Aaron Theisen

4.3k total citations · 1 hit paper
31 papers, 2.4k citations indexed

About

Aaron Theisen is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Aaron Theisen has authored 31 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Genetics, 14 papers in Molecular Biology and 11 papers in Plant Science. Recurrent topics in Aaron Theisen's work include Genomic variations and chromosomal abnormalities (25 papers), Chromosomal and Genetic Variations (11 papers) and Genomics and Rare Diseases (8 papers). Aaron Theisen is often cited by papers focused on Genomic variations and chromosomal abnormalities (25 papers), Chromosomal and Genetic Variations (11 papers) and Genomics and Rare Diseases (8 papers). Aaron Theisen collaborates with scholars based in United States, Canada and United Kingdom. Aaron Theisen's co-authors include Richard Wenstrup, Jennifer Saam, Christopher Arnell, Kelsey Moyes, Kirstin M. Roundy, Ingrid Marino, Lisa G. Shaffer, Bassem A. Bejjani, Blake C. Ballif and Catherine D. Kashork and has published in prestigious journals such as PLoS ONE, Cancer and Journal of Medical Genetics.

In The Last Decade

Aaron Theisen

31 papers receiving 2.3k citations

Hit Papers

align trajectories sort by overperformance

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.

Patients Tested at a Laboratory for Hereditary Cancer Syndromes Show an Overlap for Multiple Syndromes in Their Personal and Familial Cancer Histories

2015 1.0k citations Jennifer Saam, Christopher Arnell et al. Oncology profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Aaron Theisen United States	19	1.4k	875	761	637	520	31	2.4k
Maria Grazia Tibiletti Italy	29	503 0.4×	810 0.9×	838 1.1×	812 1.3×	469 0.9×	93	2.3k
Syed M. Jalal United States	28	1.0k 0.7×	317 0.4×	1.3k 1.7×	310 0.5×	163 0.3×	71	2.6k
Megan P. Hitchins United States	30	817 0.6×	1.2k 1.4×	1.5k 1.9×	876 1.4×	987 1.9×	66	2.8k
Janet M. Cowan United States	25	553 0.4×	169 0.2×	1.1k 1.4×	508 0.8×	305 0.6×	56	2.0k
Vaidehi Jobanputra United States	23	521 0.4×	211 0.2×	456 0.6×	234 0.4×	207 0.4×	79	1.3k
Trijnie Dijkhuizen Netherlands	24	677 0.5×	194 0.2×	801 1.1×	196 0.3×	306 0.6×	62	1.6k
Sunday M. Stray United States	11	1.3k 0.9×	428 0.5×	921 1.2×	465 0.7×	499 1.0×	14	2.2k
Jeroen Knijnenburg Netherlands	22	578 0.4×	287 0.3×	473 0.6×	153 0.2×	111 0.2×	47	1.4k
Daniel Pineda‐Alvarez United States	21	1.3k 1.0×	217 0.2×	921 1.2×	90 0.1×	219 0.4×	45	2.2k
Tom G.W. Letteboer Netherlands	16	347 0.3×	283 0.3×	410 0.5×	221 0.3×	178 0.3×	27	1.2k

Countries citing papers authored by Aaron Theisen

Since Specialization

Citations

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

Fields of papers citing papers by Aaron Theisen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aaron Theisen

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

1.

Theisen, Aaron, et al.. (2019). Chronic Ankle Instability Leads to Lower Extremity Kinematic Changes During Landing Tasks: A Systematic Review. International journal of exercise science. 12(1). 24–33. 48 indexed citations

2.

Saam, Jennifer, Christopher Arnell, Aaron Theisen, et al.. (2015). Patients Tested at a Laboratory for Hereditary Cancer Syndromes Show an Overlap for Multiple Syndromes in Their Personal and Familial Cancer Histories. Oncology. 89(5). 288–293. 1029 indexed citations breakdown →

3.

Mancini‐DiNardo, Debora, Thaddeus Judkins, Natalia Gutin, et al.. (2014). Design and validation of an oligonucleotide microarray for the detection of genomic rearrangements associated with common hereditary cancer syndromes. Journal of Experimental & Clinical Cancer Research. 33(1). 74–74. 5 indexed citations

4.

Mancini‐DiNardo, Debora, Thaddeus Judkins, Natalia Gutin, et al.. (2014). Design and validation of an oligonucleotide microarray for the detection of genomic rearrangements associated with common hereditary cancer syndromes. Journal of Experimental & Clinical Cancer Research. 33(1). 74–74. 1 indexed citations

5.

