Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
7 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion.
Mol Psychiatry. 2021 Aug;26(8):4496-4510. doi: 10.1038/s41380-020-0654-3. Epub 2020 Feb 3.
Mol Psychiatry. 2021.
PMID: 32015465
Free PMC article.
Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome.
Trevino CE, Holleman AM, Corbitt H, Maslen CL, Rosser TC, Cutler DJ, Johnston HR, Rambo-Martin BL, Oberoi J, Dooley KJ, Capone GT, Reeves RH, Cordell HJ, Keavney BD, Agopian AJ, Goldmuntz E, Gruber PJ, O'Brien JE Jr, Bittel DC, Wadhwa L, Cua CL, Moskowitz IP, Mulle JG, Epstein MP, Sherman SL, Zwick ME.
Trevino CE, et al. Among authors: holleman am.
Sci Rep. 2020 Oct 22;10(1):18051. doi: 10.1038/s41598-020-74650-4.
Sci Rep. 2020.
PMID: 33093519
Free PMC article.
Item in Clipboard
Powerful and Efficient Strategies for Genetic Association Testing of Symptom and Questionnaire Data in Psychiatric Genetic Studies.
Holleman AM, Broadaway KA, Duncan R, Todor A, Almli LM, Bradley B, Ressler KJ, Ghosh D, Mulle JG, Epstein MP.
Holleman AM, et al.
Sci Rep. 2019 May 17;9(1):7523. doi: 10.1038/s41598-019-44046-0.
Sci Rep. 2019.
PMID: 31101869
Free PMC article.
Item in Clipboard
Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome.
Trevino CE, Holleman AM, Corbitt H, Maslen CL, Rosser TC, Cutler DJ, Johnston HR, Rambo-Martin BL, Oberoi J, Dooley KJ, Capone GT, Reeves RH, Cordell HJ, Keavney BD, Agopian AJ, Goldmuntz E, Gruber PJ, O'Brien JE Jr, Bittel DC, Wadhwa L, Cua CL, Moskowitz IP, Mulle JG, Epstein MP, Sherman SL, Zwick ME.
Trevino CE, et al. Among authors: holleman am.
Sci Rep. 2021 Jul 20;11(1):15164. doi: 10.1038/s41598-021-94021-x.
Sci Rep. 2021.
PMID: 34285246
Free PMC article.
No abstract available.
Item in Clipboard
Epidemiology beyond its limits.
McCullough LE, Maliniak ML, Amin AB, Baker JM, Baliashvili D, Barberio J, Barrera CM, Brown CA, Collin LJ, Freedman AA, Gibbs DC, Haddad MB, Hall EW, Hamid S, Harrington KRV, Holleman AM, Kaufman JA, Khan MA, Labgold K, Lee VC, Malik AA, Mann LM, Marks KJ, Nelson KN, Quader ZS, Ross-Driscoll K, Sarkar S, Shah MP, Shao IY, Smith JP, Stanhope KK, Valenzuela-Lara M, Van Dyke ME, Vyas KJ, Lash TL.
McCullough LE, et al. Among authors: holleman am.
Sci Adv. 2022 Jun 10;8(23):eabn3328. doi: 10.1126/sciadv.abn3328. Epub 2022 Jun 8.
Sci Adv. 2022.
PMID: 35675391
Free PMC article.
Item in Clipboard
Rare loss of function variants in the hepatokine gene INHBE protect from abdominal obesity.
Deaton AM, Dubey A, Ward LD, Dornbos P, Flannick J; AMP-T2D-GENES Consortium; Yee E, Ticau S, Noetzli L, Parker MM, Hoffing RA, Willis C, Plekan ME, Holleman AM, Hinkle G, Fitzgerald K, Vaishnaw AK, Nioi P.
Deaton AM, et al. Among authors: holleman am.
Nat Commun. 2022 Jul 27;13(1):4319. doi: 10.1038/s41467-022-31757-8.
Nat Commun. 2022.
PMID: 35896531
Free PMC article.
Item in Clipboard
Transcript-aware analysis of rare predicted loss-of-function variants in the UK Biobank elucidate new isoform-trait associations.
Hoffing RA, Deaton AM, Holleman AM, Krohn L, LoGerfo PJ, Plekan ME, Akle Serrano S, Nioi P, Ward LD.
Hoffing RA, et al. Among authors: holleman am.
Pac Symp Biocomput. 2024;29:247-260.
Pac Symp Biocomput. 2024.
PMID: 38160284
Free article.
Item in Clipboard
Cite
Cite