Lindsay Fernández‐Rhodes

ORCID: 0000-0001-6985-423X
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Genetic Associations and Epidemiology
  • Nutrition, Genetics, and Disease
  • Genetic and phenotypic traits in livestock
  • Birth, Development, and Health
  • Cardiovascular Health and Risk Factors
  • Epigenetics and DNA Methylation
  • Genetic Mapping and Diversity in Plants and Animals
  • Obesity, Physical Activity, Diet
  • BRCA gene mutations in cancer
  • Health disparities and outcomes
  • Nutritional Studies and Diet
  • Health, Environment, Cognitive Aging
  • RNA Research and Splicing
  • Hypothalamic control of reproductive hormones
  • Hormonal Regulation and Hypertension
  • Estrogen and related hormone effects
  • Cancer-related molecular mechanisms research
  • Adipose Tissue and Metabolism
  • Racial and Ethnic Identity Research
  • Reproductive Physiology in Livestock
  • Ovarian cancer diagnosis and treatment
  • Food Security and Health in Diverse Populations
  • Neurogenetic and Muscular Disorders Research
  • Obesity and Health Practices
  • Migration, Health and Trauma

Pennsylvania State University
2017-2025

University of North Carolina at Chapel Hill
2015-2024

University of Puerto Rico at Carolina
2023

Lindsay Unified School District
2019

Public Health Department
2012-2018

National Institutes of Health
2009-2014

National Institute of Neurological Disorders and Stroke
2009-2014

10.1038/s41586-019-1310-4 article EN Nature 2019-06-01
Felix R. Day Deborah J. Thompson Hannes Helgason Daniel I. Chasman Hilary K. Finucane and 95 more Patrick Sulem Katherine S. Ruth Sean Whalen Abhishek Sarkar Eva Albrecht Elisabeth Altmaier Marzyeh Amini Caterina Barbieri Thibaud Boutin Archie Campbell Ellen W. Demerath Ayush Giri Chunyan He Jouke‐Jan Hottenga Robert Karlsson Ivana Kolčić Po−Ru Loh Kathryn L. Lunetta Massimo Mangino Marco Brumat George McMahon Sarah E. Medland Ilja M. Nolte Raymond Noordam Teresa Nutile Lavinia Paternoster Natalia Perjakova Eleonora Porcu Lynda M. Rose Katharina E. Schraut Ayellet V. Segrè Albert V. Smith Lisette Stolk Alexander Teumer Irene L. Andrulis Stefania Bandinelli Matthias W. Beckmann Javier Benı́tez Sven Bergmann Murielle Bochud Eric Boerwinkle Stig E. Bojesen Manjeet K. Bolla Judith S. Brand Hiltrud Brauch Hermann Brenner Linda Broer Thomas Brüning Julie E. Buring Harry Campbell Eulalia Catamo Stephen J. Chanock Georgia Chenevix‐Trench Tanguy Corre Fergus J. Couch Diana L. Cousminer Angela Cox Laura Crisponi Kamila Czene George Davey Smith Eco J. C. de Geus Renée de Mutsert Immaculata De Vivo Joe Dennis Peter Devilee Isabel dos‐Santos‐Silva Alison M. Dunning Johan G. Eriksson Peter A. Fasching Lindsay Fernández‐Rhodes Luigi Ferrucci Dieter Flesch‐Janys Lude Franke Marike Gabrielson Ilaria Gandin Graham G. Giles Harald Grallert Daníel F. Guðbjartsson Pascal Guénel Per Hall Emily Hallberg Ute Hamann Tamara B. Harris Catharina A. Hartman Gerardo Heiss Maartje J. Hooning John L. Hopper Frank B. Hu David J. Hunter M. Arfan Ikram Hae Kyung Im Marjo‐Riitta Järvelin Peter K. Joshi David Karasik Manolis Kellis

