Výsledky vyhledávání - Hilary C. Martin

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  1. 1
    Contribution of autosomal rare and de novo variants to sex differences in autism

    Contribution of autosomal rare and de novo variants to sex differences in autism Autor Mahmoud Koko, F. Kyle Satterstrom, Varun Warrier, Hilary C. Martin

    Vydáno 2025
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  2. 2
    The genomic history of the Middle East

    The genomic history of the Middle East Autor Mohamed A. Almarri, Marc Haber, Reem A. Lootah, Pille Hallast, Saeed Al Turki, Hilary C. Martin, Yali Xue, Chris Tyler‐Smith

    Vydáno 2021
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  3. 3
    Imperfect centered miRNA binding sites are common and can mediate repression of target mRNAs

    Imperfect centered miRNA binding sites are common and can mediate repression of target mRNAs Autor Hilary C. Martin, Shivangi Wani, Anita L Steptoe, Keerthana Krishnan, Kátia Nones, Ehsan Nourbakhsh, Alexander V. Vlassov, Sean M. Grimmond, Nicole Cloonan

    Vydáno 2014
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  4. 4
    Genome-wide association studies

    Genome-wide association studies Autor Emil Uffelmann, Qin Qin Huang, Nchangwi Syntia Munung, Jantina de Vries, Yukinori Okada, Alicia R. Martin, Hilary C. Martin, Tuuli Lappalainen, Daniëlle Posthuma

    Vydáno 2021
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  5. 5
    Reduced reproductive success is associated with selective constraint on human genes

    Reduced reproductive success is associated with selective constraint on human genes Autor Eugene J. Gardner, Matthew D. C. Neville, Kaitlin E. Samocha, Kieron Barclay, Martin Kolk, Mari Niemi, George Kirov, Hilary C. Martin, Matthew E. Hurles

    Vydáno 2022
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  6. 6
    Human Slack Potassium Channel Mutations Increase Positive Cooperativity between Individual Channels

    Human Slack Potassium Channel Mutations Increase Positive Cooperativity between Individual Channels Autor Grace Kim, Jack Kronengold, Giulia Barcia, Imran H. Quraishi, Hilary C. Martin, Edward Blair, Jenny C. Taylor, Olivier Dulac, Laurence Colleaux, Rima Nabbout, Leonard K. Kaczmarek

    Vydáno 2014
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  7. 7
    Geographical genomics of human leukocyte gene expression variation in southern Morocco

    Geographical genomics of human leukocyte gene expression variation in southern Morocco Autor Youssef Idaghdour, Wendy Czika, Kevin V. Shianna, Sang Lee, Peter M. Visscher, Hilary C. Martin, Kelci Miclaus, Sami Jadallah, David B. Goldstein, Russell D. Wolfinger, Greg Gibson

    Vydáno 2009
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  8. 8
    Integrative polygenic risk score improves the prediction accuracy of complex traits and diseases

    Integrative polygenic risk score improves the prediction accuracy of complex traits and diseases Autor Buu Truong, Leland E. Hull, Yunfeng Ruan, Qin Huang, Whitney Hornsby, Hilary C. Martin, David A. van Heel, Ying Wang, Alicia R. Martin, Sang Lee, Pradeep Natarajan

    Vydáno 2023
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  9. 9
    Integrative polygenic risk score improves the prediction accuracy of complex traits and diseases

    Integrative polygenic risk score improves the prediction accuracy of complex traits and diseases Autor Buu Truong, Leland E. Hull, Yunfeng Ruan, Qin Huang, Whitney Hornsby, Hilary C. Martin, David A. van Heel, Ying Wang, Alicia R. Martin, Sang Lee, Pradeep Natarajan

    Vydáno 2024
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  10. 10
    Widespread recessive effects on common diseases in a cohort of 44,000 British Pakistanis and Bangladeshis with high autozygosity

    Widespread recessive effects on common diseases in a cohort of 44,000 British Pakistanis and Bangladeshis with high autozygosity Autor Teng Hiang Heng, Klaudia Walter, Qin Huang, Juha Karjalainen, Mark J. Daly, Henrike Heyne, Daniel Malawsky, Georgios Kalantzis, Sarah Finer, David A. van Heel, Hilary C. Martin

    Vydáno 2025
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  11. 11
    Linear mixed model for heritability estimation that explicitly addresses environmental variation

    Linear mixed model for heritability estimation that explicitly addresses environmental variation Autor David Heckerman, Deepti Gurdasani, Carl Kadie, Cristina Pomilla, Tommy Carstensen, Hilary C. Martin, Kenneth Ekoru, Rebecca N. Nsubuga, Gerald Ssenyomo, Anatoli Kamali, Pontiano Kaleebu, Christian Widmer, Manjinder S. Sandhu

    Vydáno 2016
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  12. 12
    miR-139-5p is a regulator of metastatic pathways in breast cancer

    miR-139-5p is a regulator of metastatic pathways in breast cancer Autor Keerthana Krishnan, Anita L Steptoe, Hilary C. Martin, Diwakar R. Pattabiraman, Kátia Nones, Nicola Waddell, Mythily Mariasegaram, Peter T. Simpson, Sunil R. Lakhani, Alexander V. Vlassov, Sean M. Grimmond, Nicole Cloonan

