Tatiana Vladimirovna Markova (Tatiana Markova, T V Markova, Tatiana V Markova, Tatyana Markova)

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 17

Top Topics

Postmenopausal Women

Top Venues

International journal of molecular sciences

Molecular genetics & genomic medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Elena S Merkuryeva, Tatiana Vladimirovna Markova, Vladimir M Kenis, Olga E Agranovich, Ivan M Dan, Yulia Y Kotalevskaya, Olga A Shchagina, Oxana P Ryzhkova, Sergei S Fomenko, Elena L Dadali, Sergey I Kutsev
Presentation of Rare Phenotypes Associated with the FKBP10 Gene. Genes 15 (6) (2024)
Elena S Merkuryeva, Tatiana Vladimirovna Markova, Vladimir M Kenis, Olga E Agranovich, Ivan M Dan, Yulia Y Kotalevskaya, Olga A Shchagina, Oxana P Ryzhkova, Sergei S Fomenko, Elena L Dadali, Sergey I Kutsev
Presentation of Rare Phenotypes Associated with the FKBP10 Gene. Genes 15 (6) (2024)
Elena S Merkuryeva, Tatiana Vladimirovna Markova, Vladimir M Kenis, Olga E Agranovich, Ivan M Dan, Yulia Y Kotalevskaya, Olga A Shchagina, Oxana P Ryzhkova, Sergei S Fomenko, Elena L Dadali, Sergey I Kutsev
Presentation of Rare Phenotypes Associated with the FKBP10 Gene. Genes 15 (6) (2024)
Elena S Merkuryeva, Tatiana Vladimirovna Markova, Anton Tyurin, Diana Valeeva, Vladimir Kenis, Maria Sumina, Igor Sorokin, Olga A Shchagina, Mikhail Yurevich Skoblov, Maria Nefedova, Rita Khusainova, Ekaterina Zakharova, Elena Dadali, Sergey Kutsev
Clinical and Genetic Characteristics of Calvarial Doughnut Lesions with Bone Fragility in Three Families with a Reccurent SGMS2 Gene Variant. International journal of molecular sciences 24 (9) (2023)
Elena S Merkuryeva, Tatiana Vladimirovna Markova, Anton Tyurin, Diana Valeeva, Vladimir Kenis, Maria Sumina, Igor Sorokin, Olga A Shchagina, Mikhail Yurevich Skoblov, Maria Nefedova, Rita Khusainova, Ekaterina Zakharova, Elena Dadali, Sergey Kutsev
Clinical and Genetic Characteristics of Calvarial Doughnut Lesions with Bone Fragility in Three Families with a Reccurent SGMS2 Gene Variant. International journal of molecular sciences 24 (9) (2023)
Margarita Sharova, Tatiana Vladimirovna Markova, Maria Sumina, Marina Petukhova, Maria Bulakh, Oxana P Ryzhkova, Tatyana Nagornova, Sofya A Ionova, Andrey A Marakhonov, Elena Dadali, Sergey Kutsev
Rare IFT140-Associated Phenotype of Cranioectodermal Dysplasia and Features of Diagnostic Journey in Patients with Suspected Ciliopathies. Genes 14 (8) (2023)
Anton Tyurin, Elena Merkuryeva, Aliya Zaripova, Tatiana Vladimirovna Markova, Tatyana Nagornova, Ilya Dantsev, Dina Nadyrshina, Ekaterina Zakharova, Rita Khusainova
Does the c.-14C>T Mutation in the IFITM5 Gene Provide Identical Phenotypes for Osteogenesis Imperfecta Type V? Data from Russia and a Literature Review. Biomedicines 10 (10) (2022)
Olga Levchenko, Elena Dadali, Ludmila Bessonova, Nina Demina, Galina Rudenskaya, Galina Matyushchenko, Tatiana Vladimirovna Markova, Inga Anisimova, Natalia Semenova, Olga A Shchagina, Oxana Ryzhkova, Rena A Zinchenko, Varvara Galkina, Victoria Voinova, Sabina Nagieva, Alexander Lavrov
Complex Diagnostics of Non-Specific Intellectual Developmental Disorder. International journal of molecular sciences 23 (14) (2022)
