Michael Mitchell

11.3k total citations · 2 hit papers
177 papers, 7.8k citations indexed

About

Michael Mitchell is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Michael Mitchell has authored 177 papers receiving a total of 7.8k indexed citations (citations by other indexed papers that have themselves been cited), including 69 papers in Molecular Biology, 57 papers in Genetics and 29 papers in Surgery. Recurrent topics in Michael Mitchell's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (51 papers), Sexual Differentiation and Disorders (22 papers) and Genomics and Chromatin Dynamics (17 papers). Michael Mitchell is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (51 papers), Sexual Differentiation and Disorders (22 papers) and Genomics and Chromatin Dynamics (17 papers). Michael Mitchell collaborates with scholars based in United States, United Kingdom and France. Michael Mitchell's co-authors include David R. Anderson, Bernard Lewandowski, Colin E. Bishop, George Kovács, Nabeel A. Affara, Katherine Robinson, Lisa Gray, Marc Rodger, Clive Kearon and Philip S. Wells and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Michael Mitchell

176 papers receiving 7.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Evaluation of D-Dimer in the Diagnosis of Suspected Deep-Vein Thrombosis

2003 990 citations Philip S. Wells, David R. Anderson et al. New England Journal of Medicine profile →
Value of assessment of pretest probability of deep-vein thrombosis in clinical management

1997 764 citations David R. Anderson, Michael Mitchell et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Michael Mitchell United States	45	2.7k	2.4k	1.8k	1.3k	1.0k	177	7.8k
Matthias W. Beckmann Germany	60	3.6k 1.3×	1.4k 0.6×	239 0.1×	1.4k 1.0×	2.6k 2.5×	654	15.3k
Charles J. Lockwood United States	67	1.3k 0.5×	885 0.4×	420 0.2×	1.0k 0.8×	2.5k 2.4×	376	16.6k
David A. Lane United Kingdom	60	2.4k 0.9×	704 0.3×	2.5k 1.4×	1.8k 1.3×	44 0.0×	340	13.9k
Christopher I. Amos United States	67	7.6k 2.8×	5.3k 2.2×	65 0.0×	1.6k 1.2×	353 0.3×	544	18.6k
Stanley J. Robboy United States	54	1.3k 0.5×	945 0.4×	124 0.1×	1.8k 1.3×	2.9k 2.8×	252	9.2k
Simon Heath United States	37	2.8k 1.0×	2.4k 1.0×	124 0.1×	737 0.6×	42 0.0×	96	7.3k
Johan Askling Sweden	75	1.3k 0.5×	2.9k 1.2×	128 0.1×	2.5k 1.9×	119 0.1×	411	18.8k
Gary Moore United States	41	1.3k 0.5×	607 0.3×	387 0.2×	1.2k 0.9×	35 0.0×	252	6.8k
Judith D. Goldberg United States	66	2.4k 0.9×	1.5k 0.6×	37 0.0×	3.0k 2.3×	390 0.4×	397	16.0k
Clemens Tempfer Austria	52	1.9k 0.7×	796 0.3×	92 0.1×	2.1k 1.6×	2.6k 2.5×	374	9.2k

Countries citing papers authored by Michael Mitchell

Since Specialization

Citations

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

Fields of papers citing papers by Michael Mitchell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michael Mitchell

This figure shows the co-authorship network connecting the top 25 collaborators of Michael Mitchell. A scholar is included among the top collaborators of Michael Mitchell 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 Michael Mitchell. Michael Mitchell 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

Longepied, Guy, et al.. (2023). Spermatozoa in mice lacking the nucleoporin NUP210L show defects in head shape and motility but not in nuclear compaction or histone replacement. Clinical Genetics. 105(4). 364–375. 2 indexed citations

Moore, Gary, et al.. (2019). Recommendations for clinical laboratory testing of activated protein C resistance; communication from the SSC of the ISTH. Journal of Thrombosis and Haemostasis. 17(9). 1555–1561. 20 indexed citations

Mitchell, Michael, Michael Gattens, Kaan Kavaklı, et al.. (2018). Genotype analysis and identification of novel mutations in a multicentre cohort of patients with hereditary factor X deficiency. Blood Coagulation & Fibrinolysis. 30(1). 34–41. 7 indexed citations

Yamauchi, Yasuhiro, et al.. (2016). Two genes substitute for the mouse Y chromosome for spermatogenesis and reproduction. Science. 351(6272). 514–516. 44 indexed citations

