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Scopus Author ID: 56724168800
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Employment (2)

Children's Hospital of Philadelphia: Philadelphia, PA, US

2022-03 to present | Post Doctoral Fellow (Center for Applied Genomics)
Employment
Source: Self-asserted source
Amir Hossein Saeidian

Baylor College of Medicine - - Houston, TX: Houston, Texas, US

2023-07-01 to 2035-06-29 | LGG fellow (Molecular and Human Genetics)
Employment
Source: Self-asserted source
Amir Hossein Saeidian

Education and qualifications (1)

Thomas Jefferson University: Philadelphia, Pennsylvania, US

2017-06-01 to 2022-03 | Graduate Students (Genetics, Genomics and Cancer Biology)
Education
Source: Self-asserted source
Amir Hossein Saeidian

Works (50 of 63)

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Page 1 of 2

Secondary ACMG and non-ACMG genetic findings in a multiethnic cohort of 16,713 pediatric participants

Genetics in Medicine
2024-07 | Journal article
DOI: 10.1016/j.gim.2024.101225
Part of ISSN: 1098-3600
Contributors: Amir Hossein Saeidian; Michael E. March; Leila Youssefian; Deborah J. Watson; Esha Bhandari; Xiang Wang; Xiaonan Zhao; Nichole Marie Owen; Alanna Strong; Margaret H. Harr et al.
Source: Self-asserted source
Amir Hossein Saeidian

Multi-ancestry Genome-Wide Association Meta-Analysis Identifies Novel Loci in Atopic Dermatitis

2024-06-19 | Preprint
DOI: 10.1101/2024.06.17.24308897
Contributors: Meritxell Oliva; Mrinal K. Sarkar; Michael E. March; Amir Hossein Saeidian; Frank D. Mentch; Chen-Lin Hsieh; Fanying Tang; Ranjitha Uppala; Matthew T. Patrick; Qinmengge Li et al.
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Crossref

Whole-transcriptome Sequencing-Based Profiling of the Cutaneous Virome in Patients with Secondary Immunodeficiency

JID Innovations
2024-03 | Journal article
DOI: 10.1016/j.xjidi.2024.100278
Contributors: Leila Youssefian; Amir Hossein Saeidian; Zahra Saffarian; Mona Ariamanesh; Fahimeh Abdollahimajd; Sara Molkara; Mohammad Shahidi-Dadras; Reem Diab; Fatemeh Vahidnezhad; Sirous Zeinali et al.
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Crossref

Whole transcriptome–based skin virome profiling in typical epidermodysplasia verruciformis reveals α-, β-, and γ-HPV infections

JCI Insight
2023-03-08 | Journal article
DOI: 10.1172/jci.insight.162558
Contributors: Amir Hossein Saeidian; Leila Youssefian; Mahtab Naji; Hamidreza Mahmoudi; Samantha M. Barnada; Charles Huang; Karim Naghipoor; Amir Hozhabrpour; Jason S. Park; Flavia Manzo Margiotta et al.
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Crossref

Acquired ichthyosis, asteatotic dermatitis or xerosis? An update on pathoetiology and drug‐induced associations

Journal of the European Academy of Dermatology and Venereology
2023-01 | Journal article
DOI: 10.1111/jdv.18608
Contributors: Jason S. Park; Amir H. Saeidian; Leila Youssefian; Sylvia Hsu; Hassan Vahidnezhad; Jouni Uitto
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Crossref

Identification of risk variants related to malignant tumors in children with birth defects by whole genome sequencing.

Biomarker research
2022-11 | Journal article
DOI: 10.1186/s40364-022-00431-y
PMID: 36384586
Contributors: Liu Y; Qu HQ; Chang X; Mentch FD; Qiu H; Nguyen K; Wang X; Saeidian AH; Watson D; Glessner J et al.
Source: Self-asserted source
Amir Hossein Saeidian via Europe PubMed Central

Inherited ichthyosis as a paradigm of rare skin disorders: Genomic medicine, pathogenesis, and management.

