| Year |
Citation |
Score |
| 2018 |
Pandey A, Hale D, Das S, Goddings AL, Blakemore SJ, Viner RM. Effectiveness of Universal Self-regulation-Based Interventions in Children and Adolescents: A Systematic Review and Meta-analysis. Jama Pediatrics. PMID 29710097 DOI: 10.1001/Jamapediatrics.2018.0232 |
0.368 |
|
| 2018 |
Yassaee A, Hale D, Armitage A, Viner R. G424(P) The impact of age and dedicated age-appropriate services on transition outcomes from paediatric to adult health systems: a review of reviews Archives of Disease in Childhood. DOI: 10.1136/Archdischild-2018-Rcpch.413 |
0.312 |
|
| 2017 |
Bevilacqua L, Hale D, Barker ED, Viner R. Conduct problems trajectories and psychosocial outcomes: a systematic review and meta-analysis. European Child & Adolescent Psychiatry. PMID 28983792 DOI: 10.1007/S00787-017-1053-4 |
0.379 |
|
| 2017 |
Pandey A, Hale D, Goddings AL, Blakemore SJ, Viner R. Systematic review of effectiveness of universal self-regulation-based interventions and their effects on distal health and social outcomes in children and adolescents: review protocol. Systematic Reviews. 6: 175. PMID 28851433 DOI: 10.1186/S13643-017-0570-Z |
0.369 |
|
| 2017 |
Bevilacqua L, Hale D, Barker E, Viner R. G121(P) Conduct problems trajectories and psychosocial outcomes in early adulthood: A systematic review and meta-analysis Archives of Disease in Childhood. 102. DOI: 10.1136/Archdischild-2017-313087.120 |
0.393 |
|
| 2016 |
Yassaee A, Hale D, Armitage A, Viner R. G321 Optimising healthcare transitions for young people: A systematic review of reviews Archives of Disease in Childhood. 101. DOI: 10.1136/Archdischild-2016-310863.312 |
0.307 |
|
| 2015 |
Bonell C, Fletcher A, Fitzgerald-Yau N, Hale D, Allen E, Elbourne D, Jones R, Bond L, Wiggins M, Miners A, Legood R, Scott S, Christie D, Viner R. Initiating change locally in bullying and aggression through the school environment (INCLUSIVE): a pilot randomised controlled trial. Health Technology Assessment (Winchester, England). 19: 1-109, vii-viii. PMID 26182956 DOI: 10.3310/Hta19530 |
0.339 |
|
| 2015 |
Shackleton N, Hale D, Viner R. G491 Trends in health at the beginning of adolescence in the uk: evidence from two birth cohorts 30 years apart Archives of Disease in Childhood. 100. DOI: 10.1136/Archdischild-2015-308599.444 |
0.352 |
|
| 2014 |
Hale DR, Patalay P, Fitzgerald-Yau N, Hargreaves DS, Bond L, Görzig A, Wolpert M, Stansfeld SA, Viner RM. School-Level Variation in Health Outcomes in Adolescence: Analysis of Three Longitudinal Studies in England Prevention Science. 15: 600-610. PMID 23793374 DOI: 10.1007/s11121-013-0414-6 |
0.31 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2016 |
Bevilacqua L, Hale D, Shackleton N, Allen E, Bond L, Christie D, Elbourne D, Fitzgerald-Yau N, Fletcher A, Jones R, Legood R, Miners A, Scott S, Wiggins M, Bonell C, et al. G93(P) The role of school context and family factors in bullying and cyberbullying Archives of Disease in Childhood. 101. DOI: 10.1136/Archdischild-2016-310863.90 |
0.283 |
|
| 2015 |
Hale DR, Bevilacqua L, Viner RM. Adolescent Health and Adult Education and Employment: A Systematic Review. Pediatrics. 136: 128-40. PMID 26101362 DOI: 10.1542/peds.2014-2105 |
0.278 |
|
| 2014 |
Vallejo-Torres L, Hale D, Morris S, Viner RM. Income-related inequality in health and health-related behaviour: exploring the equalisation hypothesis. Journal of Epidemiology and Community Health. 68: 615-21. PMID 24619989 DOI: 10.1136/Jech-2013-203306 |
0.273 |
|
| 2018 |
Hale DR, Viner RM. How adolescent health influences education and employment: investigating longitudinal associations and mechanisms. Journal of Epidemiology and Community Health. PMID 29615474 DOI: 10.1136/jech-2017-209605 |
0.267 |
|
| 2019 |
Yassaee A, Hale D, Armitage A, Viner R. The Impact of Age of Transfer on Outcomes in the Transition From Pediatric to Adult Health Systems: A Systematic Review of Reviews. The Journal of Adolescent Health : Official Publication of the Society For Adolescent Medicine. PMID 30833120 DOI: 10.1016/j.jadohealth.2018.11.023 |
0.262 |
|
| 2016 |
Shackleton N, Hale D, Viner RM. Trends and socioeconomic disparities in preadolescent's health in the UK: evidence from two birth cohorts 32 years apart. Journal of Epidemiology and Community Health. 70: 140-6. PMID 26359506 DOI: 10.1136/jech-2015-205603 |
0.25 |
|
| 2014 |
Hale DR, Fitzgerald-Yau N, Viner RM. A systematic review of effective interventions for reducing multiple health risk behaviors in adolescence. American Journal of Public Health. 104: e19-41. PMID 24625172 DOI: 10.2105/AJPH.2014.301874 |
0.232 |
|
| 2017 |
Bevilacqua L, Shackleton N, Hale D, Allen E, Bond L, Christie D, Elbourne D, Fitzgerald-Yau N, Fletcher A, Jones R, Miners A, Scott S, Wiggins M, Bonell C, Viner RM. The role of family and school-level factors in bullying and cyberbullying: a cross-sectional study. Bmc Pediatrics. 17: 160. PMID 28697725 DOI: 10.1186/S12887-017-0907-8 |
0.222 |
|
| 2016 |
Hale DR, Viner RM. The correlates and course of multiple health risk behaviour in adolescence. Bmc Public Health. 16: 458. PMID 27246600 DOI: 10.1186/s12889-016-3120-z |
0.201 |
|
| 2011 |
Orsi CM, Hale DE, Lynch JL. Pediatric obesity epidemiology Current Opinion in Endocrinology, Diabetes and Obesity. 18: 14-22. PMID 21157323 DOI: 10.1097/MED.0b013e3283423de1 |
0.196 |
|
| 2015 |
Foster BA, Aquino C, Gil M, Flores G, Hale D. A randomized clinical trial of the effects of parent mentors on early childhood obesity: Study design and baseline data. Contemporary Clinical Trials. 45: 164-169. PMID 26343746 DOI: 10.1016/j.cct.2015.08.017 |
0.191 |
|
| 2016 |
Foster BA, Aquino CA, Gil M, Gelfond JA, Hale DE. A Pilot Study of Parent Mentors for Early Childhood Obesity. Journal of Obesity. 2016: 2609504. PMID 27379182 DOI: 10.1155/2016/2609504 |
0.188 |
|
| 2014 |