Patel, Yesha, Marie Lordkipanidzé, Gillian Lowe, et al.. (2014). A novel mutation in the P2Y12 receptor and a function‐reducing polymorphism in protease‐activated receptor 1 in a patient with chronic bleeding. Journal of Thrombosis and Haemostasis. 12(5). 716–725. 36 indexed citations

Mitchell, Michael, et al.. (2013). Design and development of ankle-foot prosthesis with delayed release of plantarflexion. The Journal of Rehabilitation Research and Development. 50(3). 409–409. 11 indexed citations

Ducourneau, Axel, Gilles Boëtsch, Guy Longepied, et al.. (2010). Genetic diversity on the Comoros Islands shows early seafaring as major determinant of human biocultural evolution in the Western Indian Ocean. European Journal of Human Genetics. 19(1). 89–94. 32 indexed citations

Royo, Hélène, Shantha K. Mahadevaiah, Haydn M. Prosser, et al.. (2010). Evidence that Meiotic Sex Chromosome Inactivation Is Essential for Male Fertility. Current Biology. 20(23). 2117–2123. 186 indexed citations

Longepied, Guy, Noémie Saut, Isabelle Aknin‐Seifer, et al.. (2010). Complete deletion of the AZFb interval from the Y chromosome in an oligozoospermic man. Human Reproduction. 25(10). 2655–2663. 38 indexed citations

10.

Metzler‐Guillemain, Catherine, D. Depétris, Judith Luciani, et al.. (2008). In human pachytene spermatocytes, SUMO protein is restricted to the constitutive heterochromatin. Chromosome Research. 16(5). 761–782. 28 indexed citations

11.

Das, Bibhuti B., Michael R. Recto, Christopher L. Johnsrude, et al.. (2006). Cardiac Transplantation for Pediatric Giant Cell Myocarditis. The Journal of Heart and Lung Transplantation. 25(4). 474–478. 15 indexed citations

12.

Millrain, Maggie, Diane Scott, Caroline Addey, et al.. (2005). Identification of the Immunodominant HY H2-Dk Epitope and Evaluation of the Role of Direct and Indirect Antigen Presentation in HY Responses. The Journal of Immunology. 175(11). 7209–7217. 25 indexed citations

13.

Saut, Noémie, Guy Longepied, P. Terriou, et al.. (2004). Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertility. Journal of Medical Genetics. 41(11). 814–825. 118 indexed citations

14.

Wells, Philip S., David R. Anderson, Marc Rodger, et al.. (2003). Evaluation of D-Dimer in the Diagnosis of Suspected Deep-Vein Thrombosis. New England Journal of Medicine. 349(13). 1227–1235. 990 indexed citations breakdown →

15.

Anderson, David R., M.J. Kovacs, George Kovács, et al.. (2003). Combined use of clinical assessment and d-dimer to improve the management of patients presenting to the emergency department with suspected deep vein thrombosis (the EDITED Study). Journal of Thrombosis and Haemostasis. 1(4). 645–651. 83 indexed citations

16.

Kim, Soo‐Hyun, Michael Mitchell, Hideta Fujii, Susana Llanos, & Gordon Peters. (2002). Absence of p16 ^INK4a and truncation of ARF tumor suppressors in chickens. Proceedings of the National Academy of Sciences. 100(1). 211–216. 49 indexed citations

17.

Mitchell, Michael, et al.. (1998). Osseous tumors of the foot. Clinical Imaging. 22(5). 378–378. 1 indexed citations

18.

Furlong, R. A., Carole A. Sargent, Robert P. Erickson, et al.. (1998). Characterisation of the coding sequence and fine mapping of the human DFFRY gene and comparative expression analysis and mapping to the Sxrb interval of the mouse Y chromosome of the Dffry gene. Human Molecular Genetics. 7(1). 97–107. 166 indexed citations

19.

Chiasson, Patrick M., et al.. (1997). Hip fracture surgery in Nova Scotia: a comparison of treatment provided by "generalist" general surgeons and orthopedic surgeons.. PubMed. 40(5). 383–9. 3 indexed citations

20.

Agulnik, Alexander I., Michael Mitchell, Jody L. Lerner, Diane Woods, & Colin E. Bishop. (1994). A mouse Y chromosome gene encoded by a region essential for spermatogenesis and expression of male-specific minor histocompatibility antigens. Human Molecular Genetics. 3(6). 873–878. 114 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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