Patrick Reed

ORCID: 0000-0001-7229-814X
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About
Contact & Profiles
Research Areas
  • Genomic variations and chromosomal abnormalities
  • Genomics and Rare Diseases
  • CRISPR and Genetic Engineering
  • Cancer Genomics and Diagnostics
  • Genetics and Neurodevelopmental Disorders
  • Genomics and Chromatin Dynamics
  • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
  • Renal and related cancers
  • Single-cell and spatial transcriptomics
  • DNA Repair Mechanisms
  • Genomics and Phylogenetic Studies
  • Pluripotent Stem Cells Research
  • Prenatal Screening and Diagnostics
  • Receptor Mechanisms and Signaling
  • Neuropeptides and Animal Physiology
  • Sleep and Wakefulness Research
  • Cell Image Analysis Techniques
  • interferon and immune responses
  • Mathematical Biology Tumor Growth
  • Hedgehog Signaling Pathway Studies
  • Functional Brain Connectivity Studies
  • Genetic Associations and Epidemiology
  • Memory and Neural Mechanisms
  • Fetal and Pediatric Neurological Disorders
  • Alzheimer's disease research and treatments

Salk Institute for Biological Studies
2017-2024

University of North Carolina at Chapel Hill
2023

University of Washington
2008-2010

10.1016/j.ajhg.2015.07.004 article EN publisher-specific-oa The American Journal of Human Genetics 2015-07-30
Rachel E. Rodin Yanmei Dou Minseok Kwon Maxwell A. Sherman Alissa M. D’Gama and 95 more Ryan N. Doan Lariza M. Rento Kelly M. Girskis Craig L. Bohrson Sonia N. Kim Ajay Nadig Lovelace J. Luquette D. Gulhan Christopher A. Walsh Javier Ganz Mollie B. Woodworth Pengpeng Li Rachel E. Rodin Robert Hill Sara Bizzotto Zinan Zhou Eunjung A. Lee Alison R. Barton Alissa M. D’Gama Alon Galor Craig L. Bohrson Daniel H. Kwon D. Gulhan Elaine T. Lim Isidro Cortes Lovelace J. Luquette Maxwell A. Sherman Michael E. Coulter Michael A. Lodato Peter J. Park Rebeca B. Monroy Sonia N. Kim Yanmei Dou Andrew Chess Attila Gulyás-Kovács Chaggai Rosenbluh Schahram Akbarian Ben Langmead Jeremy Thorpe Jonathan Pevsner Soonweng Cho Andrew E. Jaffe Apuã C.M. Paquola Daniel R. Weinberger Jennifer A. Erwin Jooheon Shin Richard E. Straub Rujuta Narurkar Alexej Abyzov Taejeong Bae Anjené Addington David M. Panchision Yanmei Dou Geetha Senthil Lora Bingaman Tara Dutka Thomas Lehner Laura Saucedo-Cuevas Tara Conniff Kenneth Daily Mette A. Peters Fred H. Gage Meiyan Wang Patrick Reed Sara B. Linker Alex E. Urban Bo Zhou Xiaowei Zhu Aitor Serres David Juan Inna Povolotskaya Irene Lobón Manuel Solís-Moruno Raquel García-Pérez Tomás Marquès‐Bonet Gary W. Mathern Jing Gu Joseph G. Gleeson Laurel Ball Renee D. George Tiziano Pramparo Diane A. Flasch Trenton J. Frisbie Jeffrey M. Kidd John B. Moldovan John V. Moran Kenneth Y. Kwan Ryan E. Mills Sarah B. Emery Weichen Zhou Yifan Wang Aakrosh Ratan Michael J. McConnell Flora M. Vaccarino Gianfilippo Coppola

10.1038/s41593-020-00765-6 article EN Nature Neuroscience 2021-01-11

DNA repair within neurons Humans have only a limited capacity to generate new neurons. These cells thus need errors in the genome. To better understand this process, Reid et al. developed Repair-seq, method locate genome of stem cell–derived hotspots (DRHs) were more likely occur specific genomic features such as gene bodies well formations, open chromatin, and active regulatory regions. This showed that was enriched at sites involved neuronal function identity. Furthermore, proteomic data...

