Aaron Theisen

4.3k citations

31 papers · 2.4k indexed · 1 hit paper · h-index 19

Co-authors: Richard Wenstrup Christopher Arnell Jennifer Saam Kelsey Moyes Ingrid Marino Kirstin M. Roundy Lisa G. Shaffer Bassem A. Bejjani
Topics: Genomic variations and chromosomal abnormalities (25 papers)Chromosomal and Genetic Variations (11 papers)Genomics and Rare Diseases (8 papers)
Cited by: Genetics Pathology and Forensic Medicine Cancer Research
Journals: PLoS ONE Cancer Journal of Medical Genetics
Partner nations: United States Canada United Kingdom

In The Last Decade

Aaron Theisen

31 papers receiving 2.3k 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.

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

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

#	Work	Indexed citations
1	Chronic Ankle Instability Leads to Lower Extremity Kinematic Changes During Landing Tasks: A Systematic Review 2019 ·International journal of exercise science ·Aaron Theisen,(unknown)	48
2	Patients Tested at a Laboratory for Hereditary Cancer Syndromes Show an Overlap for Multiple Syndromes in Their Personal and Familial Cancer Historiesbreakdown → 2015 ·Oncology ·Jennifer Saam,Christopher Arnell,Aaron Theisen,Kelsey Moyes,Ingrid Marino,Kirstin M. Roundy,Richard Wenstrup	1029
3	Design and validation of an oligonucleotide microarray for the detection of genomic rearrangements associated with common hereditary cancer syndromes 2014 ·Journal of Experimental & Clinical Cancer Research ·Debora Mancini‐DiNardo,Thaddeus Judkins,(unknown),(unknown),(unknown),(unknown),(unknown),Natalia Gutin,Aaron Theisen,(unknown),(unknown),Christopher Arnell,Kelsey Moyes,Benjamin B. Roa	5
4	Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problems 2011 ·Genetics in Medicine ·Trilochan Sahoo,Aaron Theisen,Jill A. Rosenfeld,Allen N. Lamb,J. Britt Ravnan,Roger A. Schultz,Beth S. Torchia,Nicholas J. Neill,Ian Casci,Bassem A. Bejjani,Lisa G. Shaffer	75
5	Microdeletion 20p12.3 involving BMP2 contributes to syndromic forms of cleft palate 2011 ·American Journal of Medical Genetics Part A ·Trilochan Sahoo,Aaron Theisen,Pedro A. Sanchez‐Lara,Michael Marble,(unknown),Beth S. Torchia,Allen N. Lamb,Bassem A. Bejjani,Lisa G. Shaffer,Yves Lacassie	53
6	Duplication of the STS region in males is a benign copy‐number variant 2011 ·American Journal of Medical Genetics Part A ·(unknown),Aaron Theisen,Lea Velsher,Erawati V. Bawle,(unknown),Nancy J. Mendelsohn,(unknown),Lisa G. Shaffer,David Chitayat	17
7	Microdeletion of Xq28 involving the AFF2 (FMR2) gene in two unrelated males with developmental delay 2011 ·American Journal of Medical Genetics Part A ·Trilochan Sahoo,Aaron Theisen,Michael Marble,Raymond C. Tervo,Jill A. Rosenfeld,Beth S. Torchia,Lisa G. Shaffer	16
8	Case series: 2q33.1 microdeletion syndrome—further delineation of the phenotype 2011 ·Journal of Medical Genetics ·Meena Balasubramanian,Kath Smith,Lina Basel‐Vanagaite,Murray Feingold,Pamela Brock,Gordon C. Gowans,Pradeep Vasudevan,Lara Cresswell,(unknown),Civonnia Harris,Neil Friedman,Rocio Moran,Holly Feret,Elaine H. Zackai,Aaron Theisen,Jill A. Rosenfeld,Michael Parker	64
9	A Genotype-First Approach for the Molecular and Clinical Characterization of Uncommon De Novo Microdeletion of 20q13.33 2010 ·PLoS ONE ·Ryan N. Traylor,Damien L. Bruno,Trent Burgess,Robert S. Wildin,(unknown),Devika Ganesamoorthy,David J. Amor,Matthew F. Hunter,Michael S. Caplan,Jill A. Rosenfeld,Aaron Theisen,Beth S. Torchia,Lisa G. Shaffer,Blake C. Ballif,Howard R. Slater	21
10	Prenatal Diagnosis Using Array CGH 2008 ·Methods in molecular biology ·Catherine D. Kashork,Aaron Theisen,Lisa G. Shaffer	10
