Hossein Najmabadi

12.8k citations

292 papers · 6.5k indexed · h-index 41

Sensory Systems top 0.2%
- Hearing, Cochlea, Tinnitus, Genetics 46
Genetics top 0.5%
- Hemoglobinopathies and Related Disorders 50
- Genetics and Neurodevelopmental Disorders 47
- Genomics and Rare Diseases 38
- Genomic variations and chromosomal abnormalities 26
Hematology top 1%
- Iron Metabolism and Disorders 42
Reproductive Medicine top 1%
Genetics top 1%
- Hemoglobinopathies and Related Disorders 50
- Genetics and Neurodevelopmental Disorders 47
- Genomics and Rare Diseases 38
- Genomic variations and chromosomal abnormalities 26
Molecular Biology
- RNA modifications and cancer 20
- Connexins and lens biology 19

Co-authors: Kimia Kahrizi Richard J. Smith Andreas Tzschach Andreas W. Kuß Masoud Garshasbi Michael S. Hildebrand Matthew R. Avenarius Roxana Kariminejad
Cited by: Sensory Systems Genetics Hematology
Partner nations: Iran United States Germany

In The Last Decade

Hossein Najmabadi

274 papers receiving 6.4k citations

Peers

Countries citing papers authored by Hossein Najmabadi

Since Specialization

Citations

This map shows the geographic impact of Hossein Najmabadi'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 Hossein Najmabadi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Hossein Najmabadi more than expected).

