Genomics is failing on diversity

Cited by (1,002)

Items 601–700 of 1,002

  1. Advancing psychiatric genetics through dissecting heterogeneity
    Karen Hodgson, Peter McGuffin, Cathryn M. Lewis · 2017 · Human Molecular Genetics
  2. Application of the ConNECT Framework to Precision Health and Health Disparities
    Usha Menon, Kimlin Tam Ashing, Mei Chang, Shannon M. Christy, Katarina Friberg Felsted, Virginia Gil Rivas, Clement K. Gwede, Qian Lü, Cathy D. Meade, Jamila Sly et al. · 2018 · Nursing Research
  3. Programmable multi-kilobase RNA editing using CRISPR-mediated trans-splicing
    Jacob de Riba Borrajo, Kamyab Javanmardi, James Griffin, Susan J. St. Martin, David Yao, Kaisle A. Hill, Paul C. Blainey, Basem Al-Shayeb · 2023 · bioRxiv (Cold Spring Harbor Laboratory)
  4. Signals in the Cells: Multimodal and Contextualized Machine Learning Foundations for Therapeutics
    Alejandro Velez-Arce, Xiang Lin, Michelle M. Li, Kexin Huang, Wenhao Gao, Tianfan Fu, Bradley L. Pentelute, M Kellis, Marinka Žitnik · 2024 · bioRxiv (Cold Spring Harbor Laboratory)
  5. The systematic assessment of completeness of public metadata accompanying omics studies in the Gene Expression Omnibus data repository
    Yu-Ning Huang, Pooja Jaiswal, Anushka Rajes, Anushka Yadav, Dottie Yu, Fangyun Liu, Grace Scheg, Emma Shih, Grigore Boldirev, Irina Nakashidze et al. · 2025 · Genome biology
  6. GWAS of QRS duration identifies new loci specific to Hispanic/Latino populations
    Brenton R. Swenson, Tin Louie, Henry J. Lin, Raúl Méndez-Giráldez, Jennifer Elizabeth Below, Cathy C. Laurie, Kathleen F. Kerr, Heather M. Highland, Timothy A. Thornton, Kelli K. Ryckman et al. · 2019 · PLoS ONE
  7. Base Editing in Human Cells to Produce Single‐Nucleotide‐Variant Clonal Cell Lines
    Carlos A. Vásquez, Quinn T. Cowan, Alexis C. Komor · 2020 · Current Protocols in Molecular Biology
  8. Towards equitable genomics governance in Africa: Guiding principles from theories of global health governance and the African moral theory of Ubuntu
    Nchangwi Syntia Munung, Jantina de Vries, Bridget Pratt · 2022 · Bioethics
  9. Clinical Decision Support for Precision Dosing: Opportunities for Enhanced Equity and Inclusion in Health Care
    Jasmine H. Hughes, Kara Woo, Ron J. Keizer, Srijib Goswami · 2022 · Clinical Pharmacology & Therapeutics
  10. Elective genomic testing: Practice resource of the National Society of Genetic Counselors
    Carrie L. Blout Zawatsky, David P Bick, Louise Bier, Birgit Funke, Matthew S. Lebo, Katie L. Lewis, Ekaterina Orlova, Emily Qian, Lauren A. Ryan, Marci L. B. Schwartz et al. · 2023 · Journal of Genetic Counseling
  11. Fast, accurate, and racially unbiased pan-cancer tumor-only variant calling with tabular machine learning
    Robert T. McLaughlin, Maansi Asthana, Marc A. Di Meo, Michele Ceccarelli, Howard J. Jacob, David L. Masica · 2023 · npj Precision Oncology
  12. Genome-wide Association Study for AKI
    Pavan K. Bhatraju, Ian B. Stanaway, Melody R. Palmer, Rajasree Menon, Jennifer A. Schaub, Steven P. Menez, Anand Srivastava, F. Perry Wilson, Krzysztof Kiryluk, Paul M. Palevsky et al. · 2023 · Kidney360
  13. Observational Data for Integrated Maternity Care: Experiences with a Data-Infrastructure for Parents and Children in the Netherlands
