Jeffrey W. Innis - Publications

University of Michigan, Ann Arbor, Ann Arbor, MI 
Genetics, Molecular Biology

41 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any innacuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2015 Mody RJ, Wu YM, Lonigro RJ, Cao X, Roychowdhury S, Vats P, Frank KM, Prensner JR, Asangani I, Palanisamy N, Dillman JR, Rabah RM, Kunju LP, Everett J, Raymond VM, ... ... Innis JW, et al. Integrative Clinical Sequencing in the Management of Refractory or Relapsed Cancer in Youth. Jama. 314: 913-25. PMID 26325560 DOI: 10.1001/jama.2015.10080  0.96
2015 Riley KN, Catalano LM, Bernat JA, Adams SD, Martin DM, Lalani SR, Patel A, Burnside RD, Innis JW, Rudd MK. Recurrent deletions and duplications of chromosome 2q11.2 and 2q13 are associated with variable outcomes. American Journal of Medical Genetics. Part A. 167: 2664-73. PMID 26227573 DOI: 10.1002/ajmg.a.37269  0.96
2015 Gee HY, Zhang F, Ashraf S, Kohl S, Sadowski CE, Vega-Warner V, Zhou W, Lovric S, Fang H, Nettleton M, Zhu JY, Hoefele J, Weber LT, Podracka L, Boor A, ... ... Innis JW, et al. KANK deficiency leads to podocyte dysfunction and nephrotic syndrome. The Journal of Clinical Investigation. 125: 2375-84. PMID 25961457 DOI: 10.1172/JCI79504  0.96
2015 Thorsson T, Russell WW, El-Kashlan N, Soemedi R, Levine J, Geisler SB, Ackley T, Tomita-Mitchell A, Rosenfeld JA, Töpf A, Tayeh M, Goodship J, Innis JW, Keavney B, Russell MW. Chromosomal Imbalances in Patients with Congenital Cardiac Defects: A Meta-analysis Reveals Novel Potential Critical Regions Involved in Heart Development. Congenital Heart Disease. 10: 193-208. PMID 24720490 DOI: 10.1111/chd.12179  0.96
2014 Russell MW, Raeker MO, Geisler SB, Thomas PE, Simmons TA, Bernat JA, Thorsson T, Innis JW. Functional analysis of candidate genes in 2q13 deletion syndrome implicates FBLN7 and TMEM87B deficiency in congenital heart defects and FBLN7 in craniofacial malformations. Human Molecular Genetics. 23: 4272-84. PMID 24694933 DOI: 10.1093/hmg/ddu144  0.96
2014 Gee HY, Otto EA, Hurd TW, Ashraf S, Chaki M, Cluckey A, Vega-Warner V, Saisawat P, Diaz KA, Fang H, Kohl S, Allen SJ, Airik R, Zhou W, Ramaswami G, ... ... Innis JL, ... ... Innis JW, et al. Whole-exome resequencing distinguishes cystic kidney diseases from phenocopies in renal ciliopathies. Kidney International. 85: 880-7. PMID 24257694 DOI: 10.1038/ki.2013.450  0.96
2013 Lehoczky JA, Thomas PE, Patrie KM, Owens KM, Villarreal LM, Galbraith K, Washburn J, Johnson CN, Gavino B, Borowsky AD, Millen KJ, Wakenight P, Law W, Van Keuren ML, Gavrilina G, ... ... Innis JW, et al. A novel intergenic ETnII-β insertion mutation causes multiple malformations in polypodia mice. Plos Genetics. 9: e1003967. PMID 24339789 DOI: 10.1371/journal.pgen.1003967  0.96
2013 Gee HY, Saisawat P, Ashraf S, Hurd TW, Vega-Warner V, Fang H, Beck BB, Gribouval O, Zhou W, Diaz KA, Natarajan S, Wiggins RC, Lovric S, Chernin G, Schoeb DS, ... ... Innis JW, et al. ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling. The Journal of Clinical Investigation. 123: 3243-53. PMID 23867502 DOI: 10.1172/JCI69134  0.96
