Jeremy Wegner

Jeremy Wegner

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Jeremy Wegner

Jeremy Wegner

Publications by authors named "Jeremy Wegner"

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Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes.

Authors:
Lindsay C Burrage John J Reynolds Nissan Vida Baratang Jennifer B Phillips Jeremy Wegner Ashley McFarquhar Martin R Higgs Audrey E Christiansen Denise G Lanza John R Seavitt Mahim Jain Xiaohui Li David A Parry Vandana Raman David Chitayat Ivan K Chinn Alison A Bertuch Lefkothea Karaviti Alan E Schlesinger Dawn Earl Michael Bamshad Ravi Savarirayan Harsha Doddapaneni Donna Muzny Shalini N Jhangiani Christine M Eng Richard A Gibbs Weimin Bi Lisa Emrick Jill A Rosenfeld John Postlethwait Monte Westerfield Mary E Dickinson Arthur L Beaudet Emmanuelle Ranza Celine Huber Valérie Cormier-Daire Wei Shen Rong Mao Jason D Heaney Jordan S Orange Débora Bertola Guilherme L Yamamoto Wagner A R Baratela Merlin G Butler Asim Ali Mehdi Adeli Daniel H Cohn Deborah Krakow Andrew P Jackson Melissa Lees Amaka C Offiah Colleen M Carlston John C Carey Grant S Stewart Carlos A Bacino Philippe M Campeau Brendan Lee

Am J Hum Genet 2019 03 14;104(3):422-438. Epub 2019 Feb 14.

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA; Texas Children's Hospital, Houston, TX 77030, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2019.01.007DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6408318PMC
March 2019

A Recurrent De Novo Heterozygous COG4 Substitution Leads to Saul-Wilson Syndrome, Disrupted Vesicular Trafficking, and Altered Proteoglycan Glycosylation.

Authors:
Carlos R Ferreira Zhi-Jie Xia Aurélie Clément David A Parry Mariska Davids Fulya Taylan Prashant Sharma Coleman T Turgeon Bernardo Blanco-Sánchez Bobby G Ng Clare V Logan Lynne A Wolfe Benjamin D Solomon Megan T Cho Ganka Douglas Daniel R Carvalho Heiko Bratke Marte Gjøl Haug Jennifer B Phillips Jeremy Wegner Michael Tiemeyer Kazuhiro Aoki Ann Nordgren Anna Hammarsjö Angela L Duker Luis Rohena Hanne Buciek Hove Jakob Ek David Adams Cynthia J Tifft Tito Onyekweli Tara Weixel Ellen Macnamara Kelly Radtke Zöe Powis Dawn Earl Melissa Gabriel Alvaro H Serrano Russi Lauren Brick Mariya Kozenko Emma Tham Kimiyo M Raymond John A Phillips George E Tiller William G Wilson Rizwan Hamid May C V Malicdan Gen Nishimura Giedre Grigelioniene Andrew Jackson Monte Westerfield Michael B Bober William A Gahl Hudson H Freeze

Am J Hum Genet 2018 10;103(4):553-567

Human Genetics Program, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA 92037, USA.

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https://linkinghub.elsevier.com/retrieve/pii/S00029297183031
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http://dx.doi.org/10.1016/j.ajhg.2018.09.003DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6174323PMC
October 2018

Grxcr1 Promotes Hair Bundle Development by Destabilizing the Physical Interaction between Harmonin and Sans Usher Syndrome Proteins.

Authors:
Bernardo Blanco-Sánchez Aurélie Clément Javier Fierro Sarah Stednitz Jennifer B Phillips Jeremy Wegner Jennifer M Panlilio Judy L Peirce Philip Washbourne Monte Westerfield

Cell Rep 2018 10;25(5):1281-1291.e4

Institute of Neuroscience, University of Oregon, Eugene, OR 97403, USA. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S22111247183156
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http://dx.doi.org/10.1016/j.celrep.2018.10.005DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6284068PMC
October 2018

Usherin defects lead to early-onset retinal dysfunction in zebrafish.

