CDC-Authored Genomics and Precision Health Publications Database
Last data update: Sep 16, 2024. (Total: 6309 publications)
| Query Trace: Jenkins MM[original query] |
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| Exome sequencing identifies novel genes underlying primary congenital glaucoma in the National Birth Defects Prevention Study
Blue EE , Moore KJ , North KE , Desrosiers TA , Carmichael SL , White JJ , Chong JX , Bamshad MJ , Jenkins MM , Almli LM , Brody LC , Freedman SF , Reefhuis J , Romitti PA , Shaw GM , Werler M , Kay DM , Browne ML , Feldkamp ML , Finnell RH , Nembhard WN , Pangilinan F , Olshan AF . Birth Defects Res 2024 116 (7) e2384 |
| Real world data are not always big data: The case for primary data collection on medication use in pregnancy in the context of birth defects research
Ailes EC , Werler MM , Howley MM , Jenkins MM , Reefhuis J . Am J Epidemiol 2024 |
| Rare variants in CAPN2 increase risk for isolated hypoplastic left heart syndrome
Blue EE , White JJ , Dush MK , Gordon WW , Wyatt BH , White P , Marvin CT , Helle E , Ojala T , Priest JR , Jenkins MM , Almli LM , Reefhuis J , Pangilinan F , Brody LC , McBride KL , Garg V , Shaw GM , Romitti PA , Nembhard WN , Browne ML , Werler MM , Kay DM , Mital S , Chong JX , Nascone-Yoder NM , Bamshad MJ . HGG Adv 2023 4 (4) 100232 |
| Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child-parent trios and a case-control design to identify novel rare variants.
Sok P , Sabo A , Almli LM , Jenkins MM , Nembhard WN , Agopian AJ , Bamshad MJ , Blue EE , Brody LC , Brown AL , Browne ML , Canfield MA , Carmichael SL , Chong JX , Dugan-Perez S , Feldkamp ML , Finnell RH , Gibbs RA , Kay DM , Lei Y , Meng Q , Moore CA , Mullikin JC , Muzny D , Olshan AF , Pangilinan F , Reefhuis J , Romitti PA , Schraw JM , Shaw GM , Werler MM , Harpavat S , Lupo PJ . Am J Med Genet A 2023 191 (6) 1546-1556 |
| Exome sequencing identifies genetic variants in anophthalmia and microphthalmia.
Li J , Yang W , Wang YJ , Ma C , Curry CJ , McGoldrick D , Nickerson DA , Chong JX , Blue EE , Mullikin JC , Reefhuis J , Nembhard WN , Romitti PA , Werler MM , Browne ML , Olshan AF , Finnell RH , Feldkamp ML , Pangilinan F , Almli LM , Bamshad MJ , Brody LC , Jenkins MM , Shaw GM . Am J Med Genet A 2022 188 (8) 2376-2388 |
| A genome-wide association study of obstructive heart defects among participants in the National Birth Defects Prevention Study.
Rashkin SR , Cleves M , Shaw GM , Nembhard WN , Nestoridi E , Jenkins MM , Romitti PA , Lou XY , Browne ML , Mitchell LE , Olshan AF , Lomangino K , Bhattacharyya S , Witte JS , Hobbs CA . Am J Med Genet A 2022 188 (8) 2303-2314 |
| Exome sequencing identifies variants in infants with sacral agenesis.
Pitsava G , Feldkamp ML , Pankratz N , Lane J , Kay DM , Conway KM , Hobbs C , Shaw GM , Reefhuis J , Jenkins MM , Almli LM , Moore C , Werler M , Browne ML , Cunniff C , Olshan AF , Pangilinan F , Brody LC , Sicko RJ , Finnell RH , Bamshad MJ , McGoldrick D , Nickerson DA , Mullikin JC , Romitti PA , Mills JL . Birth Defects Res 2022 114 (7) 215-227 |
| Exome sequencing of child-parent trios with bladder exstrophy: Findings in 26 children.
Pitsava G , Feldkamp ML , Pankratz N , Lane J , Kay DM , Conway KM , Shaw GM , Reefhuis J , Jenkins MM , Almli LM , Olshan AF , Pangilinan F , Brody LC , Sicko RJ , Hobbs CA , Bamshad M , McGoldrick D , Nickerson DA , Finnell RH , Mullikin J , Romitti PA , Mills JL . Am J Med Genet A 2021 185 (10) 3028-3041 |
| Paternal genetic variants and risk of obstructive heart defects: A parent-of-origin approach.
