Fedor A. Konovalov - Concepedia

Author

Fedor A. Konovalov

Research Centre for Medical Genetics ORCID

Also Known As

F A Konovalov, F. A Konovalov, F. A. Konovalov, F. Konovalov, F.A. Konovalov, F.А. Konovalov, Fedor A. Konovalov, Fedor Konovalov, Konovalov, F. A., Konovalov, Fedor A.

Publications

710

Citations

H-Index

Concepts

All Affiliations

Research Centre for Medical Genetics Lomonosov Moscow State University Pirogov Russian National Research Medical University Human Stem Cells Institute PJSC (Russia)Russian Children's Clinical Hospital

About

Fedor A. Konovalov is an author at Research Centre for Medical Genetics specializing in medicine, genetics, and genetic variation.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	316
2	Molecular Genetics	4	4	124
3	Biology	3	3	67
4	Neuroscience	2	2	90
5	Natural Sciences	1	1	44

Fedor A. Konovalov

Publications

508

Citations

H-Index

Page 1

	Year	Citations
Studying plant genome variation using molecular markers S. A. Gostimsky, Fedor A. Konovalov Russian Journal of Genetics Plant GeneticsGeneticsPlant Genome VariationGenetic VariationGenomics	2005	84
De novo truncating variants in the intronless IRF2BPL are responsible for developmental epileptic encephalopathy Frédéric Tran Mau‐Them, Laurent Guibaud, Laurence Duplomb, Genetics in Medicine Developmental BiologyIntronless Irf2bplDevelopmental Epileptic EncephalopathyGenetic DisorderGenetics	2018	57
Molecular markers based on LTR retrotransposons BARE-1 and Jeli uncover different strata of evolutionary relationships in diploid wheats Fedor A. Konovalov, Svetlana V. Goryunova, Aleksandra Shaturova, Molecular Genetics and Genomics BiologyPlant GeneticsMolecular MarkersMedicineGenetics	2010	44
Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles Nikolay V. Zernov, Mikhail Skoblov, Andrey V. Marakhonov, Journal of Investigative Dermatology Keratin 25Skin DevelopmentGeneticsWoolly HairDermatology	2016	38
De novo nonsense mutation in WHSC1 (NSD2) in patient with intellectual disability and dysmorphic features Ekaterina Lozier, Fedor A. Konovalov, Ilya Kanivets, Journal of Human Genetics Genetic DisorderGeneticsFragile X SpectrumPathologyDisease Gene Identification	2018	37
Genetic diversity, distribution and domestication history of the neglected GGAtAt genepool of wheat Fedor A. Konovalov, H. Knüpffer, Agostino Fricano, Theoretical and Applied Genetics	2021	37
Biallelic MFSD2A variants associated with congenital microcephaly, developmental delay, and recognizable neuroimaging features Marcello Scala, Geok Lin Chua, Cheen Fei Chin, European Journal of Human Genetics Biallelic Mfsd2a VariantsDevelopmental AnomalyDevelopmental BiologyBrain DevelopmentGenetic Disorder	2020	33
A CAPS marker set for mapping in linkage group III of pea (Pisum sativum L.). Fedor A. Konovalov, Eugenia Toshchakova, S. A. Gostimsky PubMed	2005	22
Complex Transposon Insertion as a Novel Cause of Pompe Disease Igor Bychkov, Galina Baydakova, Alexandra Filatova, International Journal of Molecular Sciences	2021	20
Ataxia with Oculomotor Apraxia Type 4 with PNKP Common “Portuguese” and Novel Mutations in Two Belarusian Families G. E. Rudenskaya, Andrey V. Marakhonov, Olga Shchagina, Journal of Pediatric Genetics	2019	19

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