Carrie J. Finno

ORCID: 0000-0001-5924-0234
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Genetic and phenotypic traits in livestock
  • Veterinary Equine Medical Research
  • Neurological diseases and metabolism
  • Molecular Biology Techniques and Applications
  • Cancer-related molecular mechanisms research
  • Muscle metabolism and nutrition
  • Genomics and Phylogenetic Studies
  • Plant Toxicity and Pharmacological Properties
  • Cardiomyopathy and Myosin Studies
  • Muscle Physiology and Disorders
  • Epigenetics and DNA Methylation
  • Genetic Mapping and Diversity in Plants and Animals
  • Exercise and Physiological Responses
  • Inflammatory Myopathies and Dermatomyositis
  • Antioxidant Activity and Oxidative Stress
  • Toxoplasma gondii Research Studies
  • Peroxisome Proliferator-Activated Receptors
  • Plant and fungal interactions
  • Genomics and Chromatin Dynamics
  • Hereditary Neurological Disorders
  • Parasitic Infections and Diagnostics
  • RNA and protein synthesis mechanisms
  • RNA modifications and cancer
  • RNA Research and Splicing
  • Cardiovascular Effects of Exercise

University of California, Davis
2016-2025

University of Kentucky
2024

University of Agriculture in Krakow
2024

University of Nebraska–Lincoln
2024

British Veterinary Association
2023

National Institutes of Health
2020

Veterinary Medical Teaching Hospital
2006-2020

Office of Dietary Supplements
2020

In-Q-Tel
2016

University of Minnesota
2003-2015

Ake T. Lu Zhe Fei Amin Haghani Todd R. Robeck Joseph A. Zoller and 95 more Caesar Z. Li Robert Lowe Qi Yan Joshua Zhang Hoang‐Giang Vu Julia Ablaeva Victoria A. Acosta-Rodríguez Danielle M. Adams Javier Almunia Ajoy Aloysius Reza Ardehali A Arneson C. Scott Baker Gareth Banks Katherine Belov Nigel C. Bennett Peter C. Black Daniel T. Blumstein Eleanor K. Bors Charles E. Breeze Robert T. Brooke Janine L. Brown Gerald G. Carter Alex Caulton Julie M. Cavin Lisa Chakrabarti Ioulia Chatzistamou Hao Chen Kai Cheng Priscila Chiavellini Oi‐Wa Choi Shannon Clarke Lisa Noelle Cooper Marie‐Laurence Cossette Joanna Day Joseph DeYoung Stacy DiRocco Christopher Dold Erin E. Ehmke Candice K. Emmons Stephan Emmrich Ebru Erbay Claire Erlacher‐Reid Chris G. Faulkes Steven H. Ferguson Carrie J. Finno Jennifer E. Flower Jean‐Michel Gaillard Eva Garde Livia Gerber Vadim N. Gladyshev Vera Gorbunova Rodolfo G. Goya Myles J.A. Grant C. B. Green Erin N. Hales M. Bradley Hanson Daniel W. Hart Martin Haulena K. Herrick Andrew N. Hogan Carolyn J. Hogg Timothy A. Hore Taosheng Huang Juan Carlos Izpisúa Belmonte Anna J. Jasinska Gareth Jones Eve Jourdain Olga Kashpur Harold L. Katcher Etsuko Katsumata Vimala Kaza Hippokratis Kiaris Michael S. Kobor Paweł Kordowitzki William R. Koski Michael Krützen Soon‐Bae Kwon Brenda Larison Sang‐Goo Lee Marina Lehmann Jean‐François Lemaître Arnold J. Levine Chunquan Li X. Li A. R. Lim David Lin D. Lindemann Tom J. Little Nicholas Macoretta Debra Maddox Craig O. Matkin Julie A. Mattison Mélanie McClure June Mergl

Abstract Aging, often considered a result of random cellular damage, can be accurately estimated using DNA methylation profiles, the foundation pan-tissue epigenetic clocks. Here, we demonstrate development universal pan-mammalian clocks, 11,754 arrays from our Mammalian Methylation Consortium, which encompass 59 tissue types across 185 mammalian species. These predictive models estimate age with high accuracy ( r > 0.96). Age deviations correlate human mortality risk, mouse somatotropic...

