R. Olney

发表

Trends in pediatric sickle cell disease-related mortality in the United States, 1983-2002.

S. Grosse, Quanhe Yang, Emad Yanni, 2009, The Journal of pediatrics.

The cost effectiveness of universal versus selective newborn screening for sickle cell disease in the US and the UK

S. Grosse, R. Olney, M. A. Baily, 2005, Applied health economics and health policy.

Preventing morbidity and mortality from sickle cell disease. A public health perspective.

R. Olney, 1999, American journal of preventive medicine.

Maternal caffeine consumption and risk of neural tube defects.

T. Burns, R. Schmidt, M. Browne, 2009, Birth defects research. Part A, Clinical and molecular teratology.

Maternal caffeine consumption and risk of congenital limb deficiencies.

T. Burns, R. Moslehi, R. Schmidt, 2012, Birth defects research. Part A, Clinical and molecular teratology.

Detection of critical congenital heart defects: Review of contributions from prenatal and newborn screening.

E. Ailes, R. Olney, M. Sontag, 2015, Seminars in perinatology.

State Legislation, Regulations, and Hospital Guidelines for Newborn Screening for Critical Congenital Heart Defects — United States, 2011–2014

James E. Kucik, R. Olney, C. Hinton, 2015, MMWR. Morbidity and mortality weekly report.

Next steps for birth defects research and prevention: The birth defects study to evaluate pregnancy exposures (BD-STEPS).

W. Nembhard, J. Reefhuis, R. Meyer, 2015, Birth defects research. Part A, Clinical and molecular teratology.

US Newborns Cost-Effectiveness of Routine Screening for Critical Congenital Heart Disease in

S. Grosse, Cora Peterson, M. Oster, 2014 .

A Public Health Economic Assessment of Hospitals' Cost to Screen Newborns for Critical Congenital Heart Disease

S. Grosse, Cora Peterson, K. V. N. Braun, 2014, Public health reports.

Results From the New Jersey Statewide Critical Congenital Heart Defects Screening Program

A. Kemper, K. Van Naarden Braun, R. Olney, 2013, Pediatrics.

Hospitalizations, costs, and mortality among infants with critical congenital heart disease: how important is timely detection?

R. Kirby, J. Tanner, S. Grosse, 2013, Birth defects research. Part A, Clinical and molecular teratology.

Rapid Implementation of Pulse Oximetry Newborn Screening to Detect Critical Congenital Heart Defects — New Jersey, 2011

Cora Peterson, K. Van Naarden Braun, R. Olney, 2013, MMWR. Morbidity and mortality weekly report.

Newborn screening for critical congenital heart disease: essential public health roles for birth defects monitoring programs.

L. Botto, R. Olney, 2012, Birth defects research. Part A, Clinical and molecular teratology.

Selected birth defects data from population-based birth defects surveillance programs in the United States, 2005–2009: Featuring critical congenital heart defects targeted for pulse oximetry screening.

Janet D Cragan, Lorenzo D Botto, Angela Lin, 2012, Birth defects research. Part A, Clinical and molecular teratology.

Trends and racial disparities in muscular dystrophy deaths in the United States, 1983–1998: An analysis of multiple cause mortality data

S. Rasmussen, A. Kenneson, J. Friedman, 2006, American journal of medical genetics. Part A.

Epidemiology of gastroschisis in metropolitan Atlanta, 1968 through 2000.

A. Correa, James E. Kucik, C. J. Alverson, 2005, Birth defects research. Part A, Clinical and molecular teratology.

Birth Defects and Genetic Disorders Among Arab Americans—Michigan, 1992–2003

G. Copeland, Emad Yanni, R. Olney, 2010, Journal of Immigrant and Minority Health.

Birth defects data from population-based birth defects surveillance programs in the United States, 2007 to 2011: highlighting orofacial clefts.

R. Kirby, Cara T Mai, M. Canfield, 2014, Birth defects research. Part A, Clinical and molecular teratology.

Self-reported maternal cigarette smoke exposure during the periconceptional period and the risk for omphalocoele.

