R. Alan Harris

ORCID: 0000-0002-7333-4752
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About
Contact & Profiles
Research Areas
  • Epigenetics and DNA Methylation
  • Chromosomal and Genetic Variations
  • Genomics and Phylogenetic Studies
  • Genomic variations and chromosomal abnormalities
  • Primate Behavior and Ecology
  • Genomics and Chromatin Dynamics
  • RNA modifications and cancer
  • Genomics and Rare Diseases
  • Birth, Development, and Health
  • Cancer-related molecular mechanisms research
  • Evolution and Genetic Dynamics
  • Cancer Genomics and Diagnostics
  • Inflammatory Bowel Disease
  • Diet and metabolism studies
  • Genetic Syndromes and Imprinting
  • MicroRNA in disease regulation
  • Single-cell and spatial transcriptomics
  • Gut microbiota and health
  • Infant Nutrition and Health
  • Neonatal Respiratory Health Research
  • T-cell and B-cell Immunology
  • Immune Cell Function and Interaction
  • CRISPR and Genetic Engineering
  • Adipose Tissue and Metabolism
  • Reproductive System and Pregnancy

Baylor Genetics
2016-2025

Baylor College of Medicine
2016-2025

NSF’s NOIRLab
2020-2024

Texas Children's Hospital
2011-2016

Livingstone College
2016

The University of Texas Health Science Center at Houston
2015

University at Albany, State University of New York
2013-2015

Albany State University
2013-2015

University of Houston
2010-2014

Magellan Aerospace (Canada)
2014

The reference human genome sequence set the stage for studies of genetic variation and its association with disease, but epigenomic lack a similar reference. To address this need, NIH Roadmap Epigenomics Consortium generated largest collection so far epigenomes primary cells tissues. Here we describe integrative analysis 111 as part programme, profiled histone modification patterns, DNA accessibility, methylation RNA expression. We establish global maps regulatory elements, define modules...

10.1038/nature14248 article EN cc-by-nc-sa Nature 2015-02-17
Richard A. Gibbs Jeffrey Rogers Michael G. Katze Roger E. Bumgarner George M. Weinstock and 95 more Elaine R. Mardis Karin Remington Robert L. Strausberg J. Craig Venter Richard K. Wilson Mark A. Batzer Carlos D. Bustamante Evan E. Eichler Matthew W. Hahn Ross C. Hardison Kateryna D. Makova Webb Miller Aleksandar Milosavljevic Robert E. Palermo Adam Siepel James M. Sikela Tony Attaway Stephanie Bell Kelly E. Bernard Christian Buhay Mimi N. Chandrabose Marvin Dao Clay Davis Kimberly D. Delehaunty Yan Ding Huyen Dinh Shannon Dugan-Rocha Lucinda A. Fulton Ramatu Ayiesha Gabisi Toni T. Garner Jennifer Godfrey Alicia Hawes Judith Hernandez Sandra Hines Michael Holder Jennifer Hume Shalini N. Jhangiani Vandita Joshi Ziad Khan Ewen F. Kirkness Andrew Cree R. Gerald Fowler Charles Lee Lora Lewis Zhangwan Li Yih-shin Liu Stephanie Moore Donna M. Muzny Lynne V. Nazareth Dinh Ngoc Ngo Geoffrey Okwuonu Grace Pai David L. Parker Heidie A. Paul Cynthia Pfannkoch Craig Pohl Yu-Hui Rogers San Juana Ruiz Aniko Sabo Jireh Santibanez Brian Schneider Scott M. Smith Erica Sodergren Amanda F. Svatek Teresa R. Utterback Selina Vattathil Wesley C. Warren Courtney White Asif Chinwalla Yucheng Feng Aaron L. Halpern LaDeana W. Hillier Xiaoqiu Huang Pat Minx Joanne O. Nelson Kymberlie Pepin Xiang Qin Granger G. Sutton Eli Venter Brian P. Walenz John W. Wallis Kim C. Worley Shiaw‐Pyng Yang Steven J.M. Jones Marco A. Marra Mariano Rocchi Jacqueline E. Schein Robert Baertsch Laura Clarke Miklós Csürös Jarret Glasscock R. Alan Harris Paul Havlak Andrew Jackson Huaiyang Jiang

The rhesus macaque (Macaca mulatta) is an abundant primate species that diverged from the ancestors of Homo sapiens about 25 million years ago. Because they are genetically and physiologically similar to humans, monkeys most widely used nonhuman in basic applied biomedical research. We determined genome sequence Indian-origin Macaca mulatta female compared data with chimpanzees humans reveal structure ancestral genomes identify evidence for positive selection lineage-specific expansions...

