| Year |
Citation |
Score |
| 2016 |
Krey JF, Drummond M, Foster S, Porsov E, Vijayakumar S, Choi D, Friderici K, Jones SM, Nuttall AL, Barr-Gillespie PG. Annexin A5 is the Most Abundant Membrane-Associated Protein in Stereocilia but is Dispensable for Hair-Bundle Development and Function. Scientific Reports. 6: 27221. PMID 27251877 DOI: 10.1038/Srep27221 |
0.729 |
|
| 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 |
0.373 |
|
| 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 |
0.354 |
|
| 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 |
0.365 |
|
| 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 |
0.71 |
|
| 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: 10.3378/027.086.0103 |
0.723 |
|
| 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 |
0.718 |
|
| 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 |
0.732 |
|
| 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 |
0.309 |
|
| 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 |
0.333 |
|
| 2012 |
Sartorato EL, Friderici K, Del Castillo I. Genetics of deafness. Genetics Research International. 2012: 562848. PMID 22567392 DOI: 10.1155/2012/562848 |
0.359 |
|
| 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 |
0.749 |
|
| 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 |
0.302 |
|
| 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 |
0.338 |
|
| 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 |
0.357 |
|
| 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 |
0.349 |
|
| 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 |
0.758 |
|
| 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 |
0.319 |
|
| 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 |
0.367 |
|
| 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 |
0.318 |
|
| 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 |
0.741 |
|
| 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 |
0.744 |
|
| 2006 |
Wilch E, Zhu M, Burkhart KB, Regier M, Elfenbein JL, Fisher RA, Friderici KH. Expression of GJB2 and GJB6 is reduced in a novel DFNB1 allele. American Journal of Human Genetics. 79: 174-9. PMID 16773579 DOI: 10.1086/505333 |
0.743 |
|
| 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 |
0.419 |
|
| 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 |
0.319 |
|
| 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 |
0.761 |
|
| 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 |
0.426 |
|
| 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 |
0.399 |
|
| 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 |
0.334 |
|
| 2002 |
Elfenbein JL, Fisher RA, Wei S, Morell RJ, Stewart C, Friedman TB, Friderici K. Audiologic aspects of the search for DFNA20: a gene causing late-onset, progressive, sensorineural hearing loss. Ear and Hearing. 22: 279-88. PMID 11527035 DOI: 10.1097/00003446-200108000-00003 |
0.364 |
|
| 2000 |
Morell RJ, Friderici KH, Wei S, Elfenbein JL, Friedman TB, Fisher RA. A new locus for late-onset, progressive, hereditary hearing loss DFNA20 maps to 17q25. Genomics. 63: 1-6. PMID 10662538 DOI: 10.1006/Geno.1999.6058 |
0.368 |
|
| 1998 |
Hoard HM, Leipprandt JR, Cavanagh KT, Truscott NK, Levene BA, Friderici KH, Jones MZ. Determination of genotypic frequency of caprine mucopolysaccharidosis IIID. Journal of Veterinary Diagnostic Investigation : Official Publication of the American Association of Veterinary Laboratory Diagnosticians, Inc. 10: 181-3. PMID 9576348 DOI: 10.1177/104063879801000212 |
0.318 |
|
| 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 |
0.342 |
|
| 1997 |
Litjens T, Bielicki J, Anson DS, Friderici K, Jones MZ, Hopwood JJ. Expression, purification and characterization of recombinant caprine N-acetylglucosamine-6-sulphatase. The Biochemical Journal. 327: 89-94. PMID 9355739 DOI: 10.1042/Bj3270089 |
0.305 |
|
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