Adverse effects of trichothiodystrophy DNA repair and transcription gene disorder on human fetal development
Moslehi, R, Signore, C, Tamura, D, Mills, JL, DiGiovanna, JJ, Tucker, MA, Troendle, J, Ueda, T, Boyle, J, Khan, SG, Oh, K-S, Goldstein, AM, Kraemer, KH
Published in Clinical genetics (01.04.2010)
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Femoral venous access is safe in burned children: An analysis of 224 catheters
Goldstein, Allan M., Weber, Joan M., Sheridan, Robert L.
Published in The Journal of pediatrics (01.03.1997)
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ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma
Gurzau, Eugene, Jakobsdottir, Margret, Magnusson, Veronica, Kumar, Rajiv, Olafsson, Jon H, Ragnarsson, Rafn, Kiemeney, Lambertus A, Thorisdottir, Kristin, Benediktsdottir, Kristrun R, Kostulas, Konstantinos, Botella-Estrada, Rafael, Gretarsdottir, Solveig, Hansson, Johan, Thorsteinsdottir, Unnur, Grasa, Matilde, Saez, Berta, Steinberg, Stacy, Rudnai, Peter, Stacey, Simon N, Gudbjartsson, Daniel F, Goldstein, Alisa M, Andres, Raquel, Mayordomo, José I, Gulcher, Jeffrey, Kong, Augustine, Sveinsdottir, Steinunn G, Sulem, Patrick, Stefansson, Kari, Rafnar, Thorunn, Koppova, Kvetoslava, Tucker, Margaret A, Juberías, Pablo, Lindblom, Annika, Nagore, Eduardo, Sigurgeirsson, Bardur, Scherer, Dominique, Soriano, Virtudes, Helgason, Agnar
Published in Nature genetics (01.07.2008)
Published in Nature genetics (01.07.2008)
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Estimated Prevalence, Tumor Spectrum, and Neurofibromatosis Type 1-Like Phenotype of CDKN2A-Related Melanoma-Astrocytoma Syndrome
Sargen, Michael R, Kim, Jung, Potjer, Thomas P, Velthuizen, Mary E, Martir-Negron, Arelis E, Odia, Yazmin, Helgadottir, Hildur, Hatton, Jessica N, Haley, Jeremy S, Thone, Gretchen, Widemann, Brigitte C, Gross, Andrea M, Yohe, Marielle E, Kaplan, Rosandra N, Shern, Jack F, Sundby, R Taylor, Astiazaran-Symonds, Esteban, Yang, Xiaohong R, Carey, David J, Tucker, Margaret A, Stewart, Douglas R, Goldstein, Alisa M
Published in JAMA dermatology (Chicago, Ill.) (01.10.2023)
Published in JAMA dermatology (Chicago, Ill.) (01.10.2023)
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Estimating CDKN2A mutation carrier probability among global familial melanoma cases using GenoMELPREDICT
Taylor, Nicholas J., Mitra, Nandita, Qian, Lu, Avril, Marie-Françoise, Bishop, D. Timothy, Bressac-de Paillerets, Brigitte, Bruno, William, Calista, Donato, Cuellar, Francisco, Cust, Anne E., Demenais, Florence, Elder, David E., Gerdes, Anne-Marie, Ghiorzo, Paola, Goldstein, Alisa M., Grazziotin, Thais C., Gruis, Nelleke A., Hansson, Johan, Harland, Mark, Hayward, Nicholas K., Hocevar, Marko, Höiom, Veronica, Holland, Elizabeth A., Ingvar, Christian, Landi, Maria Teresa, Landman, Gilles, Larre-Borges, Alejandra, Mann, Graham J., Nagore, Eduardo, Olsson, Håkan, Palmer, Jane M., Perić, Barbara, Pjanova, Dace, Pritchard, Antonia L., Puig, Susana, Schmid, Helen, van der Stoep, Nienke, Tucker, Margaret A., Wadt, Karin A.W., Yang, Xiaohong R., Newton-Bishop, Julia A., Kanetsky, Peter A.