Soileau B, Hasi M, Sebold C, Hill A, O'Donnell L, Hale DE, Cody JD. Adults with Chromosome 18 Abnormalities. Journal of Genetic Counseling. PMID 25403900 DOI: 10.1007/s10897-014-9793-5 |
0.183 |
|
| 2013 |
Hale D, Viner R. Trends in the prevalence of multiple substance use in adolescents in England, 1998-2009. Journal of Public Health (Oxford, England). 35: 367-74. PMID 23528672 DOI: 10.1093/pubmed/fdt022 |
0.181 |
|
| 2014 |
Driscoll KA, Volkening LK, Haro H, Ocean G, Wang Y, Jackson CC, Clougherty M, Hale DE, Klingensmith GJ, Laffel L, Deeb LC, Siminerio LM. Are children with type 1 diabetes safe at school? Examining parent perceptions. Pediatric Diabetes. PMID 25266418 DOI: 10.1111/Pedi.12204 |
0.175 |
|
| 2016 |
Hudak ML, Park CH, Annett RD, Hale DE, McGovern PM, McLaughlin TJ, Dole N, Kaar JL, Balsam MJ. The National Children's Study: An Introduction and Historical Overview. Pediatrics. 137: S213-8. PMID 27251867 DOI: 10.1542/Peds.2015-4410B |
0.171 |
|
| 2004 |
Hale DE. Type 2 diabetes and diabetes risk factors in children and adolescents Clinical Cornerstone. 6: 17-27. PMID 15628690 DOI: 10.1016/S1098-3597(04)80051-6 |
0.171 |
|
| 2015 |
Sebold C, Soileau B, Heard P, Carter E, O'Donnell L, Hale DE, Cody JD. Whole arm deletions of 18p: medical and developmental effects. American Journal of Medical Genetics. Part A. 167: 313-23. PMID 25586871 DOI: 10.1002/ajmg.a.36880 |
0.168 |
|
| 2016 |
Hale DE, Wyatt SB, Buka S, Cherry D, Cislo KK, Dudley DJ, McElfish PA, Norman GS, Reynolds SA, Siega-Riz AM, Wadlinger S, Walker CK, Robbins JM. The National Children's Study: Recruitment Outcomes Using the Provider-Based Recruitment Approach. Pediatrics. 137: S239-47. PMID 27251870 DOI: 10.1542/Peds.2015-4410E |
0.161 |
|
| 2005 |
Copeland KC, Becker D, Gottschalk M, Hale D. Type 2 diabetes in children and adolescents: Risk factors, diagnosis, and treatment Clinical Diabetes. 23: 181-185. DOI: 10.2337/diaclin.23.4.181 |
0.16 |
|
| 2021 |
Baweja R, Hale DE, Waxmonsky JG. Impact of CNS Stimulants for Attention-Deficit/Hyperactivity Disorder on Growth: Epidemiology and Approaches to Management in Children and Adolescents. Cns Drugs. PMID 34297331 DOI: 10.1007/s40263-021-00841-w |
0.159 |
|
| 2012 |
Willi SM, Hirst K, Jago R, Buse J, Kaufman F, El Ghormli L, Bassin S, Elliot D, Hale DE. Cardiovascular risk factors in multi-ethnic middle school students: the HEALTHY primary prevention trial. Pediatric Obesity. 7: 230-9. PMID 22461375 DOI: 10.1111/j.2047-6310.2011.00042.x |
0.157 |
|
| 2019 |
LOPEZ-ALVARENGA JC, ARYA R, CHITTOOR G, PAUL SF, PUPPALA SR, FAROOK VS, FOWLER SP, RESENDEZ RG, DIAZ-BADILLO A, LEHMAN D, MUMMIDI S, JENKINSON C, LYNCH JL, DEFRONZO RA, BLANGERO J, ... HALE DE, et al. 2093-P: Acanthosis Nigricans as a Composite Marker of Cardiometabolic Risk and Its Complex Association with Obesity and Insulin Resistance in Mexican-American Children Diabetes. 68: 2093-P. DOI: 10.2337/Db19-2093-P |
0.154 |
|
| 2004 |
Treviño RP, Yin Z, Hernandez A, Hale DE, Garcia OA, Mobley C. Impact of the Bienestar school-based diabetes mellitus prevention program on fasting capillary glucose levels: a randomized controlled trial. Archives of Pediatrics & Adolescent Medicine. 158: 911-7. PMID 15351759 DOI: 10.1001/archpedi.158.9.911 |
0.154 |
|
| 2015 |
Foster BA, Hale D. Perceptions of Weight and Health Practices in Hispanic Children: A Mixed-Methods Study. International Journal of Pediatrics. 2015: 761515. PMID 26379715 DOI: 10.1155/2015/761515 |
0.154 |
|
| 2016 |
Hutchins J, Barajas RA, Hale D, Escaname E, Lynch J. Type 2 diabetes in a 5-year-old and single center experience of type 2 diabetes in youth under 10. Pediatric Diabetes. PMID 27807935 DOI: 10.1111/pedi.12463 |
0.153 |
|
| 2011 |
Hasi M, Soileau B, Sebold C, Hill A, Hale DE, O'Donnell L, Cody JD. The role of the TCF4 gene in the phenotype of individuals with 18q segmental deletions. Human Genetics. 130: 777-87. PMID 21671075 DOI: 10.1007/s00439-011-1020-y |
0.148 |
|
| 2010 |
Sebold C, Roeder E, Zimmerman M, Soileau B, Heard P, Carter E, Schatz M, White WA, Perry B, Reinker K, O'Donnell L, Lancaster J, Li J, Hasi M, Hill A, ... ... Hale DE, et al. Tetrasomy 18p: report of the molecular and clinical findings of 43 individuals. American Journal of Medical Genetics. Part A. 152: 2164-72. PMID 20803640 DOI: 10.1002/Ajmg.A.33597 |
0.148 |
|
| 2006 |
Hale DE, Rupert G. The changing spectrum of diabetes in Mexican American youth. Reviews in Endocrine & Metabolic Disorders. 7: 163-70. PMID 17195113 DOI: 10.1007/s11154-006-9023-z |
0.146 |
|
| 2023 |
Larson CC, O'Donnell L, Soileau B, Van Riper M, Stark D, Hale DE, Cody JD. Understanding type and quality of relationships between individuals with chromosome 18 syndromes and their siblings. Journal of Genetic Counseling. PMID 37882415 DOI: 10.1002/jgc4.1823 |
0.142 |
|
| 2015 |
Cody JD, Sebold C, Heard P, Carter E, Soileau B, Hasi-Zogaj M, Hill A, Rupert D, Perry B, O'Donnell L, Gelfond J, Lancaster J, Fox PT, Hale DE. Consequences of chromsome18q deletions. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 169: 265-80. PMID 26235940 DOI: 10.1002/Ajmg.C.31446 |
0.141 |
|
| 1992 |
Ribes A, Riudor E, Navarro C, Boronat M, Marti M, Hale DE. Fatal outcome in a patient with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. Journal of Inherited Metabolic Disease. 15: 278-9. PMID 1527994 DOI: 10.1007/BF01799642 |
0.139 |
|
| 2018 |
Arya R, Farook VS, Fowler SP, Puppala S, Chittoor G, Resendez RG, Mummidi S, Vanamala J, Almasy L, Curran JE, Comuzzie AG, Lehman DM, Jenkinson CP, Lynch JL, DeFronzo RA, ... ... Hale DE, et al. Genetic and environmental (physical fitness and sedentary activity) interaction effects on cardiometabolic risk factors in Mexican American children and adolescents. Genetic Epidemiology. PMID 29460292 DOI: 10.1002/Gepi.22114 |
0.138 |
|
| 2005 |
