Works by Almli, Lynn M.

Results: 34
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    Exome sequencing identifies novel genes underlying primary congenital glaucoma in the National Birth Defects Prevention Study.

    Published in:
    Birth Defects Research, 2024, v. 116, n. 7, p. 1, doi. 10.1002/bdr2.2384
    By:
    • Blue, Elizabeth E.;
    • Moore, Kristin J.;
    • North, Kari E.;
    • Desrosiers, Tania A.;
    • Carmichael, Suzan L.;
    • White, Janson J.;
    • Chong, Jessica X.;
    • Bamshad, Michael J.;
    • Jenkins, Mary M.;
    • Almli, Lynn M.;
    • Brody, Lawrence C.;
    • Freedman, Sharon F.;
    • Reefhuis, Jennita;
    • Romitti, Paul A.;
    • Shaw, Gary M.;
    • Werler, Martha;
    • Kay, Denise M.;
    • Browne, Marilyn L.;
    • Feldkamp, Marcia L.;
    • Finnell, Richard H.
    Publication type:
    Article
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    Exome sequencing identifies variants in infants with sacral agenesis.

    Published in:
    Birth Defects Research, 2022, v. 114, n. 7, p. 215, doi. 10.1002/bdr2.1987
    By:
    • Pitsava, Georgia;
    • Feldkamp, Marcia L.;
    • Pankratz, Nathan;
    • Lane, John;
    • Kay, Denise M.;
    • Conway, Kristin M.;
    • Hobbs, Charlotte;
    • Shaw, Gary M.;
    • Reefhuis, Jennita;
    • Jenkins, Mary M.;
    • Almli, Lynn M.;
    • Moore, Cynthia;
    • Werler, Martha;
    • Browne, Marilyn L.;
    • Cunniff, Chris;
    • Olshan, Andrew F.;
    • Pangilinan, Faith;
    • Brody, Lawrence C.;
    • Sicko, Robert J.;
    • Finnell, Richard H.
    Publication type:
    Article
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    Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data.

    Published in:
    Birth Defects Research, 2019, v. 111, n. 20, p. 1618, doi. 10.1002/bdr2.1554
    By:
    • Jenkins, Mary M.;
    • Almli, Lynn M.;
    • Pangilinan, Faith;
    • Chong, Jessica X.;
    • Blue, Elizabeth E.;
    • Shapira, Stuart K.;
    • White, Janson;
    • McGoldrick, Daniel;
    • Smith, Joshua D.;
    • Mullikin, James C.;
    • Bean, Christopher J.;
    • Nembhard, Wendy N.;
    • Lou, Xiang‐Yang;
    • Shaw, Gary M.;
    • Romitti, Paul A.;
    • Keppler‐Noreuil, Kim;
    • Yazdy, Mahsa M.;
    • Kay, Denise M.;
    • Carter, Tonia C.;
    • Olshan, Andrew F.
    Publication type:
    Article
    5

    GENOME-WIDE ASSOCIATION STUDY (GWAS) AND GENOME-WIDE BY ENVIRONMENT INTERACTION STUDY (GWEIS) OF DEPRESSIVE SYMPTOMS IN AFRICAN AMERICAN AND HISPANIC/LATINA WOMEN.

    Published in:
    2016
    By:
    • Dunn, Erin C.;
    • Wiste, Anna;
    • Radmanesh, Farid;
    • Almli, Lynn M.;
    • Gogarten, Stephanie M.;
    • Sofer, Tamar;
    • Faul, Jessica D.;
    • Kardia, Sharon L. R.;
    • Smith, Jennifer A.;
    • Weir, David R.;
    • Zhao, Wei;
    • Soare, Thomas W.;
    • Mirza, Saira S.;
    • Hek, Karin;
    • Tiemeier, Henning;
    • Goveas, Joseph S.;
    • Sarto, Gloria E.;
    • Snively, Beverly M.;
    • Cornelis, Marilyn;
    • Koenen, Karestan C.
    Publication type:
    journal article
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    International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci.

