Andres Hernandez-Garcia, M.D. PhD
Picture
Andres Hernandez-Garcia, M.D. PhD
Postdoctoral Associate
Positions
- Postdoctoral Associate
-
Molecular and Human Genetics/ D. Scott Lab
Baylor College of Medicine
Houston, TX US
- INSTRUCTOR
-
SURGERY
GENERAL SURGERY
Baylor College of Medicine
HOUSTON, Texas United States
- Distinguished University Professor
-
College of Medicine
Unidad Torreon
Faculty of Medicine, Universidad Autónoma de Coahuila, México.
Torreon, Coahuila Mexico
Professor of Genetics and Professor of Medicine (Embryology). Founder of the Biomedical Research Center at Universidad Autónoma de Coahuila, México. Full time Professor Category “C” at Faculty of Medicine, Universidad Autónoma de Coahuila, Dean of the College of Medicine, Biomedical Research Center, General University Hospital and Pediatrics University Hospital of the Universidad Autónoma de Coahuila during the period of March, 1992 to March, 1996. Founder, Chairman and Consultant of Genetics Department at Faculty of Medicine and University Hospitals of Torreón, Coah. México.
- Dean of College of Medicine.
-
Universidad Autónoma de Coahuila.
Torreon, Coahuila Mexico
Working closely with subdeans of University Hospitals and Biomedical Research Center and other members of senior leadership, my primary responsibility was to oversee all educational and administrative activities across the College and University Hospitals in alignment with the mission, vision and values of the Universidad Autonoma de Coahuila. The Dean of Medical School retains primary responsibility for all the educational programs, ensuring that all programs achieve the highest standards to prepare our trainees to be leaders in their respective fields. The major responsibility of the Dean of the College of Medicine Unidad Torreon of Universidad Autonoma de Coahuila shall be that of providing active leadership in the promotion, direction and support of the clinical, educational and research activities of the University, in the maintenance of a high level of morale among the faculty, and in the encouragement of the spirit of learning among the students. In addition the Dean shall have general and primary administrative responsibility for the different programs from the College, University Hospital and Biomedical Research Center.
- Dean of University General Hospital.
-
Universidad Autónoma de Coahuila.
Torreon, Coahuila Mexico
- Dean of University Pediatric Hospital.
-
Universidad Autónoma de Coahuila.
Torreon, Coahuila Mexico
- Dean Biomedical Research Center
-
Universidad Autónoma de Coahuila.
Torreon, Coahuila Mexico
- Subdean of Centro De Investigación Biomédica.
-
Universidad Autónoma de Coahuila.
Torreon, Coahuila Mexico
- Professor
-
College of Chemistry
Unidad Cuautitlán Izcalli. Estado de México.
Universidad Nacional Autónoma de México.
México, D.F, Estado de México Mexico
Professor of Genetics
- Professor
-
School of Psychology.
Instituto Superior de Ciencia y Tecnología de la Laguna (ISCYTAC).
Universidad La Salle Laguna.
Torreon, Coahuila Mexico
Professor of Genetics and Embryology professor of Psychoendocrinology
- Scientist Staff
-
Molecular & Human Genetics.
Baylor College of Medicine
Houston, Texas United States
- Member
-
Dan L Duncan Comprehensive Cancer Center
Baylor College of Medicine
Houston, Texas United States
- Scientist Staff
-
Molecular and Human Genetics
Baylor College of Medicine
Houston, Texas United States
Education
- Residency at Unidad de Investigación Biomédica IMSS. Centro Médico Nacional. México, D.F.
- 09/1978 - Mexico, Distrito Federal Mexico
- Postdoctoral Training at BAYLOR COLLEGE OF MEDICINE
- 06/2009 - HOUSTON, Texas United States
- Postdoctoral Associate Department of Molecular & Human Genetics Baylor College of Medicine Houston, Texas, U.S.A. June 2009 to date
- Postdoctoral Fellowship at Department of Radiology/Radiation Oncology, Veterans Affairs Medical Center and Baylor College of Medicine
- 05/2001 - HOUSTON, Texas United States
- Postdoctoral Research Fellow Department of Radiology/Radiation Oncology, Veterans Affairs Medical Center and Baylor College of Medicine Houston, Texas, U.S.A. 1 August, 2000 to 31 May, 2001.
- Postdoctoral Fellowship at Texas Children’s Hospital and Baylor College of Medicine.
- 07/2000 - HOUSTON, Texas United States
- Postdoctoral Research Fellow Department of Pediatric-Hematology/ Oncology, Texas Children’s Hospital and Baylor College of Medicine. Houston, Texas, U.S.A. October 5, 1998 to 31 July, 2000.
