ИСТИНА

Milting Hendrik

Соавторы: Brodehl A., Корецкий С.Н., Мершина Е.А., Мешков А.Н., Мясников Р.П., Синицын В.Е., Stanasiuk C., Дивашук М.Г., ДРАПКИНА О.М., Жарикова А.А., Куликова О.В., Пилюс П.С., Харлап М.С. показать полностью..., Boytsov S.A., Gerull B., Gummert J., Klingel K., Laser K.T., Pohl G.M., Stein S.E., Киселева А.А., Сотникова Е.А., BARSKIY V., Drapkina O.M., Gärtner A., Gärtner A., Gärtner A., Klauke B., Klauke B., Klimushina M.V., Kudryavtseva M., Maris P., Pokrovskaya M.S., Skoblov M.Y., Sotnikova E.A., Sparber P.A., Басаргина Е.Н., Бойцов С.А., Жарикова А.В., Киселева А.А., Киселева А.В., Куликова О.Г., Марахонов А.В., Можейко Н.П., Шевченко А.О.

5 статей

Количество цитирований статей в журналах по данным Web of Science: 19, Scopus: 31

IstinaResearcherID (IRID): 188266368

Деятельность

• Статьи в журналах

  • 
    • 2021 Hemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset
    • Brodehl Andreas, Meshkov Alexey, Myasnikov Roman, Kiseleva Anna, Kulikova Olga, Klauke Bärbel, Sotnikova Evgeniia, Stanasiuk Caroline, Divashuk Mikhail, Pohl Greta Marie, Kudryavtseva Maria, Klingel Karin, Gerull Brenda, Zharikova Anastasia, Gummert Jan, Koretskiy Sergey, Schubert Stephan, Mershina Elena, Gärtner Anna, Pilus Polina, Laser Kai Thorsten, Sinitsyn Valentin, Boytsov Sergey, Drapkina Oxana, Milting Hendrik
    • в журнале International Journal of Molecular Sciences, издательство MDPI (Basel, Switzerland), том 22, № 7 DOI
  • 
    • 2021 Hemi- and homozygous loss-of-function mutations in DSG2 (Desmoglein-2) cause recessive arrhythmogenic cardiomyopathy with an early onset
    • Brodehl Andreas, Meshkov Alexey, Myasnikov Roman, Kiseleva Anna, Kulikova Olga, Klauke Bärbel, Sotnikova Evgeniia, Stanasiuk Caroline, Divashuk Mikhail, Pohl Greta Marie, Kudryavtseva Maria, Klingel Karin, Gerull Brenda, Zharikova Anastasia, Gummert Jan, Koretskiy Sergey, Schubert Stephan, Mershina Elena, Gärtner Anna, Pilus Polina, Laser Kai Thorsten, Sinitsyn Valentin, Boytsov Sergey, Drapkina Oxana, Milting Hendrik
    • в журнале International Journal of Molecular Sciences, издательство MDPI (Basel, Switzerland), том 22, № 7, с. 1-15 DOI
  • 
    • 2021 The Desmin (DES) Mutation p.A337P Is Associated with Left-Ventricular Non-Compaction Cardiomyopathy
    • Kulikova Olga, Brodehl Andreas, Kiseleva Anna, Myasnikov Roman, Meshkov Alexey, Stanasiuk Caroline, Gärtner Anna, Divashuk Mikhail, Sotnikova Evgeniia, Koretskiy Sergey, Kharlap Maria, Kozlova Viktoria, Mershina Elena, Pilus Polina, Sinitsyn Valentin, Milting Hendrik, Boytsov Sergey, Drapkina Oxana
    • в журнале Genes, издательство MDPI (Basel, Switzerland), том 12, № 1, с. 1-13 DOI
  • 
    • 2021 The Double Mutation DSG2-p.S363X and TBX20-p.D278X Is Associated with Left Ventricular Non-Compaction Cardiomyopathy: Case Report
    • Myasnikov Roman, Brodehl Andreas, Meshkov Alexey, Kulikova Olga, Kiseleva Anna, Pohl Greta Marie, Sotnikova Evgeniia, Divashuk Mikhail, Klimushina Marina, Zharikova Anastasia, Pokrovskaya Maria, Koretskiy Sergey, Kharlap Maria, Mershina Elena, Sinitsyn Valentin, Basargina Elena, Gandaeva Leila, Barskiy Vladimir, Boytsov Sergey, Milting Hendrik, Drapkina Oxana
    • в журнале International Journal of Molecular Sciences, издательство MDPI (Basel, Switzerland), том 22, № 13 DOI
  • 
    • 2019 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
    • Marakhonov Andrey V., Brodehl Andreas, Myasnikov Roman P., Sparber Peter A., Kiseleva Anna V., Kulikova Olga V., Meshkov Alexey N., Zharikova Anastasia A., Koretsky Serguey N., Kharlap Maria S., Stanasiuk Caroline, Mershina Elena A., Sinitsyn Valentin E., Shevchenko Alexey O., Mozheyko Natalia P., Drapkina Oksana M., Boytsov Sergey A., Milting Hendrik, Skoblov Mikhail Yu
    • в журнале Human Mutation, издательство John Wiley & Sons Inc. (United States), том 40, № 6, с. 734-741 DOI