Mitchel Pariani

694 total citations
13 papers, 349 citations indexed

About

Mitchel Pariani is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, Mitchel Pariani has authored 13 papers receiving a total of 349 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 3 papers in Surgery and 2 papers in Molecular Biology. Recurrent topics in Mitchel Pariani's work include Connective tissue disorders research (5 papers), Genomics and Rare Diseases (2 papers) and Aortic Disease and Treatment Approaches (2 papers). Mitchel Pariani is often cited by papers focused on Connective tissue disorders research (5 papers), Genomics and Rare Diseases (2 papers) and Aortic Disease and Treatment Approaches (2 papers). Mitchel Pariani collaborates with scholars based in United States, Italy and Canada. Mitchel Pariani's co-authors include David L. Rimoin, Eyal Reinstein, John M. Graham, Andrew Spencer, Wouter I. Schievink, Serguei Bannykh, Chloe M. Reuter, Andrea Hanson‐Kahn, Julia Platt and Elizabeth A. Harrington and has published in prestigious journals such as Scientific Reports, The American Journal of Cardiology and Journal of Neurology.

In The Last Decade

Mitchel Pariani

13 papers receiving 336 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mitchel Pariani United States	9	167	110	77	52	42	13	349
Lorna Day United Kingdom	7	115 0.7×	128 1.2×	56 0.7×	38 0.7×	36 0.9×	10	363
Cláudia B. Volpato Italy	12	99 0.6×	42 0.4×	93 1.2×	33 0.6×	112 2.7×	24	380
Janine Smith Australia	8	42 0.3×	52 0.5×	110 1.4×	24 0.5×	34 0.8×	20	253
Patricia Z. Page United States	5	126 0.8×	37 0.3×	80 1.0×	10 0.2×	103 2.5×	6	314
Andrea Guerin Canada	8	103 0.6×	57 0.5×	99 1.3×	19 0.4×	17 0.4×	30	336
Elodie Persyn United Kingdom	7	96 0.6×	23 0.2×	71 0.9×	27 0.5×	45 1.1×	7	244
Amanda F. Marvelle United States	7	126 0.8×	42 0.4×	87 1.1×	17 0.3×	38 0.9×	7	270
Kevin McCall United States	9	100 0.6×	50 0.5×	193 2.5×	67 1.3×	9 0.2×	11	354
Carole Brewer United Kingdom	8	301 1.8×	50 0.5×	191 2.5×	13 0.3×	41 1.0×	9	484
Sevcan Tuğ Bozdoğan Türkiye	10	77 0.5×	40 0.4×	86 1.1×	19 0.4×	8 0.2×	35	296

Countries citing papers authored by Mitchel Pariani

Since Specialization

Citations

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

Fields of papers citing papers by Mitchel Pariani

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mitchel Pariani

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

All Works

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13 of 13 papers shown

Algaze, Claudia, et al.. (2022). Prevalence and Outcomes of Primary Left Ventricular Dysfunction in Marfan Syndrome. The American Journal of Cardiology. 175. 119–126. 2 indexed citations

Iosef, Cristiana, Albert J Pedroza, Jason Z. Cui, et al.. (2020). Quantitative proteomics reveal lineage-specific protein profiles in iPSC-derived Marfan syndrome smooth muscle cells. Scientific Reports. 10(1). 20392–20392. 16 indexed citations

Banda, Juan M., Ashish Sarraju, Fahim Abbasi, et al.. (2019). Finding missed cases of familial hypercholesterolemia in health systems using machine learning. npj Digital Medicine. 2(1). 23–23. 77 indexed citations

Rigelsky, Christina, et al.. (2019). Genetics and Precision Medicine. Medical Clinics of North America. 103(6). 1005–1019. 8 indexed citations

Reuter, Chloe M., et al.. (2019). Understanding variants of uncertain significance in the era of multigene panels: Through the eyes of the patient. Journal of Genetic Counseling. 28(4). 878–886. 22 indexed citations

Harrington, Elizabeth A., Kyla Dunn, Mitchel Pariani, et al.. (2017). Clinically impactful differences in variant interpretation between clinicians and testing laboratories: a single-center experience. Genetics in Medicine. 20(3). 369–373. 37 indexed citations

Rimoin, David L., et al.. (2014). Echocardiographic findings in patients with spontaneous CSF leak. Journal of Neurology. 261(10). 1957–1960. 2 indexed citations

Reinstein, Eyal, Mitchel Pariani, Serguei Bannykh, David L. Rimoin, & Wouter I. Schievink. (2012). Connective tissue spectrum abnormalities associated with spontaneous cerebrospinal fluid leaks: a prospective study. European Journal of Human Genetics. 21(4). 386–390. 57 indexed citations

Reinstein, Eyal, et al.. (2012). Visceroptosis of the bowel in the hypermobility type of Ehlers–Danlos syndrome: Presentation of a rare manifestation and review of the literature. European Journal of Medical Genetics. 55(10). 548–551. 29 indexed citations

10.

Reinstein, Eyal, et al.. (2012). Early‐onset osteoarthritis in Ehlers–Danlos syndrome type VIII. American Journal of Medical Genetics Part A. 158A(4). 938–941. 10 indexed citations

11.

Kaback, Michael M., et al.. (2010). Genetic screening in the Persian Jewish community: A pilot study. Genetics in Medicine. 12(10). 628–633. 18 indexed citations

12.

Pariani, Mitchel, Andrew Spencer, John M. Graham, & David L. Rimoin. (2009). A 785 kb deletion of 3p14.1p13, including the FOXP1 gene, associated with speech delay, contractures, hypertonia and blepharophimosis. European Journal of Medical Genetics. 52(2-3). 123–127. 70 indexed citations

13.

Nardo, Bruno, Paolo Caraceni, Lorenza Puviani, et al.. (2003). 16 Successful treatment of CCL4-induced acute liver failure with portal vein arterialization in the rat. Digestive and Liver Disease. 35. A6–A6. 1 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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