- Residency at Instituto Nacional de Ciencias Medicas y Nutricion "Salvador Zubirán". INCMNSZ
- 05/1980 - Mexico, Distrito Federal Mexico
- Medical Genetics Degree Program of Specialty in Medical Genetics. Instituto Nacional de la Nutrición Salvador Zubirán., Universidad Nacional Autónoma de México. México, D. F. 1978 - 1980
- MD from Universidad Autonoma de Coahuila (UAdeC)
- 05/1978 - Saltillo, Coahuila Mexico
- Medical Doctor Degree. Universidad Autónoma de Coahuila. May 3, 1978. Number 6444/218/V., Certificate/License Number: Registration S.S.A. number 506890. Date Degree Conferred: July 18, 1978.
- PhD from Universidad Autonoma de Nuevo Leon (UANL)
- 10/2003 - Monterrey, Nuevo Leon Mexico
- Ph D. in Molecular Biology and Genetic Engineering Faculty of Medicine. Universidad Autónoma de Nuevo León. Period: 1998 to 2001. Monterrey. N.L. México. UANL. Registration Number: 133661. Registration Secretaría de Educación Pública: 4124807.
Certifications
- #6444/218/V. Certificate/License Number: Registration S.S.A.
- Universidad Autónoma de Coahuila. México
- Doctor of Medicine (M.D) Universidad Autónoma de Coahuila. México Academic average 9.0 Number 6444/218/V. Certificate/License Number: Registration S.S.A. number 506890. Date Degree Conferred: July 18, 1978.
- Medical Genetics Degree. Program of Specialty in Medical Genetics.
- (10/01/1978 - 05/31/1980)
- Instituto Nacional de la Nutrición Salvador Zubirán and Universidad Nacional Autónoma de México. México, D. F.
- Oct 1978—May 1980 Medical Genetics Degree Program of Specialty in Medical Genetics. Instituto Nacional de la Nutrición Salvador Zubirán. Universidad Nacional Autónoma de México. México, D. F.
- PhD. in Molecular Biology and Genetic Engineering
- #Registration Secretaría de Educación Pública: 412Registration Number: 133661. 4807. Date Degree Conferred: October 20, 2003. Professional Licensure: April 26, 2004
- Faculty of Medicine. Universidad Autónoma de Nuevo León. Mexico
- Oct 1998—2001 PhD. in Molecular Biology and Genetic Engineering Faculty of Medicine. Universidad Autónoma de Nuevo León. Registration Secretaría de Educación Pública: 412Registration Number: 133661. 4807. Date Degree Conferred: October 20, 2003. Professional Licensure: April 26, 2004
Honors & Awards
- Award and prize during Cardiovascular Research Institute Symposium.
- Best Abstract Award at the 4th Annual Cardiovascular Research Institute Symposium. Baylor College of Medicine. February 4, 2016. Houston, TX. USA.
- Cardiovascular Research Institute. Baylor College of Medicine. (02/2016)
- Molecular Surgeon Young Investigador Award
- 2008 Molecular Surgeon Young Investigador Award. Michael E. DeBakey Department of Surgery. Baylor College of Medicine. Nineteenth Day of December 2008. Houston, TX. USA.
- Michael E. DeBakey Department of Surgery. Baylor College of Medicine. (12/2008)
- Award National System of Researchers (SNI)
- Consejo Nacional de Ciencia y Tecnología, México. (01/2006)
- Award in Health Sciences Research
- Award in Health Sciences Research UANL-2002 by the scientific work titled Preimmunization to adenoviruses may influence the therapeutic effectiveness and toxicity of adenoviral-mediated gene therapy for cancer. Universidad Autónoma de Nuevo León. Monterrey N. L, México. September 12, 2003.
- Universidad Autónoma de Nuevo León (09/2003)
- Award in Basic Sciences Research
- Award in Basic Sciences Research Universidad Autónoma de Nuevo León. Mexico.
- Universidad Autónoma de Nuevo León (09/1987)
- Award in Clinical Research
- Award in Clinical Research. (1988.) Universidad Autónoma de Nuevo León. Mexico.
- Universidad Autónoma de Nuevo León (09/1988)
- Academic achievement scholarship
- Granted of academic performance scholarship (1991, 92, 93, 94 and 95) Universidad Autónoma de Coahuila and Secretaría de Educación Pública.
- Universidad Autónoma de Coahuila. (09/1991 - 08/1995)
- MIGUEL RAMOS ARIZPE. Medal for Academic Worth
- Granted of MIGUEL RAMOS ARIZPE. Medal for Academic Worth Universidad Autónoma de Coahuila. Saltillo, Coah. Oct. 30, 1992.