    Zoë T. M. Scheefhals, Eline Frouke de Vries, Joyce M. Molenaar, Mattijs Everard Numans, Jeroen Nathan Struijs · 2023 · International Journal of Integrated Care
  14. Towards precision nephrology: the opportunities and challenges of genomic medicine
    Jordan Gabriela Nestor, Emily Groopman, Ali G. Gharavi · 2017 · Journal of Nephrology
  15. Genetic components of human pain sensitivity: a protocol for a genome-wide association study of experimental pain in healthy volunteers
    Annina B. Schmid, Kaustubh Adhikari, Luis Miguel Ramírez, Juan Camilo Chacón-Duque, Giovanni Poletti, Carla Gallo, Francisco Rothhammer, Gabriel Bedoya, Andrés Ruiz‐Linares, David Bennett · 2019 · BMJ Open
  16. Systems Genetics for Mechanistic Discovery in Heart Diseases
    Christoph D. Rau, Aldons Jake Lusis, Yibin Wang · 2020 · Circulation Research
  17. Identifying novel genetic variants for brain amyloid deposition: a genome-wide association study in the Korean population
    Hang-Rai Kim, Sang-Hyuk Jung, Jaeho Kim, Sung Hoon Kang, Sung Hoon Kang, Song Hwangbo, Jun Pyo Kim, Beomsu Kim, Soyeon Kim, Soyeon Kim et al. · 2021 · Alzheimer s Research & Therapy
  18. Effect of Race and Ethnicity on Risk of Radiotherapy Toxicity and Implications for Radiogenomics
    Omneya Abdelkarem, Ananya Choudhury, N.G. Burnet, Holly R. Summersgill, Catharine West · 2022 · Clinical Oncology
  19. Strengthening Causal Inference in Exposomics Research: Application of Genetic Data and Methods
    Christy L. Avery, Annie Green Howard, Anna F Ballou, Victoria L. Buchanan, Jason M. Collins, Carolina G Downie, Stephanie Mulherin Engel, Mariaelisa Graff, Heather M. Highland, Moa P. Lee et al. · 2022 · Environmental Health Perspectives
  20. Psychiatric genomics, mental health equity, and intersectionality: A framework for research and practice
    Julia E. H. Brown, Jennifer L. Young, Nicole Martinez‐Martin · 2022 · Frontiers in Psychiatry
  21. Advancement in Human Face Prediction Using DNA
    Aamer Alshehhi, Aliya Almarzooqi, Khadija Alhammadi, Naoufel Werghi, Guan K. Tay, Habiba S. AlSafar · 2023 · Genes
  22. Genome-wide association study of heart rate and its variability in Hispanic/Latino cohorts
    Kathleen F. Kerr, Christy L. Avery, Henry J. Lin, Laura M. Raffield, Qian S. Zhang, Brian L. Browning, Sharon R. Browning, Matthew P. Conomos, Stephanie M. Gogarten, Cathy C. Laurie et al. · 2017 · Heart Rhythm
  23. Evaluation of the cost and effectiveness of diverse recruitment methods for a genetic screening study
    Hila Milo Rasouly, Julia Wynn, Maddalena Marasà, Rachel E. Reingold, Debanjana Chatterjee, Sheena Kapoor, Stacy E. Piva, Byum Hee Kil, Xueru Mu, Maria C. Alvarez et al. · 2019 · Genetics in Medicine
  24. Genomics of rare diseases in the Greater Middle East
    Ikram Chekroun, Shruti Shenbagam, Mohamed A. Almarri, Younes Mokrab, Mohammed J. Uddin, Omer S. Alkhnbashi, Maha Saad Zaki, Hossein Najmabadi, Kimia Kahrizi, Khalid Adnan Fakhro et al. · 2025 · Nature Genetics
  25. Enrichment analyses identify shared associations for 25 quantitative traits in over 600,000 individuals from seven diverse ancestries
    Samuel Pattillo Smith, Sahar Shahamatdar, Wei Cheng, Selena Zhang, Joseph Paik, Mariaelisa Graff, Christopher A. Haiman, Tara Cox Matise, Kari E. North, Ulrike Peters et al. · 2022 · The American Journal of Human Genetics