Cody JD, Semrud-Clikeman M, Hardies LJ, Lancaster J, Ghidoni PD, Schaub RL, Thompson NM, Wells L, Cornell JE, Love TM, Fox PT, Leach RJ, Kaye CI, Hale DE. Growth hormone benefits children with 18q deletions. American Journal of Medical Genetics. Part A. 137: 9-15. PMID 16007630 DOI: 10.1002/Ajmg.A.30848 |
0.136 |
|
| 2013 |
Belanger K, Buka S, Cherry DC, Dudley DJ, Elliott MR, Hale DE, Hertz-Picciotto I, Illuzzi JL, Paneth N, Robbins JM, Triche EW, Bracken MB. Implementing provider-based sampling for the National Children's Study: opportunities and challenges. Paediatric and Perinatal Epidemiology. 27: 20-6. PMID 23215706 DOI: 10.1111/Ppe.12005 |
0.135 |
|
| 2015 |
Hasi-Zogaj M, Sebold C, Heard P, Carter E, Soileau B, Hill A, Rupert D, Perry B, Atkinson S, O'Donnell L, Gelfond J, Lancaster J, Fox PT, Hale DE, Cody JD. A review of 18p deletions. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 169: 251-64. PMID 26250845 DOI: 10.1002/Ajmg.C.31445 |
0.132 |
|
| 2014 |
Cody JD, Hasi M, Soileau B, Heard P, Carter E, Sebold C, O'Donnell L, Perry B, Stratton RF, Hale DE. Establishing a reference group for distal 18q-: clinical description and molecular basis. Human Genetics. 133: 199-209. PMID 24092497 DOI: 10.1007/s00439-013-1364-6 |
0.13 |
|
| 2013 |
Fowler SP, Puppala S, Arya R, Chittoor G, Farook VS, Schneider J, Resendez RG, Upadhayay RP, Vandeberg J, Hunt KJ, Bradshaw B, Cersosimo E, Vandeberg JL, Almasy L, Curran JE, ... ... Hale DE, et al. Genetic epidemiology of cardiometabolic risk factors and their clustering patterns in Mexican American children and adolescents: the SAFARI Study. Human Genetics. 132: 1059-71. PMID 23736306 DOI: 10.1007/S00439-013-1315-2 |
0.13 |
|
| 2007 |
Hale DE. Estimated prevalence of hyperinsulinemia among Mexican-American adolescents in south Texas Texas Medicine. 103: 38-40. PMID 17542399 |
0.13 |
|
| 2005 |
Schaub RL, Hale DE, Rose SR, Leach RJ, Cody JD. The spectrum of thyroid abnormalities in individuals with 18q deletions Journal of Clinical Endocrinology and Metabolism. 90: 2259-2263. PMID 15671099 DOI: 10.1210/Jc.2004-1630 |
0.129 |
|
| 2012 |
Laffel L, Chang N, Grey M, Hale D, Higgins L, Hirst K, Izquierdo R, Larkin M, Macha C, Pham T, Wauters A, Weinstock RS. Metformin monotherapy in youth with recent onset type 2 diabetes: experience from the prerandomization run-in phase of the TODAY study. Pediatric Diabetes. 13: 369-75. PMID 22369102 DOI: 10.1111/j.1399-5448.2011.00846.x |
0.129 |
|
| 2005 |
Kochunov P, Lancaster J, Hardies J, Thompson PM, Woods RP, Cody JD, Hale DE, Laird A, Fox PT. Mapping structural differences of the corpus callosum in individuals with 18q deletions using targetless regional spatial normalization. Human Brain Mapping. 24: 325-31. PMID 15704090 DOI: 10.1002/Hbm.20090 |
0.128 |
|
| 2017 |
Foster BA, Escaname E, Powell TL, Larsen B, Siddiqui SK, Menchaca J, Aquino C, Ramamurthy R, Hale DE. Randomized Controlled Trial of DHA Supplementation during Pregnancy: Child Adiposity Outcomes. Nutrients. 9. PMID 28574453 DOI: 10.3390/nu9060566 |
0.127 |
|
| 2018 |
Shah AS, El Ghormli L, Gidding SS, Bacha F, Nadeau KJ, Levitt Katz LE, Tryggestad JB, Leibel N, Hale DE, Urbina EM. Prevalence of arterial stiffness in adolescents with type 2 diabetes in the TODAY cohort: Relationships to glycemic control and other risk factors. Journal of Diabetes and Its Complications. PMID 29936086 DOI: 10.1016/j.jdiacomp.2018.05.013 |
0.123 |
|
| 1999 |
Cody JD, Ghidoni PD, DuPont BR, Hale DE, Hilsenbeck SG, Stratton RF, Hoffman DS, Muller S, Schaub RL, Leach RJ, Kaye CI. Congenital anomalies and anthropometry of 42 individuals with deletions of chromosome 18q. American Journal of Medical Genetics. 85: 455-62. PMID 10405442 DOI: 10.1002/(Sici)1096-8628(19990827)85:5<455::Aid-Ajmg5>3.0.Co;2-Z |
0.121 |
|
| 2010 |
O'Donnell L, Soileau B, Heard P, Carter E, Sebold C, Gelfond J, Hale DE, Cody JD. Genetic determinants of autism in individuals with deletions of 18q. Human Genetics. 128: 155-64. PMID 20499253 DOI: 10.1007/S00439-010-0839-Y |
0.119 |
|
| 2015 |
Hasi-Zogaj M, Sebold C, Heard P, Carter E, Soileau B, Hill A, Rupert D, Perry B, Atkinson S, O'Donnell L, Gelfond J, Lancaster J, Fox PT, Hale DE, Cody JD. A review of 18p deletions American Journal of Medical Genetics, Part C: Seminars in Medical Genetics. DOI: 10.1002/ajmg.c.31445 |
0.119 |
|
| 2000 |
Hale DE, Cody JD, Baillargeon J, Schaub R, Danney MM, Leach RJ. The spectrum of growth abnormalities in children with 18q deletions Journal of Clinical Endocrinology and Metabolism. 85: 4450-4454. PMID 11134092 DOI: 10.1210/Jc.85.12.4450 |
0.117 |
|
| 2013 |
Chittoor G, Farook VS, Puppala S, Fowler SP, Schneider J, Dyer TD, Cole SA, Lynch JL, Curran JE, Almasy L, Maccluer JW, Comuzzie AG, Hale DE, Ramamurthy RS, Dudley DJ, et al. Localization of a major susceptibility locus influencing preterm birth. Molecular Human Reproduction. 19: 687-96. PMID 23689979 DOI: 10.1093/Molehr/Gat036 |
0.115 |
|
| 2017 |
Belknap A, Grosser DS, Hale DA, Lang BJ, Colley P, Benavides R, Dhiman N. Clinical uptake of antimicrobial stewardship recommendations following Nanosphere Verigene Blood Culture Gram-negative reporting. Proceedings (Baylor University. Medical Center). 30: 395-399. PMID 28966443 |
0.114 |
|
| 2015 |
Cody JD, Hale DE. Making chromosome abnormalities treatable conditions. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 169: 209-15. PMID 26351122 DOI: 10.1002/ajmg.c.31447 |
0.114 |
|
| 2019 |
Moreira A, Das H, Hasi-Zogaj M, Soileau B, Hill A, Bruder JM, Hale DE, Cody JD. Abnormal bone mineral content and density in people with tetrasomy 18p. American Journal of Medical Genetics. Part A. PMID 30637922 DOI: 10.1002/ajmg.a.61005 |
0.113 |
|
| 2005 |
Semrud-Clikeman M, Thompson NM, Schaub BL, Leach R, Hester A, Hale DE, Cody JD. Cognitive ability predicts degree of genetic abnormality in participants with 18q deletions. Journal of the International Neuropsychological Society : Jins. 11: 584-90. PMID 16212685 DOI: 10.1017/S1355617705050691 |
