Výsledky vyhledávání - Asif Javed

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  1. 1
    Phen-Gen: combining phenotype and genotype to analyze rare disorders

    Phen-Gen: combining phenotype and genotype to analyze rare disorders Autor Asif Javed, Saloni Agrawal, Pauline C. Ng

    Vydáno 2014
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  2. 2
    Ancestry informative markers for fine-scale individual assignment to worldwide populations

    Ancestry informative markers for fine-scale individual assignment to worldwide populations Autor Peristera Paschou, Joshua P. Lewis, Asif Javed, Petros Drineas

    Vydáno 2010
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  3. 3
    Occurrence of various viruses and recent evidence of SARS-CoV-2 in wastewater systems

    Occurrence of various viruses and recent evidence of SARS-CoV-2 in wastewater systems Autor Waqar Ali, Hua Zhang, Zhenglu Wang, Chuan‐Yu Chang, Asif Javed, Kamran Ali, Wei Du, Nabeel Khan Niazi, Kang Mao, Zhugen Yang

    Vydáno 2021
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  4. 4
    Rates and predictors of patient-reported cognitive side effects of antiepileptic drugs: An extended follow-up

    Rates and predictors of patient-reported cognitive side effects of antiepileptic drugs: An extended follow-up Autor Asif Javed, Brian L. Cohen, Kamil Detyniecki, Lawrence J. Hirsch, Alexander Legge, Baibing Chen, Carl W. Bazil, Kenneth Kato, Richard Buchsbaum, Hyunmi Choi

    Vydáno 2015
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  5. 5
    Trends in Stroke Presentations before and during the COVID-19 Pandemic: A Meta-Analysis

    Trends in Stroke Presentations before and during the COVID-19 Pandemic: A Meta-Analysis Autor Ishaque, Noman, Butt, Asif Javed, Kamtchum-Tatuene, Joseph, Nomani, Ali Zohair, Razzaq, Sarah, Fatima, Nida, Vekhande, Chetan, Nair, Radhika, Akhtar, Naveed, Khan, Khurshid, Saqqur, Maher, Shuaib, Ashfaq

    Vydáno 2022
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  6. 6
    Chronic type I interferon signaling promotes lipid-peroxidation-driven terminal CD8+ T cell exhaustion and curtails anti-PD-1 efficacy

    Chronic type I interferon signaling promotes lipid-peroxidation-driven terminal CD8+ T cell exhaustion and curtails anti-PD-1 efficacy Autor Weixin Chen, Jia Ming Nickolas Teo, Siu Wah Yau, Melody Yee‐Man Wong, Chun‐Nam Lok, Chi‐Ming Che, Asif Javed, Yuanhua Huang, Stephanie Ma, Guang Sheng Ling

    Vydáno 2022
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  7. 7
    Drug‐resistant epilepsy in adults: Outcome trajectories after failure of two medications

    Drug‐resistant epilepsy in adults: Outcome trajectories after failure of two medications Autor Hyunmi Choi, Matthew J. Hayat, Ruiqi Zhang, Lawrence J. Hirsch, Carl W. Bazil, Anil Mendiratta, Kenneth Kato, Asif Javed, Alexander Legge, Richard Buchsbaum, Stanley R. Resor, Gary A. Heiman

    Vydáno 2016
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  8. 8
    Development of DNA barcodes for selected Acacia species by using rbcL and matK DNA markers

    Development of DNA barcodes for selected Acacia species by using rbcL and matK DNA markers Autor Muhammad Ismail, Aftab Ahmad, Muhammad Shahid Nadeem, Muhammad Asif Javed, Sultan Habibullah Khan, Iqra Khawaish, Aftab Alam Sthanadar, Sameer H. Qari, Suliman Mohammed Suliman Alghanem, Khalid Ali Khan, Muhammad Fiaz Khan, Samina Qamer

    Vydáno 2020
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  9. 9
    An integrative model of pathway convergence in genetically heterogeneous blast crisis chronic myeloid leukemia

    An integrative model of pathway convergence in genetically heterogeneous blast crisis chronic myeloid leukemia Autor Tun Kiat Ko, Asif Javed, Kian Leong Lee, Thushangi N. Pathiraja, Xingliang Liu, Simeen Malik, Sheila Soh, Xiu Ting Heng, Naoto Takahashi, Joanna Tan, Ravi Bhatia, Alexis Jiaying Khng, Wee Joo Chng, Yee Yen Sia, David A. Fruman, King Pan Ng, Zhu En Chan, Kim Jiajing Xie, Qiangze Hoi, Cheryl Xueli Chan, Audrey S.M. Teo, Oscar Velázquez Camacho, Wee Yang Meah, Chiea Chuen Khor, Chin Thing Ong, Wei Jia Wendy Soon, Patrick Tan, Pauline C. Ng, Charles Chuah, Axel M. Hillmer, S. Tiong Ong

