Increased Risk of Cancer Other Than Melanoma in CDKN2A Founder Mutation (p16-Leiden)-Positive Melanoma Families von DE SNOO, Femke A, BISHOP, D. Timothy, WILLEMZE, Rein, BREUNING, Martijn H, GRUIS, Nelleke A, BERGMAN, Wilma, VAN LEEUWEN, Inge, VAN DER DRIFT, Clasine, VAN NIEUWPOORT, Frans A, OUT-LUITING, Coby J, VASEN, Hans F, TER HUURNE, Jeanet A. C, FRANTS, Rune R

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The hemoglobinopathies, molecular disease mechanisms and diagnostics von Harteveld, Cornelis L., Achour, Ahlem, Arkesteijn, Sandra J. G., Huurne, Jeanet, Verschuren, Maaike, Bhagwandien‐Bisoen, Sharda, Schaap, Rianne, Vijfhuizen, Linda, Idrissi, Hakima, Koopmann, Tamara T.

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Loss-of-Function Variants in SUPT5H as Modifying Factors in Beta-Thalassemia von Harteveld, Cornelis L, Achour, Ahlem, Fairuz Mohd Hasan, Nik Fatma, Legebeke, Jelmer, Arkesteijn, Sandra J G, Huurne, Jeanet Ter, Verschuren, Maaike, Bhagwandien-Bisoen, Sharda, Schaap, Rianne, Vijfhuizen, Linda, Idrissi, Hakima El, Babbs, Christian, Higgs, Douglas R, Koopmann, Tamara T, Vrettou, Christina, Traeger-Synodinos, Joanne, Baas, Frank

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The first report of hemoglobin E in combination with the highly unstable alpha‐globin variant Hb Adana: The importance of molecular confirmation von Achour, Ahlem, Grouw, Elke, Erp, Femke, Arkesteijn, Sandra, Schaap, Rianne, Huurne, Jeanet ter, Bisoen, Sharda, Verschuren, Maaike, Harteveld, Cornelis L.

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Genetic testing in familial melanoma: uptake and implications von de Snoo, Femke A., Riedijk, Samantha R., van Mil, Anneke M., Bergman, Wilma, ter Huurne, Jeanet A.C., Timman, Reinier, Bertina, Wieke, Gruis, Nelleke A., Vasen, Hans F.A., van Haeringen, Arie, Breuning, Martijn H., Tibben, Aad

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A mutation hotspot at the p14ARF splice site von Harland, Mark, Taylor, Claire F, Chambers, Philip A, Kukalizch, Kairen, Randerson-Moor, Juliette A, Gruis, Nelleke A, de Snoo, Femke A, ter Huurne, Jeanet A C, Goldstein, Alisa M, Tucker, Margaret A, Bishop, D Timothy, Bishop, Julia A Newton

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From sporadic atypical nevi to familial melanoma: Risk analysis for melanoma in sporadic atypical nevus patients von de Snoo, Femke A., MD, Kroon, Marije W., MSc, Bergman, Wilma, MD, ter Huurne, Jeanet A.C., MSc, Houwing-Duistermaat, Jeanine J., PhD, van Mourik, Leny, Snels, Dyon G.C.T.M., MD, Breuning, Martijn H., MD, Willemze, Rein, MD, Frants, Rune R., PhD, Gruis, Nelleke A., PhD

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Genome-wide linkage scan for atypical nevi in p16-Leiden melanoma families von de Snoo, Femke A, Hottenga, Jouke-Jan, Gillanders, Elizabeth M, Sandkuijl, Loudewijk A, Jones, Mary Pat, Bergman, Wilma, van der Drift, Clasine, van Leeuwen, Inge, van Mourik, Lenny, Huurne, Jeanet A C ter, Frants, Rune R, Willemze, Rein, Breuning, Martijn H, Trent, Jeffrey M, Gruis, Nelleke A

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Melanocortin 1 Receptor (MC1R) Gene Variants are Associated with an Increased Risk for Cutaneous Melanoma Which is Largely Independent of Skin Type and Hair Color von Kennedy, Cornelis, ter Huurne, Jeanet, Berkhout, Marjo, Gruis, Nelleke, Bastiaens, Maarten, Bergman, W., Willemze, R., Bouwes Bavinck, Jan Nico

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Melanocortin 1 Receptor (MC1R) Variants in High Melanoma Risk Patients are Associated with Specific Dermoscopic ABCD Features von QUINT, Koen D, VAN DER RHEE, Jasper I, GRUIS, Nelleke A, TER HUURNE, Jeanet A, WOLTERBEEK, Ron, VAN DER STOEP, Nienke, BERGMAN, Wilma, KUKUTSCH, Nicole A