Fields of papers citing papers by Hossein Najmabadi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hossein Najmabadi. 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 Hossein Najmabadi. The network helps show where Hossein Najmabadi may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Hossein Najmabadi, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Hossein Najmabadi Line = papers co-authored together Hossein Najmabadi links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Improved Diagnostic Yield in Recessive Intellectual Disability Utilizing Systematic Whole Exome Sequencing Data Reanalysis Zohreh Fattahi,Ebrahim Shokouhian,Fatemeh Peymani,Mojgan Babanejad,Maryam Beheshtian,Masoud Edizadeh,Negar Molaei,Parnian Alagha,Fatemeh Ghodratpour,Fatemeh Keshavarzi,Masoumeh Goleyjani Moghadam,Sanaz Arzhangi,Kimia Kahrizi,Hossein Najmabadi	2025	1
2	Genomics of rare diseases in the Greater Middle East Ikram Chekroun,Shruti Shenbagam,Mohamed A. Almarri,Younes Mokrab,Mohammed Uddin,Omer S. Alkhnbashi,Maha S. Zaki,Hossein Najmabadi,Kimia Kahrizi,Khalid A. Fakhro,Naif A. M. Almontashiri,Fahad Ali,Uğur Özbek,Bruno Reversade,Fowzan S. Alkuraya,Alawi Alsheikh‐Ali,Ahmad Abou Tayoun	2025	1
3	Clinical and genetic diversity in Iranian individuals with RAPSN-related congenital myasthenic syndrome Aida Ghasemi,Seyed Jalaleddin Hadei,Sara KamaliZonouzi,Asghar Shahrokhi,Hossein Najmabadi,Shahriar Nafissi	2024	0
4	Core myopathy in two siblings with a biallelic variant in the CACNA1S gene—A case series study Tara Khoeini,Ariana Kariminejad,Yalda Nilipour,Armin Ariaei,Hossein Najmabadi,Mojtaba Arabshahi,Mehrshid Faraji Zonooz,Bahram Haghi Ashtiani	2024	1
5	Bi‐allelic loss of function variant in the NRCAM gene is associated with motor‐predominant axonal polyneuropathy; the second report Zohreh Elahi,Mohamad Soveyzi,Shahriar Nafissi,Yalda Nilipour,Masoumeh Goleyjani Moghadam,Elham Keshavarz,Ariana Kariminejad,Hossein Najmabadi,Zohreh Fattahi	2023	1
6	Genetic Diagnosis of Pyruvate Kinase Deficiency in Undiagnosed Iranian Patients with Severe Hemolytic Anemia, using Whole Exome Sequencing Jafar Mehrabi Sisakht,Maghsood Mehri,Hossein Najmabadi,Azita Azarkeivan,Maryam Neishabury	2022	0
7	A GLI3 variant leading to polydactyly in heterozygotes and Pallister‐Hall‐like syndrome in a homozygote Ariana Kariminejad,Siavash Ghaderi‐Sohi,Elham Keshavarz,Seyed Abolghasem Hashemi,Elham Parsimehr,Emmanuelle Szenker‐Ravi,Muznah Khatoo,Mehrshid Faraji Zonooz,Bruno Reversade,Hossein Najmabadi,Raoul C. M. Hennekam	2020	3
8	Comprehensive genotype‐phenotype correlation in AP ‐4 deficiency syndrome; Adding data from a large cohort of Iranian patients Maryam Beheshtian,Tara Akhtarkhavari,Sepideh Mehvari,Marzieh Mohseni,Zohreh Fattahi,Seyedeh Sedigheh Abedini,Sanaz Arzhangi,Mahsa Fadaee,Payman Jamali,Reza Najafipour,Vera M. Kalscheuer,Hao Hu,Hans‐Hilger Ropers,Hossein Najmabadi,Kimia Kahrizi	2020	2
9	Identification of disease‐causing variants in the EXOSC gene family underlying autosomal recessive intellectual disability in Iranian families Maryam Beheshtian,Zohreh Fattahi,Mahsa Fadaee,Raheleh Vazehan,Payman Jamali,Elham Parsimehr,Mahboubeh Kamgar,Mehrshid Faraji Zonooz,Shokouh Sadat Mahdavi,Zahra Kalhor,Sanaz Arzhangi,Seyedeh Sedigheh Abedini,Farahnaz Sabbagh Kermani,Faezeh Mojahedi,Vera M. Kalscheuer,Hans‐Hilger Ropers,Ariana Kariminejad,Hossein Najmabadi,Kimia Kahrizi	2019	6
10	A Novel Homozygous ATP8A2 Variant in a Patient With Phenotypic Features of Dysequilibrium Syndrome Amene Saghazadeh,Seyed Hassan Tonekaboni,Hossein Najmabadi,Nima Rezaei	2019	0
11	Novel CFTR Mutations in Two Iranian Families with Severe Cystic Fibrosis. Marzieh Mohseni,Mohammad Razzaghmanesh,Elham Parsi Mehr,Hanieh Zare,Maryam Beheshtian,Hossein Najmabadi	2016	4
12	Serotonin Transporter Polymorphism (5-HTTLPR) and Citalopram Effectiveness in Iranian Patients with Major Depressive Disorder Shima Sahraian,Mohammad Babashams,Pouria Rezasoltani,Hossein Najmabadi,Kimia Kahrizi,Sahel Hemmati Gorgani	2013	6
13	Epigenetically Deregulated microRNA-375 Is Involved in a Positive Feedback Loop with Estrogen Receptor α in Breast Cancer Cells Pedro de Souza Rocha Simonini,Achim Breiling,N. Vishal Gupta,Mahdi Malekpour,Mаhmoud Youns,Ramesh Omranipour,Fatemeh Malekpour,Stefano Volinia,Carlo M. Croce,Hossein Najmabadi,Sven Diederichs,Özgür Şahin,Doris Mayer,Frank Lyko,Jörg D. Hoheisel,Yasser Riazalhosseini	2010	232
14	Genotype–Phenotype Correlations in Iranian Myotonic Dystrophy Type I Patients Kimia Kahrizi,Neda Moradin,Mojtaba Azimian,Bahareh Shojasaffar,Kaveh Alavi,Shahriar Nafisi,Mandana Hasanzad,Seyed Mohammad Ebrahim Moosavi,Azadeh Shirazian,Hossein Najmabadi	2010	1
15	Clinical heterogeneity and chromosome breakage in Iranian patients suspicious of Fanconi anemia Ghasemi Firoozabadi S,Yousef Shafeghati,Elahe Keyhani,Roxana Kariminejad,Z Oloomi,Farzaneh Moosavi,Farahnaz Amini,Hossein Najmabadi,F Behiati	2007	2
16	Review: Hearing Loss Genetics Hossein Najmabadi,Kimia Kahrizi	2005	0
17	Classification of Neuromuscular Disorders Based an Clinical Criteria , Molocular and Immunohistochemisty Analysis in Tehran Pateints K Kahrizi,Yousef Shafaghati,Elaheh Keyhani,Mandana Hassan-Zad,Mojtaba A'zimiyan,Fereidoun Layeghi,Afshin Vojdani-Rowshan,John Andoni-Ortizbera,Daniel Hentay,Hossein Najmabadi	2005	0
18	Frequency of Connexin26 Gene Mutations in Autosomal Recessive Non-syndromic Deafness in Kermanshah(2002-4) Nejat Mahdieh,Karla Nishimura,Kamran Ali-Madadi,Hilda Yazdan,Saeid Kazemi,Y Riazalhosseini,Sanaz Arzhangi,Niloufar Bazazadegan,Mehdi Totonchi,Richard J. Smith,Hossein Najmabadi	2005	1
19	"Molecular Analysis of Iranian Patients with Duchenne/Becker Muscular Dystrophies" S Kheradmand,DD Farhud,Sirous Zeinali,AR Mowjoodi,Hossein Najmabadi,Farzin Pourfarzad,P Derakhshandeh	2003	1
20	Human stem cell factor promoter deoxyribonucleic acid sequence and regulation by cyclic 3',5'-adenosine monophosphate in a Sertoli cell line. Wayne E. Taylor,Hossein Najmabadi,Michael D. Strathearn,N T Jou,Michael Liebling,T B Rajavashisth,N Chanani,Le Dinh Phung,Shalender Bhasin	1996	34

About Hossein Najmabadi

Hossein Najmabadi is a scholar working on Sensory Systems, Genetics and Hematology, having authored 292 papers that have together received 6.5k indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (50 papers), Genetics and Neurodevelopmental Disorders (47 papers), Hearing, Cochlea, Tinnitus, Genetics (46 papers), Iron Metabolism and Disorders (42 papers), Genomics and Rare Diseases (38 papers), Genomic variations and chromosomal abnormalities (26 papers), RNA modifications and cancer (20 papers) and Connexins and lens biology (19 papers). The work is most often cited by research in Sensory Systems (1.0k citations), Genetics (1.1k citations) and Hematology (865 citations). Hossein Najmabadi has collaborated with scholars based in Iran, United States and Germany. Frequent co-authors include Kimia Kahrizi, Richard J. Smith, Andreas Tzschach, Andreas W. Kuß, Masoud Garshasbi, Michael S. Hildebrand, Matthew R. Avenarius, Roxana Kariminejad, Nicole C. Meyer and Seyedeh Sedigheh Abedini.

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