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CDC-Authored Genomics and Precision Health Publications Database|Home|Public Health Genomics and Precision Health Knowledge Base (PHGKB)

CDC-Authored Genomics and Precision Health Publications Database


Last data update: Oct 07, 2024. (Total: 6342 publications)
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Records 1-8 (of 8 Records)
Query Trace: Almli LM[original query]
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
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
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
Examining Individual and Synergistic Contributions of PTSD and Genetics to Blood Pressure: A Trans-Ethnic Meta-Analysis.
Sumner JA , Maihofer AX , Michopoulos V , Rothbaum AO , Almli LM , Andreassen OA , Ashley-Koch AE , Baker DG , Beckham JC , Bradley B , Breen G , Coleman JRI , Dale AM , Dennis MF , Feeny NC , Franz CE , Garrett ME , Gillespie CF , Guffanti G , Hauser MA , Hemmings SMJ , Jovanovic T , Kimbrel NA , Kremen WS , Lawford BR , Logue MW , Lori A , Lyons MJ , Maples-Keller J , Mavissakalian MR , McGlinchey RE , Mehta D , Mellor R , Milberg W , Miller MW , Morris CP , Panizzon MS , Ressler KJ , Risbrough VB , Rothbaum BO , Roy-Byrne P , Seedat S , Smith AK , Stevens JS , van den Heuvel LL , Voisey J , Young RM , Zoellner LA , Nievergelt CM , Wolf EJ .
Front Neurosci 2021 15 678503
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
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