    Vydáno 2020
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  10. 10
    Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness

    Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness Autor Stefanie Heilmann‐Heimbach, Christine Herold, Lara M. Hochfeld, Axel M. Hillmer, Dale R. Nyholt, Julian Hecker, Asif Javed, Elaine Guo Yan Chew, Sonali Pechlivanis, Dmitriy Drichel, Xiu Ting Heng, Ricardo C.H. del Rosario, Heide Fier, Ralf Paus, Rico Rueedi, Tessel E. Galesloot, Susanne Moebus, Thomas Anhalt, Shyam Prabhakar, Rui Li, Stavroula Kanoni, George Papanikolaou, Zoltán Kutalik, Panos Deloukas, Michael P. Philpott, Gérard Waeber, Tim D. Spector, Péter Vollenweider, Lambertus A. Kiemeney, George Dedoussis, J. Brent Richards, Michael Nothnagel, Nicholas G. Martin, Tim Becker, David A. Hinds, Markus M. Nöthen

    Vydáno 2017
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  11. 11
    ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorder

    ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorder Autor Lewis Williams, Asif Javed, Amin Sabri, Denise J. Morgan, Chad Huff, John Grigg, Xiu Ting Heng, Alexis Jiaying Khng, Iris H.I.M. Hollink, Margaux A. Morrison, Leah A. Owen, Katherine Anderson, Krista Kinard, Rebecca Greenlees, Danica Novacic, Sen Hou, Wadih M. Zein, George M. Rodgers, Albert T. Vitale, Neena B. Haider, Axel M. Hillmer, Pauline C. Ng, Shankaracharya, Anson Cheng, Linda Zheng, Mark C. Gillies, Marjon van Slegtenhorst, P. Martin van Hagen, Tom Missotten, Gary L. Farley, Michael Polo, J. Jeffrey Malatack, Julie Curtin, Frank Martin, Susan Arbuckle, Stephen I. Alexander, Megan Chircop, Sonia Dávila, Kathleen B. Digre, Robyn V. Jamieson, Margaret M. DeAngelis

    Vydáno 2019
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  12. 12
    De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development

    De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development Autor Christopher T. Gordon, Shifeng Xue, Gökhan Yigit, Hicham Filali, Kelan Chen, Nadine Rosin, Koh-ichiro Yoshiura, Myriam Oufadem, Tamara Beck, Ruth McGowan, Alex Magee, Janine Altmüller, Camille Dion, Hölger Thiele, Alexandra D. Gurzau, Peter Nürnberg, Dieter Meschede, W. Mühlbauer, Nobuhiko Okamoto, Vinod Varghese, Rachel Irving, Sabine Sigaudy, Denise Williams, S. Faisal Ahmed, Carine Bonnard, Mung Kei Kong, Ilham Ratbi, Nawfal Fejjal, Meriem Fikri, Siham Chafai Elalaoui, Hallvard Reigstad, Christine Bôle‐Feysot, Patrick Nitschké, Nicola Ragge, Nicolas Lévy, Gökhan Tunçbįlek, Audrey S.M. Teo, Michael L. Cunningham, Abdelaziz Sefiani, Hülya Kayserili, James M. Murphy, Chalermpong Chatdokmaiprai, Axel M. Hillmer, Duangrurdee Wattanasirichaigoon, Stanislas Lyonnet, Frédérique Magdinier, Asif Javed, Marnie E. Blewitt, Jeanne Amiel, Bernd Wollnik, Bruno Reversade

    Vydáno 2017
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  13. 13
    MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement

    MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement Autor Sandra Donkervoort, Rasha Sabouny, Pomi Yun, Laurence Gauquelin, Katherine R. Chao, Ying Hu, Iman Al Khatib, Ana Töpf, Payam Mohassel, Beryl B. Cummings, Rupleen Kaur, Dimah Saade, Steven A. Moore, Leigh B. Waddell, Michelle A. Farrar, Julia K. Goodrich, Prech Uapinyoying, H.S. Chan, Asif Javed, M. Leach, Peter Karachunski, Joline Dalton, L. Medne, A. Harper, Caroline A. Thompson, Isabelle Thiffault, Sabine Specht, Ryan E. Lamont, Carol Saunders, Hilary Racher, François Bernier, David Mowat, Nanna Witting, John Vissing, Ronald K. Hanson, Keith A. Coffman, Meagan K. Hainlen, Jillian S. Parboosingh, Amanda Carnevale, Grace Yoon, Rhonda E. Schnur, KM Boycott, Jean K. Mah, Volker Straub, A. Reghan Foley, A. Micheil Innes, Carsten G. Bönnemann, Timothy E. Shutt

