{"id":330,"date":"2021-05-23T08:54:35","date_gmt":"2021-05-23T08:54:35","guid":{"rendered":"http:\/\/liigh.unam.mx\/cgonzagaj\/?page_id=330"},"modified":"2025-07-27T07:24:22","modified_gmt":"2025-07-27T07:24:22","slug":"cgonzagajauregui","status":"publish","type":"page","link":"https:\/\/liigh.unam.mx\/cgonzagaj\/index.php\/home\/cgonzagajauregui\/","title":{"rendered":"CLAUDIA GONZAGA-JAUREGUI, PHD"},"content":{"rendered":"\n<h4 class=\"wp-block-heading\"><strong>Principal Investigator | Investigadora, LIIGH, UNAM<\/strong><\/h4>\n\n\n<div class=\"wp-block-image\">\n<figure class=\"alignleft size-large is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"768\" height=\"1024\" src=\"https:\/\/liigh.unam.mx\/cgonzagaj\/wp-content\/uploads\/2021\/02\/Gonzaga-Jauregui_Picture2018_3_bw-3-768x1024.jpg\" alt=\"\" class=\"wp-image-214\" style=\"width:267px;height:355px\" srcset=\"https:\/\/liigh.unam.mx\/cgonzagaj\/wp-content\/uploads\/2021\/02\/Gonzaga-Jauregui_Picture2018_3_bw-3-768x1024.jpg 768w, https:\/\/liigh.unam.mx\/cgonzagaj\/wp-content\/uploads\/2021\/02\/Gonzaga-Jauregui_Picture2018_3_bw-3-225x300.jpg 225w, https:\/\/liigh.unam.mx\/cgonzagaj\/wp-content\/uploads\/2021\/02\/Gonzaga-Jauregui_Picture2018_3_bw-3-1152x1536.jpg 1152w, https:\/\/liigh.unam.mx\/cgonzagaj\/wp-content\/uploads\/2021\/02\/Gonzaga-Jauregui_Picture2018_3_bw-3-1536x2048.jpg 1536w, https:\/\/liigh.unam.mx\/cgonzagaj\/wp-content\/uploads\/2021\/02\/Gonzaga-Jauregui_Picture2018_3_bw-3-scaled.jpg 1920w\" sizes=\"(max-width: 768px) 100vw, 768px\" \/><figcaption class=\"wp-element-caption\"><strong>Email: <\/strong><em>cgonzaga[at]liigh.unam.mx<\/em><br><a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/?term=gonzaga-jauregui&amp;sort=date\" target=\"_blank\" rel=\"noreferrer noopener\"><strong>Publications | Publicaciones<\/strong><\/a><br><a href=\"https:\/\/www.researchgate.net\/profile\/Claudia_Gonzaga-Jauregui2\" target=\"_blank\" rel=\"noreferrer noopener\"><strong>ResearchGate<\/strong><\/a><strong> | <\/strong><a href=\"https:\/\/scholar.google.com\/citations?user=PG-qn38AAAAJ&amp;hl=en\" target=\"_blank\" rel=\"noreferrer noopener\"><strong>Google Scholar<\/strong><\/a><br><strong>Twitter: <\/strong><em>@cgonzagaj<\/em> &amp; @GonzagajMx<\/figcaption><\/figure><\/div>\n\n\n<p>Claudia grew up in Mexico where she did her undergraduate studies in Genomic Sciences at the National Autonomous University of Mexico (UNAM). She obtained her PhD in Molecular and Human Genetics from Baylor College of Medicine, where she contributed to large population genomic studies such as HapMap 3 and pioneered the analyses of genomic sequencing data for the identification of disease genes and molecular diagnoses. Since then her research has focused on the investigation of human pathogenic and polymorphic genomic variation that contributes to human traits and diseases.