0.113 |
|
| 2007 |
Cody JD, Sebold C, Malik A, Heard P, Carter E, Crandall A, Soileau B, Semrud-Clikeman M, Cody CM, Hardies LJ, Li J, Lancaster J, Fox PT, Stratton RF, Perry B, ... Hale DE, et al. Recurrent interstitial deletions of proximal 18q: a new syndrome involving expressive speech delay. American Journal of Medical Genetics. Part A. 143: 1181-90. PMID 17486614 DOI: 10.1002/Ajmg.A.31729 |
0.111 |
|
| 2013 |
Bracken MB, Baker D, Cauley JA, Chambers C, Culhane J, Dabelea D, Dearborn D, Drews-Botsch CD, Dudley DJ, Durkin M, Entwisle B, Flick L, Hale D, Holl J, Hovell M, et al. New models for large prospective studies: is there a risk of throwing out the baby with the bathwater? American Journal of Epidemiology. 177: 285-9. PMID 23296354 DOI: 10.1093/Aje/Kws408 |
0.11 |
|
| 2014 |
Gardiner JC, Reed PL, Bonner JD, Haggerty DK, Hale DG. Incidence of hospital-acquired pressure ulcers - a population-based cohort study. International Wound Journal. PMID 25469585 DOI: 10.1111/Iwj.12386 |
0.109 |
|
| 2021 |
Mummidi S, Farook VS, Reddivari L, Hernandez-Ruiz J, Diaz-Badillo A, Fowler SP, Resendez RG, Akhtar F, Lehman DM, Jenkinson CP, Arya R, Lynch JL, Canas JA, DeFronzo RA, Hale DE, et al. Serum carotenoids and Pediatric Metabolic Index predict insulin sensitivity in Mexican American children. Scientific Reports. 11: 871. PMID 33441626 DOI: 10.1038/s41598-020-79387-8 |
0.108 |
|
| 1985 |
Hale DE, Batshaw ML, Coates PM, Frerman FE, Goodman SI, Singh I, Stanley CA. Long-chain acyl coenzyme A dehydrogenase deficiency: an inherited cause of nonketotic hypoglycemia. Pediatric Research. 19: 666-71. PMID 4022672 DOI: 10.1203/00006450-198507000-00006 |
0.107 |
|
| 2005 |
Lancaster JL, Cody JD, Andrews T, Hardies LJ, Hale DE, Fox PT. Myelination in children with partial deletions of chromosome 18q. Ajnr. American Journal of Neuroradiology. 26: 447-54. PMID 15760848 |
0.107 |
|
| 2010 |
Cody JD, Heard P, Hale D. Identification of two novel chromosome regions associated with isolated growth hormone deficiency. Journal of Pediatric Endocrinology & Metabolism : Jpem. 23: 1159-64. PMID 21284329 DOI: 10.1515/jpem.2010.181 |
0.106 |
|
| 2006 |
Wajcberg E, Thoppil N, Patel S, Fernandez M, Hale D, DeFronzo R, Cersosimo E. Comprehensive assessment of postischemic vascular reactivity in Hispanic children and adults with and without diabetes mellitus. Pediatric Diabetes. 7: 329-35. PMID 17212600 DOI: 10.1111/j.1399-5448.2006.00209.x |
0.106 |
|
| 2017 |
Farook VS, Reddivari L, Mummidi S, Puppala S, Arya R, Lopez-Alvarenga JC, Fowler SP, Chittoor G, Resendez RG, Kumar BM, Comuzzie AG, Curran JE, Lehman DM, Jenkinson CP, Lynch JL, ... ... Hale DE, et al. Genetics of serum carotenoid concentrations and their correlation with obesity-related traits in Mexican American children. The American Journal of Clinical Nutrition. PMID 28515064 DOI: 10.3945/Ajcn.116.144006 |
0.105 |
|
| 2015 |
Carter E, Heard P, Hasi M, Soileau B, Sebold C, Hale DE, Cody JD. Ring 18 molecular assessment and clinical consequences. American Journal of Medical Genetics. Part A. 167: 54-63. PMID 25339348 DOI: 10.1002/ajmg.a.36822 |
0.105 |
|
| 2013 |
White NH, Pyle L, Willi SM, Pham T, Chernausek SD, Goland R, Hale DE, Haymond MW, Nadeau KJ, Narasimhan S. Safety and tolerability of the treatment of youth-onset type 2 diabetes: The TODAY experience Diabetes Care. 36: 1765-1771. PMID 23704676 DOI: 10.2337/Dc12-2390 |
0.105 |
|
| 2018 |
Cody JD, Hasi-Zogaj M, Heard P, Hill A, Rupert D, Sebold C, Soileau B, Hale DE. The Chromosome 18 Clinical Resource Center. Molecular Genetics & Genomic Medicine. PMID 29603904 DOI: 10.1002/mgg3.385 |
0.105 |
|
| 1999 |
Treviño RP, Marshall RM, Hale DE, Rodriguez R, Baker G, Gomez J. Diabetes risk factors in low-income Mexican-American children. Diabetes Care. 22: 202-7. PMID 10333934 DOI: 10.2337/DIACARE.22.2.202 |
0.104 |
|
| 2015 |
Foster BA, Farragher J, Parker P, Hale DE. A positive deviance approach to early childhood obesity: cross-sectional characterization of positive outliers. Childhood Obesity (Print). 11: 281-8. PMID 25885174 DOI: 10.1089/chi.2014.0098 |
0.104 |
|
| 2015 |
Somerville MH, Seeff L, Hale D, O'Brien DJ. Hospitals, collaboration, and community health improvement. The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics. 43: 56-9. PMID 25846166 DOI: 10.1111/jlme.12217 |
0.103 |
|
| 2000 |
Burke JP, Duggirala R, Hale DE, Blangero J, Stern MP. Genetic basis of acanthosis nigricans in Mexican Americans and its association with phenotypes related to type 2 diabetes. Human Genetics. 106: 467-72. PMID 10914675 DOI: 10.1007/S004390000274 |
0.102 |
|
| 2013 |
Daviss WB, O'Donnell L, Soileau BT, Heard P, Carter E, Pliszka SR, Gelfond JA, Hale DE, Cody JD. Mood disorders in individuals with distal 18q deletions. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 162: 879-88. PMID 24006251 DOI: 10.1002/ajmg.b.32197 |
0.102 |
|
| 1997 |
Ghidoni PD, Hale DE, Cody JD, Gay CT, Thompson NM, McClure EB, Danney MM, Leach RJ, Kaye CI. Growth hormone deficiency associated in the 18q deletion syndrome. American Journal of Medical Genetics. 69: 7-12. PMID 9066876 DOI: 10.1002/(Sici)1096-8628(19970303)69:1<7::Aid-Ajmg2>3.0.Co;2-P |
0.102 |
|
| 2019 |
Hargreaves DS, Arora S, Viveiro C, Hale DR, Ward JL, Sherlaw-Johnson C, Viner RM, Dunkley C, Cross JH. Association of quality of paediatric epilepsy care with mortality and unplanned hospital admissions among children and young people with epilepsy in England: a national longitudinal data linkage study. The Lancet. Child & Adolescent Health. PMID 31281027 DOI: 10.1016/S2352-4642(19)30201-9 |
0.101 |
|
| 2011 |
Cody JD, Hale DE. Linking chromosome abnormality and copy number variation. American Journal of Medical Genetics. Part A. 155: 469-75. PMID 21344636 DOI: 10.1002/ajmg.a.33849 |
