Navid Almadani

1.1k total citations
45 papers, 702 citations indexed

About

Navid Almadani is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Navid Almadani has authored 45 papers receiving a total of 702 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 14 papers in Genetics and 11 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Navid Almadani's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers), Prenatal Screening and Diagnostics (9 papers) and Sexual Differentiation and Disorders (7 papers). Navid Almadani is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers), Prenatal Screening and Diagnostics (9 papers) and Sexual Differentiation and Disorders (7 papers). Navid Almadani collaborates with scholars based in Iran, France and United States. Navid Almadani's co-authors include Hamid Gourabi, Mehdi Totonchi, Hossein Najmabadi, Mahdi Malekpour, Anahita Mohseni Meybodi, Mohammad Ali Sadighi Gilani, Faezeh Mojahedi, Y. Zhang, Richard J. Smith and Ahmad Daneshi and has published in prestigious journals such as SHILAP Revista de lepidopterología, Gene and Human Reproduction.

In The Last Decade

Navid Almadani

41 papers receiving 681 citations

Peers

Countries citing papers authored by Navid Almadani

Since Specialization

Citations

This map shows the geographic impact of Navid Almadani's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Navid Almadani with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Navid Almadani more than expected).

Fields of papers citing papers by Navid Almadani

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Navid Almadani. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Navid Almadani. The network helps show where Navid Almadani may publish in the future.

