Karen H. Friderici - Publications

Michigan State University, East Lansing, MI 
Genetics, Molecular Biology

48 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, 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
2016 Kamradt JM, Nigg JT, Friderici KH, Nikolas MA. Neuropsychological performance measures as intermediate phenotypes for attention-deficit/hyperactivity disorder: A multiple mediation analysis. Development and Psychopathology. 1-14. PMID 27049476 DOI: 10.1017/S0954579416000195  0.4
2015 Nigg JT, Elmore AL, Natarajan N, Friderici KH, Nikolas MA. Variation in an Iron Metabolism Gene Moderates the Association Between Blood Lead Levels and Attention-Deficit/Hyperactivity Disorder in Children. Psychological Science. PMID 26710823 DOI: 10.1177/0956797615618365  0.4
2015 Elmore AL, Nigg JT, Friderici KH, Jernigan K, Nikolas MA. Does 5HTTLPR Genotype Moderate the Association of Family Environment With Child Attention-Deficit Hyperactivity Disorder Symptomatology? Journal of Clinical Child and Adolescent Psychology : the Official Journal For the Society of Clinical Child and Adolescent Psychology, American Psychological Association, Division 53. 1-13. PMID 25602736 DOI: 10.1080/15374416.2014.979935  0.4
2014 Rehman AU, Santos-Cortez RL, Drummond MC, Shahzad M, Lee K, Morell RJ, Ansar M, Jan A, Wang X, Aziz A, Riazuddin S, Smith JD, Wang GT, Ahmed ZM, Gul K, ... ... Friderici KH, et al. Challenges and solutions for gene identification in the presence of familial locus heterogeneity. European Journal of Human Genetics : Ejhg. PMID 25491636 DOI: 10.1038/ejhg.2014.266  0.4
2014 Bonner JD, Fisher R, Klein J, Lu Q, Wilch E, Friderici KH, Elfenbein JL, Schutte DL, Schutte BC. Pedigree structure and kinship measurements of a mid-Michigan community: a new North American population isolate identified. Human Biology. 86: 59-68. PMID 25401987 DOI: 10.1353/hub.2014.0002  0.4
2014 Lovell KL, Zhu M, Drummond MC, Switzer RC, Friderici KH. Distribution and Severity of Neuropathology in β-Mannosidase-Deficient Mice is Strain Dependent. Jimd Reports. 13: 73-81. PMID 24142277 DOI: 10.1007/8904_2013_258  0.72
2013 Drummond MC, Friderici KH. A novel actin mRNA splice variant regulates ACTG1 expression. Plos Genetics. 9: e1003743. PMID 24098136 DOI: 10.1371/journal.pgen.1003743  0.72
2013 Dang MT, Gu C, Klavanian JI, Jernigan KA, Friderici KH, Cui Y, Molina-Molina M, Ancochea J, Xaubet A, Uhal BD. Angiotensinogen promoter polymorphisms predict low diffusing capacity in U.S. and Spanish IPF cohorts. Lung. 191: 353-60. PMID 23715995 DOI: 10.1007/s00408-013-9476-2  0.4
2012 Martel MM, Nikolas M, Jernigan K, Friderici K, Nigg JT. Diversity in pathways to common childhood disruptive behavior disorders. Journal of Abnormal Child Psychology. 40: 1223-36. PMID 22584505 DOI: 10.1007/s10802-012-9646-3  0.4
2012 Drummond MC, Belyantseva IA, Friderici KH, Friedman TB. Actin in hair cells and hearing loss. Hearing Research. 288: 89-99. PMID 22200607 DOI: 10.1016/j.heares.2011.12.003  0.4
2012 Jones NM, Holzman C, Tian Y, Witkin SS, Genc M, Friderici K, Fisher R, Sezen D, Babula O, Jernigan KA, Chung H, Wirth J. Innate immune system gene polymorphisms in maternal and child genotype and risk of preterm delivery. The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians. 25: 240-7. PMID 21627550 DOI: 10.3109/14767058.2011.569614  0.4