10.1126/science.1139247 article EN Science 2007-04-12

Abstract Background Dynamic changes to the epigenome play a critical role in establishing and maintaining cellular phenotype during differentiation, but little is known about normal methylomic differences that occur between functionally distinct areas of brain. We characterized intra- inter-individual variation across whole blood multiple regions brain from donors. Results Distinct tissue-specific patterns DNA methylation were identified, with highly significant over-representation...

10.1186/gb-2012-13-6-r43 article EN cc-by Genome biology 2012-06-15

Throughout most of the mammalian genome, genetically regulated developmental programming establishes diverse yet predictable epigenetic states across differentiated cells and tissues. At metastable epialleles (MEs), conversely, epigenotype is established stochastically in early embryo then maintained lineages, resulting dramatic systemic interindividual variation regulation. In mouse, maternal nutrition affects this process, with permanent phenotypic consequences for offspring. MEs have not...

10.1371/journal.pgen.1001252 article EN cc-by PLoS Genetics 2010-12-23
Lucia Carbone R. Alan Harris Sante Gnerre Krishna R. Veeramah Belén Lorente-Galdós and 88 more John Huddleston Thomas J. Meyer Javier Herrero Christian Roos Bronwen Aken Fabio Anaclerio Nicoletta Archidiacono Carl Baker Daniel Barrell Mark A. Batzer Kathryn Beal Antoine Blancher Craig L. Bohrson Markus Brameier Michael S. Campbell Oronzo Capozzi Claudio Casola Giorgia Chiatante Andrew Cree Annette Damert Pieter J. de Jong Laura Dumas Marcos Fernández-Callejo Paul Flicek Nina V. Fuchs Marta Gut Marta Gut Matthew W. Hahn Jessica Hernandez‐Rodriguez LaDeana W. Hillier Robert Hubley Bianca Ianc Zsuzsanna Izsvák Nina G. Jablonski Laurel Johnstone Anis Karimpour‐Fard Miriam K. Konkel Dennis Kostka Nathan H. Lazar Sandra L. Lee Lora Lewis Yue Liu Devin P. Locke Swapan Mallick Fernando L. Méndez Matthieu Muffato Lynne V. Nazareth Kimberly A. Nevonen Majesta O’Bleness Cornelia Ochis Duncan T. Odom Katherine S. Pollard Javier Quilez David Reich Mariano Rocchi Gerald G. Schumann Stephen M. J. Searle James M. Sikela Gabriella Skollár Arian F. A. Smit Kemal Sönmez Boudewijn ten Hallers Elizabeth Terhune Gregg W.C. Thomas Brygg Ullmer Mario Ventura Jerilyn A. Walker Jeffrey D. Wall Lutz Walter Michelle C. Ward Sarah J. Wheelan Christopher W. Whelan Simon White Larry Wilhelm August E. Woerner Mark Yandell Baoli Zhu Michael F. Hammer Tomás Marquès‐Bonet Evan E. Eichler Lucinda A. Fulton Catrina C. Fronick Donna M. Muzny Wesley C. Warren Kim C. Worley Jeffrey Rogers Richard K. Wilson Richard A. Gibbs

Gibbons are small arboreal apes that display an accelerated rate of evolutionary chromosomal rearrangement and occupy a key node in the primate phylogeny between Old World monkeys great apes. Here we present assembly analysis northern white-cheeked gibbon (Nomascus leucogenys) genome. We describe propensity for gibbon-specific retrotransposon (LAVA) to insert into chromosome segregation genes alter transcription by providing premature termination site, suggesting possible molecular mechanism...

