| Year |
Citation |
Score |
| 2016 |
Prensner JR, Mody RJ, Wu Y, Lonigro RJ, Cao X, Roychowdhury S, Vats P, Frank KM, Asangani I, Palanisamy N, Rabah RM, Kunju LP, Everett J, Stoffel EM, Innis JW, et al. 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. DOI: 10.1158/1538-7445.Pedca15-Pr07 |
0.35 |
|
| 2014 |
Quinonez SC, Innis JW. Human HOX gene disorders. Molecular Genetics and Metabolism. 111: 4-15. PMID 24239177 DOI: 10.1016/j.ymgme.2013.10.012 |
0.353 |
|
| 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 |
0.717 |
|
| 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 |
0.372 |
|
| 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 |
0.356 |
|
| 2012 |
Quinonez SC, Hedera P, Barr M, Ackley T, Lam C, Purkayastha A, Glover TW, Innis JW. Maternal intrachromosomal insertional translocation leads to recurrent 1q21.3q23.3 deletion in two siblings. American Journal of Medical Genetics. Part A. 158: 2591-601. PMID 22903861 DOI: 10.1002/Ajmg.A.35563 |
0.315 |
|
| 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 |
0.379 |
|
| 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 |
0.425 |
|
| 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 |
0.358 |
|
| 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 |
0.34 |
|
| 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 |
0.407 |
|
| 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 |
0.324 |
|
| 2011 |
Nelson ME, Griffin GR, Innis JW, Green GE. Campomelic dysplasia: airway management in two patients and an update on clinical-molecular correlations in the head and neck. The Annals of Otology, Rhinology, and Laryngology. 120: 682-5. PMID 22097155 DOI: 10.1177/000348941112001009 |
0.321 |
|
| 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 |
0.367 |
|
| 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 |
0.343 |
|
| 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 |
0.407 |
|
| 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 |
0.358 |
|
| 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 |
0.371 |
|
| 2010 |
Boztug K, Rosenberg PS, Böhm M, Moulton T, Curtin J, Rezaei N, Corns J, Innis J, Avci Z, Tran HC, Pellier I, Gatti S, Fruge R, Parvaneh N, Darbyshire P, et al. Extended Molecular and Clinical Phenotype of Human G6PC3 Deficiency. Blood. 116: 1495-1495. DOI: 10.1182/Blood.V116.21.1495.1495 |
0.334 |
|
| 2009 |
van Bon BW, Mefford HC, Menten B, Koolen DA, Sharp AJ, Nillesen WM, Innis JW, de Ravel TJ, Mercer CL, Fichera M, Stewart H, Connell LE, Ounap K, Lachlan K, Castle B, et al. Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome. Journal of Medical Genetics. 46: 511-23. PMID 19372089 DOI: 10.1136/Jmg.2008.063412 |
0.356 |
|
| 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 |
0.337 |
|
| 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 |
0.662 |
|
| 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 |
0.736 |
|
| 2007 |
Utsch B, McCabe CD, Galbraith K, Gonzalez R, Born M, Dötsch J, Ludwig M, Reutter H, Innis JW. Molecular characterization of HOXA13 polyalanine expansion proteins in hand-foot-genital syndrome. American Journal of Medical Genetics. Part A. 143: 3161-8. PMID 17935235 DOI: 10.1002/Ajmg.A.31967 |
0.307 |
|
| 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 |
0.697 |
|
| 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 |
0.687 |
|
| 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 |
0.685 |
|
