Vlad Makarov

2.5k total citations
5 papers, 420 citations indexed

About

Vlad Makarov is a scholar working on Genetics, Molecular Biology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Vlad Makarov has authored 5 papers receiving a total of 420 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 1 paper in Molecular Biology and 1 paper in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Vlad Makarov's work include Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetic Associations and Epidemiology (3 papers). Vlad Makarov is often cited by papers focused on Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetic Associations and Epidemiology (3 papers). Vlad Makarov collaborates with scholars based in United States. Vlad Makarov's co-authors include Iuliana Ionita‐Laza, Joseph D. Buxbaum, Xihong Lin, Seunggeun Lee, Bin Xu, Joseph A. Gogos, Maria Karayiorgou, Johannes L. Roos, Benjamin A. Raby and Seungtai Yoon and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Cancer Research and The American Journal of Human Genetics.

In The Last Decade

Vlad Makarov

5 papers receiving 418 citations

Peers

Vlad Makarov

GENET

MB

EPIDE

CN

PHYSI

Ho‐Ming Luk China

Berta Almoguera Spain

Caleb Bupp United States

Ramin Badii Qatar

Redouane Boulouiz Morocco

Julie Scuffins United States

Júlia Baptista United Kingdom

Amal Hashem Saudi Arabia

Tracy Dudding‐Byth Australia

Fernando Santos Spain

Ho‐Ming Luk China

Vlad Makarov

267 ×0.9

GENET

249 ×1.2

MB

22 ×0.8

EPIDE

14 ×0.6

CN

19 ×0.9

PHYSI

Citations per year, relative to Vlad Makarov Vlad Makarov (= 1×) peers Ho‐Ming Luk

Countries citing papers authored by Vlad Makarov

Since Specialization

Citations

This map shows the geographic impact of Vlad Makarov'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 Vlad Makarov with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Vlad Makarov more than expected).

Fields of papers citing papers by Vlad Makarov

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Vlad Makarov. 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 Vlad Makarov. The network helps show where Vlad Makarov may publish in the future.

Co-authorship network of co-authors of Vlad Makarov

This figure shows the co-authorship network connecting the top 25 collaborators of Vlad Makarov. A scholar is included among the top collaborators of Vlad Makarov 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 Vlad Makarov. Vlad Makarov is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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5 of 5 papers shown

1.

Alban, Tyler, Nadeem Riaz, Vlad Makarov, et al.. (2023). Abstract 1125: Neoantigen immunogenicity landscapes and evolution of tumor ecosystems during immunotherapy with nivolumab. Cancer Research. 83(7_Supplement). 1125–1125. 1 indexed citations

2.

Ionita‐Laza, Iuliana, Seunggeun Lee, Vlad Makarov, Joseph D. Buxbaum, & Xihong Lin. (2013). Sequence Kernel Association Tests for the Combined Effect of Rare and Common Variants. The American Journal of Human Genetics. 92(6). 841–853. 285 indexed citations

3.

Ionita‐Laza, Iuliana, Bin Xu, Vlad Makarov, et al.. (2013). Scan statistic-based analysis of exome sequencing data identifies FAN1 at 15q13.3 as a susceptibility gene for schizophrenia and autism. Proceedings of the National Academy of Sciences. 111(1). 343–348. 56 indexed citations

4.

Ionita‐Laza, Iuliana, Vlad Makarov, & Joseph D. Buxbaum. (2012). Scan-Statistic Approach Identifies Clusters of Rare Disease Variants in LRP2, a Gene Linked and Associated with Autism Spectrum Disorders, in Three Datasets. The American Journal of Human Genetics. 90(6). 1002–1013. 41 indexed citations

5.

Ionita‐Laza, Iuliana, Vlad Makarov, Seungtai Yoon, et al.. (2011). Finding Disease Variants in Mendelian Disorders By Using Sequence Data: Methods and Applications. The American Journal of Human Genetics. 89(6). 701–712. 37 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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