Ariana Kariminejad

4.4k citations

100 papers · 1.5k indexed · h-index 21

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
Topics: Skin and Cellular Biology Research (16 papers)Connective tissue disorders research (11 papers)Genomic variations and chromosomal abnormalities (11 papers)
Cited by: Genetics Cell Biology
Journals: SHILAP Revista de lepidopterologíaBrain Scientific Reports
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 of co-authors of Ariana Kariminejad

This figure shows the co-authorship network connecting the top 25 collaborators of Ariana Kariminejad. A scholar is included among the top collaborators of Ariana Kariminejad 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 Ariana Kariminejad. Ariana Kariminejad 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	Core myopathy in two siblings with a biallelic variant in the CACNA1S gene—A case series study 2024 ·SHILAP Revista de lepidopterología ·(unknown),Ariana Kariminejad,Yalda Nilipour,(unknown),Hossein Najmabadi,(unknown),(unknown),(unknown)	1
2	Comprehensive copy number analysis of spinal muscular atrophy among the Iranian population 2024 ·Scientific Reports ·(unknown),Maryam Beheshtian,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Mir Davood Omrani,(unknown),Maryam Taghdiri,Isa Abdi Rad,Shahriar Nafissi,(unknown),(unknown),(unknown),(unknown),Kimia Kahrizi,Ariana Kariminejad,Hossein Najmabadi	1
3	DOK7 congenital myasthenic syndrome: case series and review of literature 2024 ·BMC Neurology ·(unknown),(unknown),(unknown),Reza Boostani,Narges Karimi,(unknown),Ariana Kariminejad,(unknown),(unknown),Shahriar Nafissi	1
4	Bi‐allelic loss of function variant in the NRCAM gene is associated with motor‐predominant axonal polyneuropathy; the second report 2023 ·Molecular Genetics & Genomic Medicine ·(unknown),(unknown),Shahriar Nafissi,Yalda Nilipour,(unknown),Elham Keshavarz,Ariana Kariminejad,Hossein Najmabadi,Zohreh Fattahi	1
5	Kindler epidermolysis bullosa-like skin phenotype and downregulated basement membrane zone gene expression in poikiloderma with neutropenia and a homozygous USB1 mutation 2021 ·Matrix Biology ·Hassan Vahidnezhad,Leila Youssefian,Amir Hossein Saeidian,Lynn M. Boyden,Andrew Touati,(unknown),(unknown),(unknown),(unknown),Soheila Sotoudeh,Lu Liu,Alyson Guy,Ariana Kariminejad,Sirous Zeinali,Keith A. Choate,John A. McGrath,Jouni Uitto	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 2021 ·Journal of Investigative Dermatology ·Hassan Vahidnezhad,Leila Youssefian,Andrew Touati,Amir Hossein Saeidian,(unknown),(unknown),(unknown),Soheila Sotoudeh,(unknown),Alyson Guy,Ariana Kariminejad,Sirous Zeinali,Lynn M. Boyden,Keith A. Choate,John A. McGrath,Jouni Uitto	2
7	A GLI3 variant leading to polydactyly in heterozygotes and Pallister‐Hall‐like syndrome in a homozygote 2020 ·Clinical Genetics ·Ariana Kariminejad,Siavash Ghaderi‐Sohi,Elham Keshavarz,(unknown),(unknown),Emmanuelle Szenker‐Ravi,Muznah Khatoo,(unknown),Bruno Reversade,Hossein Najmabadi,Raoul C. M. Hennekam	3
8	Genomics‐based treatment in a patient with two overlapping heritable skin disorders: Epidermolysis bullosa and acrodermatitis enteropathica 2020 ·Human Mutation ·Hassan Vahidnezhad,Leila Youssefian,Soheila Sotoudeh,Lu Liu,Alyson Guy,Patricia A. Lovell,Ariana Kariminejad,Sirous Zeinali,John A. McGrath,Jouni Uitto	12
9	Molecular Diagnosis of Hereditary Neuropathies by Whole Exome Sequencing and Expanding the Phenotype Spectrum 2020 ·Archives of Iranian Medicine ·(unknown),(unknown),Maryam Beheshtian,(unknown),Zohreh Fattahi,Marzieh Mohseni,Sanaz Arzhangi,Shahriar Nafissi,Ariana Kariminejad,Hossein Najmabadi,Kimia Kahrizi	9