2011 Scheid JM, Holzman CB, Jones N, Friderici KH, Jernigan KA, Symonds LL, Sikorskii A, Fisher R. Life stressors and 5-HTTLPR interaction in relation to midpregnancy depressive symptoms among African-American women. Psychiatric Genetics. 21: 271-80. PMID 22030619 DOI: 10.1097/YPG.0b013e32834603e8  0.4
2011 Schauberger EM, Ewart SL, Arshad SH, Huebner M, Karmaus W, Holloway JW, Friderici KH, Ziegler JT, Zhang H, Rose-Zerilli MJ, Barton SJ, Holgate ST, Kilpatrick JR, Harley JB, Lajoie-Kadoch S, et al. Identification of ATPAF1 as a novel candidate gene for asthma in children. The Journal of Allergy and Clinical Immunology. 128: 753-760.e11. PMID 21696813 DOI: 10.1016/j.jaci.2011.04.058  0.4
2011 Martel MM, Nikolas M, Jernigan K, Friderici K, Waldman I, Nigg JT. The dopamine receptor D4 gene (DRD4) moderates family environmental effects on ADHD. Journal of Abnormal Child Psychology. 39: 1-10. PMID 20644990 DOI: 10.1007/s10802-010-9439-5  0.4
2010 Jones NM, Holzman C, Friderici KH, Jernigan K, Chung H, Wirth J, Fisher R. Interplay of cytokine polymorphisms and bacterial vaginosis in the etiology of preterm delivery. Journal of Reproductive Immunology. 87: 82-9. PMID 20965572 DOI: 10.1016/j.jri.2010.06.158  0.4
2010 Nikolas M, Friderici K, Waldman I, Jernigan K, Nigg JT. Gene x environment interactions for ADHD: synergistic effect of 5HTTLPR genotype and youth appraisals of inter-parental conflict. Behavioral and Brain Functions : Bbf. 6: 23. PMID 20398347 DOI: 10.1186/1744-9081-6-23  0.4
2010 Bergeron SE, Zhu M, Thiem SM, Friderici KH, Rubenstein PA. Ion-dependent polymerization differences between mammalian beta- and gamma-nonmuscle actin isoforms. The Journal of Biological Chemistry. 285: 16087-95. PMID 20308063 DOI: 10.1074/jbc.M110.110130  0.4
2010 Wilch E, Azaiez H, Fisher RA, Elfenbein J, Murgia A, Birkenhäger R, Bolz H, Da Silva-Costa SM, Del Castillo I, Haaf T, Hoefsloot L, Kremer H, Kubisch C, Le Marechal C, Pandya A, ... ... Friderici KH, et al. A novel DFNB1 deletion allele supports the existence of a distant cis-regulatory region that controls GJB2 and GJB6 expression. Clinical Genetics. 78: 267-74. PMID 20236118 DOI: 10.1111/j.1399-0004.2010.01387.x  0.4
2010 Martel MM, Nikolas M, Jernigan K, Friderici K, Nigg JT. Personality mediation of genetic effects on Attention-Deficit/Hyperactivity Disorder. Journal of Abnormal Child Psychology. 38: 633-43. PMID 20146095 DOI: 10.1007/s10802-010-9392-3  0.4
2010 Nigg JT, Nikolas M, Mark Knottnerus G, Cavanagh K, Friderici K. Confirmation and extension of association of blood lead with attention-deficit/hyperactivity disorder (ADHD) and ADHD symptom domains at population-typical exposure levels. Journal of Child Psychology and Psychiatry, and Allied Disciplines. 51: 58-65. PMID 19941632 DOI: 10.1111/j.1469-7610.2009.02135.x  0.4
2009 Gargano JW, Holzman CB, Senagore PK, Reuss ML, Pathak DR, Friderici KH, Jernigan K, Fisher R. Polymorphisms in thrombophilia and renin-angiotensin system pathways, preterm delivery, and evidence of placental hemorrhage. American Journal of Obstetrics and Gynecology. 201: 317.e1-9. PMID 19733287 DOI: 10.1016/j.ajog.2009.05.060  0.4
2009 Belyantseva IA, Perrin BJ, Sonnemann KJ, Zhu M, Stepanyan R, McGee J, Frolenkov GI, Walsh EJ, Friderici KH, Friedman TB, Ervasti JM. Gamma-actin is required for cytoskeletal maintenance but not development. Proceedings of the National Academy of Sciences of the United States of America. 106: 9703-8. PMID 19497859 DOI: 10.1073/pnas.0900221106  0.4