11	In the middle of it all: a centered approach to chromosome analysis 2008 ·Expert Opinion on Medical Diagnostics ·Lisa G. Shaffer,Blake C. Ballif,Aaron Theisen,Emily A. Rorem,Bassem A. Bejjani,Beth A. Torchia	2
12	Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication 2008 ·Molecular Cytogenetics ·Blake C. Ballif,Aaron Theisen,Justine Coppinger,Gordon C. Gowans,Joseph H. Hersh,Suneeta Madan‐Khetarpal,(unknown),Raymond C. Tervo,Luis Escobar,Christopher A. Friedrich,Marie McDonald,Lindsey Campbell,Jeffrey E. Ming,Elaine H. Zackai,Bassem A. Bejjani,Lisa G. Shaffer	176
13	Identification of a previously unrecognized microdeletion syndrome of 16q11.2q12.2 2008 ·Clinical Genetics ·(unknown),Aaron Theisen,(unknown),E H Zackai,(unknown),(unknown),L.G. Shaffer	63
14	Development of a high-density pericentromeric region BAC clone set for the detection and characterization of small supernumerary marker chromosomes by array CGH 2007 ·Genetics in Medicine ·Blake C. Ballif,(unknown),(unknown),(unknown),(unknown),Emily A. Rorem,Aaron Theisen,Bassem A. Bejjani,Lisa G. Shaffer	46
15	The clinical utility of enhanced subtelomeric coverage in array CGH 2007 ·American Journal of Medical Genetics Part A ·Blake C. Ballif,(unknown),(unknown),(unknown),Aaron Theisen,Bassem A. Bejjani,Lisa G. Shaffer	60
16	The discovery of microdeletion syndromes in the post-genomic era: review of the methodology and characterization of a new 1q41q42 microdeletion syndrome 2007 ·Genetics in Medicine ·Lisa G. Shaffer,Aaron Theisen,Bassem A. Bejjani,Blake C. Ballif,Arthur S. Aylsworth,Cynthia Lim,Marie McDonald,Jay W. Ellison,Dana Kostiner,Sulagna C. Saitta,Tamim H. Shaikh	124
17	Comparative Genomic Hybridization by Microarray for the Detection of Cytogenetic Imbalance 2006 ·Methods in molecular medicine ·Małgorzata Jarmuż‐Szymczak,Blake C. Ballif,Catherine D. Kashork,Aaron Theisen,Bassem A. Bejjani,Lisa G. Shaffer	3
18	Use of targeted array‐based CGH for the clinical diagnosis of chromosomal imbalance: Is less more? 2005 ·American Journal of Medical Genetics Part A ·Bassem A. Bejjani,Reza Saleki,Blake C. Ballif,Emily A. Rorem,Kyle Sundin,Aaron Theisen,Catherine D. Kashork,Lisa G. Shaffer	155
19	Array-based comparative genomic hybridization in clinical diagnosis 2005 ·Expert Review of Molecular Diagnostics ·Bassem A. Bejjani,Aaron Theisen,Blake C. Ballif,Lisa G. Shaffer	27
20	Delineation of mechanisms and regions of dosage imbalance in complex rearrangements of 1p36 leads to a putative gene for regulation of cranial suture closure 2004 ·European Journal of Human Genetics ·Marzena Gajęcka,Wei Yu,Blake C. Ballif,Caron D. Glotzbach,(unknown),Chad A. Shaw,Catherine D. Kashork,Heidi A. Heilstedt,(unknown),Aaron Theisen,Ritva Rice,David Rice,Lisa G. Shaffer	68

About Aaron Theisen

Aaron Theisen is a scholar working on Genetics, Cancer Research and Plant Science, having authored 31 papers that have together received 2.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (25 papers), Chromosomal and Genetic Variations (11 papers) and Genomics and Rare Diseases (8 papers). The work is most often cited by research in Genetics (1.4k citations), Pathology and Forensic Medicine (875 citations) and Cancer Research (520 citations). Aaron Theisen has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include Richard Wenstrup, Christopher Arnell, Jennifer Saam, Kelsey Moyes, Ingrid Marino, Kirstin M. Roundy, Lisa G. Shaffer, Bassem A. Bejjani, Blake C. Ballif and Catherine D. Kashork. Their work appears in journals such as PLoS ONE, Cancer and Journal of Medical Genetics.

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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