Researcher
Michael Hildebrand
University of Melbourne
Statistics
105 papers found
Papers authored by Michael Hildebrand
Refreshing results…
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Hans-Henrik M. Dahl,
John Anthony Damiano,
Richard J. H. Smith,
Ingrid E. Scheffer,
Samuel F. Berkovic
Recent advances in the molecular genetics of epilepsy
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,
Qian Dong,
Jeng-Haur Chen,
Thomas O. Moninger,
Jung Min Park,
Yuzhou Zhang,
Jianyang Du,
Michael S. Hildebrand ,
Richard J. H. Smith,
Christoph O. Randak,
David A. Stoltz,
Michael J. Welsh
CFTR-deficient pigs display peripheral nervous system defects at birth
Download from doi.org
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A. Eliot Shearer,
Michael S. Hildebrand ,
E. Ann Black-Ziegelbein,
V. Nikhil Anand,
Christina M. Sloan,
Robert W. Eppsteiner,
Todd E. Scheetz,
Patrick L. M. Huygen,
Richard J. H. Smith,
Terry A. Braun,
Thomas L. Casavant
AudioGene: Predicting Hearing Loss Genotypes from Phenotypes to Guide Genetic Screening
Download from www.ncbi.nlm.nih.gov
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Jan Novy,
Anna Tostevin,
The Uk Brain Expression Consortium,
Barbara Leal,
Ellen V. S. Hessel,
Kerstin Hallmann,
Michael S. Hildebrand ,
Hans-Henrik M. Dahl
and 62 other authors
Download from orbi.ulg.ac.be
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Harini Ravi,
Swati Joshi,
Angelica C. Guiffre,
Barbara Novak,
Scott Happe,
Emily M. LeProust,
Richard Jh Smith
Pre-capture multiplexing improves efficiency and cost-effectiveness of targeted genomic enrichment
Download from link.springer.com
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Adam P. DeLuca ,
Haihong Ji,
Camille C. Dunn,
Elizabeth A. Black-Ziegelbein,
Thomas L. Casavant,
Terry A. Braun,
Todd E. Scheetz,
Steven E. Scherer,
Marlan R. Hansen ,
Bruce J. Gantz,
Richard J. H. Smith
Prediction of Cochlear Implant Performance by Genetic Mutation: The Spiral Ganglion Hypothesis
Download from www.ncbi.nlm.nih.gov
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Richard Jh Smith
Solution-based targeted genomic enrichment for precious DNA samples
Download from link.springer.com
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Kyle R. Taylor,
Adam P. DeLuca ,
Steve Scherer,
Patrick L. M. Huygen,
Todd E. Scheetz,
Terry A. Braun,
Thomas L. Casavant,
Richard J. H. Smith
Using the phenome and genome to improve genetic diagnosis for deafness
Download from onlinelibrary.wiley.com
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Corey W. Goodman,
Bruce W. Tompkins,
Todd E. Scheetz,
Michael S. Hildebrand ,
Patrick L. M. Huygen,
Richard J. H. Smith,
Terry A. Braun,
Thomas L. Casavant
AudioGene: Computer-based prediction of genetic factors involved in non-syndromic hearing impairment
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Christina M. Sloan,
Richard J. H. Smith
Download from www.ncbi.nlm.nih.gov
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Stephen S. Newton,
John A. Chiorini,
Giovanni Di Pasquale,
Richard J. H. Smith
Viral vector tropism for supporting cells in the developing murine cochlea
Download from europepmc.org
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Katharine K. Miller,
Tao Yang,
Michael S. Hildebrand ,
A. Eliot Shearer,
A. Eliot Shearer,
Adam P. DeLuca ,
Todd E. Scheetz,
Jennifer Drummond,
Steve E. Scherer,
P. Kevin Legan,
Richard J. Goodyear,
Guy P. Richardson,
Mary Ann Cheatham,
Richard J. Smith
and 1 other authors
Download from doi.org
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Arabandi Ramesh,
C. R. Srikumari Srisailapathy,
Jaap Oostrik,
Ronald J. C. Admiraal,
Harold R. Neely,
Joseph R. Latoche,
Richard J. H. Smith,
John K. Northup,
Hannie Kremer,
Jeffrey R. Holt
and 1 other authors
Download from www.nature.com
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Zubair M. Ahmed,
Gudrun Nürnberg,
Muhammad Ansar,
Sulman Basit,
Qamar Javed,
Robert J. Morell,
Nabilah Nasreen
and 29 other authors
Loss-of-Function Mutations of ILDR1 Cause Autosomal-Recessive Hearing Impairment DFNB42
Download from www.researchgate.net
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A. Eliot Shearer,
A. Eliot Shearer,
Paul J. Lockhart,
Hossein Najmabadi,
Richard J. Leventer,
George McGillivray,
David J. Amor,
Richard J. Smith,
Melanie Bahlo
Download from dx.doi.org
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Matías Morin,
Nicole C. Meyer,
Fernando Mayo,
Silvia Modamio-Hoybjor,
Angeles Mencia,
Leticia Olavarrieta,
Carmelo Morales-Angulo,
Carla J. Nishimura,
I. del Castillo,
Heather Workman,
Adam P. DeLuca ,
Ignacio del Castillo,
Kyle R. Taylor,
van Maarten Wesemael
and 18 other authors
Download from www.ncbi.nlm.nih.gov
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Kimia Kahrizi,
Catherine J. Bromhead,
A. Eliot Shearer,
A. Eliot Shearer,
Jennifer A. Webster,
Hossein Khodaei,
Rezvan Abtahi,
Niloofar Bazazzadegan,
Mojgan Babanejad,
Nooshin Nikzat,
William J. Kimberling,
Dietrich Stephan,
Partick L. M. Huygen,
Melanie Bahlo
and 2 other authors
Mutations in TMC1 are a common cause of DFNB7/11 hearing loss in the Iranian population
Download from journals.sagepub.com
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Michael S. Hildebrand ,
Kyle R. Taylor,
José Gurrola ,
Steve Scherer,
Todd E. Scheetz,
Richard J. H. Smith
Comprehensive genetic testing for hereditary hearing loss using massively parallel sequencing
Download from doi.org
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Luke Gandolfo,
A. Eliot Shearer,
A. Eliot Shearer,
Jennifer A. Webster,
Maren Jensen,
William J. Kimberling,
Dietrich Stephan,
Patrick L. M. Huygen,
Richard J. H. Smith,
Melanie Bahlo
A Novel Mutation in COCH – Implications for Genotype-Phenotype Correlations in DFNA9 Hearing Loss
Download from www.ncbi.nlm.nih.govMissing publications? Search for publications with a matching author name.