| 2006 |
Lehoczky JA, Williams ME, Innis JW. Long-range regulation of Hoxa13 in limb development Developmental Biology. 295: 387-388. DOI: 10.1016/J.Ydbio.2006.04.189 |
0.647 |
|
| 2005 |
McCabe CD, Innis JW. A genomic approach to the identification and characterization of HOXA13 functional binding elements. Nucleic Acids Research. 33: 6782-94. PMID 16321965 DOI: 10.1093/Nar/Gki979 |
0.384 |
|
| 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 |
0.338 |
|
| 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 |
0.303 |
|
| 2005 |
Misra VK, Struys EA, O'brien W, Salomons GS, Glover T, Jakobs C, Innis JW. Phenotypic heterogeneity in the presentation of D-2-hydroxyglutaric aciduria in monozygotic twins. Molecular Genetics and Metabolism. 86: 200-5. PMID 16081310 DOI: 10.1016/J.Ymgme.2005.06.005 |
0.329 |
|
| 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 |
0.34 |
|
| 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 |
0.446 |
|
| 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 |
0.735 |
|
| 2004 |
Innis JW, Hedera P. Two patients with monomelic ulnar duplication with mirror hand polydactyly: segmental Laurin-Sandrow syndrome. American Journal of Medical Genetics. Part A. 131: 77-81. PMID 15389704 DOI: 10.1002/Ajmg.A.30296 |
0.347 |
|
| 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 |
0.396 |
|
| 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 |
0.695 |
|
| 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 |
0.688 |
|
| 2003 |
Hedera P, Innis JW. Juberg-Hayward syndrome: report of a new patient with severe phenotype and novel clinical features. American Journal of Medical Genetics. Part A. 122: 257-60. PMID 12966528 DOI: 10.1002/Ajmg.A.20263 |
0.32 |
|
| 2003 |
Paznekas WA, Boyadjiev SA, Shapiro RE, Daniels O, Wollnik B, Keegan CE, Innis JW, Dinulos MB, Christian C, Hannibal MC, Jabs EW. Connexin 43 (GJA1) mutations cause the pleiotropic phenotype of oculodentodigital dysplasia. American Journal of Human Genetics. 72: 408-18. PMID 12457340 DOI: 10.1086/346090 |
0.366 |
|
| 2002 |
Innis JW, Margulies EH, Kardia S. Integrative biology and the developing limb bud. Evolution & Development. 4: 378-89. PMID 12356268 DOI: 10.1046/J.1525-142X.2002.02025.X |
0.705 |
|
| 2002 |
Hedera P, Innis JW. Possible third case of Lin-Gettig syndrome. American Journal of Medical Genetics. 110: 380-3. PMID 12116213 DOI: 10.1002/Ajmg.10460 |
0.303 |
|
| 2002 |
Innis JW, Goodman FR, Bacchelli C, Williams TM, Mortlock DP, Sateesh P, Scambler PJ, McKinnon W, Guttmacher AE. A HOXA13 allele with a missense mutation in the homeobox and a dinucleotide deletion in the promoter underlies Guttmacher syndrome. Human Mutation. 19: 573-4. PMID 11968094 DOI: 10.1002/Humu.9036 |
0.396 |
|
| 2002 |
Innis JW. Priming the search for HOX mutations. Teratology. 65: 47-9. PMID 11857505 DOI: 10.1002/Tera.10021 |
0.428 |
|
| 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 |
0.714 |
|
| 2001 |
Dagenais SL, Adam AN, Innis JW, Glover TW. A novel frameshift mutation in exon 23 of ATP7a (MNK) results in occipital horn syndrome and not in Menkes disease American Journal of Human Genetics. 69: 420-427. PMID 11431706 DOI: 10.1086/321290 |
0.348 |
|
| 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 DOI: 10.1093/Nar/29.12.E60 |
0.667 |
|
| 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 DOI: 10.1093/Bioinformatics/16.7.650 |
0.666 |
|
| 2000 |