- Universidad Autónoma de Coahuila. (10/1992)
- ASHG 2016 Annual Conference Poster Special Recognition Award.
- ASHG 2016 Annual Conference Poster Special Recognition Award. Title: “SOX7 deficiency impairs embryonic vasculogenesis and epithelial-to-mesenchymal transition during atrioventricular endocardial cushion development” which has been selected as a Reviewers' Choice Abstract, by the American Society of Human Genetics Conference Committee 2016 at Vancouver, Canada..
- American Society of Human Genetics (10/2016 - 10/2016)
- Down-regulation of Sox7 impairs epithelial-to-mesenchymal transition and endocardial cushion morphogenesis.
- Title: Down-regulation of Sox7 impairs epithelial-to-mesenchymal transition and endocardial cushion morphogenesis. ACCEPTED for a PLATFORM (oral) presentation at the 2018 American Society of Human Genetics Annual Meeting in San Diego, California from October 16-20, 2018. Presentation Type: PLATFORM (Oral Presentation) Session Number and Title: 30. Cardiac, Valvular, and Vascular Disorders Session Date: Wednesday, October 17 Session Time: 4:15 pm - 5:45 pm Presentation Time (10 minutes + 5 minutes Q&A): 5:00 PM Abstract Title: Down-regulation of Sox7 impairs epithelial-to-mesenchymal transition and endocardial cushion morphogenesis. Abstract Program Number: 80 Location: San Diego Convention Center, 111 W Harbor Dr, San Diego, CA 92101 Room: Room 6D, Upper Level
- American Society of Human Genetics (10/2018)
- SOX7 ablation in endocardium results in downregulation of WNT4 and BMP2 and abnormal endocardial cushion development
- Reviewers' Choice Poster Special Recognition Award. Title: “SOX7 ablation in endocardium results in downregulation of WNT4 and BMP2 and abnormal endocardial cushion development”, abstract scored in the top 10% of posters abstracts
- 10/2019
- Thesis: “Preimmunization to adenoviruses may influence the therapeutic effectiveness and toxicity of adenoviral-mediated gene therapy for cancer”.
- Doctoral Thesis: Awarded with the “Magna Cum Laude” honor. June 10, 2002.
- Universidad Autónoma de Nuevo León, Mexico (06/2002)
- Granted of Medal Magdalena Mondragón for Scientific Merit
- Declared distinguish citizen by my hometown Torreón Coahuila. Council Town. September 1994.
- 09/1994
- ASHG 2016 Annual Conference Poster Special Recognition Award
- ASHG 2016 Annual Conference Poster Special Recognition Award. Title: “SOX7 deficiency impairs embryonic vasculogenesis and epithelial-to-mesenchymal transition during atrioventricular endocardial cushion development” which has been selected as a Reviewers' Choice Abstract, by the American Society of Human Genetics Conference Committee 2016 at Vancouver, Canada.
- American Society of Human Genetics Conference Committee 2016 at Vancouver, Canada. (10/2016)
- Platform Conference Featured Speaker
- Platform Conference Featured Speaker: PLATFORM (oral) presentation at the 2018 American Society of Human Genetics Annual Meeting in San Diego, California from October 16-20, 2018. Down-regulation of Sox7 impairs epithelial-to-mesenchymal transition and endocardial cushion morphogenesis.
- American Society of Human Genetics r, Canada. (10/2018)
- Reviewers' Choice Poster Special Recognition Award
- Reviewers' Choice Poster Special Recognition Award. Title: “SOX7 ablation in endocardium results in downregulation of WNT4 and BMP2 and abnormal endocardial cushion development”, abstract scored in the top 10% of posters abstracts. American Society of Human Genetics Conference Committee 2019 at Houston, Texas USA.
- American Society of Human Genetics (10/2019)
- ASHG 2016 Annual Conference Poster Special Recognition Award.
- ASHG 2016 Annual Conference Poster Special Recognition Award. Title: “SOX7 deficiency impairs embryonic vasculogenesis and epithelial-to-mesenchymal transition during atrioventricular endocardial cushion development” which has been selected as a Reviewers' Choice Abstract, by the American Society of Human Genetics Conference Committee 2016 at Vancouver, Canada..
- American Society of Human Genetics (10/2016 - 10/2016)
- Platform Conference Featured Speaker
- Platform Conference Featured Speaker: PLATFORM (oral) presentation at the 2018 American Society of Human Genetics Annual Meeting in San Diego, California from October 16-20, 2018. Down-regulation of Sox7 impairs epithelial-to-mesenchymal transition and endocardial cushion morphogenesis.