2009 Housley DJ, Nikolas M, Venta PJ, Jernigan KA, Waldman ID, Nigg JT, Friderici KH. SNP discovery and haplotype analysis in the segmentally duplicated DRD5 coding region. Annals of Human Genetics. 73: 274-82. PMID 19397556 DOI: 10.1111/j.1469-1809.2009.00513.x  0.4
2009 Messaros BM, Rossano MG, Liu G, Diamond MP, Friderici K, Nummy-Jernigan K, Daly D, Puscheck E, Paneth N, Wirth JJ. Negative effects of serum p,p'-DDE on sperm parameters and modification by genetic polymorphisms. Environmental Research. 109: 457-64. PMID 19303595 DOI: 10.1016/j.envres.2009.02.009  0.4
2008 Molina-Molina M, Xaubet A, Li X, Abdul-Hafez A, Friderici K, Jernigan K, Fu W, Ding Q, Pereda J, Serrano-Mollar A, Casanova A, Rodríguez-Becerra E, Morell F, Ancochea J, Picado C, et al. Angiotensinogen gene G-6A polymorphism influences idiopathic pulmonary fibrosis disease progression European Respiratory Journal. 32: 1004-1008. PMID 18508830 DOI: 10.1183/09031936.00015808  0.4
2007 Nigg J, Nikolas M, Friderici K, Park L, Zucker RA. Genotype and neuropsychological response inhibition as resilience promoters for attention-deficit/hyperactivity disorder, oppositional defiant disorder, and conduct disorder under conditions of psychosocial adversity. Development and Psychopathology. 19: 767-86. PMID 17705902 DOI: 10.1017/S0954579407000387  0.4
2007 Scheid JM, Holzman CB, Jones N, Friderici KH, Nummy KA, Symonds LL, Sikorskii A, Regier MK, Fisher R. Depressive symptoms in mid-pregnancy, lifetime stressors and the 5-HTTLPR genotype Genes, Brain and Behavior. 6: 453-464. PMID 16965382 DOI: 10.1111/j.1601-183X.2006.00272.x  0.4
2006 Waldman ID, Nigg JT, Gizer IR, Park L, Rappley MD, Friderici K. The adrenergic receptor alpha-2A gene (ADRA2A) and neuropsychological executive functions as putative endophenotypes for childhood ADHD. Cognitive, Affective & Behavioral Neuroscience. 6: 18-30. PMID 16869226 DOI: 10.3758/CABN.6.1.18  0.4
2006 Rendtorff ND, Zhu M, Fagerheim T, Antal TL, Jones M, Teslovich TM, Gillanders EM, Barmada M, Teig E, Trent JM, Friderici KH, Stephan DA, Tranebjaerg L. A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment. European Journal of Human Genetics : Ejhg. 14: 1097-105. PMID 16773128 DOI: 10.1038/sj.ejhg.5201670  0.4
2006 Bryan KE, Wen KK, Zhu M, Rendtorff ND, Feldkamp M, Tranebjaerg L, Friderici KH, Rubenstein PA. Effects of human deafness gamma-actin mutations (DFNA20/26) on actin function. The Journal of Biological Chemistry. 281: 20129-39. PMID 16690605 DOI: 10.1074/jbc.M601514200  0.4
2006 Sedel F, Friderici K, Nummy K, Caillaud C, Chabli A, Dürr A, Lubetzki C, Agid Y. Atypical Gilles de la Tourette Syndrome with beta-mannosidase deficiency. Archives of Neurology. 63: 129-31. PMID 16401745 DOI: 10.1001/archneur.63.1.129  0.4
2006 Zhu M, Lovell KL, Patterson JS, Saunders TL, Hughes ED, Friderici KH. Beta-mannosidosis mice: a model for the human lysosomal storage disease. Human Molecular Genetics. 15: 493-500. PMID 16377659 DOI: 10.1093/hmg/ddi465  0.4
2005 Park L, Nigg JT, Waldman ID, Nummy KA, Huang-Pollock C, Rappley M, Friderici KH. Association and linkage of alpha-2A adrenergic receptor gene polymorphisms with childhood ADHD. Molecular Psychiatry. 10: 572-80. PMID 15520832 DOI: 10.1038/sj.mp.4001605  0.4
2003 Zhu M, Yang T, Wei S, DeWan AT, Morell RJ, Elfenbein JL, Fisher RA, Leal SM, Smith RJH, Friderici KH. Mutations in the γ-Actin Gene (ACTG1) Are Associated with Dominant Progressive Deafness (DFNA20/26) American Journal of Human Genetics. 73: 1082-1091. PMID 13680526 DOI: 10.1086/379286  0.4