10.1038/s43587-023-00462-6 article EN cc-by Nature Aging 2023-08-10
Amin Haghani Caesar Z. Li Todd R. Robeck Joshua Zhang Ake T. Lu and 95 more Julia Ablaeva Victoria A. Acosta-Rodríguez Danielle M. Adams Abdulaziz N. Alagaili Javier Almunia Ajoy Aloysius Nabil Amor Reza Ardehali A Arneson C. Scott Baker Gareth Banks Katherine Belov Nigel C. Bennett Peter McL. Black Daniel T. Blumstein Eleanor K. Bors Charles E. Breeze Robert T. Brooke Janine L. Brown Gerald G. Carter Alex Caulton Julie M. Cavin Lisa Chakrabarti Ioulia Chatzistamou Andreas S. Chavez Hao Chen Kaiyang Cheng Priscila Chiavellini Oi‐Wa Choi Shannon Clarke Joseph A. Cook Lisa Noelle Cooper Marie‐Laurence Cossette Joanna Day Joseph DeYoung Stacy DiRocco Christopher Dold Jonathan L. Dunnum Erin E. Ehmke Candice K. Emmons Stephan Emmrich Ebru Erbay Claire Erlacher‐Reid Chris G. Faulkes Zhe Fei Steven H. Ferguson Carrie J. Finno Jennifer E. Flower Jean‐Michel Gaillard Eva Garde Livia Gerber Vadim N. Gladyshev Rodolfo G. Goya Matthew J. Grant Carla B. Green M. Bradley Hanson Daniel W. Hart Martin Haulena Kelsey E. S. Herrick Andrew N. Hogan Carolyn J. Hogg Timothy A. Hore Taosheng Huang Juan Carlos Izpisúa Belmonte Anna J. Jasinska Gareth Jones Eve Jourdain Olga Kashpur Harold L. Katcher Etsuko Katsumata Vimala Kaza Hippokratis Kiaris Michael S. Kobor Paweł Kordowitzki William R. Koski Michael Krützen Soo Bin Kwon Brenda Larison Sang‐Goo Lee Marianne Lehmann Jean‐François Lemaître Andrew J. Levine Xinmin Li Cun Li Andrea R. Lim David Lin Dana M. Lindemann Schuyler Liphardt Thomas J. Little Nicholas Macoretta Dewey Maddox Craig O. Matkin Julie A. Mattison Matthew McClure June Mergl

Using DNA methylation profiles (

10.1126/science.abq5693 article EN Science 2023-08-10

To date, genome-scale analyses in the domestic horse have been limited by suboptimal single nucleotide polymorphism (SNP) density and uneven genomic coverage of current SNP genotyping arrays. The recent availability whole genome sequences has created opportunity to develop a next generation, high-density equine array. Using sequence from 153 individuals representing 24 distinct breeds collated genomics community, we cataloged over 23 million de novo discovered genetic variants. Leveraging...