10.1038/nature13679 article EN cc-by-nc-sa Nature 2014-09-09
Kim C. Worley Wesley C. Warren Jeffrey Rogers Devin P. Locke Donna M. Muzny and 95 more Elaine R. Mardis George M. Weinstock Suzette D. Tardif Kjersti M. Aagaard Nicoletta Archidiacono Nirmala Arul Rayan Mark A. Batzer Kathryn Beal Broňa Brejová Oronzo Capozzi Saverio B. Capuano Claudio Casola Mimi M. Chandrabose Andrew Cree Marvin Dao Pieter J. de Jong Ricardo Cruz-Herrera del Rosario Kim D. Delehaunty Huyen Dinh Evan E. Eichler Stephen Fitzgerald Paul Flicek Catherine C. Fontenot R. Gerald Fowler Catrina C. Fronick Lucinda A. Fulton Robert S. Fulton Ramatu Ayiesha Gabisi Daniel Gerlach Tina Graves Preethi H. Gunaratne Matthew W. Hahn David Haig Yi Han R. Alan Harris Javier Herrero La Deana W. Hillier Robert Hubley Jennifer F. Hughes Jennifer Hume Shalini N. Jhangiani Lynn B. Jorde Vandita Joshi Emre Karakor Miriam K. Konkel Carolin Kosiol Christie LKovar Evgenia V. Kriventseva Sandra L. Lee Lora Lewis Y. Liu John Lopez Carlos López-Otı́n Belén Lorente-Galdós Keith G. Mansfield Tomás Marquès‐Bonet Patrick Minx Doriana Misceo Joanna Moncrieff Margaret Morgan Lynne V. Nazareth Irene Newsham Ngoc B. Nguyen Geoffrey Okwuonu Shyam Prabhakar Lora Perales Ling Pu Xosé S. Puente Vı́ctor Quesada Megan C. Ranck Brian J. Raney Muthuswamy Raveendran David Rio Deiros Mariano Rocchi David Rodrı́guez Corinna N. Ross Magali Ruffier San Juana Ruiz Saba Sajjadian Jireh Santibanez Daniel R. Schrider Steve Searle Helen Skaletsky Benjamin Soibam Arian F. A. Smit Jayantha B. Tennakoon Ľubomír Tomáška Brygg Ullmer Charles E. Vejnar Mario Ventura Albert J. Vilella Tomáš Vinař Jan Vogel Jerilyn A. Walker Qing Wang

We report the whole-genome sequence of common marmoset (Callithrix jacchus). The 2.26-Gb genome a female was assembled using Sanger read data (6×) and shotgun strategy. A first analysis has permitted comparison with genomes apes Old World monkeys identification specific features that might contribute to unique biology this diminutive primate, including genetic changes may influence body size, frequent twinning chimerism. observed positive selection in growth hormone/insulin-like factor genes...

10.1038/ng.3042 article EN cc-by-nc-sa Nature Genetics 2014-07-16

A high-quality rhesus macaque genome Genome technology has improved substantially since the first full organismal genomes were generated. Applying new technology, Warren et al. refined of macaque, a model nonhuman primate. Long-read and other recent advances in sequencing applied to generate with far fewer gaps helped refine locations numbers repetitive elements. Furthermore, authors performed resequencing among populations identify genetic variability macaque. Thus, previously incomplete...

10.1126/science.abc6617 article EN Science 2020-12-18

The rich diversity of morphology and behavior displayed across primate species provides an informative context in which to study the impact genomic on fundamental biological processes. Analysis that insight into long-standing questions evolutionary conservation biology is urgent given severe threats these are facing. Here, we present high-coverage whole-genome data from 233 representing 86% genera all 16 families. This dataset was used, together with fossil calibration, create a nuclear DNA...