Co-authorship network of co-authors of Navid Almadani

This figure shows the co-authorship network connecting the top 25 collaborators of Navid Almadani. A scholar is included among the top collaborators of Navid Almadani based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Navid Almadani. Navid Almadani is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	A FSHR missense variant associated with polycystic ovary syndrome in an Iranian family with multiple affected sisters 2025 ·Molecular Biology Reports ·(unknown), (unknown), (unknown), (unknown), Navid Almadani, Seyed Abolhassan Shahzadeh Fazeli	0
2	Genetic insights into PHARC syndrome: identification of a novel frameshift mutation in ABHD12 2023 ·BMC Medical Genomics ·Ahmad Daneshi, Masoud Garshasbi, Mohammad Farhadi, Khalil Ghasemi Falavarjani, (unknown), Navid Almadani, (unknown), (unknown), Masoumeh Falah	2
3	Compound heterozygous variants in SPNS2 cause sensorineural hearing loss 2022 ·European Journal of Medical Genetics ·(unknown), Navid Almadani, Masoud Garshasbi	2
4	Novel STAG3 variant associated with primary ovarian insufficiency and non-obstructive azoospermia in an Iranian consanguineous family 2022 ·Gene ·(unknown), (unknown), Najmeh Salehi, (unknown), Navid Almadani, Mohammad Ali Sadighi Gilani, (unknown), Elahe Motevaseli, Mehdi Totonchi	15
5	Preimplantation Genetic Screening and The Success Rate of In Vitro Fertilization: A Three-Years Study on Iranian Population. 2021 ·SHILAP Revista de lepidopterología ·Mehdi Totonchi, (unknown), (unknown), Mojtaba Rezazadeh Valojerdi, Poopak Eftekhari‐Yazdi, (unknown), Navid Almadani, Anahita Mohseni Meybodi, (unknown), (unknown), Tahereh Madani, Hamid Gourabi	6
6	Kabuki Syndrome: Identification of Two Novel Variants in <b><i>KMT2D</i></b> and <b><i>KDM6A</i></b> 2021 ·Molecular Syndromology ·(unknown), (unknown), (unknown), (unknown), Navid Almadani, (unknown), Masoud Garshasbi	6
7	Identification of a Novel Splice Site Mutation in RUNX2 Gene in a Family with Rare Autosomal Dominant Cleidocranial Dysplasia 2021 ·Iranian Biomedical Journal ·(unknown), (unknown), (unknown), Navid Almadani, Masoud Garshasbi	2
8	Strategies for whole-exome sequencing analysis in a case series study of familial male infertility 2020 ·International Journal of Reproductive BioMedicine (IJRM) ·Masomeh Askari, Dor Mohammad Kordi-Tamandani, Navid Almadani, (unknown)	2
9	Novel homozygous variants in the TMC1 and CDH23 genes cause autosomal recessive nonsyndromic hearing loss 2020 ·Molecular Genetics & Genomic Medicine ·(unknown), Ehsan Razmara, (unknown), (unknown), (unknown), (unknown), Navid Almadani, (unknown), Masoud Garshasbi	1
10	Cytogenetic assessment of Iranian infertile men with undescended testis: A retrospective study 2020 ·JBRA ·Neda Sharifi, Marjan Sabbaghian, (unknown), Navid Almadani, (unknown), Anahita Mohseni Meybodi	1
11	Birth of a healthy boy following preimplantation genetic diagnosis for congenital adrenal hyperplasia 2020 ·JBRA ·(unknown), Poopak Eftekhari‐Yazdi, (unknown), (unknown), Navid Almadani, (unknown), (unknown)	2
12	Identification of a homozygous GFPT2 variant in a family with asthenozoospermia 2019 ·Gene ·Masomeh Askari, Dor Mohammad Kordi-Tamandani, Navid Almadani, Kenneth McElreavey, Mehdi Totonchi	13
13	Identification of a missense variant in CLDN2 in obstructive azoospermia 2019 ·Journal of Human Genetics ·Masomeh Askari, Razieh Karamzadeh, Naser Ansari‐Pour, Mohammad Hossein Karimi‐Jafari, Navid Almadani, Mohammad Ali Sadighi Gilani, Hamid Gourabi, Ahmad Vosough, Anahita Mohseni Meybodi, Mehdi Sadeghi, Anu Bashamboo, Ken McElreavey, Mehdi Totonchi	18
14	Truncating CHRNG mutations associated with interfamilial variability of the severity of the Escobar variant of multiple pterygium syndrome 2016 ·BMC Genetics ·Ariana Kariminejad, Navid Almadani, (unknown), Björn Olsson, Ali‐Reza Moslemi, Homa Tajsharghi	11
15	Association of MOV10L1 gene polymorphisms and male infertility in azoospermic men with complete maturation arrest 2014 ·Journal of Assisted Reproduction and Genetics ·(unknown), Mehdi Totonchi, (unknown), Mohammad Ali Sadighi Gilani, Masoud Zamani Esteki, Navid Almadani, (unknown), Hamid Gourabi	14
16	Clinical data for 185 infertile Iranian men with Y-chromosome microdeletion 2012 ·Journal of Assisted Reproduction and Genetics ·Mehdi Totonchi, Anahita Mohseni Meybodi, (unknown), (unknown), Navid Almadani, Hamid Gourabi	39
17	α-Thalassemia Mutation Analyses in Mazandaran Province, North Iran 2009 ·Hemoglobin ·Ahmad Tamaddoni, Valeh Hadavi, (unknown), (unknown), (unknown), (unknown), Navid Almadani, Christian Oberkanins, Hai‐Yang Law, Hossein Najmabadi	40
18	Clinical variability in acro‐cardio‐facial‐syndrome 2008 ·American Journal of Medical Genetics Part A ·Ariana Kariminejad, Bita Bozorgmehr, Mohammad Ali Sadighi Gilani, Navid Almadani, Mohamad Hasan Kariminejad	4
19	Elucidating the spectrum of -thalassemia mutations in Iran 2007 ·Haematologica ·Valeh Hadavi, Amir Hossein Taromchi, Mahdi Malekpour, Behnood Gholami, Hai‐Yang Law, Navid Almadani, (unknown), Farhad Sahebjam, (unknown), Roxana Kariminejad, Mohamad Hasan Kariminejad, Azita Azarkeivan, (unknown), Ahmad Tamaddoni, Helene Puehringer, Christian Oberkanins, Hossein Najmabadi	52
20	Screening of Iranian Thalassemic Families for the Most Common Deletions of the β-Globin Gene Cluster 2007 ·Hemoglobin ·Fatemehsadat Esteghamat, (unknown), Azita Azarkeivan, Farzin Pourfarzad, Navid Almadani, Hossein Najmabadi	2

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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