Anna Mikhailov

607 total citations
16 papers, 194 citations indexed

About

Anna Mikhailov is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Anna Mikhailov has authored 16 papers receiving a total of 194 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 9 papers in Molecular Biology and 6 papers in Cognitive Neuroscience. Recurrent topics in Anna Mikhailov's work include Genetics and Neurodevelopmental Disorders (9 papers), Autism Spectrum Disorder Research (6 papers) and Genomic variations and chromosomal abnormalities (4 papers). Anna Mikhailov is often cited by papers focused on Genetics and Neurodevelopmental Disorders (9 papers), Autism Spectrum Disorder Research (6 papers) and Genomic variations and chromosomal abnormalities (4 papers). Anna Mikhailov collaborates with scholars based in Canada, Pakistan and United Kingdom. Anna Mikhailov's co-authors include John B. Vincent, Abdul Noor, Christian Windpassinger, Anath C. Lionel, Muhammad Ayub, Katharina M. Roetzer, Erwin Petek, Stephen W. Scherer, Wolfgang Kaschnitz and Christian R. Marshall and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Scientific Reports.

In The Last Decade

Anna Mikhailov

14 papers receiving 192 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Anna Mikhailov Canada	7	104	102	40	24	22	16	194
Eike Wegener Germany	6	104 1.0×	116 1.1×	57 1.4×	19 0.8×	30 1.4×	7	210
Shujie Yu China	8	106 1.0×	113 1.1×	22 0.6×	26 1.1×	21 1.0×	14	202
Daji Guo China	10	70 0.7×	123 1.2×	51 1.3×	44 1.8×	36 1.6×	15	254
Hyojin Kim United States	9	94 0.9×	128 1.3×	36 0.9×	40 1.7×	23 1.0×	14	231
Emmanuelle Lagrue France	8	79 0.8×	110 1.1×	41 1.0×	64 2.7×	9 0.4×	20	229
Elly Lewerissa Netherlands	7	90 0.9×	135 1.3×	41 1.0×	50 2.1×	11 0.5×	9	228
Nicholas Rajan Belgium	8	98 0.9×	213 2.1×	39 1.0×	32 1.3×	31 1.4×	12	256
Marianna De Franceschi Italy	6	265 2.5×	201 2.0×	46 1.1×	58 2.4×	28 1.3×	6	380
Sonia Amabile Italy	6	156 1.5×	148 1.5×	33 0.8×	29 1.2×	20 0.9×	12	242

Countries citing papers authored by Anna Mikhailov

Since Specialization

Citations

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

Fields of papers citing papers by Anna Mikhailov

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Mikhailov

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

All Works

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16 of 16 papers shown

Mikhailov, Anna, et al.. (2025). Revision Interventions for Failed Proximal Interphalangeal Joint Arthroplasty: Causes and Outcomes. Traumatology and Orthopedics of Russia. 31(1). 34–42.

Mikhailov, Anna, et al.. (2024). Arthroplasty of the proximal interphalangeal joint of the hand: the current state of the problem. SHILAP Revista de lepidopterología. 30(5). 743–752. 1 indexed citations

Harripaul, Ricardo, et al.. (2024). Biallelic variants identified in 36 Pakistani families and trios with autism spectrum disorder. Scientific Reports. 14(1). 9230–9230. 1 indexed citations

Kim, Bo‐Hyun, Anna Mikhailov, Robert L. Chow, et al.. (2024). Testing the PEST hypothesis using relevant Rett mutations in MeCP2 E1 and E2 isoforms. Human Molecular Genetics. 33(21). 1833–1845. 1 indexed citations

Harripaul, Ricardo, Anna Mikhailov, Saqib Mahmood, et al.. (2022). Biallelic Loss of Function Mutation in Sodium Channel Gene SCN10A in an Autism Spectrum Disorder Trio from Pakistan. Genes. 13(9). 1633–1633. 1 indexed citations

Shah, Abdul Haleem, Ricardo Harripaul, Anna Mikhailov, et al.. (2021). Mutation Analysis of a Pakistani Oculocutaneous Albinism Family Identifies a Novel Splice Site Defect in OCA2 Gene. Pakistan Journal of Zoology. 54(3). 1 indexed citations

Epp, Jonathan R., Kirti Mittal, Taimoor I. Sheikh, et al.. (2019). Ptchd1 exon3 truncating mutations recapitulate more clinically relevant autistic-like traits in mice. IBRO Reports. 6. S507–S507. 1 indexed citations

Shah, Abdul Haleem, Ricardo Harripaul, Anna Mikhailov, et al.. (2019). Genetic studies of multiple consanguineous Pakistani families segregating oculocutaneous albinism identified novel and reported mutations. Annals of Human Genetics. 83(4). 278–284. 8 indexed citations

Harripaul, Ricardo, Anna Mikhailov, Farooq Naeem, et al.. (2017). Three Mutations in the Bilateral Frontoparietal Polymicrogyria Gene GPR56 in Pakistani Intellectual Disability Families. Journal of Pediatric Genetics. 7(2). 60–66. 12 indexed citations

10.

Vasli, Nasim, Kirti Mittal, Anna Mikhailov, et al.. (2015). Identification of a homozygous missense mutation in LRP2 and a hemizygous missense mutation in TSPYL2 in a family with mild intellectual disability. Psychiatric Genetics. 26(2). 66–73. 17 indexed citations

11.

Mittal, Kirti, Taimoor I. Sheikh, Nasim Vasli, et al.. (2014). Identification of a homozygous splice site mutation in the dynein axonemal light chain 4 gene on 22q13.1 in a large consanguineous family from Pakistan with congenital mirror movement disorder. Human Genetics. 133(11). 1419–1429. 18 indexed citations

12.

Mir, Asif, Kirti Mittal, Nasim Vasli, et al.. (2014). Truncation of the E3 ubiquitin ligase component FBXO31 causes non-syndromic autosomal recessive intellectual disability in a Pakistani family. Human Genetics. 133(8). 975–984. 17 indexed citations

13.

Orlic-Milacic, M, Anna Mikhailov, Aaron Cheung, et al.. (2014). Over-Expression of Either MECP2_e1 or MECP2_e2 in Neuronally Differentiated Cells Results in Different Patterns of Gene Expression. PLoS ONE. 9(4). e91742–e91742. 16 indexed citations

14.

Roetzer, Katharina M., Abdul Noor, Anath C. Lionel, et al.. (2014). Identification of risk genes for autism spectrum disorder through copy number variation analysis in Austrian families. Neurogenetics. 15(2). 117–127. 90 indexed citations

15.

Mikhailov, Anna, et al.. (2013). Screening of NLGN3 and NLGN4X genes in Thai children with autism spectrum disorder. Psychiatric Genetics. 24(1). 42–43. 6 indexed citations

16.

Noor, Abdul, Christian Windpassinger, Anna Mikhailov, et al.. (2008). CC2D2A, Encoding A Coiled-Coil and C2 Domain Protein, Causes Autosomal-Recessive Mental Retardation with Retinitis Pigmentosa. The American Journal of Human Genetics. 83(5). 656–656. 4 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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