H. Hayrapetyan

发表

ISSAID/EMQN Best Practice Guidelines for the Genetic Diagnosis of Monogenic Autoinflammatory Diseases in the Next-Generation Sequencing Era.

O. Ohara, E. Ben-Chetrit, I. Touitou, 2020, Clinical chemistry.

Infertility Causes and Pregnancy Outcome in Patients With Familial Mediterranean Fever and Controls

E. Ben-Chetrit, T. Sarkisian, H. Hayrapetyan, 2020, The Journal of Rheumatology.

Patient management and the association of less common familial Mediterranean fever symptoms with other disorders

T. Sarkisian, G. Amaryan, H. Hayrapetyan, 2013, Genetics in Medicine.

PYPAF1 nonsense mutation in a patient with an unusual autoinflammatory syndrome: role of PYPAF1 in inflammation.

S. Amselem, P. Duquesnoy, T. Sarkisian, 2006, Arthritis and rheumatism.

Familial Mediterranean fever among patients from Karabakh and the diagnostic value of MEFV gene analysis in all classically affected populations.

C. Cazeneuve, S. Amselem, J. Feingold, 2003, Arthritis and rheumatism.

The FKBP4 Gene, Encoding a Regulator of the Androgen Receptor Signaling Pathway, Is a Novel Candidate Gene for Androgen Insensitivity Syndrome

Brian J. Stevenson, L. Livshits, S. Nef, 2020, International journal of molecular sciences.

Serum amyloid A1 genotype associates with adult-onset familial Mediterranean fever in patients homozygous for mutation M694V.

C. Oberkanins, G. Kriegshäuser, T. Sarkisian, 2020, Rheumatology.

Very low frequency of the lactase persistence allele LCT-13910T in the Armenian population

C. Oberkanins, G. Kriegshäuser, T. Sarkisian, 2022, Annals of human biology.

Familial Mediterranean fever in Armenia in 2015: some interesting lessons.

E. Ben-Chetrit, T. Sarkisian, H. Hayrapetyan, 2015, Clinical and experimental rheumatology.

Comprehensive analysis of mutations in the MEFV gene reveal that the location and not the substitution type determines symptom severity in FMF

T. Sarkisian, H. Hayrapetyan, M. Moradian, 2017, Molecular genetics & genomic medicine.

Clinical and genetic heterogeneity in a large cohort of Armenian patients with late-onset familial Mediterranean fever

C. Oberkanins, G. Kriegshäuser, T. Sarkisian, 2018, Genetics in Medicine.

Is plasmapheresis a potential treatment for familial Mediterranean fever patients resistant or intolerant to colchicine?

E. Ben-Chetrit, T. Sarkisian, H. Hayrapetyan, 2017, International journal of rheumatic diseases.

MEFV and SAA1 genotype associations with clinical features of familial Mediterranean fever and amyloidosis in Armenia.

E. Ben-Chetrit, T. Sarkisian, H. Hayrapetyan, 2016, Clinical and Experimental Rheumatology.

Involvement of the Modifier Gene of a Human Mendelian Disorder in a Negative Selection Process

S. Amselem, P. Duquesnoy, J. Feingold, 2009, PloS one.

Is the country of living important in the phenotypic expression of E148Q mutation? The Armenian experience.

E. Ben-Chetrit, T. Sarkisian, H. Hayrapetyan, 2020, Clinical and Experimental Rheumatology.

PW01-033 – Phenotype – genotype in Armenian children with FMF

A. Tadevosyan, G. Amaryan, H. Hayrapetyan, 2013, Pediatric Rheumatology.

Identification and functional consequences of a recurrent NLRP12 missense mutation in periodic fever syndromes.

S. Amselem, P. Duquesnoy, T. Sarkisian, 2011, Arthritis and rheumatism.

Clinical and genetic heterogeneity in a large cohort of Armenian patients with late-onset familial Mediterranean fever

C. Oberkanins, G. Kriegshäuser, T. Sarkisian, 2018, Genetics in Medicine.