检索结果 - Uppala Radhakrishna

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  1. 1
    Deep Learning/Artificial Intelligence and Blood-Based DNA Epigenomic Prediction of Cerebral Palsy

    Deep Learning/Artificial Intelligence and Blood-Based DNA Epigenomic Prediction of Cerebral Palsy 由 Ray Bahado‐Singh, Sangeetha Vishweswaraiah, Buket Aydas, Nitish K. Mishra, Chittibabu Guda, Uppala Radhakrishna

    出版 2019
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  2. 2
    Genome-Wide DNA Methylation Analysis and Epigenetic Variations Associated with Congenital Aortic Valve Stenosis (AVS)

    Genome-Wide DNA Methylation Analysis and Epigenetic Variations Associated with Congenital Aortic Valve Stenosis (AVS) 由 Uppala Radhakrishna, Samet Albayrak, Zeynep Alpay-Savasan, Amna Zeb, Onur Türkoğlu, Paul Sobolewski, Ray Bahado‐Singh

    出版 2016
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  3. 3
    Impaired Molecular Mechanisms Contributing to Chronic Pain in Patients with Hidradenitis Suppurativa: Exploring Potential Biomarkers and Therapeutic Targets

    Impaired Molecular Mechanisms Contributing to Chronic Pain in Patients with Hidradenitis Suppurativa: Exploring Potential Biomarkers and Therapeutic Targets 由 Uppala Radhakrishna, Murali R. Kuracha, Iltefat Hamzavi, Nazia Saiyed, Jignesh Prajapati, Rakesh Rawal, Lavanya V. Uppala, Giovanni Damiani, Uppala Ratnamala, Swapan K. Nath

    出版 2025
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  4. 4
    Localization of a Gene for Keratoconus to a 5.6-Mb Interval on 13q32

    Localization of a Gene for Keratoconus to a 5.6-Mb Interval on 13q32 由 Marzena Gajęcka, Uppala Radhakrishna, Daniel Winters, Swapan K. Nath, Małgorzata Rydzanicz, Uppala Ratnamala, Kimberly Ewing, Andrea Molinari, Jose A. Pitarque, Kwanghyuk Lee, Suzanne M. Leal, Bassem A. Bejjani

    出版 2009
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  5. 5
    Peutz-Jeghers Syndrome: Confirmation of Linkage to Chromosome 19p13.3 and Identification of a Potential Second Locus, on 19q13.4

    Peutz-Jeghers Syndrome: Confirmation of Linkage to Chromosome 19p13.3 and Identification of a Potential Second Locus, on 19q13.4 由 Hamid Mehenni, Jean-Louis Blouin, Uppala Radhakrishna, Shiv Shanker Bhardwaj, Kamla Bhardwaj, Vishal Dixit, Kent F. Richards, Ambrosio Bermejo‐Fenoll, Antonio Silva Leal, Ranjan Raval, Stylianos E. Antonarakis

    出版 1997
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  6. 6
    Placental epigenetics for evaluation of fetal congenital heart defects: Ventricular Septal Defect (VSD)

    Placental epigenetics for evaluation of fetal congenital heart defects: Ventricular Septal Defect (VSD) 由 Uppala Radhakrishna, Samet Albayrak, Rita Zafra, Baraa Alosh, Sangeetha Vishweswaraiah, Avinash M. Veerappa, Deepthi Mahishi, Nazia Saiyed, Nitish K. Mishra, Chittibabu Guda, Rouba Ali‐Fehmi, Ray Bahado‐Singh

    出版 2019
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  7. 7
    The Phenotypic Spectrum of GLI3 Morphopathies Includes Autosomal Dominant Preaxial Polydactyly Type-IV and Postaxial Polydactyly Type-A/B; No Phenotype Prediction from the Position of GLI3 Mutations

    The Phenotypic Spectrum of GLI3 Morphopathies Includes Autosomal Dominant Preaxial Polydactyly Type-IV and Postaxial Polydactyly Type-A/B; No Phenotype Prediction from the Position... 由 Uppala Radhakrishna, Dorothea Bornholdt, Hamish S. Scott, Uday C. Patel, Colette Rossier, Hartmut Engel, Armand Bottani, Divya Chandal, Jean-Louis Blouin, J. V. Solanki, Karl‐Heinz Grzeschik, Stylianos E. Antonarakis

    出版 1999
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  8. 8
    Y-Chromosome Lineages Trace Diffusion of People and Languages in Southwestern Asia

    Y-Chromosome Lineages Trace Diffusion of People and Languages in Southwestern Asia 由 Lluı́s Quintana-Murci, Csilla Krausz, Tatiana Zerjal, S.Hamid Sayar, Michael F. Hammer, S. Qasim Mehdi, Qasim Ayub, Raheel Qamar, Aisha Mohyuddin, Uppala Radhakrishna, Mark A. Jobling, Chris Tyler‐Smith, Ken McElreavey

    出版 2001
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  9. 9
    Artificial Intelligence and Circulating Cell-Free DNA Methylation Profiling: Mechanism and Detection of Alzheimer’s Disease

    Artificial Intelligence and Circulating Cell-Free DNA Methylation Profiling: Mechanism and Detection of Alzheimer’s Disease 由 Ray Bahado‐Singh, Uppala Radhakrishna, Juozas Gordevičius, Buket Aydas, Ali Yılmaz, Faryal Jafar, Khaled Imam, Michael Maddens, Kshetra Challapalli, Raghu Metpally, Wade H. Berrettini, Richard C. Crist, Stewart F. Graham, Sangeetha Vishweswaraiah