L. Botto, P. Romitti, M. Feldkamp, 2014, Paediatric and perinatal epidemiology.

Descriptive and risk factor analysis for choanal atresia: The National Birth Defects Prevention Study, 1997-2007.

A. Siega-Riz, J. Carey, T. Burns, 2014, European journal of medical genetics.

Differences in risk factors for second and third degree hypospadias in the national birth defects prevention study.

I. V. van Rooij, N. Roeleveld, M. M. van Gelder, 2014, Birth defects research. Part A, Clinical and molecular teratology.

Periconceptional maternal alcohol consumption and neural tube defects.

Jennifer A. Makelarski, A. Olshan, A. Siega-Riz, 2013, Birth defects research. Part A, Clinical and molecular teratology.

Hypospadias and maternal intake of phytoestrogens.

G. Shaw, M. Cogswell, A. Correa, 2013, American journal of epidemiology.

Maternal medication and herbal use and risk for hypospadias: data from the National Birth Defects Prevention Study, 1997–2007

M. Werler, J. Reefhuis, M. Honein, 2013, Pharmacoepidemiology and drug safety.

Maternal periconceptional exposure to cigarette smoking and congenital limb deficiencies.

M. Werler, L. Holmes, P. Romitti, 2013, Paediatric and perinatal epidemiology.

Contribution Hypospadias and Maternal Intake of Phytoestrogens

G. Shaw, M. Cogswell, A. Correa, 2013 .

Nutritional factors and hypospadias risks.

G. Shaw, R. Munger, A. Correa, 2012, Paediatric and perinatal epidemiology.

Spina bifida subtypes and sub‐phenotypes by maternal race/ethnicity in the National Birth Defects Prevention Study

G. Shaw, C. Moore, L. E. Mitchell, 2012, American journal of medical genetics. Part A.

Maternal Asthma Medication Use and the Risk of Selected Birth Defects

Shao Lin, M. Browne, P. Romitti, 2012, Pediatrics.

Maternal occupational pesticide exposure and risk of hypospadias in the National Birth Defects Prevention Study.

Carissa M Rocheleau, W. Sanderson, P. Stewart, 2011, Birth defects research. Part A, Clinical and molecular teratology.

Maternal self-reported genital tract infections during pregnancy and the risk of selected birth defects.

A. Mitchell, Tonia C Carter, P. Romitti, 2011, Birth defects research. Part A, Clinical and molecular teratology.

Antihypertensive Medication Use During Pregnancy and the Risk of Cardiovascular Malformations

M. Werler, A. Mitchell, A. Lin, 2009, Hypertension.

Anencephaly and spina bifida among Hispanics: maternal, sociodemographic, and acculturation factors in the National Birth Defects Prevention Study.

G. Shaw, M. Canfield, S. Carmichael, 2009, Birth defects research. Part A, Clinical and molecular teratology.

Maternal corticosteroid use and hypospadias.

G. Shaw, M. Werler, S. Carmichael, 2009, The Journal of pediatrics.

Hypospadias and intake of nutrients related to one-carbon metabolism.

G. Shaw, A. Correa, S. Carmichael, 2009, The Journal of urology.

Maternal nutrient intake and risks for transverse and longitudinal limb deficiencies: data from the National Birth Defects Prevention Study, 1997-2003.

G. Shaw, J. Robitaille, S. Carmichael, 2009, Birth defects research. Part A, Clinical and molecular teratology.

Maternal asthma medication use and the risk of gastroschisis.

Shao Lin, P. Romitti, J. P. Munsie, 2008, American journal of epidemiology.

Maternal reports of family history from the National Birth Defects Prevention Study, 1997–2001

R. Green, J. Reefhuis, L. Botto, 2008, Genetics in Medicine.

Maternal reproductive and demographic characteristics as risk factors for hypospadias.

G. Shaw, S. Carmichael, E. Lammer, 2007, Paediatric and perinatal epidemiology.

Hypospadias and maternal exposures to cigarette smoke.

G. Shaw, S. Carmichael, E. Lammer, 2005, Paediatric and perinatal epidemiology.

The return of thalidomide: are birth defects surveillance systems ready?

