Anna L. Mitchell

1.0k total citations
24 papers, 535 citations indexed

About

Anna L. Mitchell is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Anna L. Mitchell has authored 24 papers receiving a total of 535 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 7 papers in Molecular Biology and 6 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Anna L. Mitchell's work include Connective tissue disorders research (7 papers), Prenatal Screening and Diagnostics (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Anna L. Mitchell is often cited by papers focused on Connective tissue disorders research (7 papers), Prenatal Screening and Diagnostics (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). Anna L. Mitchell collaborates with scholars based in United States, France and Australia. Anna L. Mitchell's co-authors include Kosuke Izumi, Marilyn C. Jones, Laura Konczal, Peter H. Byers, Ulrike Schwarze, Rebecca Darrah, Frank J. Jacono, Anne L. Matthews, Teresa A. Smolarek and Mitchell L. Drumm and has published in prestigious journals such as Nucleic Acids Research, The American Journal of Human Genetics and The Journal of Pediatrics.

In The Last Decade

Anna L. Mitchell

23 papers receiving 510 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anna L. Mitchell United States 14 324 176 127 56 42 24 535
Edmond G. Lemire Canada 14 202 0.6× 240 1.4× 142 1.1× 76 1.4× 67 1.6× 42 616
Anita Wischmeijer Italy 16 333 1.0× 260 1.5× 96 0.8× 96 1.7× 71 1.7× 29 622
Carolyn Applegate United States 17 270 0.8× 328 1.9× 146 1.1× 43 0.8× 57 1.4× 24 821
Karen J. Harrison Canada 10 252 0.8× 248 1.4× 77 0.6× 88 1.6× 43 1.0× 17 461
François Cartault France 12 208 0.6× 257 1.5× 114 0.9× 27 0.5× 80 1.9× 31 552
Gülen Eda Ütine Türkiye 14 373 1.2× 367 2.1× 71 0.6× 77 1.4× 66 1.6× 114 715
Marie‐Ange Delrue France 15 258 0.8× 291 1.7× 75 0.6× 37 0.7× 106 2.5× 30 590
Enikö K. Pivnick United States 11 228 0.7× 223 1.3× 120 0.9× 42 0.8× 67 1.6× 28 660
Rossella Capolino Italy 18 369 1.1× 449 2.6× 84 0.7× 53 0.9× 92 2.2× 56 825
Chin‐To Fong United States 11 197 0.6× 282 1.6× 58 0.5× 65 1.2× 35 0.8× 22 738