10.1126/science.abn7829 article EN Science 2023-06-01
Hong Gao Tobias Hamp Jeffrey M. Ede Joshua G. Schraiber Jeremy F. McRae and 92 more Moriel Singer‐Berk Yanshen Yang Anastasia S. D. Dietrich Petko Fiziev Lukas F. K. Kuderna Laksshman Sundaram Yibing Wu Aashish N. Adhikari Yair Field Chen Chen Serafim Batzoglou François Aguet Gabrielle Lemire Rebecca Reimers Daniel J. Balick Mareike C. Janiak Martin Kuhlwilm Joseph D. Orkin Shivakumara Manu Alejandro Valenzuela Juraj Bergman Marjolaine Rousselle Felipe Ennes Silva Lídia Águeda Julie Blanc Marta Gut Dorien de Vries Ian Goodhead R. Alan Harris Muthuswamy Raveendran Axel Jensen Idriss S. Chuma Julie E. Horvath Christina Hvilsom David Juan Peter Frandsen Fabiano Rodrigues de Melo Fabrício Bertuol Hazel Byrne Iracilda Sampaio Izeni Pires Farias João Valsecchi Mariluce Rezende Messias Maria Nazareth Ferreira da Silva Mihir Trivedi Rogério Vieira Rossi Tomas Hrbek Nicole Andriaholinirina C. Rabarivola Alphonse Zaramody Clifford J. Jolly Jane E. Phillips‐Conroy Gregory K. Wilkerson Christian R. Abee Joe H. Simmons Eduardo Fernández‐Duque Sree Kanthaswamy Fekadu Shiferaw Dong‐Dong Wu Long Zhou Yong Shao Guojie Zhang Julius D. Keyyu Sascha Knauf Minh Đức Lê Esther Lizano Stefan Merker Arcadi Navarro Thomas Bataillon Tilo Nadler Chiea Chuen Khor Jessica Lee Patrick Tan Weng Khong Lim Andrew C. Kitchener Dietmar Zinner Marta Gut Amanda Melin Katerina Guschanski Mikkel Heide Schierup Robin M. D. Beck Govindhaswamy Umapathy Christian Roos Jean P. Boubli Monkol Lek Shamil Sunyaev Anne O’Donnell‐Luria Heidi L. Rehm Jinbo Xu Jeffrey Rogers Tomás Marquès‐Bonet Kyle Kai‐How Farh

Personalized genome sequencing has revealed millions of genetic differences between individuals, but our understanding their clinical relevance remains largely incomplete. To systematically decipher the effects human variants, we obtained whole-genome data for 809 individuals from 233 primate species and identified 4.3 million common protein-altering variants with orthologs in humans. We show that these can be inferred to have nondeleterious humans based on presence at high allele...

10.1126/science.abn8197 article EN Science 2023-06-01

While CD4+ T cell depletion is key to disease progression in people living with HIV and SIV-infected macaques, the mechanisms underlying this remain incompletely understood, most death involving uninfected cells. In contrast, SIV infection of "natural" hosts such as sooty mangabeys does not cause AIDS despite high-level viremia. Here, we report that CARD8 inflammasome activated immediately after entry by viral protease encapsulated incoming virions. Sensing activity leads rapid pyroptosis...

10.1016/j.cell.2024.01.048 article EN cc-by Cell 2024-02-01

MicroRNAs (miRNAs) are short, non-coding RNAs that target and silence protein coding genes through 3′-UTR elements. Evidence increasingly assigns an immunosuppressive role for miRNAs in immunity, but relatively few have been studied, overall understanding of the importance these regulatory transcripts complex <i>in vivo</i> systems is lacking. Here we applied multiple technologies to globally analyze miRNA expression function allergic lung disease, experimental model asthma. Deep sequencing...

10.1074/jbc.m110.145698 article EN cc-by Journal of Biological Chemistry 2010-07-15

Fifteen patients with a variety of myoclonic syndromes were studied clinically, pharmacologically, and physiologically. CSF tryptophan, 5HIAA, HVA also measured. Of these patients, 8 improved to varying degrees by therapy 5HTP, tryptophan in combination MAOI (but not alone), clonazepam. This group included 6 cases post-anoxic myoclonus, one case post-traumatic myoclonus undiagnosed non-progressive focal epilepsy. In this low levels 5HIAA found compared non-responsive controls. Two dysynergia...