    出版 2022
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  10. 10
    Refinement of the X-linked Nonsyndromic High-Grade Myopia Locus MYP1 on Xq28 and Exclusion of 13 Known Positional Candidate Genes by Direct Sequencing

    Refinement of the X-linked Nonsyndromic High-Grade Myopia Locus MYP1 on Xq28 and Exclusion of 13 Known Positional Candidate Genes by Direct Sequencing 由 Ratnamala, Uppala, Lyle, Robert, Rawal, Rakesh, Singh, Raminder, Vishnupriya, Satti, Himabindu, Pamini, Rao, Vittal, Aggarwal, Somesh, Paluru, Prasuna, Bartoloni, Lucia, Young, Terri L., Paoloni-Giacobino, Ariane, Morris, Michael A., Nath, Swapan K., Antonarakis, Stylianos E., Uppala, Radhakrishna

    出版 2011
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  11. 11
    Human Male Infertility Associated with Mutations in NR5A1 Encoding Steroidogenic Factor 1

    Human Male Infertility Associated with Mutations in NR5A1 Encoding Steroidogenic Factor 1 由 Anu Bashamboo, Bruno Ferraz‐de‐Souza, Diana Lourenço, Lin Lin, Neil J. Sebire, Debbie Montjean, Joëlle Bignon-Topalovic, Jacqueline Mandelbaum, Jean‐Pierre Siffroi, Sophie Christin‐Maître, Uppala Radhakrishna, Hassan Rouba, Célia Ravel, Jacob-S. Seeler, John C. Achermann, Ken McElreavey

    出版 2010
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  12. 12
    Insertion of β-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness

    Insertion of β-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness 由 Hamish S. Scott, Jun Kudoh, Marie Wattenhofer‐Donzé, Kazunori Shibuya, Asher Berry, Roman Chrast, Michel Guipponi, Jun Wang, Kazuhiko Kawasaki, Shuichi Asakawa, Satoshi Minoshima, Farah Younus, S. Qasim Mehdi, Uppala Radhakrishna, Marie-Pierre Papasavvas, Corinne Gehrig, Colette Rossier, Michael Korostishevsky, Andreas Gal, Nobuyoshi Shimizu, Batsheva Bonné‐Tamir, Stylianos E. Antonarakis

    出版 2001
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  13. 13
    Primary ciliary dyskinesia: a genome-wide linkage analysis reveals extensive locus heterogeneity

    Primary ciliary dyskinesia: a genome-wide linkage analysis reveals extensive locus heterogeneity 由 J-L Blouin, Maggie Meeks, Uppala Radhakrishna, AJ Sainsbury, Chris Gehring, G Duriaux Saïl, Lucia Bartoloni, V H Dombi, Angela O'Rawe, Amanda J. Walne, E. Chung, BA Afzelius, M Armengot, Mark Jorissen, DV Schidlow, Lionel Van Maldergem, H. Walt, R M Gardiner, Daniela Probst, P A Guerne, CD Delozier-Blanchet, Stylianos E. Antonarakis

    出版 2000
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  14. 14
    Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part III: Bipolar Disorder

    Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part III: Bipolar Disorder 由 Ricardo Segurado, Sevilla D. Detera‐Wadleigh, Douglas F. Levinson, Cathryn M. Lewis, Michael Gill, John I. Nürnberger, Nick Craddock, J. Raymond DePaulo, Miron Baron, Elliot S. Gershon, Jenny Ekholm, Sven Cichon, Gustavo Turecki, Stephan Claes, John R. Kelsoe, Peter R. Schofield, Renee F. Badenhop, J Morissette, Hilary Coon, Douglas Blackwood, L. Alison McInnes, Tatiana Foroud, Howard J. Edenberg, Theodore Reich, John P. Rice, Alison Goate, Melvin G. McInnis, Francis J. McMahon, Judith A. Badner, Lynn R. Goldin, Phillip R. Bennett, Virginia L. Willour, Peter P. Zandi, Jianjun Liu, Conrad Gilliam, Suh‐Hang Hank Juo, Wade H. Berrettini, Takeo Yoshikawa, Leena Peltonen, Jouko Lönnqvist, Markus M. Nöthen, Johannes Schumacher, Christine Windemuth, Marcella Rietschel, Peter Propping, Wolfgang Maier, Martin Alda, Paul Grof, Guy A. Rouleau, Jurgen Del‐Favero, Christine Van Broeckhoven, Julien Mendlewicz, Rolf Adolfsson, M. Anne Spence, Hermann Luebbert, Linda J. Adams, Jennifer A. Donald, Philip B. Mitchell, Nicholas Barden, Éric Shink, William Byerley, Walter Muir, Peter M. Visscher, Stuart MacGregor, Hugh Gurling, Gursharan Kalsi, Andrew McQuillin, Michael Escamilla, Victor I. Reus, Pedro León, Nelson B. Freimer, H. Ewald, Torben A. Kruse, Ole Mors, Uppala Radhakrishna, Jean‐Louis Blouin, Stylianos E. Antonarakis, Nurten Akarsu

    出版 2003
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