Roman P Myasnikov (R P Myasnikov, Roman Myasnikov)

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 10

Top Venues

International journal of molecular sciences

Genes

Terapevticheskii arkhiv

Human mutation

National Research Centre for Preventive Medicine

Federal State Institution Russian Cardiology Research Complex Institute of Clinical Cardiology (PHD)

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

Affiliation History

National Research Centre for Preventive Medicine

Russia

Scientist, cardiologist

Federal State Institution Russian Cardiology Research Complex Institute of Clinical Cardiology

Russia

cardiologist

Sklifosovsky Research Institute of Emergency Care

Russia

Cardiologist :: Cardiology residence of the block of intensive therapy

Sklifosovsky Research Institute of Emergency Care

Russia

nurse :: block of intensive therapy

Education History

Federal State Institution Russian Cardiology Research Complex Institute of Clinical Cardiology Oct 01 2006 - Aug 31 2009

Russia

PHD :: Cardiology

Publications

Anna A Bukaeva, Roman P Myasnikov, Olga V Kulikova, Alexey Nikolaevich Meshkov, Anna Vitalievna Kiseleva, Anna Petukhova, Evgenia Zotova, Peter A Sparber, Alexandra Ershova, Evgeniia Sotnikova, Maria Kudryavtseva, Anastasia Zharikova, Sergey N Koretskiy, Elena Mershina, Vasily E Ramensky, Marija Zaicenoka, Yuri Vyatkin, Alisa Muraveva, Alexandra A Abisheva, Tatiana Nikityuk, Valentin E Sinitsyn, Mikhail G Divashuk, Elena Dadali, Maria Pokrovskaya, Oxana Drapkina
A Rare Coincidence of Three Inherited Diseases in a Family with Cardiomyopathy and Multiple Extracardiac Abnormalities. International journal of molecular sciences 25 (14) (2024)
Anna A Bukaeva, Roman P Myasnikov, Olga V Kulikova, Alexey Nikolaevich Meshkov, Anna Vitalievna Kiseleva, Anna Petukhova, Evgenia Zotova, Peter A Sparber, Alexandra Ershova, Evgeniia Sotnikova, Maria Kudryavtseva, Anastasia Zharikova, Sergey N Koretskiy, Elena Mershina, Vasily E Ramensky, Marija Zaicenoka, Yuri Vyatkin, Alisa Muraveva, Alexandra A Abisheva, Tatiana Nikityuk, Valentin E Sinitsyn, Mikhail G Divashuk, Elena Dadali, Maria Pokrovskaya, Oxana Drapkina
A Rare Coincidence of Three Inherited Diseases in a Family with Cardiomyopathy and Multiple Extracardiac Abnormalities. International journal of molecular sciences 25 (14) (2024)
Anna A Bukaeva, Roman P Myasnikov, Olga V Kulikova, Alexey Nikolaevich Meshkov, Anna Vitalievna Kiseleva, Anna Petukhova, Evgenia Zotova, Peter A Sparber, Alexandra Ershova, Evgeniia Sotnikova, Maria Kudryavtseva, Anastasia Zharikova, Sergey N Koretskiy, Elena Mershina, Vasily E Ramensky, Marija Zaicenoka, Yuri Vyatkin, Alisa Muraveva, Alexandra A Abisheva, Tatiana Nikityuk, Valentin E Sinitsyn, Mikhail G Divashuk, Elena Dadali, Maria Pokrovskaya, Oxana Drapkina
A Rare Coincidence of Three Inherited Diseases in a Family with Cardiomyopathy and Multiple Extracardiac Abnormalities. International journal of molecular sciences 25 (14) (2024)
Roman P Myasnikov, Olga V Kulikova, Alexey Nikolaevich Meshkov, Anna A Bukaeva, Anna Vitalievna Kiseleva, Alexandra I Ershova, Anna V Petukhova, Mikhail G Divashuk, Evgenia D Zotova, Evgeniia A Sotnikova, Alexandra A Abisheva, Alisa V Muraveva, Sergey N Koretskiy, Sergey V Popov, Marina V Utkina, Ekaterina A Snigir, Sergey I Mitrofanov, Ksenia D Konureeva, Elena A Mershina, Valentin E Sinitsyn, Sergey M Yudin, Oxana M Drapkina
A Splice Variant of the <i>MYH7</i> Gene Is Causative in a Family with Isolated Left Ventricular Noncompaction Cardiomyopathy. Genes 13 (10) (2022)