- American Society of Human Genetics (10/2018 - 10/2018)
- Reviewers' Choice Poster Special Recognition Award
- Reviewers' Choice Poster Special Recognition Award. Title: “SOX7 ablation in endocardium results in downregulation of WNT4 and BMP2 and abnormal endocardial cushion development”, abstract scored in the top 10% of posters abstracts. American Society of Human Genetics Conference Committee 2019 at Houston, Texas USA.
- American Society of Human Genetics (10/2019 - 10/2019)
Websites
ORCID strives to enable transparent and trustworthy connections between researchers, their contributions, and their affiliations by providing a unique, persistent identifier for individuals to use as they engage in research, scholarship, and innovation activities.
Houston, TX - Apr 14, 2016
One in 5,000 babies is born missing a small amount of genetic material from the tip of chromosome 1, a region called 1p36. Missing genes in the 1p36 region is a relatively common cause of intellectual disability. These children may also have delayed development, seizures, heart and kidney defects, and problems with vision and hearing. The number and severity of these medical conditions varies greatly among children with 1p36 deletions. Scientists think that one reason for this variability is that the genes that are missing from the 1p36 region are not the same in each individual. Knowing which genes are actually involved in the development of this syndrome would help physicians predict the type of medical conditions a child with a 1p36 deletion might encounter and would make it easier to create individualized care plans for these patients. In a paper published today in the American Journal of Human Genetics, a multidisciplinary team including Baylor College of Medicine researchers has determined that mutations in one gene, RERE, can cause many of the features associated with 1p36 deletions.
“This discovery is important for the parents of the children with this syndrome because it answers one of their most pressing questions, what are the problems that my child is likely to have?” said Dr. Daryl A. Scott, associate professor of molecular and human genetics and molecular physiology and biophysics at Baylor and one of the two senior authors of this report.
Scott worked closely with Dr. Elliot H. Sherr, the other senior author of the paper, Sherr’s team from the department of neurology at the University of California, San Francisco, and other physicians and scientists from around the world to identify 10 patients with mutations in RERE, which is located in the 1p36 region. These patients had medical problems that were very similar to those of patients in which dozens of 1p36 genes are deleted.
“We are the first to provide evidence that RERE mutations alone can cause developmental problems typical of 1p36 deletions. RERE is important in early development,” said Scott.
This discovery is the culmination of 10 years of research in mice and other animal models. Scott and colleagues demonstrated that, in mice, Rere mutations alone result in the animals having many of the characteristics observed in patients with 1p36 deletion syndrome. However, it was impossible to prove that RERE could play the same role in humans. “One of the big surprises of our paper is that just one gene can cause many of the problems observed when the tip of chromosome 1 is deleted,” said Scott. “We anticipate that this finding will be of particular interest to the parents in the 1p36 Deletion Support & Awareness group.”
In addition, the research is a boon to families of children with RERE mutations, who know for the first time the reason their children share this group of developmental disabilities.
“Just having an answer can be hugely beneficial for families,” said Sherr, a practicing neurologist who works closely with these patients and their families. “Of course, getting a genetic answer is just the first step, but for the longest time we didn’t even have that much. It gives these families hope that we can move forward.”
Sherr is also with the department of pediatrics at UCSF.
The next step in Scott’s research will be to focus on the role of RERE in the development of the brain, heart, eye and other organs.
The following researchers also contributed to these research: Brieana Fregeau, Department of Neurology, University of California, San Francisco; Bum Jun Kim, Andrés Hernández-García, Jill A. Rosenfeld, and Seema R. Lalani, Department of Molecular and Human Genetics, Baylor; Valerie K. Jordan, Department of Molecular Physiology and Biophysics, Baylor; Megan T. Cho, Rhonda E. Schnur, Kristin G. Monaghan, and Jane Juusola, GeneDx, Gaithersburg, MD; Elizabeth Bhoj and Elaine H. Zackai, Division of Genetics, Children’s Hospital of Philadelphia; Stephanie Sacharow, Division of Medical Genetics, Boston Children’s Hospital; Kristin Barañano, Department of Neurology, Johns Hopkins University School of Medicine; Danielle G.M. Bosch and Bert B.A. de Vries Department of Human genetics, Radboud University Medical Center, The Netherlands; Kristin Lindstrom, Philip James and Peggy Kulch, Division of Genetics and Metabolism, Phoenix Children’s Hospital; Dani?lle G.M. Bosch, Bartiméus Institute for the Visually Impaired, The Netherlands, and the Department of Cognitive Neuroscience, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, The Netherlands; Mieke M. van Haelst, Koen L.I. van Gassen and Ellen van Binsbergen, Department of Genetics, University Medical Center Utrecht, The Netherlands; A. James Barkovich, Department of Radiology, University of California, San Francisco; and Audrey Schroeder, division of genetics, University of Rochester Medical Center, Rochester, NY.