<\/p>\n\n\n\n<p>Her research focuses on family-based analyses of rare and common genetic disorders to identify pathogenic variation and novel genes associated with disease to better understand the molecular architectures and pathophysiology of genetic disorders. Claudia believes that the application and understanding of human genetics and genomics can lead to improved treatments and the realization of precision genomic medicine. Because the beginning of precision medicine is an accurate genetic diagnosis, Claudia has dedicated great part of her career to the study and identification of novel genes responsible for rare genetic disorders to provide molecular answers to patients with undiagnosed diseases. She has co-authored and co-edited the first text book focused on the application of genomic approaches to the study of rare genetic diseases.<\/p>\n\n\n\n<p>Read more about the release of <strong><em>&#8220;Genomics of Rare Diseases: Understanding Disease Genetics Using Genomic Approaches&#8221;<\/em><\/strong> <a href=\"https:\/\/liigh.unam.mx\/cgonzagaj\/index.php\/news\/\" target=\"_blank\" rel=\"noreferrer noopener\">here<\/a>.<\/p>\n\n\n\n<p>Claudia is also a passionate advocate for science education and literacy. She participates in her &#8220;spare time&#8221; in educational and science outreach activities such as DNA Day, Skype a Scientist, and ASHG outreach activities to inspire new generations of students to pursue careers in science, especially girls and young female students. Read more about Dr. Gonzaga-Jauregui&#8217;s work in science education and outreach <a rel=\"noreferrer noopener\" href=\"https:\/\/www.ashg.org\/careers-learning\/career-interviews\/get-to-know-claudia-gonzaga-jauregui\/\" target=\"_blank\">here<\/a>.<\/p>\n\n\n\n<hr class=\"wp-block-separator has-text-color has-background is-style-wide\" style=\"background-color:#2f0840;color:#2f0840\"\/>\n\n\n\n<p>La Dra. Claudia Gonzaga J\u00e1uregui es originaria de la Ciudad de M\u00e9xico. Estudi\u00f3 la Licenciatura en Ciencias Gen\u00f3micas (LCG) de la Universidad Nacional Aut\u00f3noma de M\u00e9xico (UNAM). Posteriormente realiz\u00f3 sus estudios de doctorado en Gen\u00e9tica Molecular y Humana en el Baylor College of Medicine en Houston, Texas, Estados Unidos donde contribuy\u00f3 a estudios de variaci\u00f3n en poblaciones del mundo a trav\u00e9s del proyecto HapMap 3, as\u00ed como varios otros estudios relacionados a enfermedades Mendelianas. Claudia ha sido pionera en la implementaci\u00f3n y an\u00e1lisis de abordajes gen\u00f3micos para el estudio de enfermedades gen\u00e9ticas, mediante los cuales ha identificado y publicado m\u00e1s de 20 genes asociados a enfermedades raras no identificadas previamente. La Dra. Gonzaga-Jauregui es Investigadora Nacional Nivel I del SNI, CONACYT.<\/p>\n\n\n\n<p>Claudia tambi\u00e9n participa activamente en actividades de educaci\u00f3n y difusi\u00f3n de la ciencia en Estados Unidos y M\u00e9xico. Ella es miembro fundador de M\u00e1s Ciencia Por M\u00e9xico, una organizaci\u00f3n civil enfocada en promover el conocimiento y avance de la ciencia en sus diferentes \u00e1reas. Tambi\u00e9n participa en actividades de difusi\u00f3n como el concurso de ensayo con motivo del D\u00eda del ADN y da pl\u00e1ticas vocacionales a estudiantes interesados en carreras en ciencias biom\u00e9dicas.