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Edgar A. Otto

Edgar A. Otto,University of Michigan,Genetics & Genealogy,Urology,Anatomy

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Edgar A. Otto

University of Michigan

Publications: 71 | Citations: 2056

Fields: Genetics & Genealogy, Urology, Anatomy

Collaborated with 540 co-authors from 1996 to 2012 | Cited by 4527 authors

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Publications (71)

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Identification of two novel CAKUT-causing genes by massively parallel exon resequencing of candidate genes in patients with unilateral renal agenesis

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Journal: Kidney International - KIDNEY INT , vol. 81, no. 2, pp. 196-200, 2012

Mutation analysis in Bardet–Biedl syndrome by DNA pooling and massively parallel resequencing in 105 individuals (Citations: 7)

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Journal: Human Genetics - HUM GENET , vol. 129, no. 1, pp. 79-90, 2011

A transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition (Citations: 2)

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Journal: Nature Genetics - NAT GENET , vol. 43, no. 8, pp. 776-784, 2011

TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum (Citations: 1)

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Journal: Nature Genetics - NAT GENET , vol. 43, no. 3, pp. 189-196, 2011

Exome capture and massively parallel sequencing identifies a novel HPSE2 mutation in a Saudi Arabian child with Ochoa (urofacial) syndrome (Citations: 1)

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Journal: Journal of Pediatric Urology , vol. 7, no. 5, pp. 569-573, 2011

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Citations (2056 times by 989 publications)

CEP41 is mutated in Joubert syndrome and is required for tubulin glutamylation at the cilium

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Journal: Nature Genetics - NAT GENET , vol. 44, no. 2, pp. 193-199, 2012

In search of triallelism in Bardet-Biedl syndrome

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Journal: European Journal of Human Genetics - EUR J HUMAN GENET , vol. 20, no. 4, pp. 420-427, 2012

Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis

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Journal: Kidney International - KIDNEY INT , vol. 81, no. 1, pp. 94-99, 2012

SDCCAG8 Obesity Alleles and Reduced Weight Loss After a Lifestyle Intervention in Overweight Children and Adolescents

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Journal: Obesity , vol. 20, no. 2, pp. 466-470, 2012

Identification of two novel CAKUT-causing genes by massively parallel exon resequencing of candidate genes in patients with unilateral renal agenesis

, , , , , , , , , ,

Journal: Kidney International - KIDNEY INT , vol. 81, no. 2, pp. 196-200, 2012

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Co-authors (540)

Journals (21)

Keywords (172)

Edgar A. Otto,University of Michigan,Genetics & Genealogy,Urology,Anatomy

Publications (71)

BibTeX | RIS | RefWorks Download

Identification of two novel CAKUT-causing genes by massively parallel exon resequencing of candidate genes in patients with unilateral renal agenesis

Mutation analysis in Bardet–Biedl syndrome by DNA pooling and massively parallel resequencing in 105 individuals (Citations: 7)

A transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition (Citations: 2)

TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum (Citations: 1)

Exome capture and massively parallel sequencing identifies a novel HPSE2 mutation in a Saudi Arabian child with Ochoa (urofacial) syndrome (Citations: 1)

Citations (2056 times by 989 publications)

CEP41 is mutated in Joubert syndrome and is required for tubulin glutamylation at the cilium

In search of triallelism in Bardet-Biedl syndrome

Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis

SDCCAG8 Obesity Alleles and Reduced Weight Loss After a Lifestyle Intervention in Overweight Children and Adolescents

Identification of two novel CAKUT-causing genes by massively parallel exon resequencing of candidate genes in patients with unilateral renal agenesis


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Edgar A. Otto,University of Michigan,Genetics & Genealogy,Urology,Anatomy

Publications (71) BibTeX | RIS | RefWorks Download

Mutation analysis in Bardet–Biedl syndrome by DNA pooling and massively parallel resequencing in 105 individuals (Citations: 7)

A transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition (Citations: 2)

TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum (Citations: 1)

Exome capture and massively parallel sequencing identifies a novel HPSE2 mutation in a Saudi Arabian child with Ochoa (urofacial) syndrome (Citations: 1)

Publications (71)

BibTeX | RIS | RefWorks Download