M. Michael Barmada

18.3k total citations
112 papers, 4.3k citations indexed

About

M. Michael Barmada is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, M. Michael Barmada has authored 112 papers receiving a total of 4.3k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Genetics, 38 papers in Molecular Biology and 37 papers in Surgery. Recurrent topics in M. Michael Barmada's work include Genetic Associations and Epidemiology (23 papers), Pancreatitis Pathology and Treatment (22 papers) and Pancreatic and Hepatic Oncology Research (16 papers). M. Michael Barmada is often cited by papers focused on Genetic Associations and Epidemiology (23 papers), Pancreatitis Pathology and Treatment (22 papers) and Pancreatic and Hepatic Oncology Research (16 papers). M. Michael Barmada collaborates with scholars based in United States, Italy and United Kingdom. M. Michael Barmada's co-authors include David C. Whitcomb, Roland H. Pfützer, Richard H. Duerr, M. Ilyas Kamboh, Véronique D. Morinville, Mark E. Lowe, Daniel E. Weeks, F. Yesim Demirci, Shyam Visweswaran and Robert E. Ferrell and has published in prestigious journals such as Circulation, Gastroenterology and PLoS ONE.

In The Last Decade

M. Michael Barmada

111 papers receiving 4.2k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
M. Michael Barmada United States	34	1.4k	1.2k	995	788	629	112	4.3k
Moshe Z. Papa Israel	37	902 0.6×	1.3k 1.1×	505 0.5×	909 1.2×	482 0.8×	111	4.3k
Roberto Pola Italy	32	813 0.6×	1.7k 1.4×	493 0.5×	473 0.6×	410 0.7×	134	4.3k
Jae Hoon Chung South Korea	47	2.2k 1.5×	1.6k 1.3×	1.0k 1.0×	1.0k 1.3×	288 0.5×	305	7.4k
Lennart Friis‐Hansen Denmark	35	1.1k 0.8×	1.8k 1.5×	424 0.4×	715 0.9×	408 0.6×	149	4.6k
William E. Russell United States	37	1.7k 1.2×	2.2k 1.8×	1.1k 1.1×	1.4k 1.8×	293 0.5×	90	6.3k
Angela Brooks‐Wilson Canada	31	1.4k 1.0×	1.8k 1.4×	455 0.5×	1.2k 1.5×	385 0.6×	99	4.1k
Ryohei Katoh Japan	45	1.4k 1.0×	1.9k 1.6×	887 0.9×	1.1k 1.4×	600 1.0×	211	6.7k
Ross McManus Ireland	34	674 0.5×	914 0.7×	1.3k 1.3×	429 0.5×	511 0.8×	102	4.2k
Paul G. Walfish Canada	44	1.6k 1.1×	1.1k 0.9×	1.4k 1.4×	811 1.0×	368 0.6×	160	6.2k
Elisabet Guinó Spain	29	469 0.3×	1.9k 1.5×	801 0.8×	1.2k 1.5×	329 0.5×	58	4.7k

Countries citing papers authored by M. Michael Barmada

Since Specialization

Citations

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

Fields of papers citing papers by M. Michael Barmada

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Michael Barmada

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

All Works

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20 of 20 papers shown

Orlova, Ekaterina, Andrew Yeh, Min Shi, et al.. (2018). Genetic association and differential expression of PITX2 with acute appendicitis. Human Genetics. 138(1). 37–47. 12 indexed citations

Yücesoy, Berran, M. Michael Barmada, Victor J. Johnson, et al.. (2016). Genetic Basis of Irritant Susceptibility in Health Care Workers. Journal of Occupational and Environmental Medicine. 58(8). 753–759. 6 indexed citations

Wang, Xingbin, et al.. (2015). Genetic contribution of SCARB1 variants to lipid traits in African Blacks: a candidate gene association study. BMC Medical Genetics. 16(1). 106–106. 12 indexed citations

Rosenthal, Samantha L., M. Michael Barmada, Xingbin Wang, F. Yesim Demirci, & M. Ilyas Kamboh. (2014). Connecting the Dots: Potential of Data Integration to Identify Regulatory SNPs in Late-Onset Alzheimer's Disease GWAS Findings. PLoS ONE. 9(4). e95152–e95152. 35 indexed citations