    Published in:
    Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-12576-w
    By:
    • Nievergelt, Caroline M.;
    • Maihofer, Adam X.;
    • Klengel, Torsten;
    • Atkinson, Elizabeth G.;
    • Chen, Chia-Yen;
    • Choi, Karmel W.;
    • Coleman, Jonathan R. I.;
    • Dalvie, Shareefa;
    • Duncan, Laramie E.;
    • Gelernter, Joel;
    • Levey, Daniel F.;
    • Logue, Mark W.;
    • Polimanti, Renato;
    • Provost, Allison C.;
    • Ratanatharathorn, Andrew;
    • Stein, Murray B.;
    • Torres, Katy;
    • Aiello, Allison E.;
    • Almli, Lynn M.;
    • Amstadter, Ananda B.
    Publication type:
    Article
    10

    Genome-wide identification of DNA methylation QTLs in whole blood highlights pathways for cardiovascular disease.

    Published in:
    Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-12228-z
    By:
    • Huan, Tianxiao;
    • Joehanes, Roby;
    • Song, Ci;
    • Peng, Fen;
    • Guo, Yichen;
    • Mendelson, Michael;
    • Yao, Chen;
    • Liu, Chunyu;
    • Ma, Jiantao;
    • Richard, Melissa;
    • Agha, Golareh;
    • Guan, Weihua;
    • Almli, Lynn M.;
    • Conneely, Karen N.;
    • Keefe, Joshua;
    • Hwang, Shih-Jen;
    • Johnson, Andrew D.;
    • Fornage, Myriam;
    • Liang, Liming;
    • Levy, Daniel
    Publication type:
    Article
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    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.

    Published in:
    American Journal of Medical Genetics. Part A, 2023, v. 191, n. 6, p. 1546, doi. 10.1002/ajmg.a.63185
    By:
    • Sok, Pagna;
    • Sabo, Aniko;
    • Almli, Lynn M.;
    • Jenkins, Mary M.;
    • Nembhard, Wendy N.;
    • Agopian, A. J.;
    • Bamshad, Michael J.;
    • Blue, Elizabeth E.;
    • Brody, Lawrence C.;
    • Brown, Austin L.;
    • Browne, Marilyn L.;
    • Canfield, Mark A.;
    • Carmichael, Suzan L.;
    • Chong, Jessica X.;
    • Dugan‐Perez, Shannon;
    • Feldkamp, Marcia L.;
    • Finnell, Richard H.;
    • Gibbs, Richard A.;
    • Kay, Denise M.;
    • Lei, Yunping
    Publication type:
    Article
    14

    Exome sequencing identifies genetic variants in anophthalmia and microphthalmia.

    Published in:
    American Journal of Medical Genetics. Part A, 2022, v. 188, n. 8, p. 2376, doi. 10.1002/ajmg.a.62874
    By:
    • Li, Jingjing;
    • Yang, Wei;
    • Wang, Yuejun Jessie;
    • Ma, Chen;
    • Curry, Cynthia J.;
    • McGoldrick, Daniel;
    • Nickerson, Deborah A.;
    • Chong, Jessica X.;
    • Blue, Elizabeth E.;
    • Mullikin, James C.;
    • Reefhuis, Jennita;
    • Nembhard, Wendy N.;
    • Romitti, Paul A.;
    • Werler, Martha M.;
    • Browne, Marilyn L.;
    • Olshan, Andrew F.;
    • Finnell, Richard H.;
    • Feldkamp, Marcia L.;
    • Pangilinan, Faith;
    • Almli, Lynn M.
    Publication type:
    Article
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    Problematic alcohol use associates with sodium channel and clathrin linker 1 (SCLT1) in trauma-exposed populations.

