| ATP release after partial hepatectomy regulates liver regeneration in the rat E Gonzales, B Julien, V Serrière-Lanneau, A Nicou, I Doignon, ... Journal of hepatology 52 (1), 54-62, 2010 | 121 | 2010 |
| Mouse model reveals the role of SOX7 in the development of congenital diaphragmatic hernia associated with recurrent deletions of 8p23. 1 MJ Wat, TF Beck, A Hernández-García, Z Yu, D Veenma, M Garcia, ... Human molecular genetics 21 (18), 4115-4125, 2012 | 98 | 2012 |
| De novo mutations of RERE cause a genetic syndrome with features that overlap those associated with proximal 1p36 deletions B Fregeau, BJ Kim, A Hernández-García, VK Jordan, MT Cho, RE Schnur, ... The American Journal of Human Genetics 98 (5), 963-970, 2016 | 90 | 2016 |
| Impact of preimmunization on adenoviral vector expression and toxicity in a subcutaneous mouse cancer model MT Vlachaki, A Hernandez-Garcia, M Ittmann, M Chhikara, LK Aguilar, ... Molecular Therapy 6 (3), 342-348, 2002 | 75 | 2002 |
| Identification of critical regions and candidate genes for cardiovascular malformations and cardiomyopathy associated with deletions of chromosome 1p36 HP Zaveri, TF Beck, A Hernández-García, KE Shelly, T Montgomery, ... PloS one 9 (1), e85600, 2014 | 67 | 2014 |
| SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females FC Radio, K Pang, A Ciolfi, MA Levy, A Hernández-García, L Pedace, ... The American Journal of Human Genetics 108 (3), 502-516, 2021 | 61 | 2021 |
| An allelic series of mice reveals a role for RERE in the development of multiple organs affected in chromosome 1p36 deletions BJ Kim, HP Zaveri, OA Shchelochkov, Z Yu, A Hernández-García, ... PLoS One 8 (2), e57460, 2013 | 51 | 2013 |
| Serum lead, cadmium, and zinc levels in newborns with neural tube defects from a polluted zone in Mexico. VA Martínez-Ordaz, VM Velasco-Rodríguez, A Hernández-García, ... Reproductive Toxicology (Elmsford, NY) 19 (2), 149-154, 2004 | 49 | 2004 |
| P2Y2 purinergic receptor activation is essential for efficient hepatocyte proliferation in response to partial hepatectomy BC Tackett, H Sun, Y Mei, JP Maynard, S Cheruvu, A Mani, ... American Journal of Physiology-Gastrointestinal and Liver Physiology 307 (11 …, 2014 | 46 | 2014 |
| Missense variants in the histone acetyltransferase complex component gene TRRAP cause autism and syndromic intellectual disability B Cogné, S Ehresmann, E Beauregard-Lacroix, J Rousseau, T Besnard, ... The American Journal of Human Genetics 104 (3), 530-541, 2019 | 43 | 2019 |
| Gerodermia osteodysplastica hereditaria: report of three affected brothers and literature review. RGJ Lisker R, Hernández A, Martínez-Lavin M, Mutchinick O, Armas C, Reyes P Am J Med Genet. 3 (4), :389-95., 1979 | 34 | 1979 |
| Congenital heart defects and left ventricular non-compaction in males with loss-of-function variants in NONO DA Scott, A Hernandez-Garcia, MS Azamian, VK Jordan, BJ Kim, ... Journal of medical genetics 54 (1), 47-53, 2017 | 31 | 2017 |
| Clinical exome sequencing data reveal high diagnostic yields for congenital diaphragmatic hernia plus (CDH+) and new phenotypic expansions involving CDH TM Scott, IM Campbell, A Hernandez-Garcia, SR Lalani, P Liu, CA Shaw, ... Journal of medical genetics 59 (3), 270-278, 2022 | 30 | 2022 |
| FBN1 contributing to familial congenital diaphragmatic hernia TF Beck, PM Campeau, SN Jhangiani, T Gambin, AH Li, R Abo‐Zahrah, ... American Journal of Medical Genetics Part A 167 (4), 831-836, 2015 | 26 | 2015 |
| Competencia clínica del médico familiar en hipertensión arterial sistémica HA García, VL Viniegra Rev Invest Clin 51 (2), 93-8, 1999 | 23 | 1999 |
| Further delineation of the phenotypic spectrum associated with hemizygous loss‐of‐function variants in NONO M Sewani, K Nugent, PR Blackburn, JM Tarnowski, A Hernandez‐Garcia, ... American Journal of Medical Genetics Part A 182 (4), 652-658, 2020 | 18 | 2020 |
| The role of FREM2 and FRAS1 in the development of congenital diaphragmatic hernia VK Jordan, TF Beck, A Hernandez-Garcia, PN Kundert, BJ Kim, ... Human Molecular Genetics 27 (12), 2064-2075, 2018 | 17 | 2018 |
| Novel Frem1-Related Mouse Phenotypes and Evidence of Genetic Interactions with Gata4 and Slit3 TF Beck, OA Shchelochkov, Z Yu, BJ Kim, A Hernandez-Garcia, HP Zaveri, ... PLoS One 8 (3), e58830, 2013 | 17 | 2013 |
| Contribution of LPP copy number and sequence changes to esophageal atresia, tracheoesophageal fistula, and VACTERL association A Hernández‐García, E Brosens, HP Zaveri, EM de Jong, Z Yu, ... American Journal of Medical Genetics-Part A 158 (7), 1785, 2012 | 17 | 2012 |
| Prioritization of candidate genes for congenital diaphragmatic hernia in a critical region on chromosome 4p16 using a machine-learning algorithm DA Callaway, IM Campbell, SR Stover, A Hernandez-Garcia, ... Journal of pediatric genetics 7 (04), 164-173, 2018 | 16 | 2018 |