10.1126/science.abb9032 article EN Science 2021-04-01
Taejeong Bae Liana Fasching Yifan Wang Joo Heon Shin Milovan Šuvakov and 95 more Yeongjun Jang Scott Norton Caroline Dias Jessica Mariani Alexandre Jourdon Feinan Wu Arijit Panda Reenal Pattni Yasmine Chahine Rebecca C. Yeh Rosalinda C. Roberts Anita Hüttner Joel E. Kleinman Thomas M. Hyde Richard E. Straub Christopher A. Walsh Alexander E. Urban James F. Leckman Daniel R. Weinberger Flora M. Vaccarino Alexej Abyzov Christopher A. Walsh Peter J. Park Nenad Šestan Daniel R. Weinberger John V. Moran Fred H. Gage Flora M. Vaccarino Joseph G. Gleeson Gary W. Mathern Eric Courchesne Subhojit Roy Andrew Chess Schahram Akbarian Sara Bizzotto Michael E. Coulter Caroline Dias Alissa M. D’Gama Javier Ganz Robert Hill August Yue Huang Sattar Khoshkhoo Sonia Kim Alice Lee Michael A. Lodato Eduardo A. Maury Michael Miller Rebeca Borges-Monroy Rachel E. Rodin Zinan Zhou Craig L. Bohrson Chong Chu Isidro Cortés‐Ciriano Yanmei Dou Alon Galor D. Gulhan Min‐Seok Kwon Joe Luquette Maxwell A. Sherman Vinay Viswanadham Attila Jones Chaggai Rosenbluh Sean Cho Ben Langmead Jeremy Thorpe Jennifer A. Erwin Andrew E. Jaffe Michael J. McConnell Rujuta Narurkar Apuã C.M. Paquola Jooheon Shin Richard E. Straub Alexej Abyzov Taejeong Bae Yeongjun Jang Yifan Wang Cindy Molitor Mette A. Peters Sara B. Linker Patrick Reed Meiyan Wang Alexander E. Urban Bo Zhou Xiaowei Zhu Reenal Pattni Aitor Serres Amero David Juan Irene Lobón Tomás Marquès‐Bonet Manuel Solis Moruno Raquel García Pérez Inna Povolotskaya Eduardo Soriano Danny Antaki Dan Averbuj

We analyzed 131 human brains (44 neurotypical, 19 with Tourette syndrome, 9 schizophrenia, and 59 autism) for somatic mutations after whole genome sequencing to a depth of more than 200×. Typically, had 20 60 detectable single-nucleotide mutations, but ~6% harbored hundreds mutations. Hypermutability was associated age damaging in genes implicated cancers and, some brains, reflected vivo clonal expansions. Somatic duplications, likely arising during development, were found ~5% normal...

10.1126/science.abm6222 article EN Science 2022-07-28

10.1038/s41586-022-04602-7 article EN Nature 2022-04-20

10.1038/s41587-022-01559-w article EN Nature Biotechnology 2023-01-02

Abstract Schizophrenia affects approximately 1% of the world population. Genetics, epigenetics, and environmental factors are known to play a role in this psychiatric disorder. While there is high concordance monozygotic twins, about half twin pairs discordant for schizophrenia. To address question how when twins occur, we have obtained fibroblasts from two schizophrenia (one sibling with while second one unaffected by schizophrenia) three healthy (both siblings healthy). We prepared iPSC...

10.1038/s41380-024-02561-1 article EN cc-by Molecular Psychiatry 2024-05-04

Abstract When somatic cells acquire complex karyotypes, they often are removed by the immune system. Mutant that evade surveillance can lead to cancer. Neurons with karyotypes arise during neurotypical brain development, but neurons almost never origin of cancers. Instead, mutations in bring about neurodevelopmental disorders, and contribute polygenic landscape neuropsychiatric neurodegenerative disease. A subset human harbors idiosyncratic copy number variants (CNVs, “CNV neurons”),...

