Dmitriy Niyazov

2.0k total citations
8 papers, 208 citations indexed

About

Dmitriy Niyazov is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, Dmitriy Niyazov has authored 8 papers receiving a total of 208 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Rheumatology. Recurrent topics in Dmitriy Niyazov's work include Genetics and Neurodevelopmental Disorders (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Amino Acid Enzymes and Metabolism (1 paper). Dmitriy Niyazov is often cited by papers focused on Genetics and Neurodevelopmental Disorders (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Amino Acid Enzymes and Metabolism (1 paper). Dmitriy Niyazov collaborates with scholars based in United States, Canada and Australia. Dmitriy Niyazov's co-authors include Lindsay B. Henderson, Carolyn Applegate, Hans T. Björnsson, Berivan Baskin, Megan T. Cho, Mark A. Tarnopolsky, Meron Azage, Wendy K. Chung, Volkan Okur and Jonathan Picker and has published in prestigious journals such as Journal of Medical Genetics, Human Genetics and Molecular Genetics and Metabolism.

In The Last Decade

Dmitriy Niyazov

8 papers receiving 208 citations

Peers

Dmitriy Niyazov

MB

GENET

CB

RHEUM

SURGE

Anne‐Marie Guerrot France

Laila Mahmoud Qatar

Stephanie Demuth Germany

Minal Menezes Australia

Jūratė Kasnauskienė Lithuania

Naomi Meeks United States

Amber Begtrup United States

Benjamin Kamien Australia

Nicolas Chatron France

Julie Kaylor United States

Anne‐Marie Guerrot France

Dmitriy Niyazov

136 ×1.0

MB

84 ×0.8

GENET

12 ×0.3

CB

18 ×1.4

RHEUM

11 ×0.8

SURGE

Citations per year, relative to Dmitriy Niyazov Dmitriy Niyazov (= 1×) peers Anne‐Marie Guerrot

Countries citing papers authored by Dmitriy Niyazov

Since Specialization

Citations

This map shows the geographic impact of Dmitriy Niyazov's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Dmitriy Niyazov with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Dmitriy Niyazov more than expected).

Fields of papers citing papers by Dmitriy Niyazov

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dmitriy Niyazov. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Dmitriy Niyazov. The network helps show where Dmitriy Niyazov may publish in the future.

Co-authorship network of co-authors of Dmitriy Niyazov

This figure shows the co-authorship network connecting the top 25 collaborators of Dmitriy Niyazov. A scholar is included among the top collaborators of Dmitriy Niyazov based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Dmitriy Niyazov. Dmitriy Niyazov is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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8 of 8 papers shown

1.

McCarthy, John, Chun‐An Chen, Jane C. Edmond, et al.. (2020). Phenotypic expansion of Bosch–Boonstra–Schaaf optic atrophy syndrome and further evidence for genotype–phenotype correlations. American Journal of Medical Genetics Part A. 182(6). 1426–1437. 25 indexed citations

2.

Gistelinck, Charlotte, MaryAnn Weis, Jyoti Rai, et al.. (2020). Abnormal Bone Collagen Cross‐Linking in Osteogenesis Imperfecta/Bruck Syndrome Caused by Compound Heterozygous PLOD2 Mutations. JBMR Plus. 5(3). e10454–e10454. 21 indexed citations

3.

Okur, Volkan, Katrin Watschinger, Dmitriy Niyazov, et al.. (2019). Biallelic variants in AGMO with diminished enzyme activity are associated with a neurodevelopmental disorder. Human Genetics. 138(11-12). 1259–1266. 11 indexed citations

4.

Todd, Joshua J., Jessica W. Witherspoon, Tokunbor A. Lawal, et al.. (2018). Novel Variants in Individuals with RYR1-Related Congenital Myopathies: Genetic, Laboratory, and Clinical Findings. Frontiers in Neurology. 9. 118–118. 11 indexed citations

5.

Niyazov, Dmitriy, et al.. (2018). Improvement in Cardiac Function With Enzyme Replacement Therapy in a Patient With Infantile-Onset Pompe Disease. Ochsner Journal. 18(4). 413–416. 3 indexed citations

6.

Pilarowski, Genay, Hilary J. Vernon, Carolyn Applegate, et al.. (2017). Missense variants in the chromatin remodeler CHD1 are associated with neurodevelopmental disability. Journal of Medical Genetics. 55(8). 561–566. 38 indexed citations

7.

Okur, Volkan, Megan T. Cho, Lindsay B. Henderson, et al.. (2016). De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features. Human Genetics. 135(7). 699–705. 53 indexed citations

8.

Parikh, Sumit, Amel Karaa, Amy Goldstein, et al.. (2016). Solid organ transplantation in primary mitochondrial disease: Proceed with caution. Molecular Genetics and Metabolism. 118(3). 178–184. 46 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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