This work was supported by the National Institute of Neurological Disorders and Stroke grant R01 NS058721, The Netherlands Organization for Health Research and Development grant 912-12-109 and ODAS Stichting.
Sherr is a member of the clinical advisory board of Invitae and consults for Personalis. Cho, Schnur, Monaghan, and Juusola are all employees of GeneDx, which provides exome sequencing on a clinical basis. The Department of Molecular and Human Genetics at Baylor College of Medicine derives revenue from clinical laboratory testing conducted at Baylor Miraca Genetics Laboratories, which provides exome sequencing on a clinical basis.
Find an Expert
Let our media specialists help you find an expert in health, medicine, education, research and patient care.
from the labs 2016 header
Research at Baylor
Read more about research at Baylor College of Medicine in our monthly newsletter From the Labs.
Media Queries?
During business hours call: (713) 798-4710
After business hours call: (713) 775-6912
Best Abstract Awards from the Fourth Annual Symposium 2016
Congratulations to the 6 Best Abstract winners from the Fourth Annual CVRI Symposium Feb. 4, 2016 at Baylor College of Medicine! Read more about it.
People Baylor College of Medicine
Professional Development
- Elaboration of the general design of Mexican medical education
- Workshop (Participant, 1992)
- Sponsor: Asociación Mexicana de Facultades y Escuelas de Medicina, A.C.
- With the objective of evaluating and accrediting the quality of medical education in the country, the Mexican Association of Medical Schools initiated the National Programme for the Strengthening of the Quality of Medical Education (PNFCE). This programme led to the establishment of the National System of Accreditation. Medical school deans in Mexico determined the criteria for the evaluation of quality and its subsequent standards through a consensus process. The following 10 criteria resulted: general basis and educational objectives; government and institutional orientation; educational programme and academic structure; educational process assessment; students; teaching staff; institutional coherence; resources; clinical sites; and administration. Eighty-eight standards were developed in the instrument designed for the self-evaluation phase. The information resulting from the self-evaluation will be verified by a group of experts during a survey visit, which will be finalized with a report to serve as the basis for the decision to be made by the Accreditation Commission. The self-evaluation phase started in 1994. In 1996 four schools submitted their request for accreditation. As of July 1996, one survey visit has been completed and three more are programmed for the second half of the year.
- Creation of quality standards in Mexican medical education
- Workshop (Organizer, 1993)
- Sponsor: Asociación Mexicana de Facultades y Escuelas de Medicina, A.C.
- Med Educ . 1996 Sep;30(5):319-21. doi: 10.1111/j.1365-2923.1996.tb00840.x. Assessment and accreditation of Mexican medical schools J A Cordova 1, E Aguirre, A Hernández, V Hidalgo, F Domínguez, I Durante, R Jesús, O Castillo Affiliations expand PMID: 8949468 DOI: 10.1111/j.1365-2923.1996.tb00840.x Abstract With the objective of evaluating and accrediting the quality of medical education in the country, the Mexican Association of Medical Schools initiated the National Programme for the Strengthening of the Quality of Medical Education (PNFCE). This programme led to the establishment of the National System of Accreditation. Medical school deans in Mexico determined the criteria for the evaluation of quality and its subsequent standards through a consensus process. The following 10 criteria resulted: general basis and educational objectives; government and institutional orientation; educational programme and academic structure; educational process assessment; students; teaching staff; institutional coherence; resources; clinical sites; and administration. Eighty-eight standards were developed in the instrument designed for the self-evaluation phase. The information resulting from the self-evaluation will be verified by a group of experts during a survey visit, which will be finalized with a report to serve as the basis for the decision to be made by the Accreditation Commission. The self-evaluation phase started in 1994. In 1996 four schools submitted their request for accreditation. As of July 1996, one survey visit has been completed and three more are programmed for the second half of the year.
- Program Quality of Medical Education in Mexico
- Workshop (Organizer, 1993)
- Sponsor: Asociación Mexicana de Facultades y Escuelas de Medicina, A.C.
- Assessment and accreditation of Mexican medical schools J A Cordova 1, E Aguirre, A Hernández, V Hidalgo, F Domínguez, I Durante, R Jesús, O Castillo Affiliations expand PMID: 8949468 DOI: 10.1111/j.1365-2923.1996.tb00840.x
- Academic Acreditation of Medical Schools.
- Workshop (Presenter, 1994)
- Sponsor: The Liaison Committee on Medical Education and the American Medical Association
- Task Force: Academic Acreditation of Medical Schools. Sponsored by: The Liaison Committee on Medical Education and the American Medical Association. Chicago, Illinois. U.S.A. September, 11 - 16, 1994.