Authors:
Margo Dona Ralph Slijkerman Kimberly Lerner Sanne Broekman Jeremy Wegner Taylor Howat Theo Peters Lisette Hetterschijt Nanda Boon Erik de Vrieze Nasrin Sorusch Uwe Wolfrum Hannie Kremer Stephan Neuhauss Jingjing Zang Maarten Kamermans Monte Westerfield Jennifer Phillips Erwin van Wijk

Exp Eye Res 2018 08 16;173:148-159. Epub 2018 May 16.

Department of Otorhinolaryngology, Radboud University Medical Center, Geert Grooteplein 10, 6525 GA Nijmegen, The Netherlands; Donders Institute for Brain, Cognition, and Behavior, Montessorilaan 3, 6525 HR Nijmegen, The Netherlands. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S00144835183024
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http://dx.doi.org/10.1016/j.exer.2018.05.015DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6054812PMC
August 2018

Mutation of POC1B in a severe syndromic retinal ciliopathy.

Authors:
Bodo B Beck Jennifer B Phillips Malte P Bartram Jeremy Wegner Michaela Thoenes Andrea Pannes Josephina Sampson Raoul Heller Heike Göbel Friederike Koerber Antje Neugebauer Andrea Hedergott Gudrun Nürnberg Peter Nürnberg Holger Thiele Janine Altmüller Mohammad R Toliat Simon Staubach Kym M Boycott Enza Maria Valente Andreas R Janecke Tobias Eisenberger Carsten Bergmann Lars Tebbe Yang Wang Yundong Wu Andrew M Fry Monte Westerfield Uwe Wolfrum Hanno J Bolz

Hum Mutat 2014 Oct 11;35(10):1153-62. Epub 2014 Aug 11.

Institute of Human Genetics, University Hospital of Cologne, Cologne, Germany.

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http://dx.doi.org/10.1002/humu.22618DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4425427PMC
October 2014

The cone-dominant retina and the inner ear of zebrafish express the ortholog of CLRN1, the causative gene of human Usher syndrome type 3A.

Authors:
Jennifer B Phillips Hanna Västinsalo Jeremy Wegner Aurélie Clément Eeva-Marja Sankila Monte Westerfield

Gene Expr Patterns 2013 Dec 14;13(8):473-81. Epub 2013 Sep 14.

Institute of Neuroscience, 1254 University of Oregon, Eugene, OR 97403-1254, USA. Electronic address:

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http://dx.doi.org/10.1016/j.gep.2013.09.001DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3888827PMC
December 2013

Identification of differentially expressed genes in the zebrafish hypothalamic-pituitary axis.

Authors:
Sabrina Toro Jeremy Wegner Marc Muller Monte Westerfield Zoltan M Varga

Gene Expr Patterns 2009 Apr 8;9(4):200-8. Epub 2009 Jan 8.

Institute of Neuroscience, 1254 University of Oregon, Eugene, OR 97403, USA.

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http://dx.doi.org/10.1016/j.gep.2008.12.007DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2804439PMC
April 2009

Caveolin-1 is required for lateral line neuromast and notochord development.

Authors:
Susan J Nixon Adrian Carter Jeremy Wegner Charles Ferguson Matthias Floetenmeyer Jamie Riches Brian Key Monte Westerfield Robert G Parton

J Cell Sci 2007 Jul 5;120(Pt 13):2151-61. Epub 2007 Jun 5.

Institute for Molecular Bioscience, University of Queensland, Brisbane 4072, Australia.

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http://dx.doi.org/10.1242/jcs.003830DOI Listing
July 2007

Zebrafish as a model for caveolin-associated muscle disease; caveolin-3 is required for myofibril organization and muscle cell patterning.

Authors:
Susan J Nixon Jeremy Wegner Charles Ferguson Pierre-François Méry John F Hancock Peter D Currie Brian Key Monte Westerfield Robert G Parton

Hum Mol Genet 2005 Jul 11;14(13):1727-43. Epub 2005 May 11.

Institute for Molecular Bioscience, Universitky of Queensland, Brisbane 4072, Australia.

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http://dx.doi.org/10.1093/hmg/ddi179DOI Listing
July 2005