M. Khoury, L. Paulozzi, J. Erickson, 1997, American journal of medical genetics.

Epidemiology of biliary atresia: a population-based study.

M. Khoury, J. Bresee, P. Yoon, 1997, Pediatrics.

Frequency of prenatal cytogenetic diagnosis and pregnancy outcomes by maternal race–ethnicity, and the effect on the prevalence of trisomy 21, Metropolitan Atlanta, 1996–2005

S. Rasmussen, Krista S Crider, J. Cragan, 2014, American journal of medical genetics. Part A.

Development and implementation of the first national data quality standards for population-based birth defects surveillance programs in the United States

G. Copeland, R. Kirby, Cara T Mai, 2015, BMC Public Health.

Association between maternal periconceptional alcohol consumption and neural tube defects: Findings from the National Birth Defects Prevention Study, 1997-2011.

Jennifer A. Makelarski, A. Olshan, Adrienne T Hoyt, 2020, Birth defects research.

CDC Grand Rounds: Newborn screening and improved outcomes.

T. Popović, S. Terry, R. Howell, 2012, MMWR. Morbidity and mortality weekly report.

Chorionic villus sampling and transverse digital deficiencies: evidence for anatomic and gestational-age specificity of the digital deficiencies in two studies.

G. Shaw, M. Khoury, L. Edmonds, 1996, American journal of medical genetics.

Increased risk for transverse digital deficiency after chorionic villus sampling: results of the United States Multistate Case-Control Study, 1988-1992.

G. Shaw, M. Khoury, L. Edmonds, 1995, Teratology.

Health status and healthcare use in a national sample of children with sickle cell disease.

S. Boulet, M. Creary, Emad Yanni, 2010, American journal of preventive medicine.

Factors associated with high hospital resource use in a population-based study of children with orofacial clefts.

A. Allori, R. Kirby, S. Grosse, 2014, Birth defects research. Part A, Clinical and molecular teratology.

Trends in neural tube defect prevalence, folic acid fortification, and vitamin supplement use.

J. Mulinare, R. Olney, 2002, Seminars in perinatology.

Long-term speech and language developmental issues among children with Duarte galactosemia

Rani H. Singh, M. Yeargin-Allsopp, K. V. N. Braun, 2009, Genetics in Medicine.

Prevalence of developmental disabilities and receipt of special education services among children with an inborn error of metabolism.

Rani H. Singh, M. Yeargin-Allsopp, K. Van Naarden Braun, 2010, The Journal of pediatrics.

Does Periconceptional Multivitamin Use Reduce the Risk for Limb Deficiency in Offspring?

Quanhe Yang, J. Mulinare, R. Olney, 1997, Epidemiology.

The association between race/ethnicity and major birth defects in the United States, 1999-2007.

Rachel E. Rutkowski, G. Copeland, R. Kirby, 2014, American journal of public health.

TheAssociationBetweenRace/EthnicityandMajorBirth DefectsintheUnitedStates,1999-2007

Rachel E. Rutkowski, G. Copeland, R. Kirby, 2014 .

Impact of Hurricane Katrina on Newborn Screening in Louisiana

L. Lambert, M. Lobato, Emad Yanni, 2007, Pediatrics.

Trends in cytogenetic testing and identification of chromosomal abnormalities among pregnancies and children with birth defects, metropolitan Atlanta, 1968–2005

S. Rasmussen, Krista S Crider, J. Cragan, 2012, American journal of medical genetics. Part A.

Vital Signs: Update on Zika Virus–Associated Birth Defects and Evaluation of All U.S. Infants with Congenital Zika Virus Exposure — U.S. Zika Pregnancy Registry, 2016

Marie Bottomley Hartel, Angela M. Miller, Morgan F. McDonald, 2017, MMWR. Morbidity and mortality weekly report.

Differences in risk factors for 2nd and 3rd degree hypospadias in the National Birth Defects Prevention Study

N. Roeleveld, J. Reefhuis, S. Carmichael, 2015 .

Hospitalizations and associated costs in a population-based study of children with Down syndrome born in Florida.