- Medical Education.
- Seminar (Presenter, 1995)
- Sponsor: Conferencia Mundial de Educación Médica.
- Seminar: Medical Education. Conferencia Mundial de Educación Médica. Santa Fe de Bogotá, Colombia. October 2-5, 1995.
Selected Publications
- Kim BJ, Zaveri HP, Shchelochkov OA, Yu Z, Hernández-García A, Seymour ML, Oghalai JS, Pereira FA, Stockton DW, Justice MJ, Lee B, Scott DA. "An allelic series of mice reveals a role for RERE in the development of multiple organs affected in chromosome 1p36 deletions.." PLoS One.. 2013 Feb 25;8(2):Published online.
- Gonzales E, Julien B, Serrière-Lanneau V, Nicou A, Doignon I, Lagoudakis L, Garcin I, Azoulay D, Duclos-Vallée JC, Castaing D, Samuel D, Hernandez-Garcia A, Awad SS, Combettes L, Thevananther S, Tordjmann T. "ATP release after partial hepatectomy regulates liver regeneration in the rat.." J Hepatol. 2010 Jan;52(1):54-62.
- Tiana M Scott, Ian M Campbell, Andres Hernandez-Garcia, Seema R Lalani, Pengfei Liu, Chad A Shaw, Jill A Rosenfeld, Daryl A Scott "Clinical exome sequencing data reveal high diagnostic yields for congenital diaphragmatic hernia plus (CDH+) and new phenotypic expansions involving CDH." J Med Genet. 2021 Jan 18; Pubmed PMID: 33461977
- Daryl A Scott, Andres Hernandez-Garcia, Mahshid S Azamian, Valerie K Jordan, Bum Jun Kim, Molly Starkovich, Jinglan Zhang, Lee-Jun Wong, Sandra A Darilek, Amy M Breman, Yaping Yang, James R Lupski, Amyn K Jiwani, Bibhuti Das, Seema R Lalani, et al "Congenital heart defects and left ventricular non-compaction in males with loss-of-function variants in NONO." J Med Genet.. 2016 Aug 22; Pubmed PMID: 27550220
- Hernández-García A, Brosens E, Zaveri HP, de Jong EM, Yu Z, Namwanje M, Mayle A, Fernandes CJ, Lee B, Blazo M, Lalani SR, Tibboel D, de Klein A, Scott DA. "Contribution of LPP copy number and sequence changes to esophageal atresia, tracheoesophageal fistula, and VACTERL association.." Am J Med Genet A. 2012 Jul;158(7):1785-1787.
- Fregeau B, Kim BJ, Hernández-García A, Jordan VK, James P, Kulch P, Lalani SR, van Haelst MM, van Gassen KL, van Binsbergen E, Barkovich AJ, Scott DA, Sherr EH. et al "De Novo Mutations of RERE Cause a Genetic Syndrome with Features that Overlap Those Associated with Proximal 1p36 Deletions." Am J Hum Genet.. 2016 Apr 13;
- Yoel Gofin, Laura Palmer Mackay, Keren Machol, Sundeep Keswani, Lorraine Potocki, Eleonora Di Gregorio, Valeria Giorgia Naretto, Alfredo Brusco, Andres Hernandez-Garcia, Daryl A Scott "Evidence that FGFRL1 contributes to congenital diaphragmatic hernia development in humans." Am J Med Genet A. 2021 Mar;185(3):836-840..
- Beck TF, Campeau PM, Jhangiani SN, Gambin T, Li AH, Abo-Zahrah R, Jordan VK, Hernandez-Garcia A, Wiszniewski WK, Muzny D, Gibbs RA, Boerwinkle E, Lupski JR, Lee B, Reardon W, Scott DA. "FBN1 contributing to familial congenital diaphragmatic hernia.." Am J Med Genet A.. 2015 Apr;167(4):831-836.
- Sewani M, Nugent K, Blackburn PR, Tarnowski JM, Hernandez-Garcia A, Amiel J, Whalen S, Keren B, Courtin T, Rosenfeld JA, Yang Y, Patterson MC, Pichurin P, McLean SD, Scott DA. "Further delineation of the phenotypic spectrum associated with hemizygous loss-of-function variants in NONO.." Am J Med Genet A. 2020 Apr;182(4):652-658.. Pubmed PMID: 31883306
- Lisker R, Hernández A, Martínez-Lavin M, Mutchinick O, Armas C, Reyes P, Robles-Gil J. "Gerodermia osteodysplastica hereditaria: report of three affected brothers and literature review.." Am J Med Genet.. 1979;3(4):389-395.
