CDC-Authored Genomics and Precision Health Publications Database

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Last data update: Dec 05, 2023. (Total: 4799 publications since 2011)

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Records 1-10 (of 10 Records)

Query Trace: Jenkins MM[original query]
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
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