2013 Owens KM, Quinonez SC, Thomas PE, Keegan CE, Lefebvre N, Roulston D, Larsen CA, Stadler HS, Innis JW. 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. PMID 23532960 DOI: 10.1002/ajmg.a.35843  0.96
2012 Bernier FP, Caluseriu O, Ng S, Schwartzentruber J, Buckingham KJ, Innes AM, Jabs EW, Innis JW, Schuette JL, Gorski JL, Byers PH, Andelfinger G, Siu V, Lauzon J, Fernandez BA, et al. Haploinsufficiency of SF3B4, a component of the pre-mRNA spliceosomal complex, causes Nager syndrome. American Journal of Human Genetics. 90: 925-33. PMID 22541558 DOI: 10.1016/j.ajhg.2012.04.004  0.96
2012 Butler MG, Dagenais SL, Garcia-Perez JL, Brouillard P, Vikkula M, Strouse P, Innis JW, Glover TW. 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. PMID 22407726 DOI: 10.1002/ajmg.a.35229  0.96
2012 Xu W, Ahmad A, Dagenais S, Iyer RK, Innis JW. Chromosome 4q deletion syndrome: narrowing the cardiovascular critical region to 4q32.2-q34.3. American Journal of Medical Genetics. Part A. 158: 635-40. PMID 22302627 DOI: 10.1002/ajmg.a.34425  0.96
2012 Boztug K, Rosenberg PS, Dorda M, Banka S, Moulton T, Curtin J, Rezaei N, Corns J, Innis JW, Avci Z, Tran HC, Pellier I, Pierani P, Fruge R, Parvaneh N, et al. 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. PMID 22050868 DOI: 10.1016/j.jpeds.2011.09.019  0.96
2012 Saisawat P, Tasic V, Vega-Warner V, Kehinde EO, Günther B, Airik R, Innis JW, Hoskins BE, Hoefele J, Otto EA, Hildebrandt F. Identification of two novel CAKUT-causing genes by massively parallel exon resequencing of candidate genes in patients with unilateral renal agenesis Kidney International. 81: 196-200. PMID 21900877 DOI: 10.1038/ki.2011.315  0.96
2011 Roychowdhury S, Iyer MK, Robinson DR, Lonigro RJ, Wu YM, Cao X, Kalyana-Sundaram S, Sam L, Balbin OA, Quist MJ, Barrette T, Everett J, Siddiqui J, Kunju LP, Navone N, ... ... Innis JW, et al. Personalized oncology through integrative high-throughput sequencing: a pilot study. Science Translational Medicine. 3: 111ra121. PMID 22133722 DOI: 10.1126/scitranslmed.3003161  0.96
2011 Talkowski ME, Mullegama SV, Rosenfeld JA, van Bon BW, Shen Y, Repnikova EA, Gastier-Foster J, Thrush DL, Kathiresan S, Ruderfer DM, Chiang C, Hanscom C, Ernst C, Lindgren AM, Morton CC, ... ... Innis JW, et al. Assessment of 2q23.1 microdeletion syndrome implicates MBD5 as a single causal locus of intellectual disability, epilepsy, and autism spectrum disorder. American Journal of Human Genetics. 89: 551-63. PMID 21981781 DOI: 10.1016/j.ajhg.2011.09.011  0.96
2011 Al Badr W, Al Bader S, Otto E, Hildebrandt F, Ackley T, Peng W, Xu J, Li J, Owens KM, Bloom D, Innis JW. Exome capture and massively parallel sequencing identifies a novel HPSE2 mutation in a Saudi Arabian child with Ochoa (urofacial) syndrome Journal of Pediatric Urology. 7: 569-573. PMID 21450525 DOI: 10.1016/j.jpurol.2011.02.034  0.96