  26. Evaluating the Generalizability and Reproducibility of Scientific Research
    Sue Sun Yom, Curtiland Deville, Marjan Boerma, David J. Carlson, Salma K. Jabbour, Lisa C. Braverman · 2022 · International Journal of Radiation Oncology*Biology*Physics
  27. Bioinformatic Challenges Detecting Genetic Variation in Precision Medicine Programs
    Matthew A. Field · 2022 · Frontiers in Medicine
  28. Somatic targeted mutation profiling of colorectal cancer precursor lesions
    Wellington dos Santos, Mariana Bisarro dos Reis, Jun Porto, Ana Carolina de Carvalho, Marcus Matsushita, Gabriela da Silva Oliveira, Kari Juhani Syrjänen, Rui Manuel Reis, Denise Peixoto Guimarães · 2022 · BMC Medical Genomics
  29. Population Genetics of the European Roma—A Review
    Giacomo Francesco Ena, Julen Aizpurua-Iraola, Neus Font‐Porterias, Francesc Calafell, David Comas · 2022 · Genes
  30. Feasibility of preemptive pharmacogenetic testing and improvement of medication treatment satisfaction among medically underserved patients
    Christelle Lteif, Elizabeth Eddy, Joshua Terrell, Larisa H. Cavallari, John Z. Malaty, Julio D. Duarte · 2023 · Clinical and Translational Science
  31. To weight or not to weight? The effect of selection bias in 3 large electronic health record-linked biobanks and recommendations for practice
    Maxwell Salvatore, Ritoban Kundu, Xu Shi, Christopher Ryan Friese, Seunggeun Lee, Lars G. Fritsche, Alison M. Mondul, David A. Hanauer, Celeste Leigh Pearce, Bhramar Mukherjee · 2024 · Journal of the American Medical Informatics Association
  32. Association Study Confirmed Three Breast Cancer-Specific Molecular Subtype-Associated Susceptibility Loci in Chinese Han Women
    Yihui Xu, Mengyun Chen, Chenchen Liu, Xiaowei Zhang, Wei Li, Huaidong Cheng, Jun Wei Zhu, Mingjun Zhang, Zhendong Chen, Bo Zhang · 2017 · The Oncologist
  33. Genetic Knowledge within a National Australian Sample: Comparisons with Other Diverse Populations
    Ilan Dar‐Nimrod, Georgia MacNevin, Alexandra Godwin, Kate E. Lynch, Tali Magory Cohen, Asha Ganesan, James S. Morandini · 2018 · Public Health Genomics
  34. Ethical and Legal Considerations for the Inclusion of Underserved and Underrepresented Immigrant Populations in Precision Health and Genomic Research in the United States
    Jennifer K. Wagner · 2019 · Ethnicity & Disease
  35. Recruiting diversity where it exists: The Alabama Genomic Health Initiative
    Thomas May, Ashley D. Cannon, Irene Moss, Mariko Nakano‐Okuno, Sharonda Hardy, Edrika L. Miskell, Whitley V. Kelley, William A. Curry, Kelly M. East, Aras Acemgil et al. · 2020 · Journal of Genetic Counseling
  36. How Can Law and Policy Advance Quality in Genomic Analysis and Interpretation for Clinical Care?
    Barbara J. Evans, Gail H. Javitt, Ralph Hall, Megan Robertson, Pilar N. Ossorio, Susan M. Wolf, Thomas M. Morgan, Ellen Wright Clayton, for the LawSeq Quality Task Force · 2020 · The Journal of Law Medicine & Ethics
  37. Minding the gap in HIV host genetics: opportunities and challenges
    Shanelle N. Gingras, David Tang, Jeffrey F. Tuff, Paul J. McLaren · 2020 · Human Genetics
  38. Genetic Diversity and Low Stratification of the Population of the United Arab Emirates
    Guan K. Tay, Andreas Henschel, Gihan Daw Elbait, Habiba S. AlSafar · 2020 · Frontiers in Genetics