    Vydáno 2013
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  13. 13
    MicroRNA-182-5p targets a network of genes involved in DNA repair

    MicroRNA-182-5p targets a network of genes involved in DNA repair Autor Keerthana Krishnan, Anita L Steptoe, Hilary C. Martin, Shivangi Wani, Kátia Nones, Nicola Waddell, Mythily Mariasegaram, Peter T. Simpson, Sunil R. Lakhani, Brian Gabrielli, Alexander V. Vlassov, Nicole Cloonan, Sean M. Grimmond

    Vydáno 2012
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  14. 14
    Integrating polygenic risk scores in the prediction of type 2 diabetes risk and subtypes in British Pakistanis and Bangladeshis: A population-based cohort study

    Integrating polygenic risk scores in the prediction of type 2 diabetes risk and subtypes in British Pakistanis and Bangladeshis: A population-based cohort study Autor Sam Hodgson, Qin Qin Huang, Neneh Sallah, Chris Griffiths, William G. Newman, Richard C. Trembath, John Wright, R. Thomas Lumbers, Karoline Kuchenbaecker, David A. van Heel, Rohini Mathur, Hilary C. Martin, Sarah Finer

    Vydáno 2022
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  15. 15
    Application of whole genome and RNA sequencing to investigate the genomic landscape of common variable immunodeficiency disorders

    Application of whole genome and RNA sequencing to investigate the genomic landscape of common variable immunodeficiency disorders Autor Pauline A. van Schouwenburg, Emma E. Davenport, Anne‐Kathrin Kienzler, Ishita Marwah, Benjamin Wright, Mary Lucas, Tomas Malinauskas, Hilary C. Martin, Helen Lockstone, Jean‐Baptiste Cazier, Helen Chapel, Julian C. Knight, Smita Y. Patel

    Vydáno 2015
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  16. 16
    Fine-scale population structure and demographic history of British Pakistanis

    Fine-scale population structure and demographic history of British Pakistanis Autor Elena Arciero, Sufyan Abid Dogra, Daniel Malawsky, Massimo Mezzavilla, Theofanis Tsismentzoglou, Qin Qin Huang, Karen A. Hunt, Dan Mason, Saghira Malik Sharif, David A. van Heel, Eamonn Sheridan, John Wright, Neil Small, Shai Carmi, Mark M. Iles, Hilary C. Martin

    Vydáno 2021
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  17. 17
    Cohort Profile: East London Genes & Health (ELGH), a community-based population genomics and health study in British Bangladeshi and British Pakistani people

    Cohort Profile: East London Genes & Health (ELGH), a community-based population genomics and health study in British Bangladeshi and British Pakistani people Autor Sarah Finer, Hilary C. Martin, Ahsan Khan, Karen A. Hunt, Beverley MacLaughlin, Zaheer Ahmed, Richard Ashcroft, Ceri Durham, Daniel G. MacArthur, Mark I. McCarthy, John Robson, Bhavi Trivedi, Chris Griffiths, John Wright, Richard C. Trembath, David A. van Heel

    Vydáno 2019
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  18. 18
    Transferability of genetic loci and polygenic scores for cardiometabolic traits in British Pakistani and Bangladeshi individuals

    Transferability of genetic loci and polygenic scores for cardiometabolic traits in British Pakistani and Bangladeshi individuals Autor Qin Qin Huang, Neneh Sallah, Diana Dunca, Bhavi Trivedi, Karen A. Hunt, Sam Hodgson, Samuel A. Lambert, Elena Arciero, John Wright, Chris Griffiths, Richard C. Trembath, Harry Hemingway, Michael Inouye, Sarah Finer, David A. van Heel, R. Thomas Lumbers, Hilary C. Martin, Karoline Kuchenbaecker

    Vydáno 2022
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  19. 19
    Common genetic variants contribute to risk of rare severe neurodevelopmental disorders

    Common genetic variants contribute to risk of rare severe neurodevelopmental disorders Autor Mari Niemi, Hilary C. Martin, Daniel L Rice, Giuseppe Gallone, Scott D. Gordon, Martin Kelemen, Kerrie McAloney, Jeremy F. McRae, Elizabeth J. Radford, Sui Yu, Jozef Gécz, Nicholas G. Martin, Caroline F. Wright, David Fitzpatrick, Helen V. Firth, Matthew E. Hurles, Jeffrey C. Barrett

    Vydáno 2018
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  20. 20
    Influence of autozygosity on common disease risk across the phenotypic spectrum

    Influence of autozygosity on common disease risk across the phenotypic spectrum Autor Daniel Malawsky, Eva van Walree, Benjamin Meir Jacobs, Teng Hiang Heng, Qin Huang, Ataf Sabir, Saadia Rahman, Saghira Malik Sharif, Ahsan Khan, Maša Umićević Mirkov, Hiroyuki Kuwahara, Xin Gao, Fowzan S. Alkuraya, Daniëlle Posthuma, William G. Newman, Chris Griffiths, Rohini Mathur, David A. van Heel, Sarah Finer, Jared O’Connell, Hilary C. Martin

    Vydáno 2023
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