10	Identification of disease‐causing variants in the EXOSC gene family underlying autosomal recessive intellectual disability in Iranian families 2019 ·Clinical Genetics ·Maryam Beheshtian,Zohreh Fattahi,(unknown),(unknown),Payman Jamali,(unknown),(unknown),(unknown),(unknown),(unknown),Sanaz Arzhangi,Seyedeh Sedigheh Abedini,(unknown),Faezeh Mojahedi,Vera M. Kalscheuer,Hans‐Hilger Ropers,Ariana Kariminejad,Hossein Najmabadi,Kimia Kahrizi	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 2018 ·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	24
12	A novel autosomal recessiveGJB2-associated disorder: Ichthyosis follicularis, bilateral severe sensorineural hearing loss, and punctate palmoplantar keratoderma 2018 ·Human Mutation ·Leila Youssefian,Hassan Vahidnezhad,Amir Hossein Saeidian,Hamidreza Mahmoudi,Razieh Karamzadeh,Ariana Kariminejad,Jianhe Huang,Leping Li,(unknown),Paolo Fortina,Sirous Zeinali,Thomas W. White,Jouni Uitto	12
13	Discriminative Features in Three Autosomal Recessive Cutis Laxa Syndromes: Cutis Laxa IIA, Cutis Laxa IIB, and Geroderma Osteoplastica 2017 ·International Journal of Molecular Sciences ·Ariana Kariminejad,(unknown),Bita Bozorgmehr,Alireza Ghanadan,(unknown),(unknown),Faezeh Mojahedi,Aria Setoodeh,Abigail Loh,(unknown),Nathalie Escande‐Beillard,Fransiska Malfait,Bruno Reversade,Thatjana Gardeitchik,Éva Morava	15
14	Increased Endoplasmic Reticulum Stress in patients with Congenital Liver Fibrosis caused by germline mutations in a Protein Disulfide Isomerase 2017 ·Mechanisms of Development ·Poh Hui Chia,Ariana Kariminejad,Patrick Rump,Bruno Reversade	1
15	Novel mutations and a severe neurological phenotype in Sjögren-Larsson syndrome patients from Iran 2017 ·European Journal of Medical Genetics ·Ariana Kariminejad,(unknown),Bita Bozorgmehr,Elham Keshavarz,Mohamad Hasan Kariminejad,(unknown),William B. Rizzo	5
16	Characterizing a Cohort of α-Thalassemia Couples Collected During Screening for Hemoglobinopathies: 14 Years of an Iranian Experience 2014 ·Hemoglobin ·Nima Hafezi‐Nejad,Mohsen Khosravi,(unknown),Ariana Kariminejad,Valeh Hadavi,Christian Oberkanins,Azita Azarkeivan,Hossein Najmabadi	8
17	11q14.1‐11q22.1 deletion in a 1‐year‐old male with minor dysmorphic features 2010 ·American Journal of Medical Genetics Part A ·Ariana Kariminejad,Roxana Kariminejad,Andreas Tzschach,(unknown),(unknown),Reinhard Ullmann,Hans‐Hilger Ropers,Mohamad Hasan Kariminejad	4
18	Complete COL1A1 allele deletions in osteogenesis imperfecta 2010 ·Genetics in Medicine ·Fleur S. van Dijk,(unknown),Ariana Kariminejad,Carlo Marcelis,Astrid S. Plomp,Pauline Terhal,Hanne Meijers‐Heijboer,Marjan M. Weiss,Rick R. van Rijn,Jan M. Cobben,Gerard Pals	33
19	A case of megalencephalic leukoencephalopathy with subcortical cysts in an Iranian consanguineous family. 2009 ·Iranian Journal of Pediatrics ·Mahmoud Reza Ashrafi,Ariana Kariminejad,Houman Alizadeh,Bita Bozorgmehr,(unknown),(unknown)	1
20	Comparison of Early and Mid-Trimester Amniocentesis in 1459 Amniotic Fluid Cultures 2006 ·(unknown),Ariana Kariminejad,(unknown),(unknown),(unknown),(unknown),(unknown),Roxana Kariminejad,Fatemeh Ramezanzadeh,(unknown)	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) and Genomic variations and chromosomal abnormalities (11 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.

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