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A comparison of CDKN2A mutation detection within the Melanoma Genetics Consortium (GenoMEL) von Harland, Mark, Goldstein, Alisa M, Kukalizch, Kairen, Taylor, Claire, Hogg, David, Puig, Susana, Badenas, Celia, Gruis, Nelleke, ter Huurne, Jeanet, Bergman, Wilma, Hayward, Nicholas K, Stark, Mitchell, Tsao, Hensin, Tucker, Margaret A, Landi, Maria Teresa, Scarra, Giovanna Bianchi, Ghiorzo, Paola, Kanetsky, Peter A, Elder, David, Mann, Graham J, Holland, Elizabeth A, Bishop, D. Timothy, Newton Bishop, Julia

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A new gene associated with a β-thalassemia phenotype: the observation of variants in SUPT5H von Achour, Ahlem, Koopmann, Tamara, Castel, Rob, Santen, Gijs W.E., den Hollander, Nicolette, Knijnenburg, Jeroen, Ruivenkamp, Claudia A.L., Arkesteijn, Sandra G.J., ter Huurne, Jeanet, Bisoen, Sharda, Verschuren, Maaike, Vijfhuizen, Linda, Schaap, Rianne, Grimbergen, Anneliese, Slomp, Jennichjen, Traeger-Synodinos, Joanne, Vrettou, Christina, Pissard, Serge, Galacteros, Frederic, Baas, Frank, Harteveld, Cornelis L.

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Calibration by commutable control materials is able to reduce inter-method differences of current high-performance methods for HbA2 von Paleari, Renata, Ceriotti, Ferruccio, Harteveld, Cornelis L., Strollo, Marta, Bakker-Verweij, Greet, ter Huurne, Jeanet, Bisoen, Sharda, Mosca, Andrea

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Genome-wide association study identifies novel loci predisposing to cutaneous melanoma von Amos, Christopher I., Wang, Li-E, Lee, Jeffrey E., Gershenwald, Jeffrey E., Chen, Wei V., Fang, Shenying, Kosoy, Roman, Zhang, Mingfeng, Qureshi, Abrar A., Vattathil, Selina, Schacherer, Christopher W., Gardner, Julie M., Wang, Yuling, Tim Bishop, D., Barrett, Jennifer H., MacGregor, Stuart, Hayward, Nicholas K., Martin, Nicholas G., Duffy, David L., Mann, Graham J., Cust, Anne, Hopper, John, Brown, Kevin M., Grimm, Elizabeth A., Xu, Yaji, Han, Younghun, Jing, Kaiyan, McHugh, Caitlin, Laurie, Cathy C., Doheny, Kim F., Pugh, Elizabeth W., Seldin, Michael F., Han, Jiali, Wei, Qingyi

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Genome-wide linkage scan for atypical nevi in p16-Leiden melanoma families von De Snoo, Femke A, Hottenga, Jouke-jan, Gillanders, Elizabeth M, Sandkuijl, Lodewijk A, Jones, Mary Pat, Bergman, Wilma, Van Der Drift, Clasine, Van Leeuwen, Inge, Van Mourik, Leny, Huurne, Jeanet A C Ter, Frants, Rune R, Willemze, Rein, Breuning, Martijn H, Trent, Jeffrey M, Gruis, Nelleke A

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Alpha Thalassemia Screening in Multiethnic Population in Northern Europe Using Hb Bart's Immunochromatographic Test von Nik Mohd Hasan, Nik Fatma Fairuz, Arkesteijn, Sandra J G, Ter Huurne, Jeanet, Verschuren, Maaike, Bhagwandien-Bisoen, Sharda, Schaap, Rianne, Vijfhuizen, Linda, El Idrissi, Hakima, Koopmann, Tamara T, Harteveld, Cornelis L

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Calibration by commutable control materials is able to reduce inter-method differences of current high-performance methods for HbA 2 von Paleari, Renata, Ceriotti, Ferruccio, Harteveld, Cornelis L., Strollo, Marta, Bakker-Verweij, Greet, ter Huurne, Jeanet, Bisoen, Sharda, Mosca, Andrea

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Calibration by commutable control materials is able to reduce inter-method differences of current high-performance methods for HbA 2 von Paleari, Renata, Ceriotti, Ferruccio, Harteveld, Cornelis L, Strollo, Marta, Bakker-Verweij, Greet, Ter Huurne, Jeanet, Bisoen, Sharda, Mosca, Andrea

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Pathway-based analysis of a melanoma genome-wide association study: analysis of genes related to tumour-immunosuppression von Schoof, Nils, Iles, Mark M, Bishop, D Timothy, Newton-Bishop, Julia A, Barrett, Jennifer H

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Erratum: Genome-wide linkage scan for atypical nevi in p16-Leiden melanoma families von de Snoo, Femke A, Hottenga, Jouke-Jan, Gillanders, Elizabeth M, Sandkuijl, Lodewijk A, Jones, Mary Pat, Bergman, Wilma, van der Drift, Clasine, van Leeuwen, Inge, van Mourik, Leny, Huurne, Jeanet A C ter, Frants, Rune R, Willemze, Rein, Breuning, Martijn H, Trent, Jeffrey M, Gruis, Nelleke A

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