10.1093/brain/100.3.455 article EN Brain 1977-01-01

While breast milk has unique health advantages for infants, the mechanisms by which it regulates physiology of newborns are incompletely understood. miRNAs have been described as functioning transcellularly, and previously isolated in cell-free exosomal form from bodily liquids (serum, saliva, urine) tissues, including mammary tissue. We hypothesized that general, fat globules particular, contain significant numbers known limited novel miRNA species detectable with massively parallel...

10.1371/journal.pone.0050564 article EN cc-by PLoS ONE 2013-02-13

In nonhuman primates, we previously demonstrated that a maternal high-fat diet (MHFD) induces fetal nonalcoholic fatty liver disease (NAFLD) and alters the metabolome. These changes are accompanied by altered acetylation of histone H3 (H3K14ac). However, mechanism behind this alteration in remains unknown. As SIRT1 is both lysine deacetylase crucial sensor cellular metabolism, hypothesized may be involved epigenomic alterations. Here show utero exposure to MHFD, but not obesity per se,...

10.1096/fj.12-212878 article EN The FASEB Journal 2012-09-14

Nuage are amorphous ultrastructural granules in the cytoplasm of male germ cells as divergent Drosophila, Xenopus, and Homo sapiens. Most nuage cytoplasmic ribonucleoprotein structures implicated diverse RNA metabolism including regulation PIWI-interacting (piRNA) synthesis by PIWI family (i.e., MILI, MIWI2, MIWI). MILI is prominent embryonic early post-natal also called germinal that often associated with mitochondria intermitochondrial cement. We find GASZ (Germ cell protein Ankyrin...

10.1371/journal.pgen.1000635 article EN cc-by PLoS Genetics 2009-09-03

Developmental epigenetic changes, such as DNA methylation, have been recognized potential pathogenic factors in inflammatory bowel diseases, the hallmark of which is an exaggerated immune response against luminal microbes. A methyl-donor (MD) diet can modify methylation at select murine genomic loci during early development. The components MDs are routinely incorporated into prenatal human supplements. Therefore, we studied effects maternal MD supplementation on offspring colitis...

10.1093/hmg/ddr044 article EN Human Molecular Genetics 2011-02-04

Small non-coding RNAs, such as microRNAs (miRNAs), are involved in diverse biological processes including organ development and tissue differentiation. Global disruption of miRNA biogenesis Dicer knockout mice disrupts early embryogenesis primordial germ cell formation. However, the role miRNAs folliculogenesis is poorly understood. In order to identify a full transcriptome set small RNAs expressed newborn (NB) ovary, we extracted RNA fraction from mouse NB ovary tissues subjected it massive...

10.1093/molehr/gaq017 article EN Molecular Human Reproduction 2010-03-09

The connection between intestinal micro-biota and host physiology is increasingly becoming recognized. details of this dynamic interaction, however, remain to be explored. Toll-like receptor 2 (Tlr2) important for its role in bacterial recognition, inflammation, obesity-related metabolic changes. Therefore, we sought determine the epigenomic metagenomic consequences Tlr2 deficiency colonic mucosa mice gain insights into biological pathways that shape interface gut mammalian host. Colonic...

10.1096/fj.10-172205 article EN The FASEB Journal 2011-01-12

Inflammatory bowel diseases (IBDs) are heterogeneous disorders with complex aetiology. Quantitative genetic studies suggest that only a small proportion of the disease variance observed in IBD is accounted for by variation, indicating potential role differential epigenetic regulation The aim this study was to assess genome-wide DNA methylation changes specifically associated ulcerative colitis (UC), Crohn's (CD) and activity.DNA quantified peripheral blood mononuclear cells (PBMCs) from 149...

10.1093/ecco-jcc/jjv176 article EN Journal of Crohn s and Colitis 2015-09-28

Abstract Zika virus (ZIKV) is an emerging mosquito-borne ( Aedes genus) arbovirus of the Flaviviridae family. Although ZIKV has been predominately associated with a mild or asymptomatic dengue-like disease, its appearance in Americas accompanied by multi-fold increase reported incidence fetal microcephaly and brain malformations. The source mode vertical transmission from mother to fetus presumptively transplacental, although causal link explaining interval delay between maternal symptoms...

10.1038/srep41389 article EN cc-by Scientific Reports 2017-01-27
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