M. Bamshad

881 total citations
9 papers, 590 citations indexed

About

M. Bamshad is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, M. Bamshad has authored 9 papers receiving a total of 590 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Genetics and 1 paper in Genetics. Recurrent topics in M. Bamshad's work include Forensic and Genetic Research (4 papers), Genetic diversity and population structure (3 papers) and RNA and protein synthesis mechanisms (2 papers). M. Bamshad is often cited by papers focused on Forensic and Genetic Research (4 papers), Genetic diversity and population structure (3 papers) and RNA and protein synthesis mechanisms (2 papers). M. Bamshad collaborates with scholars based in United States, Poland and India. M. Bamshad's co-authors include W. Scott Watkins, Lynn B. Jorde, Alan R. Rogers, Alice Ward Racca, F. Steven Korte, Anita E. Beck, Michael Regnier, L. B. Jorde, Parimal Das and P. Govinda Reddy and has published in prestigious journals such as Genome Research, Human Molecular Genetics and Molecular Biology and Evolution.

In The Last Decade

M. Bamshad

9 papers receiving 562 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M. Bamshad United States	7	374	197	59	56	33	9	590
Marc Bauchet United States	6	657 1.8×	245 1.2×	47 0.8×	53 0.9×	14 0.4×	6	877
Vincenza Colonna Italy	18	311 0.8×	249 1.3×	43 0.7×	23 0.4×	44 1.3×	40	678
Saioa López United Kingdom	14	226 0.6×	186 0.9×	51 0.9×	23 0.4×	25 0.8×	25	653
Marc Pybus Spain	13	437 1.2×	308 1.6×	96 1.6×	43 0.8×	30 0.9×	24	738
Xuebin Qi China	16	533 1.4×	258 1.3×	98 1.7×	39 0.7×	31 0.9×	28	838
William Beggs United States	11	462 1.2×	296 1.5×	46 0.8×	35 0.6×	47 1.4×	18	823
Bryndís Yngvadóttir United Kingdom	13	478 1.3×	321 1.6×	33 0.6×	17 0.3×	29 0.9×	18	832
Godfrey Lema Tanzania	7	1.0k 2.7×	375 1.9×	131 2.2×	33 0.6×	94 2.8×	8	1.5k
Rumi Kondo Japan	12	195 0.5×	179 0.9×	36 0.6×	41 0.7×	28 0.8×	14	428
Abra Brisbin United States	12	525 1.4×	223 1.1×	131 2.2×	27 0.5×	35 1.1×	18	928

Countries citing papers authored by M. Bamshad

Since Specialization

Citations

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

Fields of papers citing papers by M. Bamshad

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

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

All Works

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9 of 9 papers shown

1.

Racca, Alice Ward, et al.. (2015). The embryonic myosin R672C mutation that underlies Freeman-Sheldon syndrome impairs cross-bridge detachment and cycling in adult skeletal muscle. Human Molecular Genetics. 24(12). 3348–3358. 37 indexed citations

2.

Santos‐Cortez, Regie Lyn P., Kwanghyuk Lee, Arnaud P. J. Giese, et al.. (2014). Adenylate cyclase 1 (ADCY1) mutations cause recessive hearing impairment in humans and defects in hair cell function and hearing in zebrafish. Human Molecular Genetics. 23(12). 3289–3298. 39 indexed citations

3.

Huff, Chad D., Yingying Zhang, Chandler Gatenbee, et al.. (2011). Crohn's Disease and Genetic Hitchhiking at IBD5. Molecular Biology and Evolution. 29(1). 101–111. 41 indexed citations

4.

Watkins, W. Scott, R. Thara, Bryan Mowry, et al.. (2008). Genetic variation in South Indian castes: evidence from Y-chromosome, mitochondrial, and autosomal polymorphisms. BMC Genetics. 9(1). 86–86. 35 indexed citations

5.

Bamshad, M.. (2001). Genetic Evidence on the Origins of Indian Caste Populations. Genome Research. 11(6). 994–1004. 266 indexed citations

6.

Watkins, W. Scott, M. Bamshad, Missy Dixon, et al.. (1999). Multiple origins of the mtDNA 9-bp deletion in populations of South India. American Journal of Physical Anthropology. 109(2). 147–158. 48 indexed citations

7.

Watkins, W. Scott, M. Bamshad, Missy Dixon, et al.. (1999). Multiple origins of the mtDNA 9‐bp deletion in populations of South India. American Journal of Physical Anthropology. 109(2). 147–158. 3 indexed citations

8.

Rogers, Alan R., et al.. (1996). Mitochondrial mismatch analysis is insensitive to the mutational process. Molecular Biology and Evolution. 13(7). 895–902. 117 indexed citations

9.

Bamshad, M. & Melinda A. Novak. (1992). Interactions of Mothers with Partners of Different Sexes in Meadow Voles and Prairie Voles. Journal of Mammalogy. 73(2). 303–311. 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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