| Characterization of impulsivity in suicide completers: clinical, behavioral and psychosocial dimensions H Zouk, M Tousignant, M Seguin, A Lesage, G Turecki Journal of affective disorders 92 (2-3), 195-204, 2006 | 286 | 2006 |
| The effect of genetic variation of the serotonin 1B receptor gene on impulsive aggressive behavior and suicide H Zouk, A McGirr, V Lebel, C Benkelfat, G Rouleau, G Turecki American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 144 …, 2007 | 102 | 2007 |
| Harmonizing clinical sequencing and interpretation for the eMERGE III network H Zouk, E Venner, NJ Lennon, DM Muzny, D Abrams, S Adunyah, ... The American Journal of Human Genetics 105 (3), 588-605, 2019 | 93 | 2019 |
| Frequency of genomic secondary findings among 21,915 eMERGE network participants AS Gordon, H Zouk, E Venner, CM Eng, BH Funke, LM Amendola, ... Genetics in Medicine 22 (9), 1470-1477, 2020 | 79 | 2020 |
| Variant classification concordance using the ACMG-AMP variant interpretation guidelines across nine genomic implementation research studies LM Amendola, K Muenzen, LG Biesecker, KM Bowling, GM Cooper, ... The American Journal of Human Genetics 107 (5), 932-941, 2020 | 55 | 2020 |
| Returning actionable genomic results in a research biobank: Analytic validity, clinical implementation, and resource utilization CLB Zawatsky, N Shah, K Machini, E Perez, KD Christensen, H Zouk, ... The American Journal of Human Genetics 108 (12), 2224-2237, 2021 | 43 | 2021 |
| Retrospective analysis of clinical genetic testing in pediatric primary dilated cardiomyopathy: testing outcomes and the effects of variant reclassification D Quiat, L Witkowski, H Zouk, KP Daly, AE Roberts Journal of the American Heart Association 9 (11), e016195, 2020 | 37 | 2020 |
| The landscape of reported VUS in multi-gene panel and genomic testing: Time for a change HL Rehm, JT Alaimo, S Aradhya, P Bayrak-Toydemir, H Best, R Brandon, ... Genetics in Medicine 25 (12), 100947, 2023 | 30 | 2023 |
| Association of pathogenic variants in hereditary cancer genes with multiple diseases C Zeng, LA Bastarache, R Tao, E Venner, S Hebbring, JD Andujar, ... JAMA oncology 8 (6), 835-844, 2022 | 30 | 2022 |
| X chromosome and suicide LM Fiori, H Zouk, C Himmelman, G Turecki Molecular psychiatry 16 (2), 216-226, 2011 | 27 | 2011 |
| Study of transcriptional effects in Cis at the IFIH1 locus H Zouk, L Marchand, C Polychronakos PloS one 5 (7), e11564, 2010 | 22 | 2010 |
| Genomic considerations for FHIR®; eMERGE implementation lessons M Murugan, LJ Babb, CO Taylor, LV Rasmussen, RR Freimuth, E Venner, ... Journal of biomedical informatics 118, 103795, 2021 | 21 | 2021 |
| The genetic architecture of Plakophilin 2 cardiomyopathy AM Dries, A Kirillova, CM Reuter, J Garcia, H Zouk, M Hawley, B Murray, ... Genetics in Medicine 23 (10), 1961-1968, 2021 | 20 | 2021 |
| Functional evaluation of the role of C-type lectin domain family 16A at the chromosome 16p13 locus H Zouk, E D'hennezel, X Du, H Ounissi-Benkalha, CA Piccirillo, ... Clinical & Experimental Immunology 175 (3), 485-497, 2014 | 20 | 2014 |
| An assessment of the role of vinculin loss of function variants in inherited cardiomyopathy MH Hawley, N Almontashiri, LG Biesecker, N Berger, WK Chung, J Garcia, ... Human mutation 41 (9), 1577-1587, 2020 | 13 | 2020 |
| Functional characterization of the Thr946Ala SNP at the type 1 diabetes IFIH1 locus H Zouk, L Marchand, Q Li, C Polychronakos Autoimmunity 47 (1), 40-45, 2014 | 12 | 2014 |
| Familial hypercholesterolemia in the electronic medical records and genomics network: prevalence, penetrance, cardiovascular risk, and outcomes after return of results O Dikilitas, A Sherafati, S Saadatagah, BA Satterfield, DC Kochan, ... Circulation: Genomic and Precision Medicine 16 (2), e003816, 2023 | 7 | 2023 |
| Reanalysis of eMERGE phase III sequence variants in 10,500 participants and infrastructure to support the automated return of knowledge updates H Zouk, W Yu, A Oza, M Hawley, PKV Kumar, C Koch, LM Mahanta, ... Genetics in Medicine 24 (2), 454-462, 2022 | 7 | 2022 |
| Unique variant spectrum in a Jordanian cohort with inherited retinal dystrophies B Azab, Z Dardas, D Aburizeg, M Al-Bdour, M Abu-Ameerh, T Saleh, ... Genes 12 (4), 593, 2021 | 5 | 2021 |
| Rates of actionable genetic findings in individuals with colorectal cancer or polyps ascertained from a community medical setting AS Gordon, EA Rosenthal, DS Carrell, LM Amendola, MO Dorschner, ... The American Journal of Human Genetics 105 (3), 526-533, 2019 | 4 | 2019 |