Zheng, Xiaojing, F. Yesim Demirci, M. Michael Barmada, et al.. (2014). A Rare Duplication on Chromosome 16p11.2 Is Identified in Patients with Psychosis in Alzheimer's Disease. PLoS ONE. 9(11). e111462–e111462. 13 indexed citations

Wang, Wei, Al‐Walid Mohsen, Guy Uechi, et al.. (2014). Complex changes in the liver mitochondrial proteome of short chain acyl-CoA dehydrogenase deficient mice. Molecular Genetics and Metabolism. 112(1). 30–39. 12 indexed citations

Barmada, M. Michael, et al.. (2014). The application of network label propagation to rank biomarkers in genome-wide Alzheimer’s data. BMC Genomics. 15(1). 282–282. 15 indexed citations

Wang, Xingbin, John E. Hokanson, Richard F. Hamman, et al.. (2013). Lipoprotein lipase gene sequencing and plasma lipid profile. Journal of Lipid Research. 55(1). 85–93. 16 indexed citations

Brehm, John M., Edna Acosta‐Pérez, Lambertus Klei, et al.. (2012). Vitamin D Insufficiency and Severe Asthma Exacerbations in Puerto Rican Children. American Journal of Respiratory and Critical Care Medicine. 186(2). 140–146. 169 indexed citations

10.

Brehm, John M., Edna Acosta‐Pérez, Lambertus Klei, et al.. (2012). African ancestry and lung function in Puerto Rican children. Journal of Allergy and Clinical Immunology. 129(6). 1484–1490.e6. 74 indexed citations

11.

Minster, Ryan L., F. Yesim Demirci, M. Michael Barmada, et al.. (2011). Replication study of genome‐wide associated SNPs with late‐onset Alzheimer's disease. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 156(4). 507–512. 16 indexed citations

12.

Yashin, Anatoli I., Konstantin G. Arbeev, Alexander M. Kulminski, et al.. (2010). “Predicting” parental longevity from offspring endophenotypes: Data from the Long Life Family Study (LLFS). Mechanisms of Ageing and Development. 131(3). 215–222. 16 indexed citations

13.

Aoun, Elie, Chung‐Chou H. Chang, Julia B. Greer, et al.. (2008). Pathways to Injury in Chronic Pancreatitis: Decoding the Role of the High-Risk SPINK1 N34S Haplotype Using Meta-Analysis. PLoS ONE. 3(4). e2003–e2003. 87 indexed citations

14.

Nelson, Tracy L., et al.. (2007). Association of the peroxisome proliferator–activated receptor γ gene with type 2 diabetes mellitus varies by physical activity among non-Hispanic whites from Colorado. Metabolism. 56(3). 388–393. 24 indexed citations

15.

Nelson, T., Tasha E. Fingerlin, Laura Moss, et al.. (2007). The Peroxisome Proliferator-activated Receptor Gamma Coactivator-1 Alpha Gene (PGC-1α) is Not Associated with Type 2 Diabetes Mellitus or Body Mass Index Among Hispanic and Non Hispanic Whites from Colorado. Experimental and Clinical Endocrinology & Diabetes. 115(4). 268–275. 15 indexed citations

16.

Dressman, Devin, Mary Ellen Ahearn, Kemal O. Yariz, et al.. (2007). X-linked infantile spinal muscular atrophy: Clinical definition and molecular mapping. Genetics in Medicine. 9(1). 52–60. 23 indexed citations

17.

Rendtorff, Nanna Dahl, Mei Zhu, Toril Fagerheim, et al.. (2006). A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment. European Journal of Human Genetics. 14(10). 1097–1105. 54 indexed citations

18.

Papachristou, Georgios I., David A. Sass, Haritha Avula, et al.. (2005). Is the Monocyte Chemotactic Protein-1 −2518 G Allele a Risk Factor for Severe Acute Pancreatitis?. Clinical Gastroenterology and Hepatology. 3(5). 475–481. 64 indexed citations

19.

Kerrison, John, M. Reza Vagefi, M. Michael Barmada, & Irene H. Maumenee. (1999). Congenital Motor Nystagmus Linked to Xq26-q27. The American Journal of Human Genetics. 64(2). 600–607. 66 indexed citations

20.

Kerrison, John, et al.. (1996). A Gene for Autosomal Dominant Congenital Nystagmus Localizes to 6p12. Genomics. 33(3). 523–526. 45 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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