Erik C. Thorland - Concepedia

Author

Erik C. Thorland

Also Known As

E C Thorland, E. C. THORLAND, E.C. Thorland, ERIK C. THORLAND, Erik C Thorland, Erik C. Thorland, Erik Thorland, Patricia Simmons

123

Publications

10.8K

Citations

H-Index

103

Concepts

All Affiliations

Mayo Clinic Mayo Clinic in Arizona WinnMed Mayo Clinic in Florida University of Utah

About

Erik C. Thorland is an author at Mayo Clinic specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	25	30	6.2K
2	Public Health	11	11	3.6K
3	Engineering	3	3	421
4	Natural Sciences	2	2	238
5	Allergy	1	1	93

Erik C. Thorland

Publications

7.5K

Citations

H-Index

Page 1

	Year	Citations
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) Erin Rooney Riggs, Erica Andersen, Athena M. Cherry, Genetics in Medicine Clinical Genome ResourceGenetic TestingTechnical StandardsMedicineGenetics	2019	1.7K
American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants Hutton M. Kearney, Erik C. Thorland, Kerry K. Brown, Genetics in Medicine Genetic TestingGenetic DisorderMedicineGeneticsAmerican College	2011	949
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities Erin B. Kaminsky, Vineith Kaul, Justin Paschall, Genetics in Medicine Intellectual ImpairmentPsychiatryGenetic DisorderGeneticsDisability	2011	444
Microduplication 22q11.2, an Emerging Syndrome: Clinical, Cytogenetic, and Molecular Analysis of Thirteen Patients Regina Ensenauer, Adewale Adeyinka, Heather C. Flynn, The American Journal of Human Genetics CytogeneticsGenetic DisorderGeneticsMolecular AnalysisPathology	2003	376
The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies Claire Redin, Harrison Brand, Ryan L. Collins, Nature Genetics Human Congenital AnomaliesDevelopmental AnomalyDevelopmental BiologyCytogeneticsGenomic Landscape	2016	346
Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia Daniel Moreno‐De‐Luca, Jennifer G. Mullé, Erin B. Kaminsky, The American Journal of Human Genetics	2010	331
The genomic landscape of small intestine neuroendocrine tumors Michaela S. Banck, Rahul Kanwar, Amit Kulkarni, Journal of Clinical Investigation EngineeringPathologyCancer BiologyTumor BiologyEndocrine Oncology	2013	320
Common fragile sites are preferential targets for HPV16 integrations in cervical tumors Erik C. Thorland, Shannon L Myers, Bobbie S. Gostout Oncogene Cervical Cancer ManagementCervical CancerHpv16 IntegrationsHuman Papillomavirus VaccinesPathology	2003	247
Integrations of the hepatitis B virus (HBV) and human papillomavirus (HPV) into the human telomerase reverse transcriptase (hTERT) gene in liver and cervical cancers Matthew J. Ferber, Damian P. Montoya, Cecilia Yu, Oncogene Cervical CancerViral HepatitisPathologyMolecular BiologyVirology	2003	233
Human papillomavirus type 16 integrations in cervical tumors frequently occur in common fragile sites. Erik C. Thorland, Shannon L Myers, David H. Persing, PubMed PathologyMolecular BiologyCytopathologyMolecular GeneticsCancer-associated Virus	2000	201

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