    Published in:
    2018
    By:
    • Almli, Lynn M.;
    • Lori, Adriana;
    • Meyers, Jacquelyn L.;
    • Shin, Jaemin;
    • Fani, Negar;
    • Maihofer, Adam X.;
    • Nievergelt, Caroline M.;
    • Smith, Alicia K.;
    • Mercer, Kristina B.;
    • Kerley, Kimberly;
    • Leveille, Jennifer M.;
    • Feng, Hao;
    • Abu‐Amara, Duna;
    • Flory, Janine D.;
    • Yehuda, Rachel;
    • Marmar, Charles R.;
    • Baker, Dewleen G.;
    • Bradley, Bekh;
    • Koenen, Karestan C.;
    • Conneely, Karen N.
    Publication type:
    journal article
    17

    A putative causal relationship between genetically determined female body shape and posttraumatic stress disorder.

    Published in:
    Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0491-4
    By:
    • Polimanti, Renato;
    • Amstadter, Ananda B.;
    • Stein, Murray B.;
    • Almli, Lynn M.;
    • Baker, Dewleen G.;
    • Bierut, Laura J.;
    • Bradley, Bekh;
    • Farrer, Lindsay A.;
    • Johnson, Eric O.;
    • King, Anthony;
    • Kranzler, Henry R.;
    • Maihofer, Adam X.;
    • Rice, John P.;
    • Roberts, Andrea L.;
    • Saccone, Nancy L.;
    • Hongyu Zhao;
    • Liberzon, Israel;
    • Ressler, Kerry J.;
    • Nievergelt, Caroline M.;
    • Koenen, Karestan C.
    Publication type:
    Article
    18

    A genome-wide identified risk variant for PTSD is a methylation quantitative trait locus and confers decreased cortical activation to fearful faces.

    Published in:
    American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2015, v. 168B, n. 5, p. 327, doi. 10.1002/ajmg.b.32315
    By:
    • Almli, Lynn M.;
    • Stevens, Jennifer S.;
    • Smith, Alicia K.;
    • Kilaru, Varun;
    • Meng, Qian;
    • Flory, Janine;
    • Abu‐Amara, Duna;
    • Hammamieh, Rasha;
    • Yang, Ruoting;
    • Mercer, Kristina B.;
    • Binder, Elizabeth B.;
    • Bradley, Bekh;
    • Hamilton, Steven;
    • Jett, Marti;
    • Yehuda, Rachel;
    • Marmar, Charles R.;
    • Ressler, Kerry J.
    Publication type:
    Article
    19

    Sex Dependent Influence of a Functional Polymorphism in Steroid 5-α-Reductase Type 2 (SRD5A2) on Post-Traumatic Stress Symptoms.

    Published in:
    American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2013, v. 162B, n. 3, p. 283, doi. 10.1002/ajmg.b.32147
    By:
    • Gillespie, Charles F.;
    • Almli, Lynn M.;
    • Smith, Alicia K.;
    • Bradley, Bekh;
    • Kerley, Kimberly;
    • Crain, Daniel F.;
    • Mercer, Kristina B.;
    • Weiss, Tamara;
    • Phifer, Justine;
    • Tang, Yilang;
    • Cubells, Joseph F.;
    • Binder, Elisabeth B.;
    • Conneely, Karen N.;
    • Ressler, Kerry J.
    Publication type:
    Article
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    Corrigendum: DICER1 and microRNA regulation in post-traumatic stress disorder with comorbid depression.

    Published in:
    Nature Communications, 2016, v. 7, n. 3, p. 10958, doi. 10.1038/ncomms10958
    By:
    • Wingo, Aliza P.;
    • Almli, Lynn M.;
    • Stevens, Jennifer S.;
    • Klengel, Torsten;
    • Uddin, Monica;
    • Li, Yujing;
    • Bustamante, Angela C.;
    • Lori, Adriana;
    • Koen, Nastassja;
    • Stein, Dan J.;
    • Smith, Alicia K.;
    • Aiello, Allison E.;
    • Koenen, Karestan C.;
    • Wildman, Derek E.;
    • Galea, Sandro;
    • Bradley, Bekh;
    • Binder, Elisabeth B.;
    • Jin, Peng;
    • Gibson, Greg;
    • Ressler, Kerry J.
    Publication type:
    Article
    22

    DICER1 and microRNA regulation in post-traumatic stress disorder with comorbid depression.

