Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Tariq, Faquih"'
Autor:
Tariq Faquih, Dennis O. Mook‐Kanamori, Frits R. Rosendaal, Trevor Baglin, Ko Willems van Dijk, Astrid vanHylckama Vlieg
Publikováno v:
Research and Practice in Thrombosis and Haemostasis, Vol 5, Iss 4, Pp n/a-n/a (2021)
Abstract Background Venous thromboembolism (VTE) is a complex disease with an incidence rate of about 1 in 1000 per year. Despite the availability of validated biomarkers for VTE, unprovoked events account for 50% of first events. Therefore, emerging
Externí odkaz:
https://doaj.org/article/83b83b04aef3441c9c80f51eeee98771
Autor:
Tariq Faquih, Maarten van Smeden, Jiao Luo, Saskia le Cessie, Gabi Kastenmüller, Jan Krumsiek, Raymond Noordam, Diana van Heemst, Frits R. Rosendaal, Astrid van Hylckama Vlieg, Ko Willems van Dijk, Dennis O. Mook-Kanamori
Publikováno v:
Metabolites, Vol 10, Iss 12, p 486 (2020)
Metabolomics studies have seen a steady growth due to the development and implementation of affordable and high-quality metabolomics platforms. In large metabolite panels, measurement values are frequently missing and, if neglected or sub-optimally i
Externí odkaz:
https://doaj.org/article/2d55b2c17fdd468aae948fb6888cdd2d
Autor:
Daniel DiCorpo, Jessica LeClair, Joanne B. Cole, Chloé Sarnowski, Fariba Ahmadizar, Lawrence F. Bielak, Anneke Blokstra, Erwin P. Bottinger, Layal Chaker, Yii-Der I. Chen, Ye Chen, Paul S. de Vries, Tariq Faquih, Mohsen Ghanbari, Valborg Gudmundsdottir, Xiuqing Guo, Natalie R. Hasbani, Dorina Ibi, M. Arfan Ikram, Maryam Kavousi, Hampton L. Leonard, Aaron Leong, Josep M. Mercader, Alanna C. Morrison, Girish N. Nadkarni, Mike A. Nalls, Raymond Noordam, Michael Preuss, Jennifer A. Smith, Stella Trompet, Petra Vissink, Jie Yao, Wei Zhao, Eric Boerwinkle, Mark O. Goodarzi, Vilmundur Gudnason, J. Wouter Jukema, Sharon L.R. Kardia, Ruth J.F. Loos, Ching-Ti Liu, Alisa K. Manning, Dennis Mook-Kanamori, James S. Pankow, H. Susan J. Picavet, Naveed Sattar, Eleanor M. Simonsick, W.M. Monique Verschuren, Ko Willems van Dijk, Jose C. Florez, Jerome I. Rotter, James B. Meigs, Josée Dupuis, Miriam S. Udler
Publikováno v:
Diabetes Care, 45(3), 674-683. American Diabetes Association Inc.
Diabetes Care, 45(3), 674-683. AMER DIABETES ASSOC
Diabetes care, vol 45, iss 3
Diabetes Care, 45(3), 674-683. AMER DIABETES ASSOC
Diabetes care, vol 45, iss 3
OBJECTIVE Type 2 diabetes (T2D) has heterogeneous patient clinical characteristics and outcomes. In previous work, we investigated the genetic basis of this heterogeneity by clustering 94 T2D genetic loci using their associations with 47 diabetes-rel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2071a39f7af63c7cf6308cce075ffb70
https://pure.eur.nl/en/publications/ca7db71b-8949-4784-b971-58aeefa45afc
https://pure.eur.nl/en/publications/ca7db71b-8949-4784-b971-58aeefa45afc
Autor:
Trevor Baglin, Astrid van Hylckama Vlieg, Frits R. Rosendaal, Ko Willems van Dijk, Tariq Faquih, Dennis O. Mook-Kanamori
Publikováno v:
Research and Practice in Thrombosis and Haemostasis
Research and Practice in Thrombosis and Haemostasis, Vol 5, Iss 4, Pp n/a-n/a (2021)
RESEARCH AND PRACTICE IN THROMBOSIS AND HAEMOSTASIS
Research and Practice in Thrombosis and Haemostasis, 5(4). WILEY
Research and Practice in Thrombosis and Haemostasis, Vol 5, Iss 4, Pp n/a-n/a (2021)
RESEARCH AND PRACTICE IN THROMBOSIS AND HAEMOSTASIS
Research and Practice in Thrombosis and Haemostasis, 5(4). WILEY
Background Venous thromboembolism (VTE) is a complex disease with an incidence rate of about 1 in 1000 per year. Despite the availability of validated biomarkers for VTE, unprovoked events account for 50% of first events. Therefore, emerging high‐t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1a81e373c6ee28ea5d0fdc9e71a3b75
http://europepmc.org/articles/PMC8110437
http://europepmc.org/articles/PMC8110437
Autor:
Diana van Heemst, Gabi Kastenmüller, Saskia le Cessie, Jiao Luo, Frits R. Rosendaal, Ko Willems van Dijk, Dennis O. Mook-Kanamori, Raymond Noordam, Maarten van Smeden, Jan Krumsiek, Tariq Faquih, Astrid van Hylckama Vlieg
Publikováno v:
Metabolites, Vol 10, Iss 486, p 486 (2020)
Metabolites, 10(12). MDPI
Metabolites
Metabolites 10, 1-23:E486 (2020)
Volume 10
Issue 12
Metabolites, 10(12). MDPI
Metabolites
Metabolites 10, 1-23:E486 (2020)
Volume 10
Issue 12
Metabolomics studies have seen a steady growth due to the development and implementation of affordable and high-quality metabolomics platforms. In large metabolite panels, measurement values are frequently missing and, if neglected or sub-optimally i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73fc7ac8fb6d9af1fe1d2a106bf75e9c
https://www.mdpi.com/2218-1989/10/12/486
https://www.mdpi.com/2218-1989/10/12/486
Autor:
M. Kloppenburg, J.H. von Hegedus, M. Ghorasaini, M. Loef, Frank P. Kroon, Tariq Faquih, M. Giera, Andreea Ioan-Facsinay
Publikováno v:
Osteoarthritis and Cartilage. 29:S141-S142
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8eee86a9668c146803780b0f48f9343d
https://doi.org/10.1016/j.joca.2021.02.200
https://doi.org/10.1016/j.joca.2021.02.200
Autor:
Tariq Faquih, Dorota Monies, Mohamed El-Kalioby, Ewa Goljan, Nada Al-Tassan, Mohamed Abouelhoda, Basma S. AlAbdulaziz, Khalid Al Abdelrahman, Shazia Subhani, Mohammad Shagrani, Jessica Burkholder, Fowzan S. Alkuraya, Nejat Mazhar, Dieter C. Broering, Renad Albar
Publikováno v:
Clinical Genetics. 92:52-61
Advanced cholestatic liver disease is a leading referral to pediatric liver transplant centers. Recent advances in the genetic classification of this group of disorders promise a highly personalized management although the genetic heterogeneity also
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c9807f652d4a4654100a5e6fdb6235d0
https://doi.org/10.1111/cge.12959
https://doi.org/10.1111/cge.12959
Autor:
Abeer E. Mustafa, Batoul Baz, Amna Magrashi, Tariq Faquih, Eman A.A. Al Yemni, Jameela Shinwari, Dorota Monies, Shazia Subhani, Nada Al-Tassan, Amjad Jabaan, Basma S. AlAbdulaziz, Wafa Ali, Mohamed Abouelhoda, Ewa Goljan, Bashayer R. Al-Mubarak, Thamer Alkhairallah, Mohamed H Al-Hamed, Renad Albar, Saeed Bohlega
Publikováno v:
Scientific Reports
Scientific Reports, Vol 9, Iss 1, Pp 1-9 (2019)
Scientific Reports, Vol 9, Iss 1, Pp 1-9 (2019)
Genetic studies of the familial forms of Parkinson’s disease (PD) have identified a number of causative genes with an established role in its pathogenesis. These genes only explain a fraction of the diagnosed cases. The emergence of Next Generation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a0c9ababf99a7aada65657951f292c7
http://europepmc.org/articles/PMC6399448
http://europepmc.org/articles/PMC6399448
Autor:
Mohamed Abouelhoda, John A. Sayer, Maha Alnemer, Dorota Monies, Maha Tulbah, Nada Al-Tassan, Salma Majid, Haya Al-Jurayb, Ahmed Alahmed, Mamdouh Albaqumi, Brian F. Meyer, Nada Alsahan, Dania S. Khalil, Mohamed H Al-Hamed, Basma Al Abdulaziz, Faisal S. BinHumaid, Rania Abudraz, Wesam Kurdi, Mohamed El-Kalioby, Noel Edwards, Asma I. Tahir, Zainab Alabdullah, Rubina Khan, Tariq Faquih
Publikováno v:
Journal of Medical Genetics
Background Inherited cystic kidney disorders are a common cause of end-stage renal disease. Over 50 ciliopathy genes, which encode proteins that influence the structure and function of the primary cilia, are implicated in cystic kidney disease. Metho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2f95f0d1dfcafd00aaf7b2bf67d7639
https://doi.org/10.1136/jmedgenet-2015-103469
https://doi.org/10.1136/jmedgenet-2015-103469
Autor:
Abeer E, Mustafa, Tariq, Faquih, Batoul, Baz, Rana, Kattan, Abdulelah, Al-Issa, Asma I, Tahir, Faiqa, Imtiaz, Khushnooda, Ramzan, Moeenaldeen, Al-Sayed, Mohammed, Alowain, Zuhair, Al-Hassnan, Hamad, Al-Zaidan, Mohamed, Abouelhoda, Bashayer R, Al-Mubarak, Nada A, Al Tassan
Publikováno v:
Genes
Quick and accurate molecular testing is necessary for the better management of many inherited diseases. Recent technological advances in various next generation sequencing (NGS) platforms, such as target panel-based sequencing, has enabled comprehens
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a9c3ecec698ab3c70d0f4ef00ced60e7
https://pubmed.ncbi.nlm.nih.gov/29789446
https://pubmed.ncbi.nlm.nih.gov/29789446