Retraction: 'Genotyping of CYP2C19 polymorphisms and its clinical validation in the ethnic Arab population', by T. Tayeb, Dana H. Bakheet, Khaled Zaza, Salma M. Wakil and Nduna Dzimiri

England: Blackwell Publishing Ltd

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Mendelian randomisation implicates hyperlipidaemia as a risk factor for colorectal cancer

Rodriguez‐Broadbent, Henry ; Law, Philip J. ; Sud, Amit ; Palin, Kimmo ; Tuupanen, Sari ; Gylfe, Alexandra ; Hänninen, Ulrika A. ; Cajuso, Tatiana ; Tanskanen, Tomas ; Kondelin, Johanna ; Kaasinen, Eevi ; Sarin, Antti‐Pekka ; Ripatti, Samuli ; Eriksson, Johan G. ; Rissanen, Harri ; Knekt, Paul ; Pukkala, Eero ; Jousilahti, Pekka ; Salomaa, Veikko ; Palotie, Aarno ; Renkonen‐Sinisalo, Laura ; Lepistö, Anna ; Böhm, Jan ; Mecklin, Jukka‐Pekka ; Al‐Tassan, Nada A. ; Palles, Claire ; Martin, Lynn ; Barclay, Ella ; Farrington, Susan M. ; Timofeeva, Maria N. ; Meyer, Brian F. ; Wakil, Salma M. ; Campbell, Harry ; Smith, Christopher G. ; Idziaszczyk, Shelley ; Maughan, Timothy S. ; Kaplan, Richard ; Kerr, Rachel ; Kerr, David ; Passarelli, Michael N. ; Figueiredo, Jane C. ; Buchanan, Daniel D. ; Win, Aung K. ; Hopper, John L. ; Jenkins, Mark A. ; Lindor, Noralane M. ; Newcomb, Polly A. ; Gallinger, Steven ; Conti, David ; Schumacher, Fred ; Casey, Graham ; Aaltonen, Lauri A. ; Cheadle, Jeremy P. ; Tomlinson, Ian P. ; Dunlop, Malcolm G. ; Houlston, Richard S.

United States: Wiley Subscription Services, Inc

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Genome‐wide association study and meta‐analysis in Northern European populations replicate multiple colorectal cancer risk loci

Tanskanen, Tomas ; van den Berg, Linda ; Välimäki, Niko ; Aavikko, Mervi ; Ness‐Jensen, Eivind ; Hveem, Kristian ; Wettergren, Yvonne ; Bexe Lindskog, Elinor ; Tõnisson, Neeme ; Metspalu, Andres ; Silander, Kaisa ; Orlando, Giulia ; Law, Philip J. ; Tuupanen, Sari ; Gylfe, Alexandra E. ; Hänninen, Ulrika A. ; Cajuso, Tatiana ; Kondelin, Johanna ; Sarin, Antti‐Pekka ; Pukkala, Eero ; Jousilahti, Pekka ; Salomaa, Veikko ; Ripatti, Samuli ; Palotie, Aarno ; Järvinen, Heikki ; Renkonen‐Sinisalo, Laura ; Lepistö, Anna ; Böhm, Jan ; Mecklin, Jukka‐Pekka ; Al‐Tassan, Nada A. ; Palles, Claire ; Martin, Lynn ; Barclay, Ella ; Tenesa, Albert ; Farrington, Susan M. ; Timofeeva, Maria N. ; Meyer, Brian F. ; Wakil, Salma M. ; Campbell, Harry ; Smith, Christopher G. ; Idziaszczyk, Shelley ; Maughan, Tim S. ; Kaplan, Richard ; Kerr, Rachel ; Kerr, David ; Buchanan, Daniel D. ; Win, Aung K. ; Hopper, John ; Jenkins, Mark A. ; Newcomb, Polly A. ; Gallinger, Steve ; Conti, David ; Schumacher, Fredrick R. ; Casey, Graham ; Cheadle, Jeremy P. ; Dunlop, Malcolm G. ; Tomlinson, Ian P. ; Houlston, Richard S. ; Palin, Kimmo ; Aaltonen, Lauri A.

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Novel mutations in TGM1 and ABCA12 cause autosomal recessive congenital ichthyosis in five Saudi families

Wakil, Salma M. ; Binamer, Yousef ; Al-Dossari, Haya ; Al-Humaidy, Rawan ; Thuraya, Rula Al ; Khalifa, Ola ; Finsterer, Josef ; Meyer, Brian F. ; Al Owain, Mohammed

England: Blackwell Publishing Ltd

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Exome sequencing identifies novel NTRK1 mutations in patients with HSAN‐IV phenotype

Altassan, Ruqaiah ; Saud, Haya Al ; Masoodi, Tariq Ahmad ; Dosssari, Haya Al ; Khalifa, Ola ; Al‐Zaidan, Hamad ; Sakati, Nadia ; Rhabeeni, Zuhair ; Al‐Hassnan, Zuhair ; Binamer, Yousef ; Alhashemi, Nadia ; Wade, William ; Al‐Zayed, Zayed ; Al‐Sayed, Moeen ; Al‐Muhaizea, Mohamed A. ; Meyer, Brian ; Al‐Owain, Mohammad ; Wakil, Salma M.

United States: Wiley Subscription Services, Inc

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Genotyping of CYP2C19 polymorphisms and its clinical validation in the ethnic Arab population

Tayeb, Hamsa T. ; Bakheet, Dana H. ; Zaza, Khaled ; Wakil, Salma M. ; Dzimiri, Nduna

England: Blackwell Publishing Ltd

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Novel copy number variants and major limb reduction malformation: Report of three cases

Shamseldin, Hanan E. ; Anazi, Shams ; Wakil, Salma M. ; Faqeih, Eissa ; El Khashab, Heba Y. ; Salih, Mustafa A. ; Al-Qattan, Mohammad M. ; Hashem, Mais ; Alsedairy, Haifa ; Alkuraya, Fowzan S.

United States: Blackwell Publishing Ltd

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Genetic Study of Saudi Diabetes (GSSD): significant association of the KCNJ11 E23K polymorphism with type 2 diabetes

Alsmadi, Osama ; Al-Rubeaan, Khalid ; Wakil, Salma M. ; Imtiaz, Faiqa ; Mohamed, Gamal ; Al-Saud, Haya ; Al-Saud, Nouran Abu ; Aldaghri, Nasser ; Mohammad, Shahinaz ; Meyer, Brian F

Chichester, UK: John Wiley & Sons, Ltd

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Prevalence and profile of mutations associated with lamivudine therapy in Indian patients with chronic hepatitis B in the surface and polymerase genes of hepatitis B virus

Wakil, Salma M. ; Kazim, Syed N. ; Khan, Luqman A. ; Raisuddin, Sheikh ; Parvez, Mohammad K. ; Guptan, Rajkumar C. ; Thakur, Varsha ; Hasnain, Seyed E. ; Sarin, Shiv K.

New York: Wiley Subscription Services, Inc., A Wiley Company

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Novel mutations in TGM 1 and ABCA 12 cause autosomal recessive congenital ichthyosis in five Saudi families

Wakil, Salma M. ; Binamer, Yousef ; Al‐Dossari, Haya ; Al‐Humaidy, Rawan ; Thuraya, Rula Al ; Khalifa, Ola ; Finsterer, Josef ; Meyer, Brian F. ; Al Owain, Mohammed

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