Published in Journal of the American Academy of Dermatology (01.08.2019)
Published in Journal of the American Academy of Dermatology (01.08.2019)
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Phenocopies in melanoma-prone families with germ-line CDKN2A mutations
Helgadottir, Hildur, Olsson, Håkan, Tucker, Margaret A, Yang, Xiaohong R, Höiom, Veronica, Goldstein, Alisa M
Published in Genetics in medicine (01.09.2018)
Published in Genetics in medicine (01.09.2018)
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Common sequence variants on 20q11.22 confer melanoma susceptibility
Hansson, Johan, Kefford, Richard F, Hopper, John L, Iyadurai, Kelly, Whiteman, David, Stark, Mitchell, Giles, Graham G, Aitken, Joanne F, Zhao, Zhen Zhen, Jetann, Jodie, Bishop, Julia Newton, Gillanders, Elizabeth M, Puig, Susana, Craig, David W, MacGregor, Stuart, Hayward, Nicholas K, Holland, Elizabeth A, Brown, Kevin M, Demenais, Florence, K Henders, Anjali, Cust, Anne E, Green, Adele, Mann, Graham J, Montgomery, Grant W, Schmid, Helen, Ghiorzo, Paola, Homer, Nils, Gruis, Nelleke A, Armstrong, Bruce K, Goldstein, Alisa M, Duffy, David L, Ferguson, Megan, Trent, Jeffrey M, Stephan, Dietrich A, Martin, Nicholas G, Thomas, Shane, Campbell, Megan J, Elder, David E, Maskiell, Judith A, Olsson, Håkan
Published in Nature genetics (01.07.2008)
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Novel loss-of-function variant in DENND5A impedes melanosomal cargo transport and predisposes to familial cutaneous melanoma
Yang, Muyi, Johnsson, Per, Bräutigam, Lars, Yang, Xiaohong R., Thrane, Kim, Gao, Jiwei, Tobin, Nicholas P., Zhou, Yitian, Yu, Rong, Nagy, Noemi, Engström, Pär G., Tuominen, Rainer, Eriksson, Hanna, Lundeberg, Joakim, Tucker, Margaret A., Goldstein, Alisa M., Egyhazi-Brage, Suzanne, Zhao, Jian, Cao, Yihai, Höiom, Veronica
Published in Genetics in medicine (01.01.2022)
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Characterization of T gene sequence variants and germline duplications in familial and sporadic chordoma
Kelley, Michael J., Shi, Jianxin, Ballew, Bari, Hyland, Paula L., Li, Wen-Qing, Rotunno, Melissa, Alcorta, David A., Liebsch, Norbert J., Mitchell, Jason, Bass, Sara, Roberson, David, Boland, Joseph, Cullen, Michael, He, Ji, Burdette, Laurie, Yeager, Meredith, Chanock, Stephen J., Parry, Dilys M., Goldstein, Alisa M., Yang, Xiaohong R.
Published in Human genetics (01.10.2014)
Published in Human genetics (01.10.2014)
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Major surgical conditions of childhood and their lifelong implications: comprehensive review
Cullis, Paul S, Fouad, Dina, Goldstein, Allan M, Wong, Kenneth K Y, Boonthai, Ampaipan, Lobos, Pablo, Pakarinen, Mikko P, Losty, Paul D
Published in BJS open (08.05.2024)
Published in BJS open (08.05.2024)
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Association of MC1R Variants and Host Phenotypes With Melanoma Risk in CDKN2A Mutation Carriers: A GenoMEL Study
Demenais, F., Mohamdi, H., Chaudru, V., Goldstein, A. M., Newton Bishop, J. A., Bishop, D. T., Kanetsky, P. A., Hayward, N. K., Gillanders, E., Elder, D. E., Avril, M. F., Azizi, E., van Belle, P., Bergman, W., Bianchi-Scarrà, G., Bressac-de Paillerets, B., Calista, D., Carrera, C., Hansson, J., Harland, M., Hogg, D., Höiom, V., Holland, E. A., Ingvar, C., Landi, M. T., Lang, J. M., Mackie, R. M., Mann, G. J., Ming, M. E., Njauw, C. J., Olsson, H., Palmer, J., Pastorino, L., Puig, S., Randerson-Moor, J., Stark, M., Tsao, H., Tucker, M. A., van der Velden, P., Yang, X. R., Gruis, N.
Published in JNCI : Journal of the National Cancer Institute (20.10.2010)
Published in JNCI : Journal of the National Cancer Institute (20.10.2010)
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Chordoma: Incidence and Survival Patterns in the United States, 1973-1995
McMaster, Mary L., Goldstein, Alisa M., Bromley, Christina M., Ishibe, Naoko, Parry, Dilys M.