Journal of the American Academy of Dermatology
2022-08 | Journal article
DOI: 10.1016/j.jaad.2022.08.012
PMID: 35963288
Contributors: Park JS; Saeidian AH; Youssefian L; Kondratuk KE; Pride HB; Vahidnezhad H; Uitto J
Source: Self-asserted source
Amir Hossein Saeidian via Europe PubMed Central

Mutation update: The spectra of PLEC sequence variants and related plectinopathies.

Human mutation
2022-07 | Journal article
DOI: 10.1002/humu.24434
PMID: 35815343
Contributors: Vahidnezhad H; Youssefian L; Harvey N; Tavasoli AR; Saeidian AH; Sotoudeh S; Varghaei A; Mahmoudi H; Mansouri P; Mozafari N et al.
Source: Self-asserted source
Amir Hossein Saeidian via Europe PubMed Central

Recalcitrant Warts, Epidermodysplasia Verruciformis, and the Tree-Man Syndrome: Phenotypic Spectrum of Cutaneous Human Papillomavirus Infections at the Intersection of Genetic Variability of Viral and Human Genomes

Journal of Investigative Dermatology
2022-05 | Journal article
DOI: 10.1016/j.jid.2021.10.029
Contributors: Jouni Uitto; Amir Hossein Saeidian; Leila Youssefian; Zahra Saffarian; Jean-Laurent Casanova; Vivien Béziat; Emmanuelle Jouanguy; Hassan Vahidnezhad
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Crossref

Pathomechanisms of epidermolysis bullosa: Beyond structural proteins.

Matrix biology : journal of the International Society for Matrix Biology
2022-04 | Journal article
DOI: 10.1016/j.matbio.2022.04.007
PMID: 35504439
Contributors: Harvey N; Youssefian L; Saeidian AH; Vahidnezhad H; Uitto J
Source: Self-asserted source
Amir Hossein Saeidian via Europe PubMed Central

Whole-transcriptome sequencing-based concomitant detection of viral and human genetic determinants of cutaneous lesions.

JCI insight
2022-04 | Journal article
DOI: 10.1172/jci.insight.156021
PMID: 35316210
PMC: PMC9089792
Contributors: Saeidian AH; Youssefian L; Huang CY; Palizban F; Naji M; Saffarian Z; Mahmoudi H; Goodarzi A; Sotoudeh S; Vahidnezhad F et al.
Source: Self-asserted source
Amir Hossein Saeidian via Europe PubMed Central

ENPP1 variants in patients with GACI and PXE expand the clinical and genetic heterogeneity of heritable disorders of ectopic calcification

PLOS Genetics
2022-04-28 | Journal article
DOI: 10.1371/journal.pgen.1010192
Contributors: Douglas Ralph; Melissa Wasserstein; Yvonne Nitschke; Michael A. Levine; Matthew Caffet; Tamara Wurst; Amir Hossein Saeidian; Leila Youssefian; Hassan Vahidnezhad; Sharon F. Terry et al.
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Crossref

Recalcitrant Cutaneous Warts in a Family with Inherited ICOS Deficiency.

The Journal of investigative dermatology
2022-03-08 | Journal article
DOI: 10.1016/j.jid.2022.02.011
PMID: 35276224
Source: Self-asserted source
Amir Hossein Saeidian
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Genetic heterogeneity of heritable ectopic mineralization disorders in a large international cohort.

Genetics in medicine : official journal of the American College of Medical Genetics
2022-01-01 | Journal article
DOI: 10.1016/j.gim.2021.08.011
PMID: 34906475
Source: Self-asserted source
Amir Hossein Saeidian
grade
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Homozygous MEFV Gene Variant and Pyrin-Associated Autoinflammation With Neutrophilic Dermatosis: A Family With a Novel Autosomal Recessive Mode of Inheritance.

