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De novo nonsense mutation in WHSC1 (NSD2) in patient with intellectual disability and dysmorphic features

Journal of human genetics, 2018-07, Vol.63 (8), p.919-922

2018

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Expanding the phenotype of CRYAA nucleotide variants to a complex presentation of anterior segment dysgenesis

Orphanet journal of rare diseases, 2020-08, Vol.15 (1), p.1-207, Article 207

2020

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Genetic Variant c.245A>G (p.Asn82Ser) in GIPC3 Gene Is a Frequent Cause of Hereditary Nonsyndromic Sensorineural Hearing Loss in Chuvash Population

Genes, 2021-05, Vol.12 (6), p.820

2021

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Primary microcephaly case from the Karachay-Cherkess Republic poses an additional support for microcephaly and Seckel syndrome spectrum disorders

BMC medical genomics, 2018-02, Vol.11 (Suppl 1), p.8-8, Article 8

2018

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Molecular markers based on LTR retrotransposons BARE-1 and Jeli uncover different strata of evolutionary relationships in diploid wheats

Molecular genetics and genomics : MGG, 2010-06, Vol.283 (6), p.551-563

2010

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Genetic diversity, distribution and domestication history of the neglected GGAtAt genepool of wheat

Theoretical and applied genetics, 2022-03, Vol.135 (3), p.755-776

2022

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Autosomal recessive cataract (CTRCT18) in the Yakut population isolate of Eastern Siberia: a novel founder variant in the FYCO1 gene

European journal of human genetics : EJHG, 2021-06, Vol.29 (6), p.965-976

2021

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Correction to: Genetic diversity, distribution and domestication history of the neglected GGAtAt genepool of wheat

Theoretical and applied genetics, 2021-10, Vol.134 (10), p.3493-3493

2021

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Mutation in PHACTR1 associated with multifocal epilepsy with infantile spasms and hypsarrhythmia

Clinical genetics, 2021-05, Vol.99 (5), p.673-683

2021

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Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles

Journal of investigative dermatology, 2016-06, Vol.136 (6), p.1097-1105

2016

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Analysis of genetic diversity and evolutionary relationships among hexaploid wheats Triticum L. using LTR-retrotransposon-based molecular markers

Genetic resources and crop evolution, 2018, Vol.65 (1), p.187-198

2018

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Ataxia with Oculomotor Apraxia Type 4 with PNKP Common “Portuguese” and Novel Mutations in Two Belarusian Families

Journal of pediatric genetics (Birmingham, Ala.), 2019-06, Vol.8 (2), p.058-062

2019

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Intrafamilial Phenotypic Variability of Collagen VI-Related Myopathy Due to a New Mutation in the COL6A1 Gene

Journal of neuromuscular diseases, 2021-01, Vol.8 (2), p.273-285

2021

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Long terminal repeat retrotransposon Jeli provides multiple genetic markers for common wheat (Triticum aestivum)

Plant genetic resources: characterization and utilization, 2011-07, Vol.9 (2), p.163-165

2011

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Correction to: Genetic diversity, distribution and domestication history of the neglected GGA.sup.tA.sup.t genepool of wheat

Theoretical and applied genetics, 2021-10, Vol.134 (10), p.3493

2021

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Genetic diversity, distribution and domestication history of the neglected GGA.sup.tA.sup.t genepool of wheat

Theoretical and applied genetics, 2022-03, Vol.135 (3), p.755

2022

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Genetic diversity, distribution and domestication history of the neglected GGA t A t genepool of wheat

Theoretical and applied genetics, 2022-03, Vol.135 (3), p.755

2022

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Conserved microRNAs and Flipons Shape Gene Expression during Development by Altering Promoter Conformations

International journal of molecular sciences, 2023-03, Vol.24 (5), p.4884

2023

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Secret Agency of the Provincial Gendarmerie at the Beginning of the 20th Century (on the Materials of the Vologda Provincial Gendarme Department)