<\/p>\n\n\n\n<hr class=\"wp-block-separator has-text-color has-background is-style-wide\" style=\"background-color:#2f0840;color:#2f0840\"\/>\n\n\n\n<h4 class=\"wp-block-heading\"><strong><strong>Publication Highlights<\/strong> | <strong>Art\u00edculos Cient\u00edficos de Inter\u00e9s<\/strong>:<\/strong><\/h4>\n\n\n\n<ul>\n<li>Miller BR*, <strong>Gonzaga-Jauregui C*<\/strong>, Brigatti KW*, de Jong J, Breese RS, Ko SY, Puffenberger EG, Van Hout C, et al. A rare variant in GPR156 associated with depression in a Mennonite pedigree causes habenula hyperactivity and stress sensitivity in mice. <em>PNAS<\/em>. 2025. PMID: <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/40228124\/\">40228124<\/a>.<\/li>\n\n\n\n<li>Flores-Ocampo V, Lim AW-Y, Ogonowski NS, Garc\u00eda-Mar\u00edn LM, Ong J-S, Yeow D, <strong>Gonzaga-Jauregui C<\/strong>, Kumar KR, Renter\u00eda ME. Population-Specific Differences in Pathogenic Variants of Genes Associated with Monogenic Parkinson\u2019s Disease. <em>Genes<\/em>. 2025. PMID:\u00a0<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/40282414\/\">40282414<\/a>.<\/li>\n\n\n\n<li>Fernandez-Luna L, Aguilar-Perez C, Grochowski CM, Mehaffey M, Carvalho CMB, <strong>Gonzaga-Jauregui C<\/strong>. Genome-wide maps of highly-similar intrachromosomal repeats that can mediate ectopic recombination in three human genome assemblies. <em>HGG Adv. <\/em>2025. PMID: <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/39722459\/\">39722459<\/a>.<\/li>\n\n\n\n<li>Calvo-Aspiros CE, <strong>Gonzaga-Jauregui C<\/strong>, First year results and insights from the Mexican Rare Disease Patient Registry. <em>Rare<\/em>. 2024; <a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S2950008724000292\">100046<\/a>.<\/li>\n\n\n\n<li><strong>Gonzaga-Jauregui C<\/strong>, Moreno-Salgado R, Tovar-Casas J, Navarrete-Mart\u00ednez JI. Newborn screening in Mexico and Latin America: present and future. <em>Rare Dis Orphan Drugs J<\/em> 2024; <a href=\"https:\/\/www.oaepublish.com\/articles\/rdodj.2024.02\">3:23<\/a>.<\/li>\n\n\n\n<li>Liu Z, Xin B, Smith IN, Sency V, [&#8230;], <strong>Gonzaga-Jauregui C*<\/strong>, Zhang B*, Wang H*. Hemizygous variants in protein phosphatase 1 regulatory subunit 3F (PPP1R3F) are associated with a neurodevelopmental disorder characterized by developmental delay, intellectual disability, and autistic features. <em>Hum Mol Genet.<\/em> 2023. PMID: <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/37531237\/\">37531237<\/a>.<\/li>\n\n\n\n<li>Novembre J, Stein C, Asgari S, <strong>Gonzaga-Jauregui C<\/strong>, Landstrom A, Lemke A, Li J, Mighton C, Taylor M, Tishkoff S. Addressing the challenges of polygenic scores in human genetic research. <em>Am J Hum Genet.<\/em> 2022. PMID: <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/36459976\/\" target=\"_blank\" rel=\"noreferrer noopener\">36459976<\/a>.<\/li>\n\n\n\n<li>Lemke AA, Esplin ED, Goldenberg AJ, <strong>Gonzaga-Jauregui C<\/strong>, Hanchard NA, et al. Addressing underrepresentation in genomics research through community engagement. <em>Am J Hum Genet.<\/em> 2022. PMID: <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/36055208\/\" target=\"_blank\" rel=\"noreferrer noopener\">36055208<\/a>.<\/li>\n\n\n\n<li>Kurolap A, Kreuder F, <strong>Gonzaga-Jauregui C<\/strong>, Duvdevani MP, Harel T, et al. Bi-allelic variants in neuronal cell adhesion molecule cause a neurodevelopmental disorder characterized by developmental delay, hypotonia, neuropathy\/spasticity. <em>Am J Hum Genet. <\/em>2022. PMID: <a rel=\"noreferrer noopener\" href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/35108495\/\" target=\"_blank\">35108495<\/a>.