R. Kirby, J. Tanner, S. Grosse, 2014, Birth defects research. Part A, Clinical and molecular teratology.

Newborn screening for sickle cell disease: public health impact and evaluation

R. Olney, 2000 .

Storage and use of residual dried blood spots from state newborn screening programs.

M. Lindegren, C. Moore, W. H. Hannon, 2006, The Journal of pediatrics.

Prevalence of Congenital Hypothyroidism—Current Trends and Future Directions: Workshop Summary

S. Grosse, R. Vogt, R. Olney, 2010, Pediatrics.

Adrenoleukodystrophy Newborn Screening in California Since 2016: Programmatic Outcomes and Follow-Up

S. Sciortino, R. Olney, Hao Tang, 2021, International journal of neonatal screening.

Sickle hemoglobin (HbS) allele and sickle cell disease: a HuGE review.

A. Ashley-Koch, Quanhe Yang, R. Olney, 2000, American journal of epidemiology.

California's experience with SMA newborn screening: A successful path to early intervention.

S. Sciortino, R. Olney, D. Mathur, 2022, Journal of neuromuscular diseases.

Population-Based Surveillance for Birth Defects Potentially Related to Zika Virus Infection - 22 States and Territories, January 2016-June 2017.

C. Moore, Nina E Forestieri, S. Gilboa, 2020, MMWR. Morbidity and mortality weekly report.

Survival of infants diagnosed with encephalocele in Atlanta, 1979-98.

A. Correa, L. Wong, C. Siffel, 2003, Paediatric and perinatal epidemiology.

Guidelines for case classification for the National Birth Defects Prevention Study.

S. Rasmussen, L. Holmes, C. Moore, 2003, Birth defects research. Part A, Clinical and molecular teratology.

Maternal progestin intake and risk of hypospadias.

G. Shaw, M. Croughan, S. Carmichael, 2005, Archives of pediatrics & adolescent medicine.

Exclusion of progressive brain disorders of childhood for a cerebral palsy monitoring system: a public health perspective.

N. Doernberg, R. Olney, Nancy S. Doernberg, 2014, Journal of registry management.

Use of selective serotonin-reuptake inhibitors in pregnancy and the risk of birth defects.

Jennita Reefhuis, S. Rasmussen, J. Reefhuis, 2007, The New England journal of medicine.

Goldenhar syndrome among infants born in military hospitals to Gulf War veterans.

L D Edmonds, L. Edmonds, C. Moore, 1997, Teratology.

Bladder exstrophy: An epidemiologic study from the International Clearinghouse for Birth Defects Surveillance and Research, and an overview of the literature

S. Bianca, A. Pierini, G. Scarano, 2011, American journal of medical genetics. Part C, Seminars in medical genetics.

The First Year Experience of Newborn Screening for Pompe Disease in California

S. Sciortino, R. Olney, D. Mathur, 2020, International journal of neonatal screening.

Characterization of β-globin haplotypes using blood spots from a population-based cohort of newborns with homozygous HbS

C. Nash, M. Caggana, R. Olney, 2002, Genetics in Medicine.

Limb/pelvis hypoplasia/aplasia with skull defect (Schinzel phocomelia): distinctive features and prenatal detection.

H. Hoyme, A. Madan, R. Olney, 2001, American journal of medical genetics.

Contribution of birth defects and genetic diseases to pediatric hospitalizations. A population-based study.

M J Khoury, M. Khoury, P. Yoon, 1997, Archives of pediatrics & adolescent medicine.

Role of Family Medical History Information in Pediatric Primary Care and Public Health: Introduction

P. Yoon, Paula W Yoon, R. Olney, 2007, Pediatrics.

A case-control study of maternal alcohol consumption and intrauterine growth retardation.

M. Khoury, A. Correa, J. Erickson, 2001, Annals of epidemiology.

Vitamin supplements and the risk for congenital anomalies other than neural tube defects

J. Erickson, L. Botto, R. Olney, 2004, American journal of medical genetics. Part C, Seminars in medical genetics.

Association of paternal age and risk for major congenital anomalies from the National Birth Defects Prevention Study, 1997 to 2004.