    Vydáno 2019
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  14. 14
    Correction to: Origins, admixture and founder lineages in European Roma

    Correction to: Origins, admixture and founder lineages in European Roma Autor Begoña Martínez‐Cruz, Isabel Mendizabal, Christine Harmant, Rosario de Pablo, Mihai Ioana, Dora Angelicheva, Anastasia Kouvatsi, Halyna Makukh, Mihai G. Netea, Horolma Pamjav, Andrea Zalán, Ivailo Tournev, Elena Marushiaková, Vesselin Popov, Jaume Bertranpetit, Luba Kalaydjieva, Lluı́s Quintana-Murci, David Comas, Jin Li, Hui Li, Shilin Li, Pandikumar Swamikrishnan, Asif Javed, Laxmi Parida, Ajay K. Royyuru, R. John Mitchell, Pierre Zalloua, Syama Adhikarla, Arun Kumar, Ganesh Prasad, Ramasamy Pitchappan, Arun Varatharajan Santhakumari, Kavitha Valampuri, R. Spencer Wells, Miguel G. Vilar, Himla Soodyall, Elena Balanovska, Oleg Balanovsky, Chris Tyler‐Smith, Fabrício R. Santos, Jaume Bertranpetit, Marc Haber, Marta Melé, David Comas, Christina Adler, Alan Cooper, Clio S. I. Der Sarkissian, Wolfgang Haak, Matthew E. Kaplan, Nirav Merchant, Colin Renfrew, Andrew Clarke, Elizabeth Matisoo‐Smith, Jill B. Gaieski, Theodore G. Schurr

    Vydáno 2021
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  15. 15
    Y-chromosome analysis reveals genetic divergence and new founding native lineages in Athapaskan- and Eskimoan-speaking populations

    Y-chromosome analysis reveals genetic divergence and new founding native lineages in Athapaskan- and Eskimoan-speaking populations Autor Matthew C. Dulik, Amanda C. Owings, Jill B. Gaieski, Miguel G. Vilar, Alestine Andre, Crystal Lennie, Mary Adele Mackenzie, Ingrid Kritsch, Sharon Snowshoe, Ruth Wright, James P. Martin, Nancy Gibson, T. Daniel Andrews, Theodore G. Schurr, Syama Adhikarla, Christina Adler, Elena Balanovska, Oleg Balanovsky, Jaume Bertranpetit, Andrew Clarke, David Comas, Alan Cooper, Clio S. I. Der Sarkissian, ArunKumar GaneshPrasad, Wolfgang Haak, Marc Haber, Angela Hobbs, Asif Javed, Jin Li, Matthew E. Kaplan, Shilin Li, Begoña Martínez‐Cruz, Elizabeth Matisoo‐Smith, Marta Melé, Nirav Merchant, R. John Mitchell, Laxmi Parida, Ramasamy Pitchappan, Daniel E. Platt, Lluís Quintana‐Murci, Colin Renfrew, Daniela R. Lacerda, Ajay K. Royyuru, Fabrício R. Santos, Himla Soodyall, David F. Soria Hernanz, Pandikumar Swamikrishnan, Chris Tyler‐Smith, Arun Varatharajan Santhakumari, Pedro Paulo Vieira, R. Spencer Wells, Pierre Zalloua, Janet Ziegle

    Vydáno 2012
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  16. 16
    Aboriginal Australian mitochondrial genome variation – an increased understanding of population antiquity and diversity

    Aboriginal Australian mitochondrial genome variation – an increased understanding of population antiquity and diversity Autor Nano Nagle, Mannis van Oven, Stephen Wilcox, Sheila van Holst Pellekaan, Chris Tyler‐Smith, Yali Xue, Kaye N. Ballantyne, Leah Wilcox, Luka Papac, Karen Cooke, Roland A.H. van Oorschot, Peter McAllister, Lesley Williams, Manfred Kayser, R. John Mitchell, Syama Adhikarla, Christina Adler, Elena Balanovska, Oleg Balanovsky, Jaume Bertranpetit, Andrew Clarke, David Comas, Alan Cooper, Clio S. I. Der Sarkissian, Matthew C. Dulik, Jill B. Gaieski, ArunKumar GaneshPrasad, Wolfgang Haak, Marc Haber, Angela Hobbs, Asif Javed, Jin Li, Matthew E. Kaplan, Shilin Li, Begoña Martínez‐Cruz, Elizabeth Matisoo‐Smith, Marta Melé, Nirav Merchant, Amanda C. Owings, Laxmi Parida, Ramasamy Pitchappan, Daniel E. Platt, Lluís Quintana‐Murci, Colin Renfrew, Ajay K. Royyuru, Arun Varatharajan Santhakumari, Fabrício R. Santos, Theodore G. Schurr, Himla Soodyall, David F. Soria Hernanz, Pandikumar Swamikrishnan, Miguel G. Vilar, R. Spencer Wells, Pierre Zalloua, Janet Ziegle

