri-Yekta A. Salehi N, et al. Sci Rep. 2021 Sep 27;11(1):19089. doi: 10.1038/s41598-021-98267-3. Sci Rep. 2021. PMID: 34580317 Free PMC article.

8

A rare frameshift mutation in SYCP1 is associated with human male infertility.

Nabi S, Askari M, Rezaei-Gazik M, Salehi N, Almadani N, Tahamtani Y, Totonchi M. Nabi S, et al. Among authors: salehi n. Mol Hum Reprod. 2022 Apr 1;28(4):gaac009. doi: 10.1093/molehr/gaac009. Mol Hum Reprod. 2022. PMID: 35377450

9

Profiling of Initial Available SARS-CoV-2 Sequences from Iranian Related COVID-19 Patients.

Salehi N, Amiri-Yekta A, Totonchi M. Salehi N, et al. Cell J. 2020 Jul;22(Suppl 1):148-150. doi: 10.22074/cellj.2020.7524. Epub 2020 Jul 18. Cell J. 2020. PMID: 32779445 Free PMC article.

10

A Novel Missense Variant in Actin Binding Domain of MYH7 Is Associated With Left Ventricular Noncompaction.

Hesaraki M, Bora U, Pahlavan S, Salehi N, Mousavi SA, Barekat M, Rasouli SJ, Baharvand H, Ozhan G, Totonchi M. Hesaraki M, et al. Among authors: salehi n. Front Cardiovasc Med. 2022 Apr 8;9:839862. doi: 10.3389/fcvm.2022.839862. eCollection 2022. Front Cardiovasc Med. 2022. PMID: 35463789 Free PMC article.

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