0.101 |
|
| 1997 |
Cody JD, Hale DE, Brkanac Z, Kaye CI, Leach RJ. Growth hormone insufficiency associated with haploinsufficiency at 18q23. American Journal of Medical Genetics. 71: 420-5. PMID 9286448 DOI: 10.1002/(Sici)1096-8628(19970905)71:4<420::Aid-Ajmg9>3.0.Co;2-X |
0.101 |
|
| 1990 |
Catzeflis C, Bachmann C, Hale DE, Coates PM, Wiesmann U, Colombo JP, Joris F, Délèze G. Early diagnosis and treatment of neonatal medium-chain acyl-CoA dehydrogenase deficiency: report of two siblings. European Journal of Pediatrics. 149: 577-81. PMID 2347356 DOI: 10.1007/BF01957697 |
0.099 |
|
| 2014 |
Forman MR, Zhu Y, Hernandez LM, Himes JH, Dong Y, Danish RK, James KE, Caulfield LE, Kerver JM, Arab L, Voss P, Hale DE, Kanafani N, Hirschfeld S. Arm span and ulnar length are reliable and accurate estimates of recumbent length and height in a multiethnic population of infants and children under 6 years of age. The Journal of Nutrition. 144: 1480-7. PMID 25031329 DOI: 10.3945/Jn.114.194340 |
0.098 |
|
| 2015 |
Farook VS, Reddivari L, Chittoor G, Puppala S, Arya R, Fowler SP, Hunt KJ, Curran JE, Comuzzie AG, Lehman DM, Jenkinson CP, Lynch JL, DeFronzo RA, Blangero J, Hale DE, et al. Metabolites as novel biomarkers for childhood obesity-related traits in Mexican-American children. Pediatric Obesity. 10: 320-7. PMID 25405847 DOI: 10.1111/Ijpo.270 |
0.098 |
|
| 2015 |
Cody JD, Sebold C, Heard P, Carter E, Soileau B, Hasi-Zogaj M, Hill A, Rupert D, Perry B, O'Donnell L, Gelfond J, Lancaster J, Fox PT, Hale DE. Consequences of chromsome18q deletions American Journal of Medical Genetics, Part C: Seminars in Medical Genetics. DOI: 10.1002/ajmg.c.31446 |
0.098 |
|
| 1992 |
Kelly DP, Hale DE, Rutledge SL, Ogden ML, Whelan AJ, Zhang Z, Strauss AW. Molecular basis of inherited medium-chain acyl-CoA dehydrogenase deficiency causing sudden child death. Journal of Inherited Metabolic Disease. 15: 171-80. PMID 1356169 DOI: 10.1007/Bf01799626 |
0.097 |
|
| 2003 |
Gunn SR, Mohammed M, Reveles XT, Viskochil DH, Palumbos JC, Johnson-Pais TL, Hale DE, Lancaster JL, Hardies LJ, Boespflug-Tanguy O, Cody JD, Leach RJ. Molecular characterization of a patient with central nervous system dysmyelination and cryptic unbalanced translocation between chromosomes 4q and 18q. American Journal of Medical Genetics. Part A. 120: 127-35. PMID 12794705 DOI: 10.1002/Ajmg.A.20026 |
0.096 |
|
| 1983 |
Stanley CA, Hale DE, Coates PM, Hall CL, Corkey BE, Yang W, Kelley RI, Gonzales EL, Williamson JR, Baker L. Medium-chain acyl-CoA dehydrogenase deficiency in children with non-ketotic hypoglycemia and low carnitine levels Pediatric Research. 17: 877-884. PMID 6646897 DOI: 10.1203/00006450-198311000-00008 |
0.095 |
|
| 2004 |
Hale DE, Kiess W. Insulins and oral hypoglycemic medications. Pediatric Endocrinology Reviews : Per. 2: 153-62. PMID 16456494 |
0.093 |
|
| 2009 |
Heard PL, Carter EM, Crandall AC, Sebold C, Hale DE, Cody JD. High resolution genomic analysis of 18q- using oligo-microarray comparative genomic hybridization (aCGH). American Journal of Medical Genetics. Part A. 149: 1431-7. PMID 19533772 DOI: 10.1002/ajmg.a.32900 |
0.092 |
|
| 1986 |
Treem WR, Witzleben CA, Piccoli DA, Stanley CA, Hale DE, Coates PM, Watkins JB. Medium-chain and long-chain acyl CoA dehydrogenase deficiency: clinical, pathologic and ultrastructural differentiation from Reye's syndrome. Hepatology (Baltimore, Md.). 6: 1270-8. PMID 3793003 DOI: 10.1002/hep.1840060608 |
0.092 |
|
| 1999 |
Cody JD, Reveles XT, Hale DE, Lehman D, Coon H, Leach RJ. Haplosufficiency of the melanocortin-4 receptor gene in individuals with deletions of 18q Human Genetics. 105: 424-427. PMID 10598807 DOI: 10.1007/S004390051125 |
0.092 |
|
| 1999 |
Hale DE, Gomez JE. Type 2 Diabetes Risk Factors in Mexican-American Youth Pediatric Research. 45: 90A-90A. DOI: 10.1203/00006450-199904020-00535 |
0.091 |
|
| 1995 |
Bhala A, Willi SM, Rinaldo P, Bennett MJ, Schmidt-Sommerfeld E, Hale DE. Clinical and biochemical characterization of short-chain acyl-coenzyme A dehydrogenase deficiency The Journal of Pediatrics. 126: 910-915. PMID 7776094 DOI: 10.1016/S0022-3476(95)70207-5 |
0.091 |
|
| 2017 |
Manning A, Highland HM, Gasser J, Sim X, Tukiainen T, Fontanillas P, Grarup N, Rivas MA, Mahajan A, Locke AE, Cingolani P, Pers TH, Viñuela A, Brown AA, Wu Y, ... ... Hale DE, et al. A Low-Frequency Inactivating Akt2 Variant Enriched in the Finnish Population is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk. Diabetes. PMID 28341696 DOI: 10.2337/Db16-1329 |
0.09 |
|
| 1994 |
Stanley CA, Hale DE. Genetic disorders of mitochondrial fatty acid oxidation Current Opinion in Pediatrics. 6: 476-481. PMID 7951672 DOI: 10.1097/00008480-199408000-00021 |
0.089 |
|
| 2011 |
White WA, Schatz MP, Sebold C, Hale DE, Cody J. Ophthalmic manifestations of tetrasomy 18p. Journal of Aapos : the Official Publication of the American Association For Pediatric Ophthalmology and Strabismus / American Association For Pediatric Ophthalmology and Strabismus. 15: 268-71. PMID 21665505 DOI: 10.1016/j.jaapos.2011.02.011 |
0.089 |
|
| 2020 |
Oser TK, Oser SM, Parascando JA, Grisolano LA, Krishna KB, Hale DE, Litchman M, Majidi S, Haidet P. Challenges and Successes in Raising a Child with Type 1 Diabetes and Autism Spectrum Disorder: Mixed Methods Study. Journal of Medical Internet Research. PMID 32217508 DOI: 10.2196/17184 |
0.089 |
|
| 2009 |
Cody JD, Heard PL, Crandall AC, Carter EM, Li J, Hardies LJ, Lancaster J, Perry B, Stratton RF, Sebold C, Schaub RL, Soileau B, Hill A, Hasi M, Fox PT, ... Hale DE, et al. Narrowing critical regions and determining penetrance for selected 18q- phenotypes. American Journal of Medical Genetics. Part A. 149: 1421-30. PMID 19533771 DOI: 10.1002/Ajmg.A.32899 |
0.088 |
|
| 2016 |