Patel J , Bircan E , Tang X , Orloff M , Hobbs CA , Browne ML , Botto LD , Finnell RH , Jenkins MM , Olshan A , Romitti PA , Shaw GM , Werler MM , Li J , Nembhard WN . PLoS Genet 2021 17 (3) e1009413 |
| A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosis.
Justice CM , Cuellar A , Bala K , Sabourin JA , Cunningham ML , Crawford K , Phipps JM , Zhou Y , Cilliers D , Byren JC , Johnson D , Wall SA , Morton JEV , Noons P , Sweeney E , Weber A , Rees KEM , Wilson LC , Simeonov E , Kaneva R , Yaneva N , Georgiev K , Bussarsky A , Senders C , Zwienenberg M , Boggan J , Roscioli T , Tamburrini G , Barba M , Conway K , Sheffield VC , Brody L , Mills JL , Kay D , Sicko RJ , Langlois PH , Tittle RK , Botto LD , Jenkins MM , LaSalle JM , Lattanzi W , Wilkie AOM , Wilson AF , Romitti PA , Boyadjiev SA . Hum Genet 2020 139 (8) 1077-1090 |
| Genome-wide association studies of structural birth defects: A review and commentary.
Lupo PJ , Mitchell LE , Jenkins MM . Birth Defects Res 2019 111 (18) 1329-1342 |
| Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data.
Jenkins MM , Almli LM , Pangilinan F , Chong JX , Blue EE , Shapira SK , White J , McGoldrick D , Smith JD , Mullikin JC , Bean CJ , Nembhard WN , Lou XY , Shaw GM , Romitti PA , Keppler-Noreuil K , Yazdy MM , Kay DM , Carter TC , Olshan AF , Moore KJ , Nascone-Yoder N , Finnell RH , Lupo PJ , Feldkamp ML , Nickerson DA , Bamshad MJ , Brody LC , Reefhuis J . Birth Defects Res 2019 111 (20) 1618-1632 |
| Impact of sample collection participation on the validity of estimated measures of association in the National Birth Defects Prevention Study when assessing gene-environment interactions.
Jenkins MM , Reefhuis J , Herring AH , Honein MA . Genet Epidemiol 2017 41 (8) 834-843 |
| A Population-Based Study of Effects of Genetic Loci on Orofacial Clefts.
Moreno Uribe LM , Fomina T , Munger RG , Romitti PA , Jenkins MM , Gjessing HK , Gjerdevik M , Christensen K , Wilcox AJ , Murray JC , Lie RT , Wehby GL . J Dent Res 2017 96 (11) 22034517716914 |
| Challenges in Studying Modifiable Risk Factors for Birth Defects.
Tinker SC , Gilboa S , Reefhuis J , Jenkins MM , Schaeffer M , Moore CA . Curr Epidemiol Rep 2015 2 (1) 23-30 |
| Maternal smoking, xenobiotic metabolizing enzyme gene variants, and gastroschisis risk.
Jenkins MM , Reefhuis J , Gallagher ML , Mulle JG , Hoffmann TJ , Koontz DA , Sturchio C , Rasmussen SA , Witte JS , Richter P , Honein MA . Am J Med Genet A 2014 164A (6) 1454-63 |
| Qualitative assessment of study materials and communication strategies used in studies that include DNA collection.
Jenkins MM , Reed-Gross E , Barfield WD , Prue CE , Gallagher ML , Rasmussen SA , Honein MA . Am J Med Genet A 2011 155A (11) 2721-31 |
| Evaluation of mailed pediatric buccal cytobrushes for use in a case-control study of birth defects.
Gallagher ML , Sturchio C , Smith A , Koontz D , Jenkins MM , Honein MA , Rasmussen SA . Birth Defects Res A Clin Mol Teratol 2011 91 (7) 642-8 |
| Maternal attitudes toward DNA collection for gene-environment studies: a qualitative research study
Jenkins MM , Reed-Gross E , Rasmussen SA , Barfield WD , Prue CE , Gallagher ML , Honein MA . Am J Med Genet A 2009 149A (11) 2378-86 |
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