Roman P Myasnikov, Anna A Bukaeva, Olga V Kulikova, Alexey Nikolaevich Meshkov, Anna Vitalievna Kiseleva, Alexandra Ershova, Anna Petukhova, Mikhail G Divashuk, Evgenia D Zotova, Evgeniia Sotnikova, Anastasia Alexandrovna Zharikova, Anastasia Zharikova, Yuri Vyatkin, Vasily Ramensky, Alexandra A Abisheva, Alisa Muraveva, Sergey N Koretskiy, Maria Kudryavtseva, Sergey Popov, Marina Utkina, Elena Mershina, Valentin E Sinitsyn, Evgeniya Kogan, Olga Blagova, Oxana Drapkina
A Case of Severe Left-Ventricular Noncompaction Associated with Splicing Altering Variant in the FHOD3 Gene. Genes 13 (2) (2022)
Roman P Myasnikov, Andreas Brodehl, Alexey Nikolaevich Meshkov, Olga V Kulikova, Anna Vitalievna Kiseleva, Greta Marie Pohl, Evgeniia Sotnikova, Mikhail G Divashuk, Marina Vyacheslavovna Klimushina, Anastasia Zharikova, Maria Pokrovskaya, Sergey N Koretskiy, Anastasia Alexandrovna Zharikova, Elena Mershina, Valentin E Sinitsyn, Elena Basargina, Leila Gandaeva, Vladimir Barskiy, Sergey Boytsov, Hendrik Milting, Oxana Drapkina
The Double Mutation DSG2-p.S363X and TBX20-p.D278X Is Associated with Left Ventricular Non-Compaction Cardiomyopathy: Case Report. International journal of molecular sciences 22 (13) (2021)
Olga V Kulikova, Roman P Myasnikov, Elena A Mershina, P S Pilus, Sergey N Koretskiy, Alexey Nikolaevich Meshkov, Anna Vitalievna Kiseleva, Anastasia Alexandrovna Zharikova, Valentin E Sinitsyn, N A Sdvigova, L A Gandaeva, V I Barskiy, Y V Derevnina, O P Zharova, E N Basargina, Sergey A Boytsov, Oxana Mikhailovna Drapkina
[Familial left ventricular noncompaction: phenotypes and clinical course. Results of the multicenter registry]. Terapevticheskii arkhiv 93 (4) (2021)
Olga V Kulikova, Andreas Brodehl, Anna Vitalievna Kiseleva, Roman P Myasnikov, Alexey Nikolaevich Meshkov, Caroline Stanasiuk, Anna Gärtner, Mikhail G Divashuk, Evgeniia Andreevna Sotnikova, Sergey Koretskiy, Anastasia Alexandrovna Zharikova, Viktoria Kozlova, Elena A Mershina, Polina Pilus, Valentin E Sinitsyn, Hendrik Milting, Sergey Boytsov, Oksana M Drapkina
The Desmin (DES) Mutation p.A337P Is Associated with Left-Ventricular Non-Compaction Cardiomyopathy. Genes 12 (1) (2021)
Andreas Brodehl, Alexey Nikolaevich Meshkov, Roman P Myasnikov, Anna Vitalievna Kiseleva, Olga V Kulikova, Bärbel Klauke, Evgeniia Sotnikova, Caroline Stanasiuk, Mikhail G Divashuk, Greta Marie Pohl, Maria Kudryavtseva, Karin Klingel, Brenda Gerull, Anastasia Zharikova, Jan Gummert, Sergey N Koretskiy, Stephan Schubert, Elena A Mershina, Anna Gärtner, Polina Pilus, Kai Thorsten Laser, Valentin E Sinitsyn, Sergey Boytsov, Oksana M Drapkina, Hendrik Milting
Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset. International journal of molecular sciences 22 (7) (2021)
Andrey A Marakhonov, Andreas Brodehl, Roman P Myasnikov, Peter A Sparber, Anna V Kiseleva, Olga V Kulikova, Alexey N Meshkov, Anastasia A Zharikova, Serguey N Koretsky, Anastasia Alexandrovna Zharikova, Caroline Stanasiuk, Elena A Mershina, Valentin E Sinitsyn, Alexey O Shevchenko, Natalia P Mozheyko, Oksana M Drapkina, Sergey A Boytsov, Andreas Brodehl, Mikhail Yurevich Skoblov
Noncompaction cardiomyopathy is caused by a novel in-frame desmin (DES) deletion mutation within the 1A coiled-coil rod segment leading to a severe filament assembly defect. Human mutation 40 (6) (2019)

Roman P Myasnikov.css-eqlu8i{font-size:small;padding-left:4px;} (R P Myasnikov, Roman Myasnikov)

Publication Activity (10 Years)

Top Topics

Top Venues

Roman P Myasnikov (R P Myasnikov, Roman Myasnikov)