Fuchsberger C, Flannick J, Teslovich TM, Mahajan A, Agarwala V, Gaulton KJ, Ma C, Fontanillas P, Moutsianas L, McCarthy DJ, Rivas MA, Perry JR, Sim X, Blackwell TW, Robertson NR, ... ... Hale DE, et al. The genetic architecture of type 2 diabetes. Nature. PMID 27398621 DOI: 10.1038/Nature18642 |
0.087 |
|
| 2010 |
Newstead A, Walden G, Trevino R, Cody J, Hale D. 095 WALKING PILOT STUDY IN ADULTS WITH CHROMOSOME 18Q DELETIONS Parkinsonism & Related Disorders. 16: S28. DOI: 10.1016/S1353-8020(10)70096-1 |
0.086 |
|
| 2018 |
OSER T, OSER SM, BANGALORE KRISHNA K, HALE DE. Raising a Child with Type 1 Diabetes and Autism—Using Social Media to Identify Barriers and Facilitators Diabetes. 67: 872-P. DOI: 10.2337/DB18-872-P |
0.086 |
|
| 1995 |
Sims HF, Brackett JC, Powell CK, Treem WR, Hale DE, Bennett MJ, Gibson B, Shapiro S, Strauss AW. The molecular basis of pediatric long chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancy. Proceedings of the National Academy of Sciences of the United States of America. 92: 841-5. PMID 7846063 DOI: 10.1073/Pnas.92.3.841 |
0.084 |
|
| 2015 |
Newstead A, Walden J, Cody J, Hale D. Balance and locomotor characteristics in young adults with 18q deficiency Physiotherapy. 101: e1082. DOI: 10.1016/J.PHYSIO.2015.03.1971 |
0.084 |
|
| 2020 |
Lopez-Alvarenga JC, Chittoor G, Paul SFD, Puppala S, Farook VS, Fowler SP, Resendez RG, Hernandez-Ruiz J, Diaz-Badillo A, Salazar D, Garza DD, Lehman DM, Mummidi S, Arya R, Jenkinson CP, ... ... Hale DE, et al. Acanthosis nigricans as a composite marker of cardiometabolic risk and its complex association with obesity and insulin resistance in Mexican American children. Plos One. 15: e0240467. PMID 33057385 DOI: 10.1371/journal.pone.0240467 |
0.084 |
|
| 1985 |
Coates PM, Hale DE, Stanley CA, Corkey BE, Cortner JA. Genetic deficiency of medium-chain acyl coenzyme a dehydrogenase: Studies in cultured skin fibroblasts and peripheral mononuclear leukocytes Pediatric Research. 19: 671-676. PMID 4022673 DOI: 10.1203/00006450-198507000-00007 |
0.083 |
|
| 1998 |
Hale DE, Cody JD, Schaub RL, Kaye CI, Leach RJ. Thyrotropin (TSH) Response to Thyrotropin Releasing Hormone (TRH) in Children with 18q-Syndrome † 434 Pediatric Research. 43: 77-77. DOI: 10.1203/00006450-199804001-00455 |
0.081 |
|
| 1998 |
Hale DE, Cody JD, Schaub RL, Kaye CI, Leach RJ. Prolactin (PRL) Response to Thyrotropin Releasing Hormone (TRH) in Children with 18q- Syndrome † 432 Pediatric Research. 43: 76-76. DOI: 10.1203/00006450-199804001-00453 |
0.081 |
|
| 2021 |
Waxmonsky JG, Pelham WE, Baweja R, Hale D, Pelham WE. Predictors of Changes in Height, Weight, and Body Mass Index After Initiation of Central Nervous System Stimulants in Children with Attention Deficit Hyperactivity Disorder. The Journal of Pediatrics. PMID 34571023 DOI: 10.1016/j.jpeds.2021.09.030 |
0.08 |
|
| 1988 |
Rinaldo P, O'Shea JJ, Coates PM, Hale DE, Stanley CA, Tanaka K. Medium-chain acyl-CoA dehydrogenase deficiency. Diagnosis by stable-isotope dilution measurement of urinary n-hexanoylglycine and 3-phenylpropionylglycine New England Journal of Medicine. 319: 1308-1313. PMID 3054550 DOI: 10.1056/Nejm198811173192003 |
0.08 |
|
| 2010 |
Zavala J, Ramirez M, Medina R, Heard P, Carter E, Crandall A, Hale D, Cody J, Escamilla M. Psychiatric syndromes in individuals with chromosome 18 abnormalities. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 837-45. PMID 19927307 DOI: 10.1002/ajmg.b.31047 |
0.08 |
|
| 2019 |
MUMMIDI S, HERNANDEZ-RUIZ J, FAROOK VS, REDDIVARI L, DIAZ-BADILLO A, FOWLER SP, RESENDEZ RG, AKHTAR F, LEHMAN D, JENKINSON C, ARYA R, LYNCH JL, DEFRONZO RA, HALE DE, BLANGERO J, et al. 1337-P: Prediction of Insulin Sensitivity Using Serum Carotenoid Concentrations and Pediatric Metabolic Index in Mexican-American Children Diabetes. 68: 1337-P. DOI: 10.2337/Db19-1337-P |
0.079 |
|
| 1999 |
Cody JD, Ghidoni PD, Dupont BR, Hale DE, Hilsenbeck SG, Stratton RF, Hoffman DS, Muller S, Schaub RL, Leach RJ, Kaye CI. Congenital Anomalies and Anthropometry of 42 Individuals with Deletions of Chromosome 18q Pediatric Research. 45: 136-136. DOI: 10.1203/00006450-199904020-00811 |
0.079 |
|
| 1988 |
Corkey BE, Hale DE, Glennon MC, Kelley RI, Coates PM, Kilpatrick L, Stanley CA. Relationship between unusual hepatic acyl coenzyme A profiles and the pathogenesis of Reye syndrome Journal of Clinical Investigation. 82: 782-788. PMID 3417871 DOI: 10.1172/Jci113679 |
0.078 |
|
| 1993 |
Stanley CA, Berry GT, Bennett MJ, Willi SM, Treem WR, Hale DE. Renal handling of carnitine in secondary Carnitine deficiency disorders Pediatric Research. 34: 89-97. PMID 8356025 DOI: 10.1203/00006450-199307000-00021 |
0.078 |
|
| 1984 |
Hale DE, Williamson JR. THE ADENINE NUCLEOTIDE (AdN) TRANSLOCASE (T): A ROLE IN DEVELOPMENTAL CHANGES Pediatric Research. 18: 139-139. DOI: 10.1203/00006450-198404001-00275 |
0.078 |
|
| 1988 |
Schwenk WF, Hale DE, Haymond MW. Decreased fasting free fatty acids with L-carnitine in children with carnitine deficiency. Pediatric Research. 23: 491-4. PMID 3290828 DOI: 10.1203/00006450-198805000-00011 |
0.078 |
|
| 2008 |
Horbinski C, Carter EM, Heard PL, Sathanoori M, Hu J, Vockley J, Gunn S, Hale DE, Surti U, Cody JD. Molecular and clinical characterization of a recurrent cryptic unbalanced t(4q;18q) resulting in an 18q deletion and 4q duplication. American Journal of Medical Genetics. Part A. 146: 2898-904. PMID 18932219 DOI: 10.1002/Ajmg.A.32557 |
0.078 |
|
| 1988 |
Coates PM, Hale DE, Finocchiaro G, Tanaka K, Winter SC. Genetic deficiency of short-chain acyl-coenzyme A dehydrogenase in cultured fibroblasts from a patient with muscle carnitine deficiency and severe skeletal muscle weakness. The Journal of Clinical Investigation. 81: 171-5. PMID 3335634 DOI: 10.1172/JCI113290 |
0.078 |
|
| 1988 |
Treem WR, Stanley CA, Finegold DN, Hale DE, Coates PM. Primary carnitine deficiency due to a failure of carnitine transport in kidney, muscle, and fibroblasts New England Journal of Medicine. 319: 1331-1336. PMID 3185635 DOI: 10.1056/NEJM198811173192006 |