- A. Hernandez-Garcia · S. Thevananther · S.S. Awad "Identification of a Novel Epidermal Growth Factor Receptor (EGFR) Binding Activity of Cyclin D1 Promoter During HepG2 Cell Proliferation and in Human Hepatocellular Carcinoma." Journal of Surgical Research. 2009 Feb;151(2):188-189.
- Zaveri HP, Beck TF, Hernández-García A, Shelly KE, Montgomery T, van Haeringen A, Anderlid BM, Patel C, Goel H, Houge G, Morrow BE, Cheung SW, Lalani SR, Scott DA "Identification of critical regions and candidate genes for cardiovascular malformations and cardiomyopathy associated with deletions of chromosome 1p36.." PLoS One. 2014 Jan 15;9(1):PLoS One. 2014;.
- Hernandez-Garcia A, Vlachaki MT, Ittmann M, Chhikara M, Aguilar LK, Zhu X, Teh BS, Butler EB, Woo S, Thompson TC, Barrera-Saldana H, Aguilar-Cordova E. "Impact of preimmunization on adenoviral vector expression and toxicity in a subcutaneous mouse cancer model.." Mol Ther. 2002 Sep;6(3):342-348.
- Gómez-Arroyo S1, Hernández-García A, Villalobos-Pietrini R. "Induction of sister-chromatid exchanges in Vicia faba by arsenic-contaminated drinking water.." Mutat Res.. 1988 Jul;208(3):219-224.
- Benjamin Cogne´, Sophie Ehresmann, Eliane Beauregard-Lacroix, Justine Rousseau, Thomas Besnard, Thomas Garcia, Slave´ Petrovski, Shiri Avni, Kirsty McWalter, Patrick R. Blackburn, Daryl A. Scott, Andres Hernandez-Garcia, et al.. "Missense Variants in the Histone Acetyltransferase Complex Component Gene TRRAP Cause Autism and Syndromic Intellectual Disability.." Am J Hum Genet.. 2019 Mar 7;104(3):530-541. Pubmed PMID: 30827496
- Benjamin Cogné, Sophie Ehresmann, Eliane Beauregard-Lacroix , Justine Rousseau, "et al" "Missense Variants in the Histone Acetyltransferase Complex Component Gene TRRAP Cause Autism and Syndromic Intellectual Disability.." Am J Hum Genet. 2019 Mar 7;104(3):530-541.. Pubmed PMID: 30827496
- Wat MJ, Beck TF, Hernández-García A, Yu Z, Veenma D, Garcia M, Holder AM, Wat JJ, Chen Y, Mohila CA, Lally KP, Dickinson M, Tibboel D, de Klein A, Lee B, Scott DA. "Mouse model reveals the role of SOX7 in the development of congenital diaphragmatic hernia associated with recurrent deletions of 8p23.1.." Hum Mol Genet.. 2012 Sep 15;21(18):4115-25..
- Beck TF, Shchelochkov OA, Yu Z, Kim BJ, Hernández-García A, Zaveri HP, Bishop C, Overbeek PA, Stockton DW, Justice MJ, Scott DA. "Novel frem1-related mouse phenotypes and evidence of genetic interactions with gata4 and slit3.." PLoS One.. 2013 Mar 11;8(3):Published online.
- Ken Saida, Tokiko Fukuda, Daryl A Scott, Toru Sengoku, Kazuhiro Ogata, Annarita Nicosia, Andres Hernandez-Garcia, Seema R Lalani, Mahshid S Azamian, “et al” "OTUD5 Variants Associated With X-Linked Intellectual Disability and Congenital Malformation." Front Cell Dev Biol. 2021 Mar 3;9(631428) Pubmed PMID: 33748114
- Tackett BC, Sun H, Mei Y, Maynard JP, Cheruvu S, Mani A, Hernandez-Garcia A, Vigneswaran N, Karpen SJ, Thevananther S. "P2Y2 purinergic receptor activation is essential for efficient hepatocyte proliferation in response to partial hepatectomy.." Am J Physiol Gastrointest Liver Physiol.. 2014 Dec 1;3007(11):1073-87.
- Sepúlveda J1, Gutiérrez F, Moreno M, Hernández A. "Peroxisomal proliferation induced by treatment with clofibrate in a patient with a peroxisomal disease.." Cell Biochem Biophys.. 2000;32:329-332.
- Narasimhaswamy S Belaguli · Mao Zhang · Andres-Hernandez Garcia · David H Berger "PIAS1 is a GATA4 SUMO ligase that regulates GATA4-dependent intestinal promoters independent of SUMO ligase activity and GATA4 sumoylation.." PLOS ONE. 2012 Apr;7(4):Published: Apri.
