Christin Collins - Concepedia

Author

Christin Collins

PerkinElmer (United States)

Also Known As

C Collins, CHRISTIN D. COLLINS, Christin Collins, Christin D Collins, Christin D. Collins

Publications

1.1K

Citations

H-Index

Concepts

All Affiliations

PerkinElmer (United States)Boston Children's Hospital Harvard University Emory University Center for Systems Biology

About

Christin Collins is an author at PerkinElmer (United States) specializing in medicine, genetics, and molecular diagnostics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	388
2	Public Health	2	2	234
3	Biostatistics	2	2	234
4	Engineering	1	1	39
5	Genetic Medicine	1	1	65

Christin Collins

Publications

Citations

H-Index

Page 1

	Year	Citations
Genetic landscape and novel disease mechanisms from a large <scp>LGMD</scp> cohort of 4656 patients Babi Ramesh Reddy Nallamilli, Samya Chakravorty, Akanchha Kesari, Annals of Clinical and Translational Neurology	2018	181
Characteristics and Predictive Value of Blood Transcriptome Signature in Males with Autism Spectrum Disorders Sek Won Kong, Christin Collins, Yuko Shimizu‐Motohashi, PLoS ONE Autism Spectrum DisordersGeneticsAsd DetectionGenetic EpidemiologyHuman Polymorphism	2012	169
A comprehensive genomic approach for neuromuscular diseases gives a high diagnostic yield Arunkanth Ankala, Cristina da Silva, Francesca Gualandi, Annals of Neurology	2014	166
Gene Expression Associated With Interferon Alfa Antiviral Activity in An Hcv Replicon Cell Line Haizhen Zhu, Hongshan Zhao, Christin Collins, Hepatology	2003	106
Comparative RNA editing in autistic and neurotypical cerebella Alal Eran, Jin Billy Li, Kayla Vatalaro, Molecular Psychiatry Syndromic AutismGeneticsComparative Rna EditingAutismNeuroscience	2012	69
Scaling resolution of variant classification differences in ClinVar between 41 clinical laboratories through an outlier approach Steven M. Harrison, Jill Dolinksy, Wenjie Chen, Human Mutation Genetic EpidemiologyDiagnosisPathologyDatabasesClinical Laboratories	2018	65
MCT8 Deficiency Davide Tonduti, Adeline Vanderver, Angela Berardinelli, Journal of Child Neurology	2012	57
Lack of correlation between the levels of soluble cytotoxic T-lymphocyte associated antigen-4 (CTLA-4) and the CT-60 genotypes Sharad Purohit, Robert H. Podolsky, Christin Collins, Journal of Autoimmune Diseases	2005	56
Molecular diagnostic testing for congenital disorders of glycosylation (CDG): Detection rate for single gene testing and next generation sequencing panel testing Melanie A. Jones, Devin Rhodenizer, Cristina da Silva, Molecular Genetics and Metabolism Genetic TestingNext GenerationMendelian DisorderGenetic DisorderMedicine	2013	46
Copy number variant discrepancy resolution using the ClinGen dosage sensitivity map results in updated clinical interpretations in ClinVar Erin Rooney Riggs, Tristan Nelson, Andrew Merz, Human Mutation	2018	42

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