Goodman FR, Bacchelli C, Brady AF, Brueton LA, Fryns JP, Mortlock DP, Innis JW, Holmes LB, Donnenfeld AE, Feingold M, Beemer FA, Hennekam RC, Scambler PJ. Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome. American Journal of Human Genetics. 67: 197-202. PMID 10839976 DOI: 10.1086/302961 |
0.354 |
|
| 2000 |
Celli J, Van Beusekom E, Hennekam RCM, Gallardo ME, Smeets DFCM, Rodríguez De Córdoba S, Innis JW, Frydman M, König R, Kingston H, Tolmie J, Govaerts LCP, Van Bokhoven H, Brunner HG. Familial syndromic esophageal atresia maps to 2p23-p24 American Journal of Human Genetics. 66: 436-444. PMID 10677303 DOI: 10.1086/302779 |
0.38 |
|
| 2000 |
Mortlock DP, Sateesh P, Innis JW. Evolution of N-terminal sequences of the vertebrate HOXA13 protein. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 11: 151-8. PMID 10656931 DOI: 10.1007/S003350010029 |
0.367 |
|
| 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 |
0.691 |
|
| 2000 |
Margulies EH, Innis JW. Building arms or legs with molecular models. Pediatric Research. 47: 2-3. PMID 10625073 DOI: 10.1203/00006450-200001000-00002 |
0.634 |
|
| 1999 |
Post LC, Innis JW. Infertility in Adult Hypodactyly Mice Is Associated with Hypoplasia of Distal Reproductive Structures Biology of Reproduction. 61: 1402-1408. PMID 10569982 DOI: 10.1095/Biolreprod61.6.1402 |
0.324 |
|
| 1999 |
Post LC, Innis JW. Altered Hox expression and increased cell death distinguish Hypodactyly from Hoxa13 null mice. The International Journal of Developmental Biology. 43: 287-294. DOI: 10.1387/Ijdb.10470645 |
0.405 |
|
| 1998 |
Innis JW. Role of HOX genes in human development. Current Opinion in Pediatrics. 9: 617-22. PMID 9425595 DOI: 10.1097/00008480-199712000-00011 |
0.42 |
|
| 1997 |
Kondo T, Zákány J, Innis JW, Duboule D. Of fingers, toes and penises. Nature. 390: 29. PMID 9363887 DOI: 10.1038/36234 |
0.434 |
|
| 1997 |
Innis JW, Asher JH, Liang Y, Wang A, Wilke CM, Dierick HA, Kazen-Gillespie K, Sheldon S, Glover TW, Friedman TB. Exclusion of BMP6 as a candidate gene for cleidocranial dysplasia. American Journal of Medical Genetics. 71: 292-7. PMID 9268099 DOI: 10.1002/(Sici)1096-8628(19970822)71:3<292::Aid-Ajmg9>3.0.Co;2-W |
0.386 |
|
| 1997 |
Innis JW, Asher JH, Poznanski AK, Sheldon S. Autosomal dominant microcephaly with normal intelligence, short palpebral fissures, and digital anomalies. American Journal of Medical Genetics. 71: 150-5. PMID 9217213 DOI: 10.1002/(Sici)1096-8628(19970808)71:2<150::Aid-Ajmg6>3.0.Co;2-1 |
0.337 |
|
| 1997 |
Mortlock DP, Innis JW. Mutation of HOXA13 in hand-foot-genital syndrome. Nature Genetics. 15: 179-80. PMID 9020844 DOI: 10.1038/Ng0297-179 |
0.37 |
|
| 1996 |
Mortlock DP, Nelson MR, Innis JW. An efficient method for isolating putative promoters and 5'-transcribed sequences from large genomic clones. Genome Research. 6: 327-35. PMID 8723725 DOI: 10.1101/Gr.6.4.327 |
0.315 |
|
| 1996 |
Griffith AJ, Arts A, Downs C, Innis JW, Shepard NT, Sheldon S, Gebarski SS. Familial large vestibular aqueduct syndrome. The Laryngoscope. 106: 960-5. PMID 8699909 DOI: 10.1097/00005537-199608000-00009 |
0.328 |
|
| 1996 |
Mortlock DP, Post LC, Innis JW. The molecular basis of hypodactyly (Hd): a deletion in Hoxa 13 leads to arrest of digital arch formation. Nature Genetics. 13: 284-9. PMID 8673126 DOI: 10.1038/Ng0796-284 |
0.43 |
|
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