  39. How biased is our validation (data) for AS relationships?
    Lars Prehn, Anja Feldmann · 2021 · ACM Internet Measurement Conference (IMC)
  40. Looking back and thinking forwards — 15 years of cardiology and cardiovascular research
    Jonathan M. Kalman, Sergio Lavandero, Felix Mahfoud, Matthias Nahrendorf, Magdi Habib Yacoub, Dong Hui Zhao · 2019 · Nature Reviews Cardiology
  41. Reinventing Neuroaging Research in the Digital Age
    Matthew J. Huentelman, Joshua S. Talboom, Candace R. Lewis, Zhao Chen, Carol Ann Barnes · 2019 · Trends in Neurosciences
  42. The practical utility of genetic screening in school settings
    Jeffrey A. Shero, Wilhelmina van Dijk, Ashley A. Edwards, Christopher W. Schatschneider, Emily Jane Solari, Sara Ann Hart · 2021 · npj Science of Learning
  43. Vitamin D levels, brain volume, and genetic architecture in patients with psychosis
    Akiah Ottesen Berg, Kjetil Nordbø Jørgensen, Mari Nerhus, Lavinia Athanasiu, Alice B. Popejoy, Francesco Bettella, Linn Bonaventure Norbom, Tiril Pedersen Gurholt, Sandra Rinne Dahl, Ole A. Andreassen et al. · 2018 · PLoS ONE
  44. Human Genetics and Genomics in South Africa: Ethical, Legal and Social Implications
    Academy of Science of South Africa, Department of Science and Technology · 2018
  45. Indigenous Data Sovereignty in Genomics and Human Genetics: Genomic Equity and Justice for Indigenous Peoples
    Nicole Britney Halmai, Riley I. Taitingfong, Lydia L. Jennings, Joseph Yracheta, Ibrahim Garba, Justin R. Lund, Caleigh A. Curley, Katrina G. Claw, Maile M. Taualii, Nanibaa’ A. Garrison et al. · 2025 · Annual Review of Genomics and Human Genetics
  46. The Consortium for Genomic Diversity, Ancestry, and Health in Colombia (CÓDIGO): building local capacity in genomics and bioinformatics
    Leonardo Mariño‐Ramírez, Shivam Sharma, James Matthew Hamilton, Thanh Long Nguyen, Sonali A. Gupta, Aravinth Venkatesh Natarajan, Shashwat Deepali Nagar, Jay Landon Menuey, Wei‐An Chen, Adalberto Sánchez et al. · 2025 · Communications Biology
  47. Philanthrocapitalism and Global Health
    James Wilson · 2021 · Cambridge University Press eBooks
  48. African Global Representation in Biomedical Sciences
    Nicola Mulder, Lyndon J. Zass, Yosr Hamdi, Houcemeddine Othman, Sumir Panji, Imane Allali, Yasmina Jaufeerally Fakim · 2021 · Annual Review of Biomedical Data Science
  49. The genetic and evolutionary basis of gene expression variation in East Africans
    Derek E. Kelly, Shweta Ramdas, Rong Ma, Renata Rawlings-Goss, Gregory R. Grant, Alessia Ranciaro, Jibril B Hirbo, William R. Beggs, Meredith Yeager, Stephen Jacob Chanock et al. · 2023 · Genome biology
  50. Polygenic Risk Score Associates With Atherosclerotic Plaque Characteristics at Autopsy
    Anne Cornelissen, Neel V. Gadhoke, Kathleen A. Ryan, Chani J. Hodonsky, Rebecca Mitchell, Nathan A. Bihlmeyer, ThuyVy Duong, Zhifen Chen, Armelle Dikongue, Atsushi Sakamoto et al. · 2023 · Arteriosclerosis Thrombosis and Vascular Biology
  51. Evaluating NetMHCpan performance on non-European HLA alleles not present in training data
    Thomas Karl Atkins, Arnav Solanki, George Vasmatzis, James L. Cornette, Marc D. Riedel · 2024 · Frontiers in Immunology
  52. Population specific genetic heterogeneity of familial hypercholesterolemia in South Africa