A. Olshan, O. Devine, Krista S Crider, 2010, Annals of epidemiology.

Trisomies 13 and 18: Population prevalences, characteristics, and prenatal diagnosis, metropolitan Atlanta, 1994–2003

Krista S Crider, J. Cragan, R. Olney, 2008, American journal of medical genetics. Part A.

Multistate study of the epidemiology of clubfoot.

M. Strickland, S. E. Parker, Cara T Mai, 2009, Birth defects research. Part A, Clinical and molecular teratology.

Population-based surveillance for rare congenital and inherited disorders: models and challenges.

Krista S Crider, R. Olney, J. M. Jackson, 2010, Advances in experimental medicine and biology.

Renal defects and limb deficiencies in 197 infants: Is it possible to define the “acrorenal syndrome”?

C. Stoll, A. Rosano, P. Mastroiacovo, 2004, American journal of medical genetics. Part A.

Cystic fibrosis deaths in the United States from 1979 through 1991. An analysis using multiple-cause mortality data.

D. Mannino, R. Olney, C. Halliburton, 1996, Archives of pediatrics & adolescent medicine.

Maternal periconceptional alcohol consumption and congenital limb deficiencies.

L. Holmes, P. Romitti, R. Olney, 2014, Birth defects research. Part A, Clinical and molecular teratology.

Late detection of critical congenital heart disease among US infants: estimation of the potential impact of proposed universal screening using pulse oximetry.

G. Shaw, S. Gilboa, D. Fixler, 2014, JAMA pediatrics.

Cost-Effectiveness of Routine Screening for Critical Congenital Heart Disease in US Newborns

S. Grosse, Cora Peterson, M. Oster, 2013, Pediatrics.

Factors Associated With Late Detection of Critical Congenital Heart Disease in Newborns

R. Kirby, J. Tanner, S. Grosse, 2013, Pediatrics.

Limb defects associated with major congenital anomalies: clinical and epidemiological study from the International Clearinghouse for Birth Defects Monitoring Systems.

M. Khoury, C. Stoll, G. Zampino, 2000, American journal of medical genetics.

THE SEVENTEENTH DATA RELEASE OF THE SLOAN DIGITAL SKY SURVEYS: COMPLETE RELEASE OF MANGA, MASTAR AND APOGEE-2 DATA

Pablo Vera Alfaro, D. A. García-Hernández, J. A. Vázquez-Mata, 2022 .

On the symmetry of limb deficiencies among children with multiple congenital anomalies.

M. Khoury, E. Bermejo, C. Stoll, 2001, Annales de genetique.

EPIDEMIOLOGIC STUDY OF INFANTS WITH BILIARY ATRESIA. AUTHORS' REPLY

M. Khoury, M. Davenport, J. Bresee, 1998 .

Maternal hypertension, antihypertensive medication use, and the risk of severe hypospadias.

M. Werler, A. Mitchell, A. Correa, 2008, Birth defects research. Part A, Clinical and molecular teratology.

Maternal report of fever from cold or flu during early pregnancy and the risk for noncardiac birth defects, National Birth Defects Prevention Study, 1997-2011.

R. Finnell, J. Hecht, M. Canfield, 2018, Birth defects research.

Caffeine, selected metabolic gene variants, and risk for neural tube defects.

J. Murray, T. Burns, R. Schmidt, 2010, Birth defects research. Part A, Clinical and molecular teratology.

Harlequin Ichthyosis among the Navajo: Counseling issues

R. Olney, P. Olney, 1993, Journal of Genetic Counseling.

Developing a public health-tracking system for follow-up of newborn screening metabolic conditions: a four-state pilot project structure and initial findings

Cara T Mai, Ying Wang, L. Botto, 2013, Genetics in Medicine.

Use of Family History Information for Neural Tube Defect Prevention

R. Green, R. Olney, J. Ehrhardt, 2011 .

Maternal periconceptional occupational pesticide exposure and neural tube defects.

Jennifer A. Makelarski, Carissa M Rocheleau, G. Shaw, 2014, Birth defects research. Part A, Clinical and molecular teratology.