Sahoo, Trilochan, Aaron Theisen, Jill A. Rosenfeld, et al.. (2011). Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problems. Genetics in Medicine. 13(10). 868–880. 75 indexed citations

6.

Sahoo, Trilochan, Aaron Theisen, Pedro A. Sanchez‐Lara, et al.. (2011). Microdeletion 20p12.3 involving BMP2 contributes to syndromic forms of cleft palate. American Journal of Medical Genetics Part A. 155(7). 1646–1653. 53 indexed citations

7.

Theisen, Aaron, Lea Velsher, Erawati V. Bawle, et al.. (2011). Duplication of the STS region in males is a benign copy‐number variant. American Journal of Medical Genetics Part A. 155(8). 1972–1975. 17 indexed citations

8.

Sahoo, Trilochan, Aaron Theisen, Michael Marble, et al.. (2011). Microdeletion of Xq28 involving the AFF2 (FMR2) gene in two unrelated males with developmental delay. American Journal of Medical Genetics Part A. 155(12). 3110–3115. 16 indexed citations

9.

Traylor, Ryan N., Damien L. Bruno, Trent Burgess, et al.. (2010). A Genotype-First Approach for the Molecular and Clinical Characterization of Uncommon De Novo Microdeletion of 20q13.33. PLoS ONE. 5(8). e12462–e12462. 21 indexed citations

10.

Kashork, Catherine D., Aaron Theisen, & Lisa G. Shaffer. (2010). Diagnosis of Cryptic Chromosomal Syndromes by Fluorescence In Situ Hybridization (FISH). Current Protocols in Human Genetics. 67(1). 2 indexed citations

11.

Ballif, Blake C., Aaron Theisen, Justine Coppinger, et al.. (2008). Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication. Molecular Cytogenetics. 1(1). 8–8. 176 indexed citations

12.

Shaffer, Lisa G., Justine Coppinger, Sarah Alliman, et al.. (2008). Comparison of microarray‐based detection rates for cytogenetic abnormalities in prenatal and neonatal specimens. Prenatal Diagnosis. 28(9). 789–795. 102 indexed citations

13.

Kashork, Catherine D., Aaron Theisen, & Lisa G. Shaffer. (2008). Prenatal Diagnosis Using Array CGH. Methods in molecular biology. 444. 59–70. 10 indexed citations

14.

Theisen, Aaron, et al.. (2008). Identification of a previously unrecognized microdeletion syndrome of 16q11.2q12.2. Clinical Genetics. 74(5). 469–475. 63 indexed citations

15.

Shaffer, Lisa G., Blake C. Ballif, Aaron Theisen, et al.. (2008). In the middle of it all: a centered approach to chromosome analysis. Expert Opinion on Medical Diagnostics. 2(2). 221–229. 2 indexed citations

16.

Ballif, Blake C., et al.. (2007). Development of a high-density pericentromeric region BAC clone set for the detection and characterization of small supernumerary marker chromosomes by array CGH. Genetics in Medicine. 9(3). 150–162. 46 indexed citations

17.

Shaffer, Lisa G., Aaron Theisen, Bassem A. Bejjani, et al.. (2007). The discovery of microdeletion syndromes in the post-genomic era: review of the methodology and characterization of a new 1q41q42 microdeletion syndrome. Genetics in Medicine. 9(9). 607–616. 124 indexed citations

18.

Jarmuż‐Szymczak, Małgorzata, Blake C. Ballif, Catherine D. Kashork, et al.. (2006). Comparative Genomic Hybridization by Microarray for the Detection of Cytogenetic Imbalance. Methods in molecular medicine. 128. 23–31. 3 indexed citations

19.

Bejjani, Bassem A., Reza Saleki, Blake C. Ballif, et al.. (2005). Use of targeted array‐based CGH for the clinical diagnosis of chromosomal imbalance: Is less more?. American Journal of Medical Genetics Part A. 134A(3). 259–267. 155 indexed citations

20.

Gajęcka, Marzena, Wei Yu, Blake C. Ballif, et al.. (2004). Delineation of mechanisms and regions of dosage imbalance in complex rearrangements of 1p36 leads to a putative gene for regulation of cranial suture closure. European Journal of Human Genetics. 13(2). 139–149. 68 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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