2011 Nelson M, Quinonez S, Ackley T, Iyer RK, Innis JW. Multiple congenital anomalies and developmental delay in a boy associated with a de novo 16p13.3 deletion. American Journal of Medical Genetics. Part A. 155: 612-7. PMID 21344629 DOI: 10.1002/ajmg.a.33808  0.96
2011 Reis LM, Tyler RC, Schilter KF, Abdul-Rahman O, Innis JW, Kozel BA, Schneider AS, Bardakjian TM, Lose EJ, Martin DM, Broeckel U, Semina EV. BMP4 loss-of-function mutations in developmental eye disorders including SHORT syndrome. Human Genetics. 130: 495-504. PMID 21340693 DOI: 10.1007/s00439-011-0968-y  0.96
2011 Bedoyan JK, Lesperance MM, Ackley T, Iyer RK, Innis JW, Misra VK. A complex 6p25 rearrangement in a child with multiple epiphyseal dysplasia. American Journal of Medical Genetics. Part A. 155: 154-63. PMID 21204225 DOI: 10.1002/ajmg.a.33751  0.96
2008 Brunetti-Pierri N, Berg JS, Scaglia F, Belmont J, Bacino CA, Sahoo T, Lalani SR, Graham B, Lee B, Shinawi M, Shen J, Kang SH, Pursley A, Lotze T, Kennedy G, ... ... Innis JW, et al. Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities. Nature Genetics. 40: 1466-71. PMID 19029900 DOI: 10.1038/ng.279  0.96
2008 Lehoczky JA, Innis JW. Expanded HOXA13 polyalanine tracts in a monotreme Evolution and Development. 10: 433-438. PMID 18638320 DOI: 10.1111/j.1525-142X.2008.00254.x  0.96
2008 Lehoczky JA, Innis JW. BAC transgenic analysis reveals enhancers sufficient for Hoxa13 and neighborhood gene expression in mouse embryonic distal limbs and genital bud Evolution and Development. 10: 421-432. PMID 18638319 DOI: 10.1111/j.1525-142X.2008.00253.x  0.96
2007 Lehoczky JA, Innis JW. A mouse transgene drives embryonic dorsal posterior commissure expression Transgenic Research. 16: 823-828. PMID 17549599 DOI: 10.1007/s11248-007-9104-0  0.96
2006 Lehoczky JA, Cai WW, Douglas JA, Moran JL, Beier DR, Innis JW. Description and genetic mapping of Polypodia: an X-linked dominant mouse mutant with ectopic caudal limbs and other malformations. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 17: 903-13. PMID 16964440 DOI: 10.1007/s00335-006-0041-7  0.96
2006 Williams ME, Lehoczky JA, Innis JW. A group 13 homeodomain is neither necessary nor sufficient for posterior prevalence in the mouse limb. Developmental Biology. 297: 493-507. PMID 16806154 DOI: 10.1016/j.ydbio.2006.05.027  0.96
2005 McDermott DA, Bressan MC, He J, Lee JS, Aftimos S, Brueckner M, Gilbert F, Graham GE, Hannibal MC, Innis JW, Pierpont ME, Raas-Rothschild A, Shanske AL, Smith WE, Spencer RH, et al. TBX5 genetic testing validates strict clinical criteria for Holt-Oram syndrome. Pediatric Research. 58: 981-6. PMID 16183809 DOI: 10.1203/01.PDR.0000182593.95441.64  0.96
2005 Williams TM, Williams ME, Heaton JH, Gelehrter TD, Innis JW. Group 13 HOX proteins interact with the MH2 domain of R-Smads and modulate Smad transcriptional activation functions independent of HOX DNA-binding capability. Nucleic Acids Research. 33: 4475-84. PMID 16087734 DOI: 10.1093/nar/gki761  0.52
2005 DeScipio C, Kaur M, Yaeger D, Innis JW, Spinner NB, Jackson LG, Krantz ID. Chromosome rearrangements in cornelia de Lange syndrome (CdLS): report of a der(3)t(3;12)(p25.3;p13.3) in two half sibs with features of CdLS and review of reported CdLS cases with chromosome rearrangements. American Journal of Medical Genetics. Part A. 137: 276-82. PMID 16075459 DOI: 10.1002/ajmg.a.30857  0.96
