Ariana Kariminejad

4.4k citations

100 papers · 1.5k indexed · h-index 21

Genetics top 2%
- Connective tissue disorders research 11
- Genomic variations and chromosomal abnormalities 11
- Neurogenetic and Muscular Disorders Research 8
- Genomics and Rare Diseases 6
Cell Biology top 5%
- Skin and Cellular Biology Research 16
Genetics top 10%
- Connective tissue disorders research 11
- Genomic variations and chromosomal abnormalities 11
- Neurogenetic and Muscular Disorders Research 8
- Genomics and Rare Diseases 6
Molecular Biology top 10%
- RNA regulation and disease 8
Developmental Biology top 10%
Pediatrics, Perinatology and Child Health
- Prenatal Screening and Diagnostics 7
Cellular and Molecular Neuroscience
- Hereditary Neurological Disorders 7

Co-authors: Hossein Najmabadi Rick R. van Rijn Gerard Pals Fleur S. van Dijk Linda M. Reis Elena V. Semina J. M. Cobben Peter G. J. Nikkels
Cited by: Genetics Cell Biology
Journals: SHILAP Revista de lepidopterología (3 papers)Brain (1 paper)Scientific Reports (3 papers)
Partner nations: Iran United States Netherlands

In The Last Decade

Ariana Kariminejad

96 papers receiving 1.4k citations

Peers

Countries citing papers authored by Ariana Kariminejad

Since Specialization

Citations

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

Fields of papers citing papers by Ariana Kariminejad

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Ariana Kariminejad, 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 Ariana Kariminejad Line = papers co-authored together Ariana Kariminejad links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work
1	Core myopathy in two siblings with a biallelic variant in the CACNA1S gene—A case series study SHILAP Revista de lepidopterología ·Tara Khoeini,Ariana Kariminejad,Yalda Nilipour,Armin Ariaei,Hossein Najmabadi,Mojtaba Arabshahi,Mehrshid Faraji Zonooz,Bahram Haghi Ashtiani	2024	1
2	Comprehensive copy number analysis of spinal muscular atrophy among the Iranian population Scientific Reports ·Ali Khanbazi,Maryam Beheshtian,Maryam Azad,Masoumeh Akbari Kelishomi,Fariba Afroozan,Fatemeh Fatehi,Khadijeh Noudehi,Shima Zamanian Najafabadi,Mir Davood Omrani,Haleh Habibi,Maryam Taghdiri,Isa Abdi Rad,Shahriar Nafissi,Aria Jankhah,Hilda Yazdan,P. Daneshmand,Shadan Saberi,Kimia Kahrizi,Ariana Kariminejad,Hossein Najmabadi	2024	1
3	DOK7 congenital myasthenic syndrome: case series and review of literature BMC Neurology ·Bentolhoda Ziaadini,Bardyia Ghaderi Yazdi,Elham Dirandeh,Reza Boostani,Narges Karimi,Akram Panahi,Ariana Kariminejad,Mahsa Fadaee,Fatemeh Ahangari,Shahriar Nafissi	2024	1
4	Bi‐allelic loss of function variant in the NRCAM gene is associated with motor‐predominant axonal polyneuropathy; the second report Molecular Genetics & Genomic Medicine ·Zohreh Elahi,Mohamad Soveyzi,Shahriar Nafissi,Yalda Nilipour,Masoumeh Goleyjani Moghadam,Elham Keshavarz,Ariana Kariminejad,Hossein Najmabadi,Zohreh Fattahi	2023	1
5	Kindler epidermolysis bullosa-like skin phenotype and downregulated basement membrane zone gene expression in poikiloderma with neutropenia and a homozygous USB1 mutation Matrix Biology ·Hassan Vahidnezhad,Leila Youssefian,Amir Hossein Saeidian,Lynn M. Boyden,Andrew Touati,Nailah Harvey,Mahtab Naji,Masoud Zabihi,Mohammadreza Barzegar,Soheila Sotoudeh,Lu Liu,Alyson Guy,Ariana Kariminejad,Sirous Zeinali,Keith A. Choate,John A. McGrath,Jouni Uitto	2021	5
6	186 Kindler epidermolysis bullosa-like skin phenotype and downregulated basement membrane zone gene expression in poikiloderma with neutropenia and a homozygous USB1 mutation Journal of Investigative Dermatology ·Hassan Vahidnezhad,Leila Youssefian,Andrew Touati,Amir Hossein Saeidian,Nailah Harvey,Masoud Zabihi,Mohammadreza Barzegar,Soheila Sotoudeh,L. Liu,Alyson Guy,Ariana Kariminejad,Sirous Zeinali,Lynn M. Boyden,Keith A. Choate,John A. McGrath,Jouni Uitto	2021	2
7	A GLI3 variant leading to polydactyly in heterozygotes and Pallister‐Hall‐like syndrome in a homozygote Clinical Genetics ·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	Genomics‐based treatment in a patient with two overlapping heritable skin disorders: Epidermolysis bullosa and acrodermatitis enteropathica Human Mutation ·Hassan Vahidnezhad,Leila Youssefian,Soheila Sotoudeh,Lu Liu,Alyson Guy,Patricia A. Lovell,Ariana Kariminejad,Sirous Zeinali,John A. McGrath,Jouni Uitto	2020	12
9	Molecular Diagnosis of Hereditary Neuropathies by Whole Exome Sequencing and Expanding the Phenotype Spectrum Archives of Iranian Medicine ·Sara Taghizadeh,Raheleh Vazehan,Maryam Beheshtian,Farnaz Sadeghinia,Zohreh Fattahi,Marzieh Mohseni,Sanaz Arzhangi,Shahriar Nafissi,Ariana Kariminejad,Hossein Najmabadi,Kimia Kahrizi	2020	9
