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Jeffrey W. Innis

Affiliations: 
University of Michigan, Ann Arbor, Ann Arbor, MI 
Area:
Genetics, Molecular Biology
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"Jeffrey Innis"
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Elliott H. Margulies grad student 2001 University of Michigan
Jessica A. Lehoczky grad student 2007 University of Michigan

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Publications

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Prensner JR, Mody RJ, Wu Y, et al. (2016) Abstract PR07: The landscape of molecular aberrations in pediatric and young adult cancer patients undergoing clinical sequencing for disease management: Novel biological findings from the Peds-MiOncoSeq study Cancer Research. 76
Quinonez SC, Innis JW. (2014) Human HOX gene disorders. Molecular Genetics and Metabolism. 111: 4-15
Lehoczky JA, Thomas PE, Patrie KM, et al. (2013) A novel intergenic ETnII-β insertion mutation causes multiple malformations in polypodia mice. Plos Genetics. 9: e1003967
Gee HY, Saisawat P, Ashraf S, et al. (2013) ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling. The Journal of Clinical Investigation. 123: 3243-53
Owens KM, Quinonez SC, Thomas PE, et al. (2013) Analysis of de novo HOXA13 polyalanine expansions supports replication slippage without repair in their generation. American Journal of Medical Genetics. Part A. 161: 1019-27
Quinonez SC, Hedera P, Barr M, et al. (2012) Maternal intrachromosomal insertional translocation leads to recurrent 1q21.3q23.3 deletion in two siblings. American Journal of Medical Genetics. Part A. 158: 2591-601
Bernier FP, Caluseriu O, Ng S, et al. (2012) Haploinsufficiency of SF3B4, a component of the pre-mRNA spliceosomal complex, causes Nager syndrome. American Journal of Human Genetics. 90: 925-33
Butler MG, Dagenais SL, Garcia-Perez JL, et al. (2012) Microcephaly, intellectual impairment, bilateral vesicoureteral reflux, distichiasis, and glomuvenous malformations associated with a 16q24.3 contiguous gene deletion and a Glomulin mutation. American Journal of Medical Genetics. Part A. 158: 839-49
Xu W, Ahmad A, Dagenais S, et al. (2012) Chromosome 4q deletion syndrome: narrowing the cardiovascular critical region to 4q32.2-q34.3. American Journal of Medical Genetics. Part A. 158: 635-40
Boztug K, Rosenberg PS, Dorda M, et al. (2012) Extended spectrum of human glucose-6-phosphatase catalytic subunit 3 deficiency: novel genotypes and phenotypic variability in severe congenital neutropenia. The Journal of Pediatrics. 160: 679-683.e2
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