    Vydáno 2017
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  17. 17
    Neolithic mitochondrial haplogroup H genomes and the genetic origins of Europeans

    Neolithic mitochondrial haplogroup H genomes and the genetic origins of Europeans Autor Paul Brotherton, Wolfgang Haak, Jennifer E.L. Templeton, Guido Brandt, Julien Soubrier, Christina Adler, Stephen M. Richards, Clio Der Sarkissian, Robert Ganslmeier, Susanne Friederich, Veit Dresely, Mannis van Oven, Rosalie Kenyon, Mark B. Van der Hoek, Jonas Korlach, Khai Luong, Simon Y. W. Ho, Lluís Quintana‐Murci, Doron M. Behar, Harald Meller, Kurt W. Alt, Alan Cooper, Syama Adhikarla, Arun Kumar Ganesh Prasad, Ramasamy Pitchappan, Arun Varatharajan Santhakumari, Elena Balanovska, Oleg Balanovsky, Jaume Bertranpetit, David Comas, Begoña Martínez‐Cruz, Marta Melé, Andrew Clarke, Elizabeth Matisoo‐Smith, Matthew C. Dulik, Jill B. Gaieski, Amanda C. Owings, Theodore G. Schurr, Miguel G. Vilar, Angela Hobbs, Himla Soodyall, Asif Javed, Laxmi Parida, Daniel E. Platt, Ajay K. Royyuru, Jin Li, Shilin Li, Matthew E. Kaplan, Nirav Merchant, R. John Mitchell, Colin Renfrew, Daniela R. Lacerda, Fabrício R. Santos, David F. Soria Hernanz, R. Spencer Wells, Pandikumar Swamikrishnan, Chris Tyler‐Smith, Pedro Paulo Vieira, Janet Ziegle

    Vydáno 2013
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  18. 18
    Large-Scale Whole-Genome Sequencing of Three Diverse Asian Populations in Singapore

    Large-Scale Whole-Genome Sequencing of Three Diverse Asian Populations in Singapore Autor Degang Wu, Jinzhuang Dou, Xiaoran Chai, Claire Bellis, Andreas Wilm, Chih Chuan Shih, Wendy Wei Jia Soon, Nicolas Bertin, Clarabelle Bitong Lin, Chiea Chuen Khor, Michael DeGiorgio, Shanshan Cheng, Li Bao, Neerja Karnani, William Ying Khee Hwang, Sonia Dávila, Patrick Tan, Asim Shabbir, Angela Moh, Eng‐King Tan, Jia Nee Foo, Liuh Ling Goh, Khai Pang Leong, Roger Foo, Carolyn S.P. Lam, Mark Richards, Ching‐Yu Cheng, Tin Aung, Tien Yin Wong, Huck‐Hui Ng, Jianjun Liu, Chaolong Wang, Matthew Ackers‐Johnson, Edita Aliwarga, Kenneth Ban, Denis Bertrand, John C. Chambers, Dana Leng Hui Chan, Cheryl Xue Li Chan, Miao Li Chee, Miao Ling Chee, Pauline Chen, Yunxin Chen, Elaine Guo Yan Chew, Wen Jie Chew, Lynn Hui Yun Chiam, Jenny Pek Ching Chong, I-Ly Joanna Chua, Stuart A. Cook, Wei Dai, Rajkumar Dorajoo, Chuan-Sheng Foo, Rick Siow Mong Goh, Axel M. Hillmer, Ishak D. Irwan, Fazlur Jaufeerally, Asif Javed, Justin Jeyakani, John Tat Hung Koh, Jia Yu Koh, Pavitra Krishnaswamy, Jyn Ling Kuan, Kumari Neelam, Ai Shan Lee, Seow Eng Lee, Lee Sheldon, Yen Ling Lee, See Ting Leong, Zheng Li, Peter Yiqing Li, Jun Xian Liew, Oi Wah Liew, Su Chi Lim, Weng Khong Lim, Chia Wei Lim, Tingsen Benson Lim, Choon Kiat Lim, Seet Yoong Loh, Au Wing Lok, Calvin Chin, Shivani Majithia, Sebastian Maurer‐Stroh, Wee Yang Meah, Shi Qi Mok, Niranjan Nargarajan, Pauline C. Ng, Sarah B. Ng, Zhenyuan Ng, Jessica Yan Xia Ng, Ebonne Ng, Shi Ling Ng, Simon Nusinovici, Chin Thing Ong, Bangfen Pan, Vincent Pedergnana, Stanley Poh, Shyam Prabhakar, Kumar M. Prakash, Ivy Quek, Charumathi Sabanayagam

    Vydáno 2019
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