JAMA dermatology
2021-12 | Journal article
DOI: 10.1001/jamadermatol.2021.3899
PMID: 34643647
Contributors: Vahidnezhad H; Youssefian L; Saeidian AH; Ziaee V; Mahmoudi H; Parvaneh N; Ashjaei B; Shahrokh S; Kamyab Hesari K; Soltani Zangbar M et al.
Source: Self-asserted source
Amir Hossein Saeidian via Europe PubMed Central

Ichthyosis, psoriasiform dermatitis, and recurrent fungal infections in patients with biallelic mutations in PERP.

Journal of the European Academy of Dermatology and Venereology : JEADV
2021-12 | Journal article
DOI: 10.1111/jdv.17856
PMID: 34863005
Contributors: Youssefian L; Khodavaisy S; Khosravi-Bachehmir F; Park JS; Saeidian AH; Mahmoudi H; Saffarian Z; Naraghi ZS; Kamyab-Hesari K; Zeinali S et al.
Source: Self-asserted source
Amir Hossein Saeidian via Europe PubMed Central

Homozygous ITGA3 Missense Mutation in Adults in a Family with Syndromic Epidermolysis Bullosa (ILNEB) without Pulmonary Involvement

Journal of Investigative Dermatology
2021-11 | Journal article
DOI: 10.1016/j.jid.2021.03.029
Contributors: Ágnes Kinyó; András László Kovács; Péter Degrell; Endre Kálmán; Nikoletta Nagy; Sarolta Kárpáti; Rolland Gyulai; Amir Hossein Saeidian; Leila Youssefian; Hassan Vahidnezhad et al.
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Crossref

Humans with inherited T cell CD28 deficiency are susceptible to skin papillomaviruses but are otherwise healthy.

Cell
2021-07 | Journal article
DOI: 10.1016/j.cell.2021.06.004
PMID: 34214472
Contributors: Béziat V; Rapaport F; Hu J; Titeux M; Bonnet des Claustres M; Bourgey M; Griffin H; Bandet É; Ma CS; Sherkat R et al.
Source: Self-asserted source
Amir Hossein Saeidian via Europe PubMed Central

Knockdown of SDR9C7 Impairs Epidermal Barrier Function

Journal of Investigative Dermatology
2021-07 | Journal article
DOI: 10.1016/j.jid.2020.11.030
Contributors: Leila Youssefian; Fatemeh Niaziorimi; Amir Hossein Saeidian; Andrew P. South; Farzaneh Khosravi-Bachehmir; Sadegh Khodavaisy; Hassan Vahidnezhad; Jouni Uitto
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Crossref

Genetic Predisposition to Numerous Large Ulcerating Basal Cell Carcinomas and Response to Immune Therapy.

International journal of dermatology and venereology
2021-06 | Journal article
DOI: 10.1097/jd9.0000000000000170
PMID: 34278326
PMC: PMC8265835
Contributors: Dasgeb B; Leila Y; Saeidian AH; Kang J; Shi W; Shoenberg E; Ertel A; Fortina P; Vahidnezhad H; Uitto J
Source: Self-asserted source
Amir Hossein Saeidian via Europe PubMed Central

Interpretation of genomic sequence variants in heritable skin diseases: A primer for clinicians.

Journal of the American Academy of Dermatology
2021-06 | Journal article
DOI: 10.1016/j.jaad.2021.06.013
PMID: 34118299
Contributors: Uitto J; Saeidian AH; Youssefian L; Vahidnezhad H
Source: Self-asserted source
Amir Hossein Saeidian via Europe PubMed Central

Whole-Transcriptome Analysis by RNA Sequencing for Genetic Diagnosis of Mendelian Skin Disorders in the Context of Consanguinity.

Clinical chemistry
2021-06 | Journal article
DOI: 10.1093/clinchem/hvab042
PMID: 33969388
Contributors: Youssefian L; Saeidian AH; Palizban F; Bagherieh A; Abdollahimajd F; Sotoudeh S; Mozafari N; Farahani RA; Mahmoudi H; Babashah S et al.
Source: Self-asserted source
Amir Hossein Saeidian via Europe PubMed Central

Kindler epidermolysis bullosa-like skin phenotype and downregulated basement membrane zone gene expression in poikiloderma with neutropenia and a homozygous USB1 mutation.

