Carolyn M. Yrigollen

Author

University of California, Davis ORCID

Also Known As

C.M. Yrigollen, Carolyn M Yrigollen, Carolyn M. Yrigollen, Carolyn Yrigollen, Philip E. Thuma

Publications

1.6K

Citations

H-Index

Concepts

All Affiliations

University of California, Davis Yale University University of California Davis Medical Center Lomonosov Moscow State University Karolinska Institutet

About

Carolyn M. Yrigollen is an author at University of California, Davis specializing in medicine, genetics, and fragile x spectrum.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	714
2	Public Health	2	2	35
3	Education	1	1	34
4	Engineering	1	1	42
5	Language Studies	1	1	22

Carolyn M. Yrigollen

Publications

1.5K

Citations

H-Index

Page 1

	Year	Citations
AGG interruptions within the maternal FMR1 gene reduce the risk of offspring with fragile X syndrome Carolyn M. Yrigollen, Blythe Durbin‐Johnson, Louise W. Gane, Genetics in Medicine Fragile X SyndromeDevelopmental BiologyMendelian DisorderGenetic DisorderGenetics	2012	174
Genes Controlling Affiliative Behavior as Candidate Genes for Autism Carolyn M. Yrigollen, Summer S. Han, Anna Kochetkova, Biological Psychiatry Candidate GenesSyndromic AutismGeneticsPsychiatric GeneticsAutism	2008	173
Fragile X AGG analysis provides new risk predictions for 45–69 repeat alleles Sarah L. Nolin, Sachin Sah, Anne Glicksman, American Journal of Medical Genetics Part A	2013	124
Macrophage Migration Inhibitory Factor and Autism Spectrum Disorders Elena L. Grigorenko, Summer S. Han, Carolyn M. Yrigollen, PEDIATRICS	2008	113
AGG interruptions and maternal age affect FMR1 CGG repeat allele stability during transmission Carolyn M. Yrigollen, Loreto Martorell, Blythe Durbin‐Johnson, Journal of Neurodevelopmental Disorders	2014	109
Clinical and molecular implications of mosaicism in FMR1 full mutations Dalyir Pretto, Carolyn M. Yrigollen, Hiu-Tung Tang, Frontiers in Genetics Fmr1 Promoter RegionGeneticsPathologyMolecular GeneticsDisease Gene Identification	2014	106
Association Between Polymorphisms in the Dopamine Transporter Gene and Depression Gerald J. Haeffel, Marya Getchell, Roman Koposov, Psychological Science	2008	95
Comparison of Whole-Genome DNA Methylation Patterns in Whole Blood, Saliva, and Lymphoblastoid Cell Lines Tara M. Thompson, Duaa Sharfi, Maria Lee, Behavior Genetics ChromatinDna SequencingEpigenetic ChangeGeneticsDna Methylation	2012	75
Toxicity after AAV delivery of RNAi expression constructs into nonhuman primate brain Megan S. Keiser, Paul T. Ranum, Carolyn M. Yrigollen, Nature Medicine NeurovirologyImmunologyCell DeathGene DeliveryGene Vector	2021	70
Genome-Wide Association and Exome Sequencing Study of Language Disorder in an Isolated Population Sergey A. Kornilov, Natalia Rakhlin, Roman Koposov, PEDIATRICS	2016	69

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