10.1038/ng.3841 article EN Nature Genetics 2017-04-24
Pierrick Wainschtein Deepti Jain Zhili Zheng Stella Aslibekyan Diane M. Becker and 95 more Wenjian Bi Jennifer A. Brody Jenna C. Carlson Adolfo Correa Margaret Mengmeng Du Lindsay Fernández‐Rhodes Kendra Ferrier Misa Graff Xiuqing Guo Jiang He Nancy L. Heard‐Costa Heather M. Highland Joel N. Hirschhorn Candace M Howard-Claudio Carmen R. Isasi Rebecca D. Jackson Jicai Jiang Roby Joehanes Anne E. Justice Rita R. Kalyani Sharon L. R. Kardia Ethan M. Lange Meryl S. LeBoff Seunggeun Lee Xihao Li Zilin Li Elise Lim D. Y. Lin Xihong Lin Simin Liu Yingchang Lu JoAnn E. Manson Lisa W. Martin Caitlin McHugh Julie Mikulla Solomon K. Musani Maggie Ng Deborah A. Nickerson Colin N. A. Palmer James A. Perry Ulrike Peters Michael Preuß Qibin Qi Laura M. Raffield Laura J. Rasmussen‐Torvik Alex P. Reiner Emily M. Russell Colleen M. Sitlani Jennifer A. Smith Cassandra N. Spracklen Tao Wang Zhe Wang Jennifer Wessel Hanfei Xu Mohammad Yaser Sachiko Yoneyama Kendra A. Young Jingwen Zhang Xinruo Zhang Hufeng Zhou Xiaofeng Zhu Sebastian Zoellner Namiko Abe Gonçalo R. Abecasis François Aguet Laura Almasy Álvaro Alonso Seth A. Ament Peter Anderson Pramod Anugu Deborah Applebaum‐Bowden Kristin Ardlie Dan E. Arking Allison E. Ashley‐Koch Tim Assimes Paul L. Auer Dimitrios Avramopoulos Najib Ayas Adithya Balasubramanian John Barnard Kathleen C. Barnes R. Graham Barr Emily Barron‐Casella Lucas Barwick Terri H. Beaty Gerald J. Beck Lewis C. Becker Rebecca Beer Amber L. Beitelshees Emelia J. Benjamin Takis Benos Marcos Bezerra Larry Bielak Joshua C. Bis Thomas W. Blackwell

10.1038/s41588-021-00997-7 article EN Nature Genetics 2022-03-01

Spinal and bulbar muscular atrophy is an X-linked motor neuron disease caused by a CAG repeat expansion in the androgen receptor gene. To characterize natural history define outcome measures for clinical trials, we assessed history, laboratory findings muscle strength function 57 patients with genetically confirmed disease. We also administered self-assessment questionnaires activities of daily living, quality life erectile function. found average delay over 5 years from onset weakness to...

10.1093/brain/awp258 article EN cc-by-nc Brain 2009-10-21
Katherine A. Kentistou Lena R. Kaisinger Stasa Stankovic Marc Vaudel Edson Mendes de Oliveira and 95 more Andrea Messina Robin Walters Xiaoxi Liu Alexander S Busch Hannes Helgason Deborah J Thompson Federico Santoni Konstantin M. Petricek Yassine Zouaghi Isabel Huang-Doran Daníel F. Guðbjartsson Eirik Bratland Kuang Lin Eugene J. Gardner Yajie Zhao Raina Y Jia Chikashi Terao Marjorie J Riggan Manjeet K Bolla Mojgan Yazdanpanah Nahid Yazdanpanah Jonathan P Bradfield Linda Broer Archie Campbell Daniel I. Chasman Diana L. Cousminer Nora Franceschini Lude Franke Giorgia Girotto Chunyan He Marjo‐Riitta Järvelin Peter K. Joshi Yoichiro Kamatani Robert Karlsson Jian’an Luan Kathryn L. Lunetta Reedik Mägi Massimo Mangino Sarah E. Medland Christa Meisinger Raymond Noordam Teresa Nutile Maria Pina Concas Ozren Polašek Eleonora Porcu Susan M. Ring Cinzia Sala Albert V. Smith Toshiko Tanaka Peter J. van der Most Veronique Vitart Carol A. Wang Gonneke Willemsen Marek Zygmunt Thomas U. Ahearn Irene L. Andrulis Hoda Anton-Culver Antonis C Antoniou Paul L. Auer Catriona L K Barnes Matthias W Beckmann Amy Berrington de González Natalia Bogdanova Stig E. Bojesen Hermann Brenner Julie E. Buring Federico Canzian Jenny Chang‐Claude Fergus J Couch Angela Cox Laura Crisponi Kamila Czene Mary B. Daly Ellen W. Demerath Joe Dennis Peter Devilee Immaculata De Vivo Thilo Dörk Alison M. Dunning Miriam Dwek Johan G. Eriksson Peter A. Fasching Lindsay Fernández‐Rhodes Liana Ferreli Olivia Fletcher Manuela Gago‐Dominguez Montserrat García‐Closas José A. García‐Sáenz Anna González‐Neira Harald Grallert Pascal Guénel Christopher A. Haiman Per Hall Ute Hamann Hákon Hákonarson

Abstract Pubertal timing varies considerably and is associated with later health outcomes. We performed multi-ancestry genetic analyses on ~800,000 women, identifying 1,080 signals for age at menarche. Collectively, these explained 11% of trait variance in an independent sample. Women the top bottom 1% polygenic risk exhibited ~11 ~14-fold higher risks delayed precocious puberty, respectively. identified several genes harboring rare loss-of-function variants ~200,000 including ZNF483 , which...