Matrix biology : journal of the International Society for Matrix Biology
2021-05 | Journal article
DOI: 10.1016/j.matbio.2021.05.002
PMID: 34004352
Contributors: Vahidnezhad H; Youssefian L; Saeidian AH; Boyden LM; Touati A; Harvey N; Naji M; Zabihi M; Barzegar M; Sotoudeh S et al.
Source: Self-asserted source
Amir Hossein Saeidian via Europe PubMed Central

Genotype–phenotype correlation in a large English cohort of patients with autosomal recessive ichthyosis

British Journal of Dermatology
2020 | Journal article
DOI: 10.1111/bjd.18211
EID:

2-s2.0-85071755999
Contributors: Simpson, J.K.; Martinez-Queipo, M.; Onoufriadis, A.; Tso, S.; Glass, E.; Liu, L.; Higashino, T.; Scott, W.; Tierney, C.; Simpson, M.A. et al.
Source: Self-asserted source
Amir Hossein Saeidian via Scopus - Elsevier

Homozygous IL1RN Mutation in Siblings with Deficiency of Interleukin-1 Receptor Antagonist (DIRA)

Journal of Clinical Immunology
2020 | Journal article
DOI: 10.1007/s10875-020-00767-w
EID:

2-s2.0-85081747593

Part of ISBN:

15732592 02719142
Contributors: Ziaee, V.; Youssefian, L.; Faghankhani, M.; Jazayeri, A.; Saeidian, A.H.; Vahidnezhad, H.; Uitto, J.
Source: Self-asserted source
Amir Hossein Saeidian via Scopus - Elsevier

Molecular genetics of keratinization disorders – what’s new about ichthyosis

Acta Dermato-Venereologica
2020 | Journal article
DOI: 10.2340/00015555-3431
EID:

2-s2.0-85086867665

Part of ISBN:

16512057 00015555
Contributors: Uitto, J.; Youssefian, L.; Saeidian, A.H.; Vahidnezhad, H.
Source: Self-asserted source
Amir Hossein Saeidian via Scopus - Elsevier

The matriptase-prostasin proteolytic cascade in dermatologic diseases

Experimental Dermatology
2020 | Journal article
DOI: 10.1111/exd.14104
EID:

2-s2.0-85086046723

Part of ISBN:

16000625 09066705
Contributors: Touati, A.; Saeidian, A.H.; Youssefian, L.; Faghankhani, M.; Niaziorimi, F.; Pajouhanfar, S.; Vahidnezhad, H.; Uitto, J.
Source: Self-asserted source
Amir Hossein Saeidian via Scopus - Elsevier

Arrhythmogenic right ventricular cardiomyopathy in patients with biallelic JUP-associated skin fragility.

Scientific reports
2020-12 | Journal article
DOI: 10.1038/s41598-020-78344-9
PMID: 33303784
PMC: PMC7729882
Contributors: Vahidnezhad H; Youssefian L; Faghankhani M; Mozafari N; Saeidian AH; Niaziorimi F; Abdollahimajd F; Sotoudeh S; Rajabi F; Mirsafaei L et al.
Source: Self-asserted source
Amir Hossein Saeidian via Europe PubMed Central

GGCX mutations in a patient with overlapping pseudoxanthoma elasticum/cutis laxa-like phenotype.

The British journal of dermatology
2020-11 | Journal article
DOI: 10.1111/bjd.19576
PMID: 33000479
Contributors: Li D; Ryu E; Saeidian AH; Youssefian L; Oliphant E; Terry SF; Tong PL; Uitto J; Haass NK; Li Q
Source: Self-asserted source
Amir Hossein Saeidian via Europe PubMed Central

Linear basal cell nevus with a novel mosaic PTCH1 mutation

Experimental Dermatology
2020-06 | Journal article
DOI: 10.1111/exd.14101
Contributors: Amir Hossein Saeidian; Adam Cohen‐Nowak; Megan O’Donnell; Doaa Shalabi; Kathleen P. McGuinn; Leila Youssefian; Hassan Vahidnezhad; Fatemeh Niaziorimi; Bahar Dasgeb; David A. Kasper et al.
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Research Techniques Made Simple: Whole-Transcriptome Sequencing by RNA-Seq for Diagnosis of Monogenic Disorders