<\/li>\n\n\n\n<li>Salzer-Sheelo L, Fellner A, Orenstein N, Bazak L, Lev-El Halabi N, [&#8230;], <strong>Gonzaga-Jauregui C<\/strong>, Basel-Salmon L. Biallelic truncating variants in the muscular A-type lamin-interacting protein (MLIP) gene cause myopathy with hyperCKemia. <em>Am J Hum Genet<\/em>. 2022. PMID: <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/34935254\/\" target=\"_blank\" rel=\"noreferrer noopener\">34935254<\/a>.<\/li>\n\n\n\n<li>Lynch MT, Maloney KA, Pollin TI, Streeten EA, Xu H; [&#8230;], <strong>Gonzaga-Jauregui C<\/strong>, Mitchell BD. The burden of pathogenic variants in clinically actionable genes in a founder population. <em>Am J Med Genet A. <\/em>2021. PMID: <a rel=\"noreferrer noopener\" href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/34467620\/\" target=\"_blank\">34467620<\/a>.<\/li>\n\n\n\n<li>Horowitz J, Warner N, Staples J, Crowley E, Gosalia N, [&#8230;], Muise A, <strong>Gonzaga-Jauregui C<\/strong>. Mutation spectrum of <em>NOD2<\/em> reveals recessive inheritance as a main driver of Early Onset Crohn\u2019s Disease. <em>Scientific Reports<\/em>. 2021. PMID: <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/33692434\/\" target=\"_blank\" rel=\"noreferrer noopener\">33692434<\/a>.<\/li>\n\n\n\n<li>Nistala H, Dronzek J, <strong>Gonzaga-Jauregui C<\/strong>, Chim SM, Rajamani S, et al. NMIHBA results from hypomorphic PRUNE1 variants that lack short-chain exopolyphosphatase activity. <em>Hum Mol Genet<\/em>. 2021. PMID: <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/33105479\/\" target=\"_blank\" rel=\"noreferrer noopener\">33105479<\/a>.<\/li>\n\n\n\n<li><strong>Gonzaga-Jauregui C<\/strong>, Yesil G, Nistala H, Gezdirici A, Bayram Y, Nannuru KC, [&#8230;], Lupski JR*. Functional biology of the Steel syndrome founder allele and evidence for clan genomics derivation of <em>COL27A1<\/em> pathogenic alleles worldwide. <em>Eur J Hum Genet.<\/em> 2020; 28(9). PMID: <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/32376988\/\" target=\"_blank\" rel=\"noreferrer noopener\">32376988<\/a>.<\/li>\n\n\n\n<li><strong>Gonzaga-Jauregui<\/strong> <strong>C<\/strong>, Ge W, Staples J, Van Hout C, Yadav A, et al. Clinical and Molecular Prevalence of Lipodystrophy in an Unascertained Large Clinical Care Cohort. <em>Diabetes<\/em>. 2020. PMID: <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/31836692\/\" target=\"_blank\" rel=\"noreferrer noopener\">31836692<\/a>.<\/li>\n\n\n\n<li>Horn S, Au M, Basel-Salmon L, Bayrak-Toydemir P, Chapin A, Cohen L, Elting MW, Graham JM, <strong>Gonzaga-Jauregui<\/strong> <strong>C<\/strong>, Konen O, et al. <em><u>De novo<\/u><\/em> variants in PAK1 lead to intellectual disability with macrocephaly and seizures. <em>Brain<\/em>. 2019. PMID: <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/31504246\/\" target=\"_blank\" rel=\"noreferrer noopener\">31504246<\/a>.<\/li>\n\n\n\n<li>Bend R, Cohen L, Carter MT, Lyons MJ, Niyazov D, [&#8230;], Ferreira CR, <strong>Gonzaga-Jauregui<\/strong> <strong>C<\/strong>. Phenotype and mutation expansion of the PTPN23 associated disorder characterized by neurodevelopmental delay and structural brain abnormalities. <em>Eur J Hum Genet.