    Natalie Smyth, Michèle Ramsay, Frederick Johan Raal · 2018 · Current Opinion in Lipidology
  53. Motivations for Participation in Parkinson Disease Genetic Research Among Hispanics versus Non-Hispanics
    Karen Nuytemans, Clara Patricia Manrique, Aaron Uhlenberg, William K. Scott, Michael L. Cuccaro, Corneliu C. Luca, Carlos Singer, Jeffery M. Vance · 2019 · Frontiers in Genetics
  54. Understanding access to genomics in an ethnically diverse south Florida population: A comparison of demographics in odyssey and rapid whole genome sequencing programs
    Saida B. Hussain, Alexandra L. Quittner, Marilyn Brown, Ana Maria Li-Rosi · 2020 · Journal of Genetic Counseling
  55. A Meta-Analysis of the Transferability of Bone Mineral Density Genetic Loci Associations From European to African Ancestry Populations
    Michelle S. Yau, Allison L. Kuipers, Ryan Price, Aude Nicolas, Salman M. Tajuddin, Samuel K. Handelman, Liubov S Arbeeva, Alessandra Chesi, Yi‐Hsiang Hsu, Ching‐Ti Liu et al. · 2020 · Journal of Bone and Mineral Research
  56. Common genetic variation in circadian clock genes are associated with cardiovascular risk factors in an African American and Hispanic/Latino cohort
    Pablo Ignacio Salazar, Sreenivas Konda, Arvind Sridhar, Zarema H. Arbieva, Martha L. Daviglus, Dawood Darbar, Jalees Rehman · 2021 · IJC Heart & Vasculature
  57. Transcriptome-Wide Association Study of Blood Cell Traits in African Ancestry and Hispanic/Latino Populations
    Jia Wen, Munan Xie, Bryce Rowland, Jonathan D. Rosen, Quan Sun, Jiawen Carmen Chen, Amanda L. Tapia, Huijun Qian, Madeline H. Kowalski, Yue Shan et al. · 2021 · Genes
  58. The Ethics of Consent in a Shifting Genomic Ecosystem
    Sandra Soo‐Jin Lee · 2021 · Annual Review of Biomedical Data Science
  59. Access and Representation: A Narrative Review of the Disparities in Access to Clinical Trials and Precision Oncology in Black men with Prostate Cancer
    Ashanda Rosetta Patrice Esdaille, Christine Ibilibor, Arturo E. Holmes, Nynikka R. Palmer, Adam Bryant Murphy · 2021 · Urology
  60. IFITM3, FURIN, ACE1, and TNF-α Genetic Association With COVID-19 Outcomes: Systematic Review and Meta-Analysis
    João Locke Ferreira de Araújo, Diego Menezes, Renato Santana Aguiar, Renan Pedra de Souza · 2022 · Frontiers in Genetics
  61. Effects of genetic ancestry and socioeconomic deprivation on ethnic differences in serum creatinine
    Leonardo Mariño‐Ramírez, Shivam Sharma, Lavanya Rishishwar, Andrew B. Conley, Shashwat Deepali Nagar, I. King Jordan · 2022 · Gene
  62. Systematic review of genome-wide association studies of anxiety disorders and neuroticism
    Kristien van der Walt, Megan L. Campbell, Dan Joseph Stein, Shareefa Dalvie · 2022 · The World Journal of Biological Psychiatry
  63. Australian public perspectives on genomic data storage and sharing: Benefits, concerns and access preferences
    Fiona Lynch, Yan Meng, Stephanie Best, Ilias Goranitis, Julian Savulescu, Christopher Gyngell, Danya F. Vears · 2022 · European Journal of Medical Genetics
  64. Big Data in Gastroenterology Research
    Madeline A. Alizadeh, Natalia Sampaio Moura, Alyssa Schledwitz, Seema A Patil, Jacques Ravel, Jean‐Pierre Raufman · 2023 · International Journal of Molecular Sciences