    Published in:
    Nature Communications, 2015, v. 6, n. 12, p. 10106, doi. 10.1038/ncomms10106
    By:
    • Wingo, Aliza P.;
    • Almli, Lynn M.;
    • Stevens, Jennifer J.;
    • Klengel, Torsten;
    • Uddin, Monica;
    • Li, Yujing;
    • Bustamante, Angela C.;
    • Lori, Adriana;
    • Koen, Nastassja;
    • Stein, Dan J.;
    • Smith, Alicia K.;
    • Aiello, Allison E.;
    • Koenen, Karestan C.;
    • Wildman, Derek E.;
    • Galea, Sandro;
    • Bradley, Bekh;
    • Binder, Elisabeth B.;
    • Jin, Peng;
    • Gibson, Greg;
    • Ressler, Kerry J.
    Publication type:
    Article
    23

    Examining Individual and Synergistic Contributions of PTSD and Genetics to Blood Pressure: A Trans-Ethnic Meta-Analysis.

    Published in:
    Frontiers in Neuroscience, 2021, v. 15, p. 1, doi. 10.3389/fnins.2021.678503
    By:
    • Sumner, Jennifer A.;
    • Maihofer, Adam X.;
    • Michopoulos, Vasiliki;
    • Rothbaum, Alex O.;
    • Almli, Lynn M.;
    • Andreassen, Ole A.;
    • Ashley-Koch, Allison E.;
    • Baker, Dewleen G.;
    • Beckham, Jean C.;
    • Bradley, Bekh;
    • Breen, Gerome;
    • Coleman, Jonathan R. I.;
    • Dale, Anders M.;
    • Dennis, Michelle F.;
    • Feeny, Norah C.;
    • Franz, Carol E.;
    • Garrett, Melanie E.;
    • Gillespie, Charles F.;
    • Guffanti, Guia;
    • Hauser, Michael A.
    Publication type:
    Article
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    Accounting for Population Stratification in DNA Methylation Studies.

    Published in:
    Genetic Epidemiology, 2014, v. 38, n. 3, p. 231, doi. 10.1002/gepi.21789
    By:
    • Barfield, Richard T.;
    • Almli, Lynn M.;
    • Kilaru, Varun;
    • Smith, Alicia K.;
    • Mercer, Kristina B.;
    • Duncan, Richard;
    • Klengel, Torsten;
    • Mehta, Divya;
    • Binder, Elisabeth B.;
    • Epstein, Michael P.;
    • Ressler, Kerry J.;
    • Conneely, Karen N.
    Publication type:
    Article
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    Exome sequencing of child–parent trios with bladder exstrophy: Findings in 26 children.

    Published in:
    American Journal of Medical Genetics. Part A, 2021, v. 185, n. 10, p. 3028, doi. 10.1002/ajmg.a.62439
    By:
    • Pitsava, Georgia;
    • Feldkamp, Marcia L.;
    • Pankratz, Nathan;
    • Lane, John;
    • Kay, Denise M.;
    • Conway, Kristin M.;
    • Shaw, Gary M.;
    • Reefhuis, Jennita;
    • Jenkins, Mary M.;
    • Almli, Lynn M.;
    • Olshan, Andrew F.;
    • Pangilinan, Faith;
    • Brody, Lawrence C.;
    • Sicko, Robert J.;
    • Hobbs, Charlotte A.;
    • Bamshad, Mike;
    • McGoldrick, Daniel;
    • Nickerson, Deborah A.;
    • Finnell, Richard H.;
    • Mullikin, James
    Publication type:
    Article
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