10.1186/s12864-017-3943-8 article EN cc-by BMC Genomics 2017-07-27
Aimei Lu Zhe Fei Amin Haghani Todd R. Robeck Joseph A. Zoller and 95 more Chengzhang Li Robert Lowe Qi Yan Joshua Zhang Hoang‐Giang Vu Julia Ablaeva Victoria A. Acosta-Rodríguez Denise M. Adams Javier Almunia Ajoy Aloysius Reza Ardehali A Arneson C. Scott Baker Gareth Banks Katherine Belov Nigel C. Bennett Peter McL. Black Daniel T. Blumstein Eleanor K. Bors Charles E. Breeze Robert T. Brooke Janine L. Brown G. Carter Alex Caulton Julie M. Cavin Lisa Chakrabarti Ioulia Chatzistamou Hao Chen Kai Cheng Priscila Chiavellini Oi‐Wa Choi Shannon Clarke Lisa Noelle Cooper Marie‐Laurence Cossette Joanna Day Joseph DeYoung Stacy DiRocco Christopher Dold Erin E. Ehmke Candice K. Emmons Stephan Emmrich Ebru Erbay Claire Erlacher‐Reid Christopher G. Faulkes Steven H. Ferguson Carrie J. Finno Jennifer E. Flower Jean‐Michel Gaillard Eva Garde Livia Gerber Vadim N. Gladyshev Vera Gorbunova Rodolfo G. Goya Maria J. Grant C.B. Green Erin N. Hales M. Bradley Hanson Daniel W. Hart Martin Haulena K. Herrick Andrew N. Hogan Carolyn J. Hogg T.A. Hore Taosheng Huang Juan Carlos Izpisúa Belmonte Anna J. Jasinska Gareth Jones Eve Jourdain Olga Kashpur Harold L. Katcher Etsuko Katsumata Vimala Kaza Hippokratis Kiaris Michael S. Kobor Paweł Kordowitzki William R. Koski Michael Kruetzen Soon‐Bae Kwon Brenda Larison Sang‐Goo Lee Marina Lehmann Jean‐François Lemaître Andrew J. Levine Chengzhang Li X. Li A. Lim David Lin D. Lindemann Tom J. Little Nicholas Macoretta Debra Maddox Craig O. Matkin Julie A. Mattison Mélanie McClure June Mergl

ABSTRACT Aging is often perceived as a degenerative process resulting from random accrual of cellular damage over time. Despite this, age can be accurately estimated by epigenetic clocks based on DNA methylation profiles almost any tissue the body. Since such pan-tissue have been successfully developed for several different species, we hypothesized that one build pan-mammalian measure in all mammalian species. To address generated data using 11,754 arrays, each profiling up to 36 thousand...

10.1101/2021.01.18.426733 preprint EN cc-by-nc bioRxiv (Cold Spring Harbor Laboratory) 2021-01-19

The cause of immune-mediated myositis (IMM), characterized by recurrent, rapid-onset muscle atrophy in Quarter Horses (QH), is unknown. histopathologic hallmark IMM lymphocytic infiltration myofibers. purpose this study was to identify putative functional variants associated with equine IMM. A genome-wide association (GWA) performed on 36 QHs and 54 breed matched unaffected from the same environment using Equine SNP50 SNP70 genotyping arrays. mixed model analysis identified nine SNPs within...

10.1186/s13395-018-0155-0 article EN cc-by Skeletal Muscle 2018-03-06

Abstract Effective conservation and management of threatened wildlife populations require an accurate assessment age structure to estimate demographic trends population viability. Epigenetic aging models are promising developments because they individual with high accuracy, accurately predict in related species, do not invasive sampling or intensive long-term studies. Using blood biopsy samples from known plains zebras ( Equus quagga ), we model epigenetic using two approaches: the clock...

10.1038/s42003-021-02935-z article EN cc-by Communications Biology 2021-12-17

Cyathostomins are ubiquitous equine nematodes. Infection can result in larval cyathostominosis due to mass emergence. Although faecal egg count (FEC) tests provide estimates of shedding, these correlate poorly with burden and no information on mucosal/luminal larvae. Previous studies describe a serum IgG(T)-based ELISA (CT3) that exhibits utility for detection cyathostomins. Here, this is optimised/validated commercial application using sera from horses which data were available....

10.1016/j.ijpara.2023.07.001 article EN cc-by-nc-nd International Journal for Parasitology 2023-08-01

Equine neuroaxonal dystrophy/degenerative myeloencephalopathy (eNAD/EDM) is a neurodegenerative disease that primarily affects young, genetically predisposed horses are deficient in vitamin E. NAD/EDM has not previously been documented Gypsy Vanner (GVs).