  65. Cohort Profile: Extended Cohort for E-health, Environment and DNA (EXCEED)
    Catherine John, Nicola F. Reeve, Robert C. Free, Alexander T. Williams, Ioanna Ntalla, Aliki‐Eleni Farmaki, Jane Bethea, Linda M Barton, Nick R. G. Shrine, Chiara Batini et al. · 2019 · International Journal of Epidemiology
  66. Socioeconomics, race, and ethnicity in childhood cancer survival: Accessing and addressing root causes of disparities
    Meryl D. Colton, Makenzie L. Hawkins, DeLayna Goulding, Myles Cockburn, Adam L. Green · 2018 · Cancer
  67. On the cross-population generalizability of gene expression prediction models
    Kevin L. Keys, Angel C. Y. Mak, Marquitta J. White, Walter L. Eckalbar, Andrew Dahl, Joel Mefford, Anna V. Mikhaylova, María G. Contreras, Jennifer R. Elhawary, Celeste S. Eng et al. · 2019 · bioRxiv (Cold Spring Harbor Laboratory)
  68. Class-Conditional VAE-GAN for Local-Ancestry Simulation
    Daniel Mas Montserrat, Carlos D. Bustamante, Alexander G. Ioannidis · 2019 · arXiv (Cornell University)
  69. Genomic and physiological mechanisms of high-altitude adaptation in Ethiopian highlanders: a comparative perspective
    Wubalem Desta Seifu, Abreham Bekele‐Alemu, Changqing Zeng · 2025 · Frontiers in Genetics
  70. Eliciting Willingness and Beliefs towards Participation in Genetic Psychiatric Testing in Black/African American Mothers at Risk for Depression
    Rahshida Atkins, Terri-Ann Kelly, Shanda Johnson, Wanda M. Williams, Yolanda M. Nelson, Paule V. Joseph, Deirdre Jackson, Deborah King, Tiffany Stellmacher, Nisoni-Davis Halty et al. · 2020 · Behavioral Sciences
  71. Strengthening the Global Response to Infectious Disease Threats in the Twenty-First Century, with a COVID-19 Epilogue
    David E. Bloom, Daniel Cadarette · 2021 · Cambridge University Press eBooks
  72. Consent for Use of Genetic Data among US Hispanics/Latinos: Results from the Hispanic Community Health Study/ Study of Latinos
    Sara Rodrigo González, Garrett Strizich, Carmen R. Isasi, Simin Hua, Betsy Comas, Tamar Sofer, Bharat Thyagarajan, Krista M. Perreira, Gregory A. Talavera, Martha L. Daviglus et al. · 2021 · Ethnicity & Disease
  73. Polygenic Risk Score in African populations: progress and challenges
    Yagoub Adam, Suraju Sadeeq, Judit Kumuthini, Olabode Ajayi, Gordon Wells, Rotimi Solomon, Olubanke Olujoke Ogunlana, Emmanuel Adetiba, Emeka Iweala, Benedikt Brors et al. · 2022 · F1000Research
  74. Mapping ethical and social aspects of biomarker research and its application in atopic dermatitis and psoriasis: a systematic review of reason
    Marie-Christine Fritzsche, Alena Buyx, Nora Hangel · 2022 · Journal of the European Academy of Dermatology and Venereology
  75. Substance, discourse, and practice: a review of communication research on automation
    Joshua B. Barbour, Jared T. Jensen, Shelbey R. Call, Nandini Sharma · 2023 · Annals of the International Communication Association
  76. Polygenic risk scores for the prediction of common cancers in East Asians: A population-based prospective cohort study
    Peh Joo Ho, Iain Beehuat Tan, Dawn Qingqing Chong, Chiea Chuen Khor, Jian‐Min Yuan, Woon‐Puay Koh, Rajkumar Dorajoo, Jingmei Li · 2023 · eLife
  77. Genetic research with Indigenous Peoples: perspectives on governance and oversight in the US