<\/em> 2020. PMID: <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/31395947\/\" target=\"_blank\" rel=\"noreferrer noopener\">31395947<\/a>.<\/li>\n\n\n\n<li>Zhu N*, <strong>Gonzaga-Jauregui C*<\/strong>, Welch CL*, Ma L, Qi H, King AK, Krishnan U, Rosenzweig EB, Ivy DD, Austin ED, et al. Exome Sequencing in Children With Pulmonary Arterial Hypertension Demonstrates Differences Compared With Adults. <em>Circ Genom Precis Med.<\/em> 2018. PMID: <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/29631995\/\" target=\"_blank\" rel=\"noreferrer noopener\">29631995<\/a>.<\/li>\n\n\n\n<li>Tan TY, <strong>Gonzaga-Jauregui<\/strong> C, Bhoj EJ, Strauss KA, Brigatti K, et al. Monoallelic <em>BMP2<\/em> Variants Predicted to Result in Haploinsufficiency Cause Craniofacial, Skeletal, and Cardiac Features Overlapping Those of 20p12 Deletions. <em>Am J Hum Genet.<\/em> 2017. PMID: <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/29198724\/\" target=\"_blank\" rel=\"noreferrer noopener\">29198724<\/a>.<\/li>\n\n\n\n<li>Strauss KA, <strong>Gonzaga-Jauregui C<\/strong>, Brigatti KW, Williams KB, King AK, Van Hout C, [&#8230;], Shuldiner AR, Puffenberger EG. Genomic diagnostics within a medically underserved population: efficacy and implications. <em>Genet Med. <\/em>2018. PMID: <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/28726809\/\" target=\"_blank\" rel=\"noreferrer noopener\">28726809<\/a>.<\/li>\n\n\n\n<li><strong>Gonzaga-Jauregui C<\/strong>, Harel T, Gambin T, Kousi M, Griffin LB, Francescatto L, Ozes B, Karaca E, [&#8230;], Gibbs RA, Lupski JR. Exome Sequence Analysis Suggests that Genetic Burden Contributes to Phenotypic Variability and Complex Neuropathy, <em>Cell Rep. <\/em>2015. PMID:\u00a0<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/26257172\/\" target=\"_blank\" rel=\"noreferrer noopener\">26257172<\/a>.<\/li>\n\n\n\n<li><strong>Gonzaga-Jauregui C<\/strong>, Gamble CN, Yuan B, Penney S, Jhangiani S, Muzny DM, Gibbs RA, Lupski JR, Hecht JT. Mutations in <em>COL27A1<\/em> cause Steel syndrome and suggest a founder mutation effect in the Puerto Rican population. <em>Eur J Hum Genet.<\/em> 2014. PMID: <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/24986830\/\" target=\"_blank\" rel=\"noreferrer noopener\">24986830<\/a>.<\/li>\n\n\n\n<li><strong>Gonzaga-Jauregui C<\/strong>, Lupski JR, Gibbs RA; Human genome sequencing in health and disease, <em>Annual Review of Medicine<\/em>, 2012. PMID: <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/22248320\/\" target=\"_blank\" rel=\"noreferrer noopener\">22248320<\/a>.<\/li>\n\n\n\n<li>Lupski, JR, Reid JG,\u00a0 <strong>Gonzaga-Jauregui C<\/strong>, Deiros DR, Chen D, [&#8230;], Gibbs RA; Whole-Genome Sequencing in a Patient with Charcot-Marie-Tooth Neuropathy, <em>The New England Journal of Medicine<\/em>, 2010. PMID: <a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/20220177\/\" target=\"_blank\" rel=\"noreferrer noopener\">20220177<\/a>.