10.1111/jvim.17062 article EN cc-by-nc-nd Journal of Veterinary Internal Medicine 2024-04-13

Horses obtain vitamin E, an essential nutrient for neuromuscular health, through green pasture. Vitamin E dietary deficiencies can lead to diseases such as equine neuroaxonal dystrophy/equine degenerative myeloencephalopathy, motor neuron disease and deficient myopathy. Some horses are genetically susceptible developing these diseases, but not all that exhibit clinical signs. supplementation is effective at slowing or halting signs of some the damage usually irreversible, except in case...

10.12968/ukve.2023.0049 article EN UK-Vet Equine 2025-01-02

Equine spinal neurodegenerative conditions are frequently encountered in sport and racing horses may be career-ending diagnoses. To further define the spatial transcriptomic landscape of equine dorsal root ganglia (DRG) healthy adult horses, we investigated gene expression differences distinct DRG regions using GeoMx Digital Spatial Profiling from NanoString. Four human cell markers demonstrated high fidelity for cells; microtubule-associated protein 2 (MAP2), myelin basic (MBP), allograft...

10.1177/03009858241312623 article EN cc-by-nc Veterinary Pathology 2025-02-06

Abstract Anhidrosis is defined as a decreased or absent ability to sweat in response heat and exercise. In horses, this condition can increase the risk of life‐threatening hyperthermia. A prior study has suggested that equine anhidrosis associated with missense variant (rs68643109) Potassium Voltage‐Gated Channel Subfamily E Regulatory Subunit 4 ( KCNE4 ) gene. This project aimed validate association population well‐phenotyped horses determine allele frequency publicly available whole‐genome...

10.1111/age.70004 article EN cc-by Animal Genetics 2025-02-01

The Functional Annotation of Animal Genomes (FAANG) consortium aims to annotate animal genomes across species, and work in the horse has substantially contributed that goal. As part this initiative, chromatin immunoprecipitation with sequencing (ChIP-seq) was performed identify histone modifications corresponding enhancers (H3K4me1), promoters (H3K4me3), activators (H3K27ac), repressors (H3K27me3) eight tissues from two Thoroughbred stallions: adipose, parietal cortex, heart, lamina, liver,...

10.3389/fgene.2025.1534461 article EN cc-by Frontiers in Genetics 2025-02-27

Abstract Objective —To characterize onset and clinical signs of polysaccharide storage myopathy (PSSM) in a welldefined population affected Quarter Horses, identify risk factors for PSSM, determine compliance owners to dietary exercise recommendations, evaluate the efficacy recommendations. Animals —40 Horses with PSSM 37 unaffected control horses. Procedure s—Owners horses completed retrospective questionnaire concerning their horse's condition. Results —Between horses, no significant...

10.2460/ajvr.2003.64.1319 article EN American Journal of Veterinary Research 2003-10-01

To describe epidemiological, clinical, and pathological features of neuroaxonal dystrophy in Quarter Horses (QHs) on a single farm.Prospective case series. Animals-148 horses.Neurologic, pathological, toxicological evaluations were completed selected neurologically affected horses over 2-year period. Descriptive statistical analysis was performed.87 QHs 1 QH-crossbred horse affected. Most (50/88 [56.8%]) to 2 years old (median age, [range, months 34 years]). Neurologic deficits included...

10.2460/javma.239.6.823 article EN Journal of the American Veterinary Medical Association 2011-09-15

The Functional Annotation of Animal Genomes (FAANG) project aims to identify genomic regulatory elements in both sexes across multiple stages development domesticated animals. This study represents the first stage FAANG for horse, Equus caballus. A biobank 80 tissue samples, two cell lines and six body fluids was created from adult Thoroughbred mares. Ante-mortem assessments included full physical examinations, lameness, ophthalmologic neurologic evaluations. Complete blood counts serum...

10.1111/age.12717 article EN publisher-specific-oa Animal Genetics 2018-10-11
Coming Soon ...