0.076 |
|
| 1997 |
Andresen BS, Bross P, Udvari S, Kirk J, Gray G, Kmoch S, Chamoles N, Knudsen I, Winter V, Wilcken B, Yokota I, Hart K, Packman S, Harpey JP, Saudubray JM, ... Hale DE, et al. The molecular basis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in compound heterozygous patients: is there correlation between genotype and phenotype? Human Molecular Genetics. 6: 695-707. PMID 9158144 DOI: 10.1093/HMG/6.5.695 |
0.076 |
|
| 1992 |
Coates PM, Indo Y, Young D, Hale DE, Tanaka K. Immunochemical characterization of variant medium-chain acyl-CoA dehydrogenase in fibroblasts from patients with medium-chain acyl-CoA dehydrogenase deficiency. Pediatric Research. 31: 34-8. PMID 1594327 DOI: 10.1203/00006450-199201000-00006 |
0.076 |
|
| 1995 |
Tamvakopoulos CS, Willi S, Anderson VE, Hale DE. Long-Chain Acyl-CoA Profiles in Cultured Fibroblasts from Patients with Defects in Fatty Acid Oxidation Biochemical and Molecular Medicine. 55: 15-21. PMID 7551821 DOI: 10.1006/bmme.1995.1026 |
0.076 |
|
| 2014 |
Perry BP, Sebold C, Hasi M, Heard P, Carter E, Hill A, Gelfond J, Hale DE, Cody JD. Sensorineural hearing loss in people with deletions of 18q: hearing in 18q-. Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology. 35: 782-6. PMID 24662633 DOI: 10.1097/Mao.0000000000000363 |
0.076 |
|
| 1991 |
Indo Y, Coates PM, Hale DE, Tanaka K. Immunochemical characterization of variant long-chain acyl-CoA dehydrogenase in cultured fibroblasts from nine patients with long-chain acyl-CoA dehydrogenase deficiency. Pediatric Research. 30: 211-5. PMID 1945557 DOI: 10.1203/00006450-199109000-00001 |
0.076 |
|
| 2018 |
Cody JD, Heard P, Rupert D, Hasi-Zogaj M, Hill A, Sebold C, Hale DE. Chromosome 18 gene dosage map 2.0. Human Genetics. PMID 30448861 DOI: 10.1007/s00439-018-1960-6 |
0.076 |
|
| 2009 |
Cody JD, Carter EM, Sebold C, Heard PL, Hale DE. A gene dosage map of Chromosome 18: a map with clinical utility. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 11: 778-82. PMID 19745747 DOI: 10.1097/GIM.0b013e3181b6573d |
0.074 |
|
| 2015 |
Backeljauw PF, Miller BS, Dutailly P, Houchard A, Lawson E, Hale DE, Reiner B, Sperling MA. Recombinant human growth hormone plus recombinant human insulin-like growth factor-1 coadministration therapy in short children with low insulin-like growth factor-1 and growth hormone sufficiency: results from a randomized, multicenter, open-label, parallel-group, active treatment-controlled trial. Hormone Research in PæDiatrics. 83: 268-79. PMID 25765099 DOI: 10.1159/000371799 |
0.074 |
|
| 1995 |
Strauss AW, Powell CK, Hale DE, Anderson MM, Ahuja A, Brackett JC, Sims HF. Molecular basis of human mitochondrial very-long-chain acyl-CoA dehydrogenase deficiency causing cardiomyopathy and sudden death in childhood. Proceedings of the National Academy of Sciences of the United States of America. 92: 10496-500. PMID 7479827 DOI: 10.1073/Pnas.92.23.10496 |
0.074 |
|
| 1998 |
Hale DE, Danney CM, Plotkin RA, Danney MM. Non-insulin Dependent Diabetes in Youth (Type 2Y). † 433 Pediatric Research. 43: 77-77. DOI: 10.1203/00006450-199804001-00454 |
0.072 |
|
| 1997 |
Hale DE, Cornell JE, Bennett MJ. Stability of long-chain and short-chain 3-hydroxyacyl-CoA dehydrogenase activity in postmortem liver Clinical Chemistry. 43: 273-278. DOI: 10.1093/CLINCHEM/43.2.273 |
0.07 |
|
| 1994 |
Treem WR, Rinaldo P, Hale DE, Stanley CA, Millington DS, Hyams JS, Jackson S, Turnbull DM. Acute fatty liver of pregnancy and long‐chain 3‐hydroxyacyl–coenzyme A dehydrogenase deficiency Hepatology. 19: 339-345. DOI: 10.1002/Hep.1840190211 |
0.069 |
|
| 1995 |
Tein I, Donner EJ, Hale DE, Murphy EG. Clinical and neurophysiologic response of myopathy and neuropathy in long-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency to oral prednisone. Pediatric Neurology. 12: 68-76. PMID 7748366 DOI: 10.1016/0887-8994(94)00109-F |
0.068 |
|
| 1993 |
Sewell AC, Herwig J, Böhles H, Rinaldo P, Bhala A, Hale DE. A new case of short-chain acyl-CoA dehydrogenase deficiency with isolated ethylmalonic aciduria. European Journal of Pediatrics. 152: 922-924. PMID 8276024 DOI: 10.1007/Bf01957531 |
0.068 |
|
| 1992 |
Bennett MJ, Bhala A, Poirier SF, Ragni MC, Willi SM, Hale DE. When Do Gut Flora in the Newborn Produce 3-Phenylpropionic Acid? Implications for Early Diagnosis of Medium-Chain Acyl-CoA Dehydrogenase Deficiency Clinical Chemistry. 38: 278-281. DOI: 10.1093/CLINCHEM/38.2.278 |
0.068 |
|
| 1984 |
Hale DE, Corkey BE, Stanley CA. EFFECTS OF VALPROIC ACID (DEPAKENE) ON KETOGENESIS (K), GLUCONEOGENESIS (G), AND UREAGENESIS (U) BY RAT HEPATOCYTES Pediatric Research. 18: 294A-294A. DOI: 10.1203/00006450-198404001-01207 |
0.067 |
|
| 2017 |
Jason F, Fuchsberger C, Mahajan A, Teslovich TM, Agarwala V, Gaulton KJ, Caulkins L, Koesterer R, Ma C, Moutsianas L, McCarthy DJ, Rivas MA, Perry JRB, Sim X, Blackwell TW, ... ... Hale DE, et al. Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. Scientific Data. 4: 170179. PMID 29257133 DOI: 10.1038/Sdata.2017.179 |
0.067 |
|
| 2019 |
Olson CA, Carstens GE, Herring AD, Hale DS, Kayser WC, Miller RK. Effects of temperament at feedlot arrival and breed type on growth efficiency, feeding behavior, and carcass value in finishing heifers. Journal of Animal Science. PMID 30689930 DOI: 10.1093/Jas/Skz029 |
0.066 |
|
| 2018 |
Harris MK, Eastwood LC, Boykin CA, Arnold AN, Gehring KB, Hale DS, Kerth CR, Griffin DB, Savell JW, Belk KE, Woerner DR, Hasty JD, Delmore RJ, Martin JN, Lawrence TE, et al. National Beef Quality Audit-2016: assessment of cattle hide characteristics, offal condemnations, and carcass traits to determine the quality status of the market cow and bull beef industry. Translational Animal Science. 2: 37-49. PMID 32704688 DOI: 10.1093/tas/txx002 |
0.065 |
|