Journal of Investigative Dermatology
2020-06 | Journal article
DOI: 10.1016/j.jid.2020.02.032
Contributors: Amir Hossein Saeidian; Leila Youssefian; Hassan Vahidnezhad; Jouni Uitto
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Crossref
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Review for "Toll-like receptor-2 mediates systemic inflammation in gentamicin-induced rat nephrotoxicity"

2020-03 | Other
DOI: 10.1111/1440-1681.13334/v1/review1
Contributors: Amir Hossein Doustimotlagh
Source: Self-asserted source
Amir Hossein Saeidian via Crossref Metadata Search

A CIB1 Splice-Site Founder Mutation in Families with Typical Epidermodysplasia Verruciformis

Journal of Investigative Dermatology
2019 | Journal article
DOI: 10.1016/j.jid.2018.11.011
EID:

2-s2.0-85060136906
Contributors: Vahidnezhad, H.; Youssefian, L.; Saeidian, A.H.; Mansoori, B.; Jazayeri, A.; Azizpour, A.; Hesari, K.K.; Yousefi, M.; Zeinali, S.; Jouanguy, E. et al.
Source: Self-asserted source
Amir Hossein Saeidian via Scopus - Elsevier

A novel autosomal recessive GJB2-associated disorder: Ichthyosis follicularis, bilateral severe sensorineural hearing loss, and punctate palmoplantar keratoderma

Human Mutation
2019 | Journal article
DOI: 10.1002/humu.23686
EID:

2-s2.0-85057873895
Contributors: Youssefian, L.; Vahidnezhad, H.; Saeidian, A.H.; Mahmoudi, H.; Karamzadeh, R.; Kariminejad, A.; Huang, J.; Li, L.; Jannace, T.F.; Fortina, P. et al.
Source: Self-asserted source
Amir Hossein Saeidian via Scopus - Elsevier

Autosomal recessive congenital ichthyosis: Genomic landscape and phenotypic spectrum in a cohort of 125 consanguineous families

Human Mutation
2019 | Journal article
DOI: 10.1002/humu.23695
EID:

2-s2.0-85060144131
Contributors: Youssefian, L.; Vahidnezhad, H.; Saeidian, A.H.; Touati, A.; Sotoudeh, S.; Mahmoudi, H.; Mansouri, P.; Daneshpazhooh, M.; Aghazadeh, N.; Hesari, K.K. et al.
Source: Self-asserted source
Amir Hossein Saeidian via Scopus - Elsevier

Epidermodysplasia Verruciformis: Genetic Heterogeneity and EVER1 and EVER2 Mutations Revealed by Genome-Wide Analysis

Journal of Investigative Dermatology
2019 | Journal article
DOI: 10.1016/j.jid.2018.07.010
EID:

2-s2.0-85054428682
Contributors: Youssefian, L.; Vahidnezhad, H.; Mahmoudi, H.; Saeidian, A.H.; Daneshpazhooh, M.; Kamyab Hesari, K.; Zeinali, S.; de Jong, S.J.; Orth, G.; Blanchet-Bardon, C. et al.
Source: Self-asserted source
Amir Hossein Saeidian via Scopus - Elsevier

Genome-wide single nucleotide polymorphism-based autozygosity mapping facilitates identification of mutations in consanguineous families with epidermolysis bullosa

Experimental Dermatology
2019 | Journal article
DOI: 10.1111/exd.13501
EID:

2-s2.0-85042154294
Contributors: Vahidnezhad, H.; Youssefian, L.; Saeidian, A.H.; Zeinali, S.; Touati, A.; Abiri, M.; Sotoudeh, S.; Norouz-zadeh, S.; Amirinezhad, N.; Mozafari, N. et al.
Source: Self-asserted source
Amir Hossein Saeidian via Scopus - Elsevier