    Nanibaa’ A. Garrison, Stephanie Russo Carroll · 2023 · Frontiers in Research Metrics and Analytics
  78. Genomic insights for personalised care in lung cancer and smoking cessation: motivating at-risk individuals toward evidence-based health practices
    Tony Chen, Giang H. Pham, Louis W. Fox, Nina Adler, Xiaoyu Wang, Jingning Zhang, Jinyoung Byun, Younghun Han, Gretchen Saunders, Dajiang J. Liu et al. · 2024 · EBioMedicine
  79. How genomics and multi-modal AI are reshaping precision medicine
    Han Zhuang · 2025 · Frontiers in Medicine
  80. Attitudes and experiences regarding genetic research among persons of African descent
    Denise M. Scott, Veronica G. Thomas, Jane Otado, Faun Rockcliffe, Omotomilade Olopoenia, Dietrich Johnson, Shawneequa Callier · 2019 · Journal of Community Genetics
  81. Integrating stakeholder feedback in translational genomics research: an ethnographic analysis of a study protocol’s evolution
    Stephanie A. Kraft, Carmit K. McMullen, Nangel M. Lindberg, David Pham Bui, Kelly J. Shipman, Katherine Anderson, Galen Joseph, Devan M. Duenas, Kathryn M. Porter, Tia L. Kauffman et al. · 2020 · Genetics in Medicine
  82. Identifying adaptive alleles in the human genome: from selection mapping to functional validation
    Elizabeth A. Werren, Obed A. Garcia, Abigail W. Bigham · 2020 · Human Genetics
  83. Differences in MTHFR and LRRK2 variant’s association with sporadic Parkinson’s disease in Mexican Mestizos correlated to Native American ancestry
    Elizabeth Romero-Gutiérrez, Paola Vázquez-Cárdenas, Hortensia Moreno-Macías, Jose Manuel Salas-Pacheco, Teresa Tusié‐Luna, Óscar Arias-Carrión · 2021 · npj Parkinson s Disease
  84. Genomic Sequencing Results Disclosure in Diverse and Medically Underserved Populations: Themes, Challenges, and Strategies from the CSER Consortium
    Sabrina A. Suckiel, Julianne M. O’Daniel, Katherine E. Donohue, Katie M. Gallagher, Marian J. Gilmore, Laura Godfrey Hendon, Galen Joseph, Billie Rachael Lianoglou, Jennifer M. Mathews, Mary E. Norton et al. · 2021 · Journal of Personalized Medicine
  85. Mapping the Diverse and Inclusive Future of Parkinson’s Disease Genetics and Its Widespread Impact
    Inas Elsayed, Alejandro Martínez-Carrasco, Mario Cornejo‐Olivas, Sara Bandrés‐Ciga · 2021 · Genes
  86. Insights on Genetic and Environmental Factors in Parkinson’s Disease from a Regional Swedish Case-Control Cohort
    Kajsa Atterling Brolin, Sara Bandrés‐Ciga, Cornelis Blauwendraat, Håkan Widner, Per Odin, Oskar Hansson, Andreas Puschmann, Maria Swanberg · 2021 · Journal of Parkinson s Disease
  87. Imputation Performance in Latin American Populations: Improving Rare Variants Representation With the Inclusion of Native American Genomes
    Andrés Jimenez-Kaufmann, Amanda Yoon-Yee Chong, Adrián Cortés, Consuelo D. Quinto-Cortés, Selene L. Fernández-Valverde, Leticia Dolores Ferreyra-Reyes, Luis Pablo Cruz‐Hervert, Santiago Gerardo Medina-Muñoz, Mashaal Sohail, María J. Palma-Martínez et al. · 2022 · Frontiers in Genetics
  88. Molecular testing in newborn screening: VUS burden among true positives and secondary reproductive limitations via expanded carrier screening panels