10.1038/s41588-024-01798-4 article EN cc-by Nature Genetics 2024-07-01

Abstract Objective: Several genome–wide association studies (GWAS) have demonstrated that common genetic variants contribute to obesity. However, of this complex trait focused on ancestrally European populations, despite the high prevalence obesity in some minority groups. Design and Methods: As part “Population Architecture using Genomics Epidemiology (PAGE)” Consortium, we investigated between 13 GWAS‐identified single‐nucleotide polymorphisms (SNPs) BMI 69,775 subjects, including 6,149...

10.1002/oby.20268 article EN Obesity 2013-04-01

Do genetic associations identified in genome-wide association studies (GWAS) of age at menarche (AM) and natural menopause (ANM) replicate women diverse race/ancestry from the Population Architecture using Genomics Epidemiology (PAGE) Study? We replicated GWAS reproductive trait single nucleotide polymorphisms (SNPs) our European descent population found that many SNPs were also associated with AM ANM populations ancestry. Menarche mark lifespan are important risk factors for chronic...

10.1093/humrep/det071 article EN Human Reproduction 2013-03-18

Several genome-wide studies have identified loci associated with reproductive traits, such as ages of menarche and menopause, in women European ancestry. In this study, we investigated the relevance these minority US Hispanic women. We utilized data from 3468 who were genotyped a part Women's Health Initiative SNP Association Resource. replicated associations eight (LRP18, LIN28B, CENPW, INHBA, TMEM38B, ZNF483, NFAT5 OLFM2) age at menarche, two (MCM8 BRSK1/TMEM150B) menopause. The MCM8 locus...

10.1093/hmg/ddr570 article EN Human Molecular Genetics 2011-11-30

Polygenic severe obesity (body mass index [BMI] ≥40 kg/m2) has increased, especially in Hispanic/Latino populations, yet we know little about the underlying mechanistic pathways. We analyzed whole-blood multiomics data to identify genes differentially regulated Mexican Americans from Cameron County Hispanic Cohort. Our RNA sequencing analysis identified 124 significantly expressed between cases (BMI and controls <25 kg/m2); 33% replicated an independent sample same population. integrative...

10.1016/j.xgen.2025.100784 article EN cc-by-nc-nd Cell Genomics 2025-03-01

Age at menarche (AM) and age natural menopause (ANM) define the boundaries of reproductive lifespan in women. Their timing is associated with various diseases, including cancer cardiovascular disease. Genome-wide association studies have identified several genetic variants either AM or ANM populations largely European Asian descent The extent to which these associations generalize diverse remains unknown. Therefore, we sought replicate previously reported findings identify novel using...

10.1371/journal.pone.0055258 article EN cc-by PLoS ONE 2013-02-12

Summary/Abstract Genome-wide association studies (GWAS) have laid the foundation for investigations into biology of complex traits, drug development, and clinical guidelines. However, dominance European-ancestry populations in GWAS creates a biased view role human variation disease, hinders equitable translation genetic associations public health applications. The Population Architecture using Genomics Epidemiology (PAGE) study conducted 26 behavioral phenotypes 49,839 non-European...

10.1101/188094 preprint EN cc-by-nd bioRxiv (Cold Spring Harbor Laboratory) 2017-09-15

Purpose . The adult myopathy assessment tool (AMAT) is a performance-based battery comprised of functional and endurance subscales that can be completed in approximately 30 minutes without the use specialized equipment. purpose this study was to determine construct validity internal consistency AMAT with sample adults spinal bulbar muscular atrophy (SBMA). Methods assessed 56-male participants genetically confirmed SBMA (mean age, 53 ± 10 years). assessments for disease status, strength,...

10.1155/2014/873872 article EN cc-by Rehabilitation Research and Practice 2014-01-01

Obesity is a public health concern. Yet the identification of adiposity-related genetic variants among United States (US) Hispanics, which largest US minority group, remains largely unknown.To interrogate an priori list 47 (32 overall body mass and 15 central adiposity) index single-nucleotide polymorphisms (SNPs) previously studied in individuals European descent 3494 Hispanic women Women's Health Initiative SNP Association Resource (WHI SHARe).Cross-sectional analysis measured (BMI), waist...

10.1038/nutd.2013.26 article EN cc-by Nutrition and Diabetes 2013-08-26
Coming Soon ...