Inherited Interleukin 2-Inducible T-Cell (ITK) Kinase Deficiency in Siblings with Epidermodysplasia Verruciformis and Hodgkin Lymphoma

Clinical Infectious Diseases
2019 | Journal article
DOI: 10.1093/cid/ciy942
EID:

2-s2.0-85061155640
Contributors: Youssefian, L.; Vahidnezhad, H.; Yousefi, M.; Saeidian, A.H.; Azizpour, A.; Touati, A.; Nikbakht, N.; Hesari, K.K.-.; Adib-Sereshki, M.M.; Zeinali, S. et al.
Source: Self-asserted source
Amir Hossein Saeidian via Scopus - Elsevier

Inherited non-alcoholic fatty liver disease and dyslipidemia due to monoallelic ABHD5 mutations

Journal of Hepatology
2019 | Journal article
DOI: 10.1016/j.jhep.2019.03.026
EID:

2-s2.0-85066250600
Contributors: Youssefian, L.; Vahidnezhad, H.; Saeidian, A.H.; Pajouhanfar, S.; Sotoudeh, S.; Mansouri, P.; Amirkashani, D.; Zeinali, S.; Levine, M.A.; Peris, K. et al.
Source: Self-asserted source
Amir Hossein Saeidian via Scopus - Elsevier

Mutations in PLOD3, encoding lysyl hydroxylase 3, cause a complex connective tissue disorder including recessive dystrophic epidermolysis bullosa-like blistering phenotype with abnormal anchoring fibrils and type VII collagen deficiency

Matrix Biology
2019 | Journal article
DOI: 10.1016/j.matbio.2018.11.006
EID:

2-s2.0-85058421348
Contributors: Vahidnezhad, H.; Youssefian, L.; Saeidian, A.H.; Touati, A.; Pajouhanfar, S.; Baghdadi, T.; Shadmehri, A.A.; Giunta, C.; Kraenzlin, M.; Syx, D. et al.
Source: Self-asserted source
Amir Hossein Saeidian via Scopus - Elsevier

Phenotypic Spectrum of Epidermolysis Bullosa: The Paradigm of Syndromic versus Non-Syndromic Skin Fragility Disorders

Journal of Investigative Dermatology
2019 | Journal article
DOI: 10.1016/j.jid.2018.10.017
EID:

2-s2.0-85058370443
Contributors: Vahidnezhad, H.; Youssefian, L.; Saeidian, A.H.; Uitto, J.
Source: Self-asserted source
Amir Hossein Saeidian via Scopus - Elsevier

Quantitative Trait Locus and Integrative Genomics Revealed Candidate Modifier Genes for Ectopic Mineralization in Mouse Models of Pseudoxanthoma Elasticum

Journal of Investigative Dermatology
2019-12 | Journal article
DOI: 10.1016/j.jid.2019.04.023
Contributors: Qiaoli Li; Vivek M. Philip; Timothy M. Stearns; Jason A. Bubier; Benjamin L. King; Benjamin E. Low; Michael V. Wiles; Amir Hossein Saeidian; Beth A. Sundberg; Jouni Uitto et al.
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Hypotrichosis with juvenile macular dystrophy: Combination of whole‐genome sequencing and genome‐wide homozygosity mapping identifies a large deletion in CDH3 initially undetected by whole‐exome sequencing—A lesson from next‐generation sequencing

Molecular Genetics & Genomic Medicine
2019-11 | Journal article
DOI: 10.1002/mgg3.975
Contributors: Amir Hossein Saeidian; Hassan Vahidnezhad; Leila Youssefian; Soheila Sotudeh; Meisam Sargazi; Sirous Zeinali; Jouni Uitto
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Crossref
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Development and implementation of a novel panel consisting 20 markers for the detection of genetic causes of male infertility

Andrologia
2018 | Journal article
DOI: 10.1111/and.12946
EID:

2-s2.0-85039161327
Contributors: Bahrami Zadegan, S.; Dabbagh Bagheri, S.; Joudaki, A.; Samiee Aref, M.H.; Saeidian, A.H.; Abiri, M.; Zeinali, S.
Source: Self-asserted source
Amir Hossein Saeidian via Scopus - Elsevier