A. Correa, J. Khoury, Quanhe Yang, 2001 .

Maternal Caffeine Intake, Selected Metabolic Gene Variants, and Neural Tube Defects (NTDs)

T. Burns, R. Schmidt, M. Browne, 2007 .

Prenatal diagnosis of Noonan's syndrome in a female infant with spontaneous resolution of cystic hygroma and hydrops.

G. Sarto, C. Clericuzio, R. Olney, 1990, The Western journal of medicine.

First Three Years' Experience of Mucopolysaccharidosis Type I Newborn Screening in California.

S. Sciortino, R. Olney, D. Mathur, 2023, The Journal of pediatrics.

Maternal periconceptional occupational exposure to pesticides and selected musculoskeletal birth defects.

Carissa M Rocheleau, C. Kielb, Shao Lin, 2014, International journal of hygiene and environmental health.

Bladder Exstrophy: An Epidemiologic Study From the International Clearinghouse for Birth Defects Surveillance and Research, and an Overview of the Literature

S. Bianca, A. Pierini, G. Scarano, 2011 .

Trends in pediatric sickle cell disease-related mortality in the United States, 1983-2002.

S. Grosse, Quanhe Yang, Emad Yanni, 2009, The Journal of pediatrics.

Maternal periconceptional occupational pesticide exposure and neural tube defects.

Jennifer A. Makelarski, Carissa M Rocheleau, G. Shaw, 2014, Birth defects research. Part A, Clinical and molecular teratology.

Late detection of critical congenital heart disease among US infants: estimation of the potential impact of proposed universal screening using pulse oximetry.

G. Shaw, S. Gilboa, D. Fixler, 2014, JAMA pediatrics.

Hypospadias and maternal intake of phytoestrogens.

G. Shaw, M. Cogswell, A. Correa, 2013, American journal of epidemiology.

Spina bifida subtypes and sub‐phenotypes by maternal race/ethnicity in the National Birth Defects Prevention Study

G. Shaw, L. E. Mitchell, M. Canfield, 2012, American Journal of Medical Genetics. Part A.

Hypospadias and intake of nutrients related to one-carbon metabolism.

G. Shaw, A. Correa, S. Carmichael, 2009, The Journal of urology.

Rapid Implementation of Pulse Oximetry Newborn Screening to Detect Critical Congenital Heart Defects — New Jersey, 2011

Cora Peterson, K. Van Naarden Braun, R. Olney, 2013, MMWR. Morbidity and mortality weekly report.

The Seventeenth Data Release of the Sloan Digital Sky Surveys: The Seventeenth Data Release of the Sloan Digital Sky Surveys: Complete Release of MaNGA, MaStar, and APOGEE-2 Data Complete Release of MaNGA, MaStar, and APOGEE-2 Data

Pablo Vera Alfaro, D. A. García-Hernández, J. A. Vázquez-Mata, 2022 .

State Legislation, Regulations, and Hospital Guidelines for Newborn Screening for Critical Congenital Heart Defects — United States, 2011–2014

R. Olney, Jeff Hudson, Rachel Daskalov, 2015, MMWR. Morbidity and mortality weekly report.

378-S: Maternal use of Selective Serotonin Re-Uptake Inhibitors and Risk for Birth Defects

S. Rasmussen, J. Reefhuis, J. Friedman, 2005 .

Trisomies 13 and 18: Population prevalences, characteristics, and prenatal diagnosis, metropolitan Atlanta, 1994–2003

J. Cragan, R. Olney, Krista S. Crider, 2008, American journal of medical genetics. Part A.

Developing a public health-tracking system for follow-up of newborn screening metabolic conditions: a four-state pilot project structure and initial findings

Cara T Mai, Ying Wang, L. Botto, 2013, Genetics in Medicine.

(Mis)classifying limb deficiencies: Reply to "Academicians are more likely to share each other's toothbrush than each other's nomenclature (Cohen, 1982)".

P. Mastroiacovo, L. Botto, R. Olney, 1998, American journal of medical genetics.