Olga Mironovich, Nailya Galeeva, Anna Stepanova, Tatiana Markova, Maria Lalayants, Natalia Alekseeva, George Tavarkiladze, Tatiana Vladimirovna Markova, Liudmila Bessonova, Marina Petukhova, Daria Guseva, Inga Anisimova, Alexander Polyakov, Oxana P Ryzhkova, Elena Bliznetz
Spectrum of Genes for Non- GJB2 -Related Non-Syndromic Hearing Loss in the Russian Population Revealed by a Targeted Deafness Gene Panel. International journal of molecular sciences 23 (24) (2022)
Olga Mironovich, Nailya Galeeva, Anna Stepanova, Tatiana Markova, Maria Lalayants, Natalia Alekseeva, George Tavarkiladze, Tatiana Vladimirovna Markova, Liudmila Bessonova, Marina Petukhova, Daria Guseva, Inga Anisimova, Alexander Polyakov, Oxana P Ryzhkova, Elena Bliznetz
Spectrum of Genes for Non- GJB2 -Related Non-Syndromic Hearing Loss in the Russian Population Revealed by a Targeted Deafness Gene Panel. International journal of molecular sciences 23 (24) (2022)
Tatiana Vladimirovna Markova, Vladimir Kenis, Evgeniy Melchenko, Darya Guseva, Darya Osipova, Nailya Galeeva, Tatiana Nagornova, Elena Leonidovna Dadali
Clinical and genetic characterization of three Russian patients with pycnodysostosis due to pathogenic variants in the CTSK gene. Molecular genetics & genomic medicine 10 (5) (2022)
Olga A Shchagina, Valeriy Fedotov, Tatiana Vladimirovna Markova, Olga Mironovich, Oksana Ryzhkova, Tatiana Fedotova, Aleksander Polyakov
Palmoplantar Keratoderma: A Molecular Genetic Analysis of Family Cases. International journal of molecular sciences 23 (17) (2022)
Olga Mironovich, Nailya Galeeva, Anna Stepanova, Tatiana Markova, Maria Lalayants, Natalia Alekseeva, George Tavarkiladze, Tatiana Vladimirovna Markova, Liudmila Bessonova, Marina Petukhova, Daria Guseva, Inga Anisimova, Alexander Polyakov, Oxana P Ryzhkova, Elena Bliznetz
Spectrum of Genes for Non- GJB2 -Related Non-Syndromic Hearing Loss in the Russian Population Revealed by a Targeted Deafness Gene Panel. International journal of molecular sciences 23 (24) (2022)
Olga Mironovich, Nailya Galeeva, Anna Stepanova, Tatiana Markova, Maria Lalayants, Natalia Alekseeva, George Tavarkiladze, Tatiana Vladimirovna Markova, Liudmila Bessonova, Marina Petukhova, Daria Guseva, Inga Anisimova, Alexander Polyakov, Oxana P Ryzhkova, Elena Bliznetz
Spectrum of Genes for Non- GJB2 -Related Non-Syndromic Hearing Loss in the Russian Population Revealed by a Targeted Deafness Gene Panel. International journal of molecular sciences 23 (24) (2022)
Tatiana Vladimirovna Markova, Vladimir Kenis, Evgenii Melchenko, Aynur Alieva, Tatiana Nagornova, Anna A Orlova, Natalya Ogorodova, Olga A Shchagina, Alexander Polyakov, Elena Dadali, Sergey Kutsev
Clinical and Genetic Characteristics of Multiple Epiphyseal Dysplasia Type 4. Genes 13 (9) (2022)
Tatiana Vladimirovna Markova, Peter A Sparber, Artem Borovikov, Tatiana Nagornova, Elena Dadali
Clinical and genetic characterization of autosomal recessive stickler syndrome caused by novel compound heterozygous mutations in the COL9A3 gene. Molecular genetics & genomic medicine 9 (3) (2021)
G E Rudenskaya, V A Kadnikova, Oxana P Ryzhkova, L A Bessonova, E L Dadali, Daria Guseva, Tatiana Vladimirovna Markova, D N Khmelkova, Olga A Shchagina
KIF1A-related autosomal dominant spastic paraplegias (SPG30) in Russian families. BMC neurology 20 (1) (2020)