Publications by authors named "Lynn Almli"

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Maternal Myo-Inositol Intake and Congenital Heart Defects in Offspring: A Population-Based Case-Control Study.
Ruiqi Cen, L Joseph Su, Jun Ying, Mohammed S Orloff, Elijah H Bolin, Lynn M Almli

BJOG· November 2025

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Exome Sequencing to Identify Novel Susceptibility Genes for Nonsyndromic Split-Hand/Ft Malformation: A Report From the National Birth Defects Prevention Study.
Tonia C Carter, Denise M Kay, Faith Pangilinan, Lynn M Almli, Mary M Jenkins

Birth Defects Res· May 2025

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Exome sequencing identifies novel genes underlying primary congenital glaucoma in the National Birth Defects Prevention Study.
Elizabeth E Blue, Kristin J Moore, Kari E North, Tania A Desrosiers, Suzan L Carmichael, Lynn M Almli

Birth Defects Res· July 2024

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Rare variants in increase risk for isolated hypoplastic left heart syndrome.
Elizabeth E Blue, Janson J White, Michael K Dush, William W Gordon, Brent H Wyatt, Lynn M Almli

HGG Adv· October 2023

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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.
Pagna Sok, Aniko Sabo, Lynn M Almli, Mary M Jenkins, Wendy N Nembhard

Am J Med Genet A· June 2023

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Birth defects associated with paternal firefighting in the National Birth Defects Prevention Study.
Miriam R Siegel, Carissa M Rocheleau, Brittany S Hollerbach, Amel Omari, Sara A Jahnke, Lynn M Almli

Am J Ind Med· January 2023

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Exome sequencing identifies genetic variants in anophthalmia and microphthalmia.
Jingjing Li, Wei Yang, Yuejun Jessie Wang, Chen Ma, Cynthia J Curry, Lynn M Almli

Am J Med Genet A· August 2022

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Enhancing Discovery of Genetic Variants for Posttraumatic Stress Disorder Through Integration of Quantitative Phenotypes and Trauma Exposure Information.
Adam X Maihofer, Karmel W Choi, Jonathan R I Coleman, Nikolaos P Daskalakis, Christy A Denckla, Lynn M Almli

Biol Psychiatry· April 2022

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Exome sequencing identifies variants in infants with sacral agenesis.
Georgia Pitsava, Marcia L Feldkamp, Nathan Pankratz, John Lane, Denise M Kay, Lynn M Almli

Birth Defects Res· April 2022

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Exome sequencing of child-parent trios with bladder exstrophy: Findings in 26 children.
Georgia Pitsava, Marcia L Feldkamp, Nathan Pankratz, John Lane, Denise M Kay, Lynn M Almli

Am J Med Genet A· October 2021

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Examining Individual and Synergistic Contributions of PTSD and Genetics to Blood Pressure: A Trans-Ethnic Meta-Analysis.
Jennifer A Sumner, Adam X Maihofer, Vasiliki Michopoulos, Alex O Rothbaum, Lynn M Almli

Front Neurosci· June 2021

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Multi-omic biomarker identification and validation for diagnosing warzone-related post-traumatic stress disorder.
Kelsey R Dean, Rasha Hammamieh, Synthia H Mellon, Duna Abu-Amara, Janine D Flory, Lynn M Almli

Mol Psychiatry· December 2020

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Maternal occupational exposure to solvents and gastroschisis in offspring - National Birth Defects Prevention Study 1997-2011.
Nynke Spinder, Lynn M Almli, Tania A Desrosiers, Kathryn E Arnold, Jorieke E H Bergman

Occup Environ Med· March 2020

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Infant Mortality Attributable to Birth Defects - United States, 2003-2017.
Lynn M Almli, Danielle M Ely, Elizabeth C Ailes, Rahi Abouk, Scott D Grosse

MMWR Morb Mortal Wkly Rep· January 2020

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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.
Mary M Jenkins, Lynn M Almli, Faith Pangilinan, Jessica X Chong, Elizabeth E Blue

Birth Defects Res· December 2019

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International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci.
Caroline M Nievergelt, Adam X Maihofer, Torsten Klengel, Elizabeth G Atkinson, Chia-Yen Chen, Lynn M Almli

Nat Commun· October 2019

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Genome-wide identification of DNA methylation QTLs in whole blood highlights pathways for cardiovascular disease.
Tianxiao Huan, Roby Joehanes, Ci Song, Fen Peng, Yichen Guo, Lynn M Almli

Nat Commun· September 2019

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Genome-wide association study in two populations to determine genetic variants associated with Toxoplasma gondii infection and relationship to schizophrenia risk.
Alex W Wang, Dimitrios Avramopoulos, Adriana Lori, Jennifer Mulle, Karen Conneely, Lynn Almli

Prog Neuropsychopharmacol Biol Psychiatry· June 2019

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Powerful and Efficient Strategies for Genetic Association Testing of Symptom and Questionnaire Data in Psychiatric Genetic Studies.
Aaron M Holleman, K Alaine Broadaway, Richard Duncan, Andrei Todor, Lynn M Almli

Sci Rep· May 2019

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Risk of gastroschisis with maternal genitourinary infections: the US National birth defects prevention study 1997-2011.
Marcia L Feldkamp, Kathryn E Arnold, Sergey Krikov, Jennita Reefhuis, Lynn M Almli

BMJ Open· March 2019

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Problematic alcohol use associates with sodium channel and clathrin linker 1 (SCLT1) in trauma-exposed populations.
Lynn M Almli, Adriana Lori, Jacquelyn L Meyers, Jaemin Shin, Negar Fani

Addict Biol· September 2018

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Kernel machine methods for integrative analysis of genome-wide methylation and genotyping studies.
Ni Zhao, Xiang Zhan, Yen-Tsung Huang, Lynn M Almli, Alicia Smith

Genet Epidemiol· March 2018

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A putative causal relationship between genetically determined female body shape and posttraumatic stress disorder.
Renato Polimanti, Ananda B Amstadter, Murray B Stein, Lynn M Almli, Dewleen G Baker

Genome Med· November 2017

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Relationship between Toxoplasma gondii seropositivity and acoustic startle response in an inner-city population.
Nick M Massa, Erica Duncan, Tanja Jovanovic, Kimberly Kerley, Lei Weng, Lynn M Almli

Brain Behav Immun· March 2017

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Association Between Infant Mortality Attributable to Birth Defects and Payment Source for Delivery - United States, 2011-2013.
Lynn M Almli, Caroline C Alter, Rebecca B Russell, Sarah C Tinker, Penelope P Howards

MMWR Morb Mortal Wkly Rep· January 2017

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