2003 Rothrock CR, Murgia A, Sartorato EL, Leonardi E, Wei S, Lebeis SL, Yu LE, Elfenbein JL, Fisher RA, Friderici KH. Connexin 26 35delG does not represent a mutational hotspot. Human Genetics. 113: 18-23. PMID 12684873 DOI: 10.1007/s00439-003-0944-2  0.4
2002 Bedilu R, Nummy KA, Cooper A, Wevers R, Smeitink J, Kleijer WJ, Friderici KH. Variable clinical presentation of lysosomal beta-mannosidosis in patients with null mutations. Molecular Genetics and Metabolism. 77: 282-90. PMID 12468273 DOI: 10.1016/S1096-7192(02)00172-5  0.4
1999 Leipprandt JR, Chen H, Horvath JE, Qiao XT, Jones MZ, Friderici KH. Identification of a bovine beta-mannosidosis mutation and detection of two beta-mannosidase pseudogenes. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 10: 1137-41. PMID 10594236 DOI: 10.1007/s003359901179  0.4
1998 Morell RJ, Kim HJ, Hood LJ, Goforth L, Friderici K, Fisher R, Van Camp G, Berlin CI, Oddoux C, Ostrer H, Keats B, Friedman TB. Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness. The New England Journal of Medicine. 339: 1500-5. PMID 9819448 DOI: 10.1056/NEJM199811193392103  0.4
1998 Alkhayat AH, Kraemer SA, Leipprandt JR, Macek M, Kleijer WJ, Friderici KH. Human beta-mannosidase cDNA characterization and first identification of a mutation associated with human beta-mannosidosis. Human Molecular Genetics. 7: 75-83. PMID 9384606 DOI: 10.1093/hmg/7.1.75  0.4
1996 Leipprandt JR, Kraemer SA, Haithcock BE, Chen H, Dyme JL, Cavanagh KT, Friderici KH, Jones MZ. Caprine beta-mannosidase: sequencing and characterization of the cDNA and identification of the molecular defect of caprine beta-mannosidosis. Genomics. 37: 51-6. PMID 8921369 DOI: 10.1006/geno.1996.0519  0.4
1995 Chen H, Leipprandt JR, Traviss CE, Sopher BL, Jones MZ, Cavanagh KT, Friderici KH. Molecular cloning and characterization of bovine beta-mannosidase. The Journal of Biological Chemistry. 270: 3841-8. PMID 7876128 DOI: 10.1074/jbc.270.8.3841  0.4
1993 Sopher BL, Traviss CE, Cavanagh KT, Jones MZ, Friderici KH. Bovine kidney beta-mannosidase: purification and characterization. The Biochemical Journal. 289: 343-7. PMID 8424779 DOI: 10.1042/bj2890343  0.4
1990 Oh SY, Amalfitano A, Friderici K, Chen MC, Fluck MM. Low probability of double integration in transformation of nonpermissive cells by polyomavirus Journal of Virology. 64: 1304-1313. PMID 2154610  0.4
1989 Hacker DL, Friderici K, Fluck MM. A nonlethal mutation in large T antigen of polyomavirus which affects viral DNA synthesis Journal of Virology. 63: 776-781. PMID 2536103 DOI: 10.1128/jvi.63.2.776-781.1989  0.4
1986 Priehs C, Friderici K, Winberry L, Fluck MM. Properties of cells transformed by the middle T-antigen-coding region of polyomavirus Journal of Virology. 57: 211-218. PMID 3001346 DOI: 10.1128/jvi.57.1.211-218.1986  0.4
1986 Friderici K, Priehs C, Fluck MM. Superinfection rescue of an integrated defective polyomavirus genome Journal of Virology. 57: 205-210. PMID 3001345 DOI: 10.1128/jvi.57.1.205-210.1986  0.4
1985 Winberry L, Priehs C, Friderici K, Thompson M, Fluck M. Expression of proto-oncogenes in normal and papovavirus-transformed or -infected rat fibroblasts Virology. 147: 154-168. PMID 2414921 DOI: 10.1016/0042-6822(85)90235-1  0.4
1984 Friderici K, Yin Oh S, Ellis R, Guacci V, Fluck MM. Recombination induces tandem repeats of integrated viral sequences in polyoma-transformed cells Virology. 137: 67-73. PMID 6089421 DOI: 10.1016/0042-6822(84)90009-6  0.4
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