| 2015 |
Arya R, Puppala S, Farook VS, Chittoor G, Jenkinson CP, Blangero J, Hale DE, Duggirala R, Almasy L. Mapping of susceptibility genes for obesity, type 2 diabetes, and the metabolic syndrome in human populations Genome Mapping and Genomics in Human and Non-Human Primates. 181-245. DOI: 10.1007/978-3-662-46306-2_12 |
0.065 |
|
| 1999 |
Cody J, Reveles X, Hale D, Lehman D, Coon H, Leach R. Haplosufficiency of the melanocortin-4 receptor gene in individuals with deletions of 18q Human Genetics. 105: 424-427. DOI: 10.1007/s004399900147 |
0.065 |
|
| 2015 |
O'Donnell L, Soileau BT, Sebold C, Gelfond J, Hale DE, Cody JD. Tetrasomy 18p: report of cognitive and behavioral characteristics. American Journal of Medical Genetics. Part A. 167: 1474-82. PMID 25900901 DOI: 10.1002/Ajmg.A.37036 |
0.065 |
|
| 2021 |
Bogale KT, Hale DE, Schaefer E, Bangalore Krishna K. Prevalence and factors associated with diabetic ketoacidosis at diagnosis of type 1 diabetes: A report from a tertiary medical center in Central Pennsylvania. Endocrinology, Diabetes & Metabolism. 4: e00186. PMID 33855199 DOI: 10.1002/edm2.186 |
0.064 |
|
| 2018 |
Flannick J, Fuchsberger C, Mahajan A, Teslovich TM, Agarwala V, Gaulton KJ, Caulkins L, Koesterer R, Ma C, Moutsianas L, McCarthy DJ, Rivas MA, Perry JRB, Sim X, Blackwell TW, ... ... Hale DE, et al. Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. Scientific Data. 5: 180002. PMID 29360107 DOI: 10.1038/sdata.2018.2 |
0.063 |
|
| 1992 |
Stanley CA, Sunaryo F, Hale DE, Bonnefont JP, Demaugre F, Saudubray JM. Elevated plasma carnitine in the hepatic form of carnitine palmitoyltransferase-1 deficiency. Journal of Inherited Metabolic Disease. 15: 785-9. PMID 1434517 DOI: 10.1007/BF01800021 |
0.062 |
|
| 1990 |
Bennett MJ, Coates PM, Hale DE, Millington DS, Pollitt RJ, Rinaldo P, Roe CR, Tanaka K. Analysis of abnormal urinary metabolites in the newborn period in medium-chain acyl-CoA dehydrogenase deficiency. Journal of Inherited Metabolic Disease. 13: 707-715. PMID 2246856 DOI: 10.1007/Bf01799572 |
0.06 |
|
| 1991 |
Tein I, De Vivo DC, Hale DE, Clarke JT, Zinman H, Laxer R, Shore A, DiMauro S. Short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency in muscle: a new cause for recurrent myoglobinuria and encephalopathy. Annals of Neurology. 30: 415-9. PMID 1835339 DOI: 10.1002/ANA.410300315 |
0.058 |
|
| 1996 |
Bennett MJ, Hale DE, Pollitt RJ, Stanley CA, Variend S. Endocardial fibroelastosis and primary carnitine deficiency due to a defect in the plasma membrane carnitine transporter Clinical Cardiology. 19: 243-246. PMID 8674264 DOI: 10.1002/CLC.4960190320 |
0.058 |
|
| 2017 |
Hale DA, Krause JR. Plasma cell myeloma with lymphoplasmacytic morphology and cyclin D1 expression, an uncommon variant. Proceedings (Baylor University. Medical Center). 30: 192-194. PMID 28405079 |
0.058 |
|
| 1986 |
Ikeda Y, Hale DE, Keese SM, Coates PM, Tanaka K. Biosynthesis of variant medium chain acyl-CoA dehydrogenase in cultured fibroblasts from patients with medium chain acyl-CoA dehydrogenase deficiency. Pediatric Research. 20: 843-7. PMID 3748657 DOI: 10.1203/00006450-198609000-00007 |
0.056 |
|
| 1999 |
Lehman DM, Hale DE, Cody JT, Harrison JM, Leach RJ. Molecular, morphometric and functional analyses demonstrate that the growth hormone deficient little mouse is not hypomyelinated. Brain Research. Developmental Brain Research. 116: 191-9. PMID 10521563 DOI: 10.1016/S0165-3806(99)00081-4 |
0.055 |
|
| 1984 |
Hale DE, Williamson JR. Developmental changes in the adenine nucleotide translocase in the guinea pig. Journal of Biological Chemistry. 259: 8737-8742. DOI: 10.1016/s0021-9258(17)47214-0 |
0.053 |
|
| 1996 |
Isaacs JD, Sims HF, Powell CK, Bennett MJ, Hale DE, Treem WR, Strauss AW. Maternal acute fatty liver of pregnancy associated with fetal trifunctional protein deficiency: molecular characterization of a novel maternal mutant allele. Pediatric Research. 40: 393-8. PMID 8865274 DOI: 10.1203/00006450-199609000-00005 |
0.053 |
|
| 1981 |
Hale DE, Stanley CA, Baker L. 248 DEVELOPMENTAL CHANGES IN FATTY ACID OXIDATION IN NEWBOEN GUINEA PIG HEART Pediatric Research. 15: 481-481. DOI: 10.1203/00006450-198104001-00258 |
0.046 |
|
| 1990 |
Lehman TC, Hale DE, Bhala A, Thorpe C. An acyl-coenzyme A dehydrogenase assay utilizing the ferricenium ion. Analytical Biochemistry. 186: 280-4. PMID 2363500 DOI: 10.1016/0003-2697(90)90080-S |
0.039 |
|
| 1986 |
Kelley RI, Coates PM, Hale DE, Stanley CA. Metabolic Disorder Possible Cause of Reye’s Syndrome American Journal of Diseases of Children. 140: 328-329. PMID 3953520 DOI: 10.1001/archpedi.1986.02140180062019 |
0.039 |
|
| 1984 |
Coates PM, Hale DE, Stanley CA, Glasgow AM. Systemic carnitine deficiency simulating Reye syndrome The Journal of Pediatrics. 105: 679. PMID 6481556 DOI: 10.1016/S0022-3476(84)80460-6 |
0.036 |
|
| 1991 |
Bennett MJ, Hale DE, Coates PM, Stanley CA. Postmortem recognition of fatty acid oxidation disorders Fetal and Pediatric Pathology. 11: 365-370. PMID 1866359 DOI: 10.3109/15513819109064772 |
0.035 |
|
| 1992 |
Stanley CA, Hale DE, Berry GT, Deleeuw S, Boxer J, Bonnefont JP. Brief report: A deficiency of carnitine-acylcarnitine translocase in the inner mitochondrial membrane New England Journal of Medicine. 327: 19-23. PMID 1598097 DOI: 10.1056/NEJM199207023270104 |
0.033 |
|
| 2004 |
Cody JD, Hale DE. Precision in phenotyping and genotyping American Journal of Medical Genetics. Part A. 131: 313. PMID 15540176 |
0.026 |
|
| 2020 |
Hale DA, Krause JR. Unexpected lymph node finding in a patient with essential thrombocythemia. Blood. 135: 154. PMID 31917841 DOI: 10.1182/blood.2019002036 |
0.017 |
|
| 1999 |
Burke JP, Hale DE, Hazuda HP, Stern MP. A quantitative scale of acanthosis nigricans. Diabetes Care. 22: 1655-9. PMID 10526730 DOI: 10.2337/DIACARE.22.10.1655 |
0.011 |
|
| Hide low-probability matches. |