Micheil Innes

Associate Professor

University of Calgary

Canada

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Articles (13)

Year:

2024

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2024

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2024

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2022

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2021

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2021

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2020

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2020

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2020

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2020

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2020

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2020

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2020

Collaborators (4)

Rachel Schot

Erasmus University Medical Center

NETHERLANDS

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Chester Brown

Genetics Division Chief/Professor

University of Tennessee Health Science Center

UNITED STATES

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Francois Bernier

Head and Professor

University of Calgary

CANADA

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Sarah Childs

Professor

University of Calgary

CANADA

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Micheil Innes

Research Interests

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Articles (13)

Genome sequencing identifies biallelic variants in SCLT1 in a patient with syndromic nephronophthisis: Reflections on the SCLT1‐related ciliopathy spectrum

Investigations of an individual with a Marfanoid habitus, mild intellectual disability, and severe social anxiety identifies PCDHGA5 as a candidate neurodevelopmental disorder gene

Insights from the hereditary endocrine clinic

Hnrnpul1 controls transcription, splicing, and modulates skeletal and limb development in vivo

Fifty years of recognizable patterns of human malformation: Insights and opportunities

CHRNB1‐associated congenital myasthenia syndrome: Expanding the clinical spectrum

Congenital hiatal hernia segregating with a duplication in 9q22.31q22.32 in two families

Skeletal Phenotypes Due to Abnormalities in Mitochondrial Protein Homeostasis and Import

A diagnostic approach to syndromic retinal dystrophies with intellectual disability

Automated syndrome diagnosis by three-dimensional facial imaging

Channelopathies Are a Frequent Cause of Genetic Ataxias Associated with Cerebellar Atrophy

Further delineation of the clinical spectrum of KAT6B disorders and allelic series of pathogenic variants

Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients

Collaborators (4)

Rachel Schot

Chester Brown

Francois Bernier

Sarah Childs

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