- Callaway DA1, Campbell IM2, Stover SR3, Hernandez-Garcia A3, Jhangiani SN3,4, Punetha J3, Paine IS3, Posey JE3, Muzny D3,4, Lally KP5, Lupski JR3,4,6, Shaw CA3, Fernandes CJ6, Scott DA3,7. "Prioritization of Candidate Genes for Congenital Diaphragmatic Hernia in a Critical Region on Chromosome 4p16 using a Machine-Learning Algorithm.." J Pediatr Genet.. 2018 Dec 7;4:164-173. Pubmed PMID: 30430034
- Kim BJ, Zaveri HP, Jordan VK, Hernandez-Garcia A, Jacob DJ, Zamora DL, Yu W, Schwartz RJ, Scott DA "RERE deficiency leads to decreased expression of GATA4 and the development of ventricular septal defects.." Dis Model Mech.. 2018 Aug 28;11(9):1-12. Pubmed PMID: 30061196
- Carrillo-Ponce Mde L, Martínez-Ordaz VA, Velasco-Rodríguez VM, Hernández-García A, Hernández-Serrano MC, Sanmiguel F. "Serum lead, cadmium, and zinc levels in newborns with neural tube defects from a polluted zone in Mexico.." Reprod Toxicol. 2004 Dec;19(2):149-54.
- Francesca Clementina Radio, Kaifang Pang, Andrea Ciolfi, Michael A Levy, Andrés Hernández-García, "et al" "SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females." Am J Hum Genet .. 2021 Mar 4;108(3):502-516. Pubmed PMID: 33596411
- Jordan VK, Beck TF, Hernandez-Garcia A, Kundert PN, Kim BJ, Jhangiani SN, Gambin T, Starkovich M, Punetha J, Paine IS, Posey JE, Li AH, Muzny D, Hsu CW, Lashua AJ, Sun X, Fernandes CJ, Dickinson ME, Lally KP, Gibbs RA, Boerwinkle E, Lupski JR, Scott DA. "The Role of FREM2 and FRAS1 in the Development of Congenital Diaphragmatic Hernia.." Hum Mol Genet. 2028 Jun 15;12:2064-2075. Pubmed PMID: 29618029
- Miyake CY, Ehsan SA, Zhang L, Mackenzie SJ, Azamian MS, Scott DA, Hernandez-Garcia A, Lalani SR. "Early initiation of B-vitamin supplementation may reduce symptoms and explain intrafamilial variability: Insights from two sibling pairs from the TANGO2 natural history study.." Am J Med Genet A .. 2023 Sep;191(9):2433-2439. Pubmed PMID: 37421366
- Florence Petit, Mauro Longoni, Andres Hernandez-Garcia , Hagith Yonath , James R Lupski , Yufeng Shen , Wendy K Chung , Daryl A Scott, Carol J Bult , Patricia K Donahoe , Frances A High "PLS3 missense variants affecting the actin-binding domains cause X-linked congenital diaphragmatic hernia and body-wall defects." Am J Hum Genet .. 2023 Oct 5;110(10):1787-1803. Pubmed PMID: 37751738
- Hernández-García A, Pendleton KE, Kim S, Li Y, Kim BJ, Zaveri HP, Jordan VK, Berry AM, Ljungberg MC, Chen R, Lanz RB, Scott DA. "SOX7 deficiency causes ventricular septal defects through its effects on endocardial-to-mesenchymal transition and the expression of Wnt4 and Bmp2.." Hum Mol Genet .. 2023 Jun 19;32(13):2152-2161. Pubmed PMID: 37000005
- Chiang IK, Humphrey D, Mills RJ, Kaltzis P, Pachauri S, Graus M, Saha D, Wu Z, Young P, Sim CB, Davidson T, Hernandez-Garcia A, Shaw CA, Renwick A, Scott DA, Porrello ER, Wong ES, Hudson JE, Red-Horse K, Del Monte-Nieto G, Francois M. "Sox7-positive endothelial progenitors establish coronary arteries and govern ventricular compaction.." EMBO Rep .. 2023 Oct 9;24(10):e55043. Pubmed PMID: 37551717
- Hardcastle A, Berry AM, Campbell IM, Zhao X, Liu P, Gerard AE, Rosenfeld JA, Sisoudiya SD, Hernandez-Garcia A, Shaw CA, Chung WK, Scott DA. "Identifying phenotypic expansions for congenital diaphragmatic hernia plus (CDH+) using DECIPHER data.." Am J Med Genet A .. 2022 Oct;188(10):2958-2968. Pubmed PMID: 35904974
Languages
Spanish
Log In to edit your profile