2005 Williams TM, Williams ME, Kuick R, Misek D, McDonagh K, Hanash S, Innis JW. Candidate downstream regulated genes of HOX group 13 transcription factors with and without monomeric DNA binding capability. Developmental Biology. 279: 462-80. PMID 15733672 DOI: 10.1016/j.ydbio.2004.12.015  0.52
2005 Williams TM, Williams ME, Innis JW. Range of HOX/TALE superclass associations and protein domain requirements for HOXA13:MEIS interaction. Developmental Biology. 277: 457-71. PMID 15617687 DOI: 10.1016/j.ydbio.2004.10.004  0.96
2004 Lehoczky JA, Williams ME, Innis JW. Conserved expression domains for genes upstream and within the HoxA and HoxD clusters suggests a long-range enhancer existed before cluster duplication. Evolution & Development. 6: 423-30. PMID 15509224 DOI: 10.1111/j.1525-142X.2004.04050.x  0.96
2004 Innis JW, Mortlock D, Chen Z, Ludwig M, Williams ME, Williams TM, Doyle CD, Shao Z, Glynn M, Mikulic D, Lehmann K, Mundlos S, Utsch B. Polyalanine expansion in HOXA13: three new affected families and the molecular consequences in a mouse model. Human Molecular Genetics. 13: 2841-51. PMID 15385446 DOI: 10.1093/hmg/ddh306  0.52
2004 Wechsler SB, Lehoczky JA, Hall JG, Innis JW. Tibial aplasia, lower extremity mirror image polydactyly, brachyphalangy, craniofacial dysmorphism and genital hypoplasia: Further delineation and mutational analysis Clinical Dysmorphology. 13: 63-69. PMID 15057119 DOI: 10.1097/00019605-200404000-00002  0.96
2004 Keegan CE, Vilain E, Mohammed M, Lehoczky J, Dobyns WB, Archer SM, Innis JW. Microcephaly, jejunal atresia, aberrant right bronchus, ocular anomalies, and XY sex reversal. American Journal of Medical Genetics. Part A. 125: 293-8. PMID 14994240 DOI: 10.1002/ajmg.a.20455  0.96
2002 Innis JW, Margulies EH, Kardia S. Integrative biology and the developing limb bud. Evolution & Development. 4: 378-89. PMID 12356268  0.8
2001 Margulies EH, Kardia SL, Innis JW. A comparative molecular analysis of developing mouse forelimbs and hindlimbs using serial analysis of gene expression (SAGE). Genome Research. 11: 1686-98. PMID 11591645 DOI: 10.1101/gr.192601  0.8
2001 Margulies EH, Kardia SL, Innis JW. Identification and prevention of a GC content bias in SAGE libraries. Nucleic Acids Research. 29: E60-0. PMID 11410683  0.8
2000 Margulies EH, Innis JW. eSAGE: managing and analysing data generated with serial analysis of gene expression (SAGE). Bioinformatics (Oxford, England). 16: 650-1. PMID 11038335  0.8
2000 Post LC, Margulies EH, Kuo A, Innis JW. Severe limb defects in Hypodactyly mice result from the expression of a novel, mutant HOXA13 protein. Developmental Biology. 217: 290-300. PMID 10625554 DOI: 10.1006/dbio.1999.9550  0.8
2000 Margulies EH, Innis JW. Building arms or legs with molecular models. Pediatric Research. 47: 2-3. PMID 10625073  0.8
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