10.1038/s41467-024-48392-0 article EN cc-by Nature Communications 2024-05-17

10.1038/s41593-020-00767-4 article EN Nature Neuroscience 2021-01-11
Dara Tolchin J. Paige Yeager Priya Prasad Naghmeh Dorrani Alvaro Serrano Russi and 95 more Julián A. Martínez-Agosto Abdul Haseeb Marco Angelozzi Gijs W.E. Santen Claudia Ruivenkamp Saadet Mercimek‐Andrews Christel Depienne Alma Kuechler Barbara Mikat Hermann‐Josef Lüdecke Frédéric Bilan Gwenaël Le Guyader Brigitte Gilbert‐Dussardier Boris Keren Solveig Heide Damien Haye Hilde Van Esch Liesbeth Keldermans Damara Ortiz Emily Lancaster Ian D. Krantz Bryan L. Krock Kieran B. Pechter Alexandre Arkader Līvija Medne Elizabeth T. DeChene Eduardo Calpena Giada Melistaccio Andrew O.M. Wilkie Mohnish Suri Nicola Foulds Amber Begtrup Lindsay B. Henderson Cara Forster Patrick Reed Marie McDonald Allyn McConkie‐Rosell Julien Thévenon Pauline Le Tanno Charles Coutton Anne Tsai Sarah Stewart Aleš Maver Rudolf Gorazd Olivier Pichon Mathilde Nizon Benjamin Cogné Bertrand Isidor Dominique Martin–Coignard Radka Stoeva Véronique Lefebvre Cédric Le Caignec John C. Ambrose Marta Bleda F. Boardman-Pretty J. M. Boissiere C. R. Boustred Mark J. Caulfield G. C. Chan C.E.H. Craig Louise C. Daugherty Anna de Burca A. Devereau Greg Elgar Rebecca E. Foulger Tom Fowler Pedro Furió‐Tarí J.M. Hackett Dina Halai John E. Holman Tim Hubbard Dalia Kasperavičiūtė Melis Kayikci L. Lahnstein Keith A. Lawson S. E. A. Leigh Ivone Leong Fabrice Lopez F. Maleady-Crowe James Mason Ellen M. McDonagh Loukas Moutsianas M. Mueller Anna C. Need Christopher A. Odhams C. Patch D. Perez-Gil Dimitris Polychronopoulos J. Pullinger T. Rahim Augusto Rendon Tim Rogers Mina Ryten K. Savage Richard H. Scott

10.1016/j.ajhg.2020.04.015 article EN publisher-specific-oa The American Journal of Human Genetics 2020-05-21

Schizophrenia (SZ) is a serious mental illness and neuropsychiatric brain disorder with behavioral symptoms that include hallucinations, delusions, disorganized behavior, cognitive impairment. Regulation of such behaviors requires utilization neurotransmitters released to mediate cell-cell communication which are essential functions in health disease. We hypothesized SZ may involve dysregulation secreted from neurons. To gain an understanding human SZ, induced neurons (iNs) were derived...

10.1038/s41380-024-02422-x article EN cc-by Molecular Psychiatry 2024-02-02

Abstract Somatic mosaicism is defined as an occurrence of two or more populations cells having genomic sequences differing at given loci in individual who derived from a single zygote. It characteristic multicellular organisms that plays crucial role normal development and disease. To study the nature extent somatic autism spectrum disorder, bipolar focal cortical dysplasia, schizophrenia, Tourette syndrome, multi-institutional consortium called Brain Mosaicism Network (BSMN) was formed...

10.1038/s41597-023-02645-7 article EN cc-by Scientific Data 2023-11-20

As with all mathematical modeling, the scope of question to be explored determines most appropriate model. The case is no different for modeling primary brain tumors (gliomas), ranging from too simple, not accounting major feature gliomas (extensive invasion), complicated, many variables and easy way translate culture media in vitro tissue vivo. We settle on a "just right" approach which utilizes currently available magnetic resonance imaging (MRI) estimate two defining characteristics, net...

10.1142/s1793048008000642 article EN Biophysical Reviews and Letters 2008-04-01

Abstract Neurons are the longest-living cells in our bodies, becoming post-mitotic early development upon terminal differentiation. Their lack of DNA replication makes them reliant on repair mechanisms to maintain genome fidelity. These decline with age, potentially giving rise genomic dysfunction that may influence cognitive and neurodegenerative diseases. Despite this challenge, knowledge how instability emerges what neurons other long-lived have evolved protect their integrity over human...

10.1101/2020.03.25.008490 preprint EN cc-by-nc bioRxiv (Cold Spring Harbor Laboratory) 2020-03-26
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