Published in Cancer causes & control (01.01.2001)
Published in Cancer causes & control (01.01.2001)
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Mutations in SUFU predispose to medulloblastoma
Rutka, James T, Hogg, David, Taylor, Michael D, Liu, Ling, Raffel, Corey, Hui, Chi-chung, Mainprize, Todd G, Zhang, Xiaoyun, Agatep, Ron, Chiappa, Sharon, Gao, Luzhang, Lowrance, Anja, Hao, Aihau, Goldstein, Alisa M, Stavrou, Theodora, Scherer, Stephen W, Dura, Wieslaw T, Wainwright, Brandon, Squire, Jeremy A
Published in Nature genetics (01.07.2002)
Published in Nature genetics (01.07.2002)
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Geographical Variation in the Penetrance of CDKN2A Mutations for Melanoma
Bishop, D. Timothy, Demenais, Florence, Goldstein, Alisa M., Bergman, Wilma, Bishop, Julia Newton, Paillerets, Brigitte Bressac-de, Chompret, Agnès, Ghiorzo, Paola, Gruis, Nelleke, Hansson, Johan, Harland, Mark, Hayward, Nicholas, Holland, Elizabeth A., Mann, Graham J., Mantelli, Michela, Nancarrow, Derek, Platz, Anton, Tucker, Margaret A.
Published in JNCI : Journal of the National Cancer Institute (19.06.2002)
Published in JNCI : Journal of the National Cancer Institute (19.06.2002)
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Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutations
Yang, Xiaohong R., Rotunno, Melissa, Xiao, Yanzi, Ingvar, Christian, Helgadottir, Hildur, Pastorino, Lorenza, van Doorn, Remco, Bennett, Hunter, Graham, Cole, Sampson, Joshua N., Malasky, Michael, Vogt, Aurelie, Zhu, Bin, Bianchi-Scarra, Giovanna, Bruno, William, Queirolo, Paola, Fornarini, Giuseppe, Hansson, Johan, Tuominen, Rainer, Burdett, Laurie, Hicks, Belynda, Hutchinson, Amy, Jones, Kristine, Yeager, Meredith, Chanock, Stephen J., Landi, Maria Teresa, Höiom, Veronica, Olsson, Håkan, Gruis, Nelleke, Ghiorzo, Paola, Tucker, Margaret A., Goldstein, Alisa M.
Published in Human genetics (01.11.2016)
Published in Human genetics (01.11.2016)
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MC1R, ASIP, and DNA Repair in Sporadic and Familial Melanoma in a Mediterranean Population
Landi, Maria Teresa, Kanetsky, Peter A., Tsang, Shirley, Gold, Bert, Munroe, David, Rebbeck, Timothy, Swoyer, Jennifer, Ter-Minassian, Monica, Hedayati, Mohammad, Grossman, Lawrence, Goldstein, Alisa M., Calista, Donato, Pfeiffer, Ruth M.
Published in JNCI : Journal of the National Cancer Institute (06.07.2005)
Published in JNCI : Journal of the National Cancer Institute (06.07.2005)
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Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions
Barrett, Jennifer H., Taylor, John C., Bright, Chloe, Harland, Mark, Dunning, Alison M., Akslen, Lars A., Andresen, Per A., Avril, Marie‐Françoise, Azizi, Esther, Bianchi Scarrà, Giovanna, Brossard, Myriam, Brown, Kevin M., Dębniak, Tadeusz, Elder, David E., Friedman, Eitan, Ghiorzo, Paola, Gillanders, Elizabeth M., Gruis, Nelleke A., Hansson, Johan, Helsing, Per, Hočevar, Marko, Höiom, Veronica, Ingvar, Christian, Landi, Maria Teresa, Lang, Julie, Lathrop, G. Mark, Lubiński, Jan, Mackie, Rona M., Molven, Anders, Novaković, Srdjan, Olsson, Håkan, Puig, Susana, Puig‐Butille, Joan Anton, van der Stoep, Nienke, van Doorn, Remco, van Workum, Wilbert, Goldstein, Alisa M., Kanetsky, Peter A., Pharoah, Paul D. P., Demenais, Florence, Hayward, Nicholas K., Newton Bishop, Julia A., Bishop, D. Timothy, Iles, Mark M.
Published in International journal of cancer (15.03.2015)
Published in International journal of cancer (15.03.2015)
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