Erik C. Thorland

10.9k citations

61 papers · 4.2k indexed · 2 hit papers · h-index 28

Genetics top 0.5%
- Genomic variations and chromosomal abnormalities 23
- Genomics and Rare Diseases 10
- Genetics and Neurodevelopmental Disorders 6
- Genetic Syndromes and Imprinting 4
Pediatrics, Perinatology and Child Health top 1%
- Prenatal Screening and Diagnostics 9
Molecular Biology top 5%
- Epigenetics and DNA Methylation 9
- Cancer-related gene regulation 6
Cancer Research top 5%
Epidemiology top 5%
Hematology
- Hemophilia Treatment and Research 5

Co-authors: Hutton M. Kearney Sarah T. South Kerry K. Brown Fabiola Quintero‐Rivera Jeremy C. Smith Bobbie S. Gostout Erin Rooney Riggs Erica Andersen
Cited by: Genetics Pediatrics, Perinatology and Child Health Molecular Biology
Journals: Journal of Clinical Investigation (1 paper)Blood (1 paper)Neurology (1 paper)
Partner nations: United States China United Kingdom

In The Last Decade

Erik C. Thorland

59 papers receiving 4.1k citations

Hit Papers

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Peers

Countries citing papers authored by Erik C. Thorland

Since Specialization

Citations

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

Fields of papers citing papers by Erik C. Thorland

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Erik C. Thorland. 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 Erik C. Thorland. The network helps show where Erik C. Thorland may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Erik C. Thorland, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Erik C. Thorland Line = papers co-authored together Erik C. Thorland links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Follow the LINE: A novel case of dilated cardiomyopathy caused by a LINE-1 insertion in the TTN gene American Journal of Clinical Pathology ·Qiliang Ding,J. Fine,Frank T Hoffman,Michelle L. Kluge,Rhonda K. Kuennen,Sarah Thieke,Nicole L. Hoppman,Cherisse A. Marcou,Ross Rowsey,Erik C. Thorland,Linnea M. Baudhuin,Ann M. Moyer,Alessia Buglioni	2024	0
2	Interpretation and reporting of large regions of homozygosity and suspected consanguinity/uniparental disomy, 2021 revision: A technical standard of the American College of Medical Genetics and Genomics (ACMG) Genetics in Medicine ·Patrick R. Gonzales,Erica Andersen,Teneille R. Brown,Vanessa L. Horner,Juli Horwitz,Catherine Rehder,Natasha L. Rudy,Nathaniel H. Robin,Erik C. Thorland	2021	35
3	Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen)breakdown → Genetics in Medicine ·Erin Rooney Riggs,Erica Andersen,Athena M. Cherry,Sibel Kantarci,Hutton M. Kearney,Ankita Patel,Gordana Raca,Deborah Ritter,Sarah T. South,Erik C. Thorland,Daniel Pineda‐Alvarez,Swaroop Aradhya,Alastair J. Martin	2019	879
4	Patterns of homozygosity in patients with uniparental disomy: detection rate and suggested reporting thresholds for SNP microarrays Genetics in Medicine ·Nicole L. Hoppman,Kandelaria M. Rumilla,Emily Lauer,Hutton M. Kearney,Erik C. Thorland	2018	40
5	Novel de novo SPOCK1 mutation in a proband with developmental delay, microcephaly and agenesis of corpus callosum European Journal of Medical Genetics ·Radhika Dhamija,John M. Graham,Nizar Smaoui,Erik C. Thorland,Salman Kirmani	2014	20
6	The genomic landscape of small intestine neuroendocrine tumors Journal of Clinical Investigation ·Michaela S. Banck,Rahul Kanwar,Amit Kulkarni,Ganesh K. Boora,Franziska Metge,Benjamin R. Kipp,Lizhi Zhang,Erik C. Thorland,Kay Minn,Ramesh Tentu,Bruce W. Eckloff,Eric D. Wieben,Yanhong Wu,Julie M. Cunningham,David M. Nagorney,Judith A Gilbert,Matthew M. Ames,Andreas S. Beutler	2013	208
7	Reflex fluorescent in situ hybridization testing for unsuccessful product of conception cultures: A retrospective analysis of 5555 samples attempted by conventional cytogenetics and fluorescent in situ hybridization Genetics in Medicine ·Brandon M. Shearer,Erik C. Thorland,Austin W. Carlson,Syed M. Jalal,Rhett P. Ketterling	2011	53
8	American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variantsbreakdown → Genetics in Medicine ·Hutton M. Kearney,Erik C. Thorland,Kerry K. Brown,Fabiola Quintero‐Rivera,Sarah T. South	2011	643
9	A method for rapid, targeted CNV genotyping identifies rare variants associated with neurocognitive disease Genome Research ·Heather C Mefford,Gregory M. Cooper,Troy Zerr,Joshua D. Smith,Carl Baker,Neil Shafer,Erik C. Thorland,Cindy Skinner,Charles E. Schwartz,Deborah A. Nickerson,Evan E. Eichler	2009	101