10	Identification of disease‐causing variants in the EXOSC gene family underlying autosomal recessive intellectual disability in Iranian families Clinical Genetics ·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
11	Next generation sequencing identifies double homozygous mutations in two distinct genes (EXPH5 and COL17A1) in a patient with concomitant simplex and junctional epidermolysis bullosa Human Mutation ·Hassan Vahidnezhad,Leila Youssefian,Amir Hossein Saeidian,Andrew Touati,Soheila Sotoudeh,Ali Jazayeri,Alyson Guy,Patricia A. Lovell,Lu Liu,Ariana Kariminejad,John A. McGrath,Sirous Zeinali,Jouni Uitto	2018	24
12	A novel autosomal recessiveGJB2-associated disorder: Ichthyosis follicularis, bilateral severe sensorineural hearing loss, and punctate palmoplantar keratoderma Human Mutation ·Leila Youssefian,Hassan Vahidnezhad,Amir Hossein Saeidian,Hamidreza Mahmoudi,Razieh Karamzadeh,Ariana Kariminejad,Jianhe Huang,Leping Li,Thomas F. Jannace,Paolo Fortina,Sirous Zeinali,Thomas W. White,Jouni Uitto	2018	12
13	Discriminative Features in Three Autosomal Recessive Cutis Laxa Syndromes: Cutis Laxa IIA, Cutis Laxa IIB, and Geroderma Osteoplastica International Journal of Molecular Sciences ·Ariana Kariminejad,Fariba Afroozan,Bita Bozorgmehr,Alireza Ghanadan,Susan Akbaroghli,Hamid Khorram Khorshid,Faezeh Mojahedi,Aria Setoodeh,Abigail Loh,Yu Xuan Tan,Nathalie Escande‐Beillard,Fransiska Malfait,Bruno Reversade,Thatjana Gardeitchik,Éva Morava	2017	15
14	Increased Endoplasmic Reticulum Stress in patients with Congenital Liver Fibrosis caused by germline mutations in a Protein Disulfide Isomerase Mechanisms of Development ·Poh Hui Chia,Ariana Kariminejad,Patrick Rump,Bruno Reversade	2017	1
15	Novel mutations and a severe neurological phenotype in Sjögren-Larsson syndrome patients from Iran European Journal of Medical Genetics ·Ariana Kariminejad,Mohammadreza Barzgar,Bita Bozorgmehr,Elham Keshavarz,Mohamad Hasan Kariminejad,Dana S'aulis,William B. Rizzo	2017	5
16	Characterizing a Cohort of α-Thalassemia Couples Collected During Screening for Hemoglobinopathies: 14 Years of an Iranian Experience Hemoglobin ·Nima Hafezi‐Nejad,Mohsen Khosravi,Nooshin Bayat,Ariana Kariminejad,Valeh Hadavi,Christian Oberkanins,Azita Azarkeivan,Hossein Najmabadi	2014	8
17	11q14.1‐11q22.1 deletion in a 1‐year‐old male with minor dysmorphic features American Journal of Medical Genetics Part A ·Ariana Kariminejad,Roxana Kariminejad,Andreas Tzschach,Hamid Najafi,Alischo Ahmed,Reinhard Ullmann,Hans‐Hilger Ropers,Mohamad Hasan Kariminejad	2010	4
18	Complete COL1A1 allele deletions in osteogenesis imperfecta Genetics in Medicine ·Fleur S. van Dijk,Margriet Huizer,Ariana Kariminejad,Carlo Marcelis,Astrid S. Plomp,Pauline Terhal,Hanne Meijers‐Heijboer,Marjan M. Weiss,Rick R. van Rijn,Jan M. Cobben,Gerard Pals	2010	33
19	A case of megalencephalic leukoencephalopathy with subcortical cysts in an Iranian consanguineous family. Iranian Journal of Pediatrics ·Mahmoud Reza Ashrafi,Ariana Kariminejad,Houman Alizadeh,Bita Bozorgmehr,Sepideh Amoeian,Mohammad Hasan Kariminejad	2009	1
20	Comparison of Early and Mid-Trimester Amniocentesis in 1459 Amniotic Fluid Cultures Hanieh Jafarieh,Ariana Kariminejad,Ahmad Rajaee,Maryam Mirzazadeh,Nasrin Nabavinia,Farnaz Azimi,Maryam Zangeneh,Roxana Kariminejad,Fatemeh Ramezanzadeh,Mohammad Hassan Kariminejad	2006	1

About Ariana Kariminejad

Ariana Kariminejad is a scholar working on Developmental Biology, Genetics and Cell Biology, having authored 100 papers that have together received 1.5k indexed citations. Recurring topics across this work include Skin and Cellular Biology Research (16 papers), Connective tissue disorders research (11 papers), Genomic variations and chromosomal abnormalities (11 papers), RNA regulation and disease (8 papers), Neurogenetic and Muscular Disorders Research (8 papers), Prenatal Screening and Diagnostics (7 papers), Hereditary Neurological Disorders (7 papers) and Genomics and Rare Diseases (6 papers). The work is most often cited by research in Genetics (715 citations), Cell Biology (284 citations) and Genetics (128 citations). Ariana Kariminejad has collaborated with scholars based in Iran, United States and Netherlands. Frequent co-authors include Hossein Najmabadi, Rick R. van Rijn, Gerard Pals, Fleur S. van Dijk, Linda M. Reis, Elena V. Semina, J. M. Cobben, Peter G. J. Nikkels, Alessandra Maugeri and Siavash Ghaderi‐Sohi. Their work appears in journals such as SHILAP Revista de lepidopterología, Brain and Scientific Reports.

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.

Explore authors with similar magnitude of impact