Jane L Schuette

Jane L Schuette

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Jane L Schuette

Jane L Schuette

Publications by authors named "Jane L Schuette"

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Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling.

Authors:
Brett V Johnson Raman Kumar Sabrina Oishi Suzy Alexander Maria Kasherman Michelle Sanchez Vega Atma Ivancevic Alison Gardner Deepti Domingo Mark Corbett Euan Parnell Sehyoun Yoon Tracey Oh Matthew Lines Henrietta Lefroy Usha Kini Margot Van Allen Sabine Grønborg Sandra Mercier Sébastien Küry Stéphane Bézieau Laurent Pasquier Martine Raynaud Alexandra Afenjar Thierry Billette de Villemeur Boris Keren Julie Désir Lionel Van Maldergem Martina Marangoni Nicola Dikow David A Koolen Peter M VanHasselt Marjan Weiss Petra Zwijnenburg Joaquim Sa Claudia Falcao Reis Carlos López-Otín Olaya Santiago-Fernández Alberto Fernández-Jaén Anita Rauch Katharina Steindl Pascal Joset Amy Goldstein Suneeta Madan-Khetarpal Elena Infante Elaine Zackai Carey Mcdougall Vinodh Narayanan Keri Ramsey Saadet Mercimek-Andrews Loren Pena Vandana Shashi Kelly Schoch Jennifer A Sullivan Filippo Pinto E Vairo Pavel N Pichurin Sarah A Ewing Sarah S Barnett Eric W Klee M Scott Perry Mary Kay Koenig Catherine E Keegan Jane L Schuette Stephanie Asher Yezmin Perilla-Young Laurie D Smith Jill A Rosenfeld Elizabeth Bhoj Paige Kaplan Dong Li Renske Oegema Ellen van Binsbergen Bert van der Zwaag Marie Falkenberg Smeland Ioana Cutcutache Matthew Page Martin Armstrong Angela E Lin Marcie A Steeves Nicolette den Hollander Mariëtte J V Hoffer Margot R F Reijnders Serwet Demirdas Daniel C Koboldt Dennis Bartholomew Theresa Mihalic Mosher Scott E Hickey Christine Shieh Pedro A Sanchez-Lara John M Graham Kamer Tezcan G B Schaefer Noelle R Danylchuk Alexander Asamoah Kelly E Jackson Naomi Yachelevich Margaret Au Luis A Pérez-Jurado Tjitske Kleefstra Peter Penzes Stephen A Wood Thomas Burne Tyler Mark Pierson Michael Piper Jozef Gécz Lachlan A Jolly

Biol Psychiatry 2019 Jun 29. Epub 2019 Jun 29.

University of Adelaide and Robinson Research Institute, Adelaide, Australia. Electronic address:

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http://dx.doi.org/10.1016/j.biopsych.2019.05.028DOI Listing
June 2019

CTNNB1 mutation associated with familial exudative vitreoretinopathy (FEVR) phenotype.

Ophthalmic Genet 2016 12 11;37(4):468-470. Epub 2016 Mar 11.

b W.K. Kellogg Eye Center, Department of Ophthalmology and Visual Sciences , University of Michigan , Ann Arbor , Michigan , USA.

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https://www.tandfonline.com/doi/full/10.3109/13816810.2015.1
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http://dx.doi.org/10.3109/13816810.2015.1120318DOI Listing
December 2016

Duplication 2p25 in a child with clinical features of CHARGE syndrome.

Am J Med Genet A 2016 May 6;170A(5):1148-54. Epub 2016 Feb 6.

Department of Human Genetics, The University of Michigan, Ann Arbor, Michigan.

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http://dx.doi.org/10.1002/ajmg.a.37592DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5117441PMC
May 2016

Parents' Perspectives on Variants of Uncertain Significance from Chromosome Microarray Analysis.

J Genet Couns 2016 Feb 19;25(1):101-11. Epub 2015 May 19.

Department of Pediatrics and Communicable Diseases, University of Michigan, Ann Arbor, Michigan, USA.

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http://dx.doi.org/10.1007/s10897-015-9847-3DOI Listing
February 2016

Novel DICER1 mutation as cause of multinodular goiter in children.

Head Neck 2013 Dec 1;35(12):E369-71. Epub 2013 Jun 1.

Division of Pediatric Otolaryngology, Department of Otolaryngology-Head and Neck Surgery, University of Michigan Health System, Ann Arbor, Michigan.

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http://dx.doi.org/10.1002/hed.23250DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3762914PMC
December 2013

Who counsels parents of newborns who are carriers of sickle cell anemia or cystic fibrosis?

J Genet Couns 2013 Apr 18;22(2):218-25. Epub 2012 Aug 18.

Department of Pediatrics and Communicable Diseases, Child Health Evaluation and Research Unit, Division of General Pediatrics, Mott Children's Hospital, University of Michigan, 300 N. Ingalls St. 6D21, Ann Arbor, MI 48109, USA.

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http://dx.doi.org/10.1007/s10897-012-9537-3DOI Listing
April 2013

Guidelines for Writing Letters to Patients.

J Genet Couns 2002 Oct;11(5):399-418

Department of Human Genetics, University of Michigan, Ann Arbor, Michigan.

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http://dx.doi.org/10.1023/A:1016841731426DOI Listing
October 2002