Epidermolysis bullosa: Molecular pathology of connective tissue components in the cutaneous basement membrane zone

Matrix Biology
2018 | Journal article
DOI: 10.1016/j.matbio.2018.04.001
EID:

2-s2.0-85045724614
Contributors: Has, C.; Nyström, A.; Saeidian, A.H.; Bruckner-Tuderman, L.; Uitto, J.
Source: Self-asserted source
Amir Hossein Saeidian via Scopus - Elsevier

Erythrokeratoderma: a manifestation associated with multiple types of ichthyoses with different gene defects

British Journal of Dermatology
2018 | Journal article
DOI: 10.1111/bjd.16053
EID:

2-s2.0-85040797801
Contributors: Youssefian, L.; Touati, A.; Vahidnezhad, H.; Saeidian, A.H.; Sotoudeh, S.; Zeinali, S.; Uitto, J.
Source: Self-asserted source
Amir Hossein Saeidian via Scopus - Elsevier

First report of COL7A1 mutations in two patients with recessive dystrophic epidermolysis bullosa from Peru

Clinical and Experimental Dermatology
2018 | Journal article
DOI: 10.1111/ced.13400
EID:

2-s2.0-85041499560
Contributors: Saeidian, A.H.; Youssefian, L.; Rosales-Solis, G.M.; Vahidnezhad, H.; Atanasova, V.S.; Uitto, J.; South, A.P.; Salas-Alanis, J.C.
Source: Self-asserted source
Amir Hossein Saeidian via Scopus - Elsevier

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
2018 | Journal article
DOI: 10.1002/humu.23592
EID:

2-s2.0-85052432966
Contributors: Vahidnezhad, H.; Youssefian, L.; Saeidian, A.H.; Touati, A.; Sotoudeh, S.; Jazayeri, A.; Guy, A.; Lovell, P.A.; Liu, L.; Kariminejad, A. et al.
Source: Self-asserted source
Amir Hossein Saeidian via Scopus - Elsevier

Recessive mutation in tetraspanin CD151 causes Kindler syndrome-like epidermolysis bullosa with multi-systemic manifestations including nephropathy

Matrix Biology
2018 | Journal article
DOI: 10.1016/j.matbio.2017.11.003
EID:

2-s2.0-85035090558
Contributors: Vahidnezhad, H.; Youssefian, L.; Saeidian, A.H.; Mahmoudi, H.; Touati, A.; Abiri, M.; Kajbafzadeh, A.-M.; Aristodemou, S.; Liu, L.; McGrath, J.A. et al.
Source: Self-asserted source
Amir Hossein Saeidian via Scopus - Elsevier

Seven novel COL7A1 mutations identified in patients with recessive dystrophic epidermolysis bullosa from Mexico

Clinical and Experimental Dermatology
2018 | Journal article
DOI: 10.1111/ced.13407
EID:

2-s2.0-85048993603
Contributors: Saeidian, A.H.; Youssefian, L.; Moreno Trevino, M.G.; Fortuna, G.; Vahidnezhad, H.; Atanasova, V.S.; Uitto, J.; Salas-Alanis, J.C.; South, A.P.
Source: Self-asserted source
Amir Hossein Saeidian via Scopus - Elsevier
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Peer review (25 reviews for 13 publications/grants)

Review activity for BMC medical genetics (2)
Review activity for Clinical chemistry. (5)
Review activity for Clinical, cosmetic and investigational dermatology (2)
Review activity for Dermatologic therapy. (1)
Review activity for European journal of human genetics (5)
Review activity for Expert opinion on biological therapy (1)
Review activity for Gene reports. (2)
Review activity for Genetics in medicine. (1)
Review activity for Genetics in medicine. (1)
Review activity for Human mutation. (2)
Review activity for Journal of cosmetic dermatology. (1)
Review activity for Pediatric investigation. (1)
Review activity for The application of clinical genetics (1)
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