M. Maheshwari

1.8k total citations
6 papers, 359 citations indexed

About

M. Maheshwari is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, M. Maheshwari has authored 6 papers receiving a total of 359 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 2 papers in Genetics and 1 paper in Cellular and Molecular Neuroscience. Recurrent topics in M. Maheshwari's work include Genetics and Neurodevelopmental Disorders (2 papers), Amino Acid Enzymes and Metabolism (1 paper) and Genetic Syndromes and Imprinting (1 paper). M. Maheshwari is often cited by papers focused on Genetics and Neurodevelopmental Disorders (2 papers), Amino Acid Enzymes and Metabolism (1 paper) and Genetic Syndromes and Imprinting (1 paper). M. Maheshwari collaborates with scholars based in United States, Czechia and India. M. Maheshwari's co-authors include Chunyu Liu, Sevilla D. Detera‐Wadleigh, Richard A. Gibbs, Elliot S. Gershon, Judith A. Badner, Susan L. Christian, Eiji Hattori, Tom I. Bonner, Manju Ghosh and Shivaram Shastri and has published in prestigious journals such as The American Journal of Human Genetics, BMC Genomics and Human Mutation.

In The Last Decade

M. Maheshwari

6 papers receiving 346 citations

Peers

M. Maheshwari

MB

GENET

PMH

BIOCH

SS

Yasuo Kajimoto Japan

Mengchen Ye United States

Steinunn Gunnarsdottir Iceland

Claudia B. Leichtlein New Zealand

Veronica Musante Italy

Melissa Moholt-Siebert United States

Wenying Jin China

Lina Issa Germany

A. Christoforou United Kingdom

Shaomin Zhu China

Yasuo Kajimoto Japan

M. Maheshwari

251 ×1.2

MB

43 ×0.3

GENET

64 ×0.9

PMH

12 ×0.2

BIOCH

27 ×0.5

SS

Citations per year, relative to M. Maheshwari M. Maheshwari (= 1×) peers Yasuo Kajimoto

Countries citing papers authored by M. Maheshwari

Since Specialization

Citations

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

Fields of papers citing papers by M. Maheshwari

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Maheshwari

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

All Works

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6 of 6 papers shown

1.

Maheshwari, M., Jiajun Shi, Judith A. Badner, et al.. (2009). Common and rare variants of DAOA in bipolar disorder. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 150B(7). 960–966. 10 indexed citations

2.

Detera‐Wadleigh, Sevilla D., Chunyu Liu, M. Maheshwari, et al.. (2007). Sequence variation in DOCK9 and heterogeneity in bipolar disorder. Psychiatric Genetics. 17(5). 274–286. 33 indexed citations

3.

Maheshwari, M., et al.. (2003). Screening of families with autosomal recessive non‐syndromic hearing impairment (ARNSHI) for mutations in GJB2 gene: Indian scenario. American Journal of Medical Genetics Part A. 120A(2). 180–184. 55 indexed citations

4.

Hattori, Eiji, Chunyu Liu, Judith A. Badner, et al.. (2003). Polymorphisms at the G72/G30 Gene Locus, on 13q33, Are Associated with Bipolar Disorder in Two Independent Pedigree Series*. The American Journal of Human Genetics. 72(5). 1131–1140. 197 indexed citations

5.

Maheshwari, M., et al.. (2002). Mutation screening of two candidate genes from 13q32 in families affected with Bipolar disorder: human peptide transporter (SLC15A1) and human glypican5 (GPC5). BMC Genomics. 3(1). 30–30. 5 indexed citations

6.

Maheshwari, M., John W. Belmont, Rth Ho, et al.. (2002). PTPN11 Mutations in Noonan syndrome type I: detection of recurrent mutations in exons 3 and 13. Human Mutation. 20(4). 298–304. 59 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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