| Current status of newborn screening worldwide: 2015 BL Therrell, CD Padilla, JG Loeber, I Kneisser, A Saadallah, GJC Borrajo, ... Seminars in perinatology 39 (3), 171-187, 2015 | 598 | 2015 |
| Results of screening 1.9 million Texas newborns for 21-hydroxylase-deficient congenital adrenal hyperplasia BL Therrell Jr, SA Berenbaum, V Manter-Kapanke, J Simmank, K Korman, ... Pediatrics 101 (4), 583-590, 1998 | 418 | 1998 |
| Consensus statement on 21-hydroxylase deficiency from the Lawson Wilkins pediatric Endocrine Society and the European Society for Paediatric Endocrinology Joint LwPes/esPe CAH working Group The Journal of Clinical Endocrinology & Metabolism 87 (9), 4048-4053, 2002 | 302 | 2002 |
| Newborn screening for congenital adrenal hyperplasia BL Therrell Endocrinology and Metabolism Clinics 30 (1), 15-30, 2001 | 273 | 2001 |
| Trends in incidence rates of congenital hypothyroidism related to select demographic factors: data from the United States, California, Massachusetts, New York, and Texas CF Hinton, KB Harris, L Borgfeld, M Drummond-Borg, R Eaton, F Lorey, ... Pediatrics 125 (Supplement_2), S37-S47, 2010 | 245 | 2010 |
| Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: newborn screening and its relationship to the diagnosis and treatment of the disorder S Pang, A Clark, EC Neto, R Giugliani, H Dean, J Winter, JL Dhondt, ... Screening 2 (2-3), 105-139, 1993 | 213 | 1993 |
| Newborn screening in the Asia Pacific region CD Padilla, BL Therrell Journal of Inherited Metabolic Disease: Official Journal of the Society for …, 2007 | 185 | 2007 |
| Newborn screening in North America BL Therrell, J Adams Journal of Inherited Metabolic Disease: Official Journal of the Society for …, 2007 | 182 | 2007 |
| History and current status of newborn screening for hemoglobinopathies JM Benson, BL Therrell Jr Seminars in perinatology 34 (2), 134-144, 2010 | 165 | 2010 |
| US newborn screening policy dilemmas for the twenty-first century BL Therrell Jr Molecular genetics and metabolism 74 (1-2), 64-74, 2001 | 164 | 2001 |
| Guidelines for the retention, storage, and use of residual dried blood spot samples after newborn screening analysis: statement of the Council of Regional Networks for Genetic … BL Therrell, WH Hannon, KA Pass, F Lorey, C Brokopp, J Eckman, ... Biochemical and Molecular Medicine 57 (2), 116-124, 1996 | 163 | 1996 |
| Status of newborn screening programs in the United States BL Therrell, A Johnson, D Williams Pediatrics 117 (Supplement_3), S212-S252, 2006 | 142 | 2006 |
| Inborn errors of metabolism identified via newborn screening: Ten-year incidence data and costs of nutritional interventions for research agenda planning BL Therrell Jr, MA Lloyd-Puryear, KM Camp, MY Mann Molecular genetics and metabolism 113 (1-2), 14-26, 2014 | 125 | 2014 |
| Newborn screening for sickle cell diseases in the United States: a review of data spanning 2 decades BL Therrell Jr, MA Lloyd-Puryear, JR Eckman, MY Mann Seminars in perinatology 39 (3), 238-251, 2015 | 124 | 2015 |
| Guidelines for the development of comprehensive care centers for congenital adrenal hyperplasia: guidance from the CARES Foundation initiative RJ Auchus, SF Witchel, KR Leight, J Aisenberg, R Azziz, TA Bachega, ... International journal of pediatric endocrinology 2010, 1-17, 2010 | 99 | 2010 |
| US newborn screening system guidelines: statement of the Council of Regional Networks for Genetic Services BL Therrell, SR Panny, A Davidson, J Eckman, WH Hannon, MA Henson, ... Screening 1 (2), 135-147, 1992 | 91 | 1992 |
| Impact of Expanded Newborn Screening--United States, 2006. B Therrell, F Lorey, R Eaton, D Frazier, G Hoffman, C Boyle, D Green, ... MMWR: Morbidity & Mortality Weekly Report 57 (37), 2008 | 79 | 2008 |
| Communication of positive newborn screening results for sickle cell disease and sickle cell trait: variation across states PL Kavanagh, CJ Wang, BL Therrell, PG Sprinz, H Bauchner American Journal of Medical Genetics Part C: Seminars in Medical Genetics …, 2008 | 79 | 2008 |
| Long-term follow-up after diagnosis resulting from newborn screening: statement of the US Secretary of Health and Human Services' Advisory Committee on Heritable Disorders and … AR Kemper, CA Boyle, J Aceves, D Dougherty, J Figge, JL Fisch, ... Genetics in Medicine 10 (4), 259-261, 2008 | 78 | 2008 |
| National evaluation of US newborn screening system components BL Therrell, WH Hannon Mental retardation and developmental disabilities research reviews 12 (4 …, 2006 | 75 | 2006 |