Countries citing papers authored by Anna L. Mitchell

Since Specialization
Citations

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

Fields of papers citing papers by Anna L. Mitchell

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna L. Mitchell

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

All Works

20 of 20 papers shown
1.
Jajosky, Audrey N., Anna L. Mitchell, Mahmut Akgül, et al.. (2022). Identification of a Cancer-Predisposing Germline POT1 p.Ile49Metfs*7 Variant by Targeted Sequencing of a Splenic Marginal Zone Lymphoma. Genes. 13(4). 591–591. 3 indexed citations
2.
Berisha, Stela Z., et al.. (2020). Cytogenetic and molecular diagnostic testing associated with prenatal and postnatal birth defects. Birth Defects Research. 112(4). 293–306. 19 indexed citations
3.
Darrah, Rebecca, Frank J. Jacono, Neha Joshi, et al.. (2018). AGTR2 absence or antagonism prevents cystic fibrosis pulmonary manifestations. Journal of Cystic Fibrosis. 18(1). 127–134. 15 indexed citations
4.
Darrah, Rebecca, Anna L. Mitchell, Abdus Sattar, et al.. (2016). Early pulmonary disease manifestations in cystic fibrosis mice. Journal of Cystic Fibrosis. 15(6). 736–744. 31 indexed citations
5.
6.
Regalado, Ellen S., Dong Guo, Regie Lyn P. Santos‐Cortez, et al.. (2015). Pathogenic FBN1 variants in familial thoracic aortic aneurysms and dissections. Clinical Genetics. 89(6). 719–723. 17 indexed citations
7.
Zankl, Andreas, Emma L. Duncan, Paul Leo, et al.. (2014). Multicentric Carpotarsal Osteolysis Is Caused by Mutations Clustering in the Amino-Terminal Transcriptional Activation Domain of MAFB. The American Journal of Human Genetics. 94(4). 643–643. 3 indexed citations
8.
Darrah, Rebecca, Ilya Bederman, Anna L. Mitchell, et al.. (2013). Ventilatory pattern and energy expenditure are altered in cystic fibrosis mice. Journal of Cystic Fibrosis. 12(4). 345–351. 19 indexed citations
9.
Manjila, Sunil, Benjamin Miller, Balint Otvos, et al.. (2013). Moyamoya Disease Associated with Asymptomatic Mosaic Turner Syndrome: A Rare Cause of Hemorrhagic Stroke. Journal of Stroke and Cerebrovascular Diseases. 23(5). 1242–1244. 12 indexed citations
10.
Sund, Kristen L., Sarah Zimmerman, Cameron Thomas, et al.. (2012). Regions of homozygosity identified by SNP microarray analysis aid in the diagnosis of autosomal recessive disease and incidentally detect parental blood relationships. Genetics in Medicine. 15(1). 70–78. 61 indexed citations
11.
Repnikova, Elena, Caroline Astbury, Shalini C. Reshmi, et al.. (2012). Microarray comparative genomic hybridization and cytogenetic characterization of tissue‐specific mosaicism in three patients. American Journal of Medical Genetics Part A. 158A(8). 1924–1933. 17 indexed citations
12.
Zankl, Andreas, Emma L. Duncan, Paul Leo, et al.. (2012). Multicentric Carpotarsal Osteolysis Is Caused by Mutations Clustering in the Amino-Terminal Transcriptional Activation Domain of MAFB. The American Journal of Human Genetics. 90(3). 494–501. 78 indexed citations
13.
Slavin, Thomas P., et al.. (2011). Isolated skeletal malformations in a child with a small mosaic ring microduplication of 18 p11.21q11.2: Genotype–phenotype correlations. American Journal of Medical Genetics Part A. 155(3). 618–621. 3 indexed citations
14.
Mitchell, Anna L., et al.. (2011). Characterization of Tissue-Specific and Developmentally Regulated Alternative Splicing of Exon 64 in theCOL5A1Gene. Connective Tissue Research. 53(3). 267–276. 7 indexed citations
15.
Izumi, Kosuke, Laura Konczal, Anna L. Mitchell, & Marilyn C. Jones. (2011). Underlying Genetic Diagnosis of Pierre Robin Sequence: Retrospective Chart Review at Two Children’s Hospitals and a Systematic Literature Review. The Journal of Pediatrics. 160(4). 645–650.e2. 98 indexed citations
16.
Mitchell, Anna L., et al.. (2009). Molecular mechanisms of classical Ehlers-Danlos syndrome (EDS). Human Mutation. 30(6). 995–1002. 33 indexed citations
17.
18.
Doherty, Michael J., Ian A. Glass, Craig L. Bennett, et al.. (2003). An Xp; Yq Translocation Causing a Novel Contiguous Gene Syndrome in Brothers with Generalized Epilepsy, Ichthyosis, and Attention Deficits. Epilepsia. 44(12). 1529–1535. 41 indexed citations
19.
Mitchell, Anna L., et al.. (2001). Isolation of Genomic DNA from Blood Using a Novel Filter-Based DNA Purification Technology. BioTechniques. 31(1). 142–145. 6 indexed citations
20.
Andersen, Lone B., et al.. (1991). A highly polymorphic cDNA probe in theNF1gene. Nucleic Acids Research. 19(13). 3754–3754. 13 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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