<\/li>\n<\/ul>\n\n\n\n<p>Full list of publications <a rel=\"noreferrer noopener\" href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/?term=gonzaga-jauregui&amp;sort=date\" target=\"_blank\">here<\/a> | Lista completa de publicaciones <a rel=\"noreferrer noopener\" href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/?term=gonzaga-jauregui&amp;sort=date\" target=\"_blank\">aqu\u00ed<\/a>.<\/p>\n\n\n\n<hr class=\"wp-block-separator has-text-color has-background is-style-wide\" style=\"background-color:#2f0840;color:#2f0840\"\/>\n\n\n\n<p><strong>Interviews and Science Outreach | Entrevistas y Divulgaci\u00f3n de la Ciencia:<\/strong><\/p>\n\n\n\n<ul>\n<li><a href=\"https:\/\/lalupa.mx\/2025\/03\/09\/la-importancia-de-la-atencion-a-enfermedades-raras-en-mexico-y-el-mundo-claudia-gonzaga-jauregui\/\">\u201cLa importancia de la atenci\u00f3n a enfermedades raras en M\u00e9xico y el mundo\u201d<\/a>, La Lupa, 2025.<\/li>\n\n\n\n<li><a href=\"https:\/\/www.gaceta.unam.mx\/la-unam-impulsa-el-estudio-de-enfermedades-raras-en-mexico\/\">\u201cLa UNAM impulsa el estudio de enfermedades raras en M\u00e9xico\u201d<\/a>, Gaceta UNAM, 2025.<\/li>\n\n\n\n<li><a href=\"https:\/\/www.science.org\/content\/article\/rare-disease-initiative-aims-speed-diagnoses-and-treatment-latin-america\">\u201cRare disease initiative aims to speed diagnoses and treatment in Latin America\u201d<\/a>, Science Magazine, 2024.<\/li>\n\n\n\n<li><a href=\"https:\/\/www.neb.com\/en\/nebinspired-blog\/genomes-without-borders-bridging-gaps-in-health-equity\">\u201cGenomes Without Borders: Bridging Gaps in Health Equity\u201d<\/a>, NEB Inspired Blog, 2024.<\/li>\n\n\n\n<li><a href=\"https:\/\/www.neb.com\/en-us\/podcasts\/podcast-61-interview-with-claudia-gonzaga-jauregui\">&#8220;Molecular Diagnostic and Precision Medicine access in Mexico and Latin America&#8221;<\/a>. NEB Podcast Lessons from Lab and Life, Episode 61, 2024.<\/li>\n\n\n\n<li><a href=\"https:\/\/www.eluniversalqueretaro.mx\/nuestras-historias\/investigadora-de-la-unam-juriquilla-trabaja-con-la-genetica-para-estudiar-enfermedades-raras\/\">\u201cInvestigadora de la UNAM Juriquilla trabaja con la gen\u00e9tica para estudiar enfermedades raras\u201d<\/a>, El Universal Quer\u00e9taro, 2023.<\/li>\n\n\n\n<li><a href=\"https:\/\/podcasters.spotify.com\/pod\/show\/glycocast\/episodes\/Diagnostic-challenges-of-rare-disorders-in-Latin-America-e2an5vs\" target=\"_blank\" rel=\"noreferrer noopener\">\u201cDiagnostic Challenges of Rare Disorders in Latin America\u201d<\/a>. GlycoCast Podcast, 2023.<\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/effieparks.com\/podcast\/episode-193-claudia-gonzaga-jauregui\" target=\"_blank\">Once Upon A Gene Podcast: Episode 193<\/a>. Rare Diseases Podcast with Effie Parks, 2023.<\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/www.youtube.com\/watch?v=K-yaa8riOvM\" target=\"_blank\">\u201cEnfermedades Raras: Importancia del Diagn\u00f3stico Molecular de Pacientes con Enfermedades Raras y Poco Frecuentes en M\u00e9xico\u201d<\/a>. Programa \u201cSalud con los Expertos\u201d, Iniciativa Pensemos Cebras M\u00e9xico, 2023.<\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/shows.acast.com\/de-chicharos-y-habas-conversaciones-en-genetica-humana\/episodes\/reduciendo-la-subrepresentacion-de-poblaciones-no-europeas-e\" target=\"_blank\">\u201cReduciendo la subrepresentaci\u00f3n de poblaciones no europeas en estudios gen\u00f3micos\u201d<\/a>. <em>De Ch\u00edcharos y Habas: Conversaciones en Gen\u00e9tica Humana<\/em>. Podcast, 2022.