10	Fluorescence In Situ Hybridization to Visualize Genetic Abnormalities in Interphase Cells of Acinar Cell Carcinoma, Ductal Adenocarcinoma, and Islet Cell Carcinoma of the Pancreas Mayo Clinic Proceedings ·Gordon W. Dewald,Thomas C. Smyrk,Erik C. Thorland,Robert R. McWilliams,Daniel L. Van Dyke,Jeannette G. Keefe,Kimberly J. Belongie,Stephanie A. Smoley,Darlene L. Knutson,Stephanie Fink,Anne E. Wiktor,Gloria M. Petersen	2009	23
11	Malignant Melanoma in the 21st Century: The Emerging Molecular Landscape Mayo Clinic Proceedings ·Aleksandar Sekulić,Paul Haluska,Arlo J. Miller,Josep Genebriera De Lamo,Samuel Ejadi,José S. Pulido,Diva R. Salomão,Erik C. Thorland,Richard G. Vile,David C. Swanson,Barbara A. Pockaj,Susan D. Laman,Mark R. Pittelkow,Svetomir N. Markovic	2008	90
12	Overexpression of Syk tyrosine kinase in peripheral T-cell lymphomas Leukemia ·Andrew L. Feldman,D X Sun,Mark E. Law,Anne J. Novak,Ayoma D. Attygalle,Erik C. Thorland,Stephanie Fink,Julie A. Vrana,Bolette L. Caron,William G. Morice,Ellen D. Remstein,Karen L. Grogg,Paul J. Kurtin,William R. Macon,Ahmet Doǧan	2008	107
13	Incidence ofTCRandTCL1Gene Translocations and Isochromosome 7q in Peripheral T-Cell Lymphomas Using Fluorescence In Situ Hybridization American Journal of Clinical Pathology ·Andrew L. Feldman,Mark E. Law,Karen L. Grogg,Erik C. Thorland,Stephanie Fink,Paul J. Kurtin,William R. Macon,Ellen D. Remstein,Ahmet Doǧan	2008	25
14	Comprehensive validation of array comparative genomic hybridization platforms: how much is enough? Genetics in Medicine ·Erik C. Thorland,Patrick R. Gonzales,Troy J. Gliem,Anne E. Wiktor,Rhett P. Ketterling	2007	8
15	Evaluation of a commercially available focused aCGH platform for the detection of constitutional chromosome anomalies American Journal of Medical Genetics Part A ·Brandon M. Shearer,Erik C. Thorland,Patrick R. Gonzales,Rhett P. Ketterling	2007	13
16	Congenital disorder of glycosylation Ic due to a de novo deletion and an hALG-6 mutation Biochemical and Biophysical Research Communications ·Erik A. Eklund,Liangwu Sun,Samuel Yang,Romela Pasion,Erik C. Thorland,Hudson H. Freeze	2005	13
17	Common fragile sites are preferential targets for HPV16 integrations in cervical tumors Oncogene ·Erik C. Thorland,Shannon L Myers,Bobbie S. Gostout,Jeremy C. Smith	2003	195
18	Integrations of the hepatitis B virus (HBV) and human papillomavirus (HPV) into the human telomerase reverse transcriptase (hTERT) gene in liver and cervical cancers Oncogene ·Matthew J. Ferber,Damian P. Montoya,Cecilia Yu,Ileana Aderca,Andrew R. McGee,Erik C. Thorland,David M. Nagorney,Bobbie S. Gostout,Larry J. Burgart,Loreto Boix,Jordi Bruix,Brian J. McMahon,T.H. Cheung,Tony K.H. Chung,Y.F. Wong,Jeremy C. Smith,Lewis R. Roberts	2003	171
19	Cloning and characterization of the common fragile site FRA6F harboring a replicative senescence gene and frequently deleted in human tumors Oncogene ·Maria Cristina Morelli,E. Karayianni,C. Magnanini,Andrew J. Mungall,Erik C. Thorland,Massimo Negrini,Jeremy C. Smith,Giuseppe Barbanti‐Brodano	2002	74
20	Overlapping PCR for Bidirectional PCR Amplification of Specific Alleles: A Rapid One-Tube Method for Simultaneously Differentiating Homozygotes and Heterozygotes Genome Research ·Qiang Liu,Erik C. Thorland,John A. Heit,Steve S. Sommer	1997	133

About Erik C. Thorland

Erik C. Thorland is a scholar working on Genetics, Genetics and Hematology, having authored 61 papers that have together received 4.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (23 papers), Genomics and Rare Diseases (10 papers), Epigenetics and DNA Methylation (9 papers), Prenatal Screening and Diagnostics (9 papers), Cancer-related gene regulation (6 papers), Genetics and Neurodevelopmental Disorders (6 papers), Hemophilia Treatment and Research (5 papers) and Genetic Syndromes and Imprinting (4 papers). The work is most often cited by research in Genetics (2.1k citations), Pediatrics, Perinatology and Child Health (843 citations) and Molecular Biology (1.8k citations). Erik C. Thorland has collaborated with scholars based in United States, China and United Kingdom. Frequent co-authors include Hutton M. Kearney, Sarah T. South, Kerry K. Brown, Fabiola Quintero‐Rivera, Jeremy C. Smith, Bobbie S. Gostout, Erin Rooney Riggs, Erica Andersen, Swaroop Aradhya and Ankita Patel. Their work appears in journals such as Journal of Clinical Investigation, Blood and Neurology.

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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