Historia provinciae - žurnal regionalʹnoj istorii, 2019-03, Vol.3 (1), p.86-145

Konovalov, Fedor

2019

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Ruthenium-catalyzed nucleophilic fluorination of halobenzenes

Chemical communications (Cambridge, England), 2015-01, Vol.51 (70), p.13527-13530

2015

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The Trifluoromethyl Anion

Angewandte Chemie (International ed.), 2015-12, Vol.54 (50), p.15289-15293

International ed. in English, 2015

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Alloying Elements Effect on the Recrystallization Process in Magnesium-Rich Aluminum Alloy

Materials, 2022-10, Vol.15 (20), p.7062

2022

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Case Report: Complicated Molecular Diagnosis of MECP2 Gene Structural Rearrangement in a Proband with Rett Syndrome

Journal of autism and developmental disorders, 2021-06, Vol.51 (6), p.2159-2163

2021

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Complex Transposon Insertion as a Novel Cause of Pompe Disease

International journal of molecular sciences, 2021-10, Vol.22 (19), p.10887

2021

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Biallelic MFSD2A variants associated with congenital microcephaly, developmental delay, and recognizable neuroimaging features

European journal of human genetics : EJHG, 2020-11, Vol.28 (11), p.1509-1519

2020

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De novo nonsense mutation in WHSC1 (NSD2) in patient with intellectual disability and dysmorphic features

Expanding the phenotype of CRYAA nucleotide variants to a complex presentation of anterior segment dysgenesis

Genetic Variant c.245A>G (p.Asn82Ser) in GIPC3 Gene Is a Frequent Cause of Hereditary Nonsyndromic Sensorineural Hearing Loss in Chuvash Population

Primary microcephaly case from the Karachay-Cherkess Republic poses an additional support for microcephaly and Seckel syndrome spectrum disorders

Molecular markers based on LTR retrotransposons BARE-1 and Jeli uncover different strata of evolutionary relationships in diploid wheats

Genetic diversity, distribution and domestication history of the neglected GGAtAt genepool of wheat

Autosomal recessive cataract (CTRCT18) in the Yakut population isolate of Eastern Siberia: a novel founder variant in the FYCO1 gene

Correction to: Genetic diversity, distribution and domestication history of the neglected GGAtAt genepool of wheat

Mutation in PHACTR1 associated with multifocal epilepsy with infantile spasms and hypsarrhythmia

Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles

Analysis of genetic diversity and evolutionary relationships among hexaploid wheats Triticum L. using LTR-retrotransposon-based molecular markers

Ataxia with Oculomotor Apraxia Type 4 with PNKP Common “Portuguese” and Novel Mutations in Two Belarusian Families

Intrafamilial Phenotypic Variability of Collagen VI-Related Myopathy Due to a New Mutation in the COL6A1 Gene

Long terminal repeat retrotransposon Jeli provides multiple genetic markers for common wheat (Triticum aestivum)

Correction to: Genetic diversity, distribution and domestication history of the neglected GGA.sup.tA.sup.t genepool of wheat

Genetic diversity, distribution and domestication history of the neglected GGA.sup.tA.sup.t genepool of wheat

Genetic diversity, distribution and domestication history of the neglected GGA t A t genepool of wheat

Conserved microRNAs and Flipons Shape Gene Expression during Development by Altering Promoter Conformations

Secret Agency of the Provincial Gendarmerie at the Beginning of the 20th Century (on the Materials of the Vologda Provincial Gendarme Department)

Ruthenium-catalyzed nucleophilic fluorination of halobenzenes

The Trifluoromethyl Anion

Alloying Elements Effect on the Recrystallization Process in Magnesium-Rich Aluminum Alloy

Case Report: Complicated Molecular Diagnosis of MECP2 Gene Structural Rearrangement in a Proband with Rett Syndrome

Complex Transposon Insertion as a Novel Cause of Pompe Disease

Biallelic MFSD2A variants associated with congenital microcephaly, developmental delay, and recognizable neuroimaging features

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