    Sabina Cook, Emily Dunn, Jenna Kornish, Laurel Calderwood, MaryAnn W. Campion, Kristina P. Cusmano‐Ozog, Christina G. Tise · 2023 · Genetics in Medicine
  89. Copying Machine Learning Classifiers
    Irene Unceta, Jordi Nin, Oriol Pujol · 2020 · IEEE Access
  90. Potential Clinical Relevance of Differences in Allele Frequencies Found within Very Important Pharmacogenes between Hmong and East Asian Populations
    Ya‐Feng Wen, Kathleen A. Culhane‐Pera, Bharat Thyagarajan, Jeffrey R. Bishop, Heather A. Zierhut, Muaj Lo, Txia Xiong, Kerui Peng, Katherine J. Holzer, Koobmeej Lee et al. · 2019 · Pharmacotherapy The Journal of Human Pharmacology and Drug Therapy
  91. Unraveling the identity of gastric cardiac cancer
    Qin Miao Huang, Matthew D. Read, Jason S. Gold, Xiao Ping Zou · 2020 · Journal of Digestive Diseases
  92. Perspectives and preferences regarding genomic secondary findings in underrepresented prenatal and pediatric populations: A mixed-methods approach
    Shannon M. Rego, Hannah Hoban, Simon Michael Outram, Astrid N. Zamora, Flavia Chen, Nuriye Sahin‐Hodoglugil, Beatriz Anguiano, Matthew Norstad, Tiffany Yip, Billie Rachael Lianoglou et al. · 2022 · Genetics in Medicine
  93. Clinical Interpretation
    Nathanael D. Moore, Parastou Ghazi, Eliezer M. Van Allen · 2019 · Springer eBooks
  94. An African ancestry-specific nonsense variant in CD36 is associated with a higher risk of dilated cardiomyopathy
    Jennifer E. Huffman, Liam Gaziano, Zeina Reda Al Sayed, Renae Judy, Laura M. Raffield, Kiran J. Biddinger, BRIAN R. CHAREST, Anant Chopra, DAVID R. GAGNON, Xiuqing Guo et al. · 2025 · Nature Genetics
  95. Community Engagement in Precision Medicine Research: Organizational Practices and Their Impacts for Equity
    Janet K. Shim, Nicole Foti, Emily E. Vasquez, Stephanie Malia Fullerton, Michael Bentz, Melanie Jeske, Sandra Soo‐Jin Lee · 2023 · AJOB Empirical Bioethics
  96. Admixture mapping implicates 13q33.3 as ancestry-of-origin locus for Alzheimer disease in Hispanic and Latino populations
    Andréa R. V. R. Horimoto, Lisa A. Boyken, Elizabeth Blue, Kelsey E. Grinde, Rafael Albertovich Nafikov, Harkirat K. Sohi, Alejandro Q. Nato, Joshua C. Bis, Luis Ignacio Brusco, Laura Morelli et al. · 2023 · Human Genetics and Genomics Advances
  97. Do digital health interventions hold promise for stroke prevention and care in Black and Latinx populations in the United States? A scoping review
    Bianca D. Rivera, Claire Nurse, Vivek Shah, Chastidy Roldan, Adiebonye E. Jumbo, Mohammad A. Faysel, Steven R. Levine, David R. Kaufman, Aimee Afable · 2023 · BMC Public Health
  98. Dissociation of Reliability, Heritability, and Predictivity in Coarse- and Fine-Scale Functional Connectomes during Development
    Erica L. Busch, Kristina M. Rapuano, Kevin M. Anderson, Monica D. Rosenberg, Richard Watts, B.J. Casey, James V. Haxby, Ma Feilong · 2022 · Journal of Neuroscience
  99. Immunogenetic Diversity and Cancer Immunotherapy Disparities
    Noel F.C.C. de Miranda, Ferenc A. Scheeren · 2024 · Cancer Discovery
  100. Protein-truncating variant in APOL3 increases chronic kidney disease risk in epistasis with APOL1 risk alleles
    David Y. Zhang, Michael G. Levin, Jeffrey Duda, Latrice G. Landry, Walter R T Witschey, Scott M. Damrauer, Marylyn DeRiggi Ritchie, Daniel James Rader · 2024 · JCI Insight