<\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/www.elnorte.com\/buscan-registrar-a-pacientes-con-males-raros\/ar2511767\" target=\"_blank\">&#8220;Buscan registrar a pacientes con males raros&#8221;<\/a>, Diario El Norte, 2022.<\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/www.biotechniques.com\/whole-genome-studies\/identifying-the-molecular-cause-of-rare-genetic-disorders\/\" target=\"_blank\">&#8220;Identifying the molecular cause of rare genetic disorders&#8221;<\/a>, BioTechniques, 2022. <\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/www.wilsoncenter.org\/article\/normalizing-rarity-awakening-rare-diseases-latin-america\" target=\"_blank\">&#8220;Normalizing Rarity: The Awakening of Rare Diseases in Latin America&#8221;<\/a>, Wilson Center, 2022.<\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/youtu.be\/WH3JZdhWmqI\" target=\"_blank\">&#8220;The Awakening of Rare Diseases in Latin America&#8221;<\/a>, Wilson Center, 2022.<\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/www.statnews.com\/2022\/08\/11\/oxford-mexican-research-team-diversify-genomic-databases\/\" target=\"_blank\">&#8220;A team of Oxford and Mexican researchers want to diversify genomic databases. Can they end \u2018parachute science,\u2019 too?&#8221;<\/a>, STAT News, 2022.<\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/theprogressnetwork.org\/human-genome\/\" target=\"_blank\">&#8220;We have the first fully complete human genome. So what?&#8221;<\/a>, The Progress Network, 2022.<\/li>\n<\/ul>\n\n\n\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Principal Investigator | Investigadora, LIIGH, UNAM Claudia grew up in Mexico where she did her undergraduate studies in Genomic Sciences at the National Autonomous University of Mexico (UNAM). She obtained her PhD in Molecular and Human Genetics from Baylor College of Medicine, where she contributed to large population genomic studies such as HapMap 3 and &hellip;<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":187,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"_links":{"self":[{"href":"https:\/\/liigh.unam.mx\/cgonzagaj\/index.php\/wp-json\/wp\/v2\/pages\/330"}],"collection":[{"href":"https:\/\/liigh.unam.mx\/cgonzagaj\/index.php\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/liigh.unam.mx\/cgonzagaj\/index.php\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/liigh.unam.mx\/cgonzagaj\/index.php\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/liigh.unam.mx\/cgonzagaj\/index.php\/wp-json\/wp\/v2\/comments?post=330"}],"version-history":[{"count":27,"href":"https:\/\/liigh.unam.mx\/cgonzagaj\/index.php\/wp-json\/wp\/v2\/pages\/330\/revisions"}],"predecessor-version":[{"id":565,"href":"https:\/\/liigh.unam.mx\/cgonzagaj\/index.php\/wp-json\/wp\/v2\/pages\/330\/revisions\/565"}],"up":[{"embeddable":true,"href":"https:\/\/liigh.unam.mx\/cgonzagaj\/index.php\/wp-json\/wp\/v2\/pages\/187"}],"wp:attachment":[{"href":"https:\/\/liigh.unam.mx\/cgonzagaj\/index.php\/wp-json\/wp\/v2\/media?parent=330"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}