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Publications for Ansari, M

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Number of items: 8.

2017

Shaw, Natalie D; Brand, Harrison; Kupchinsky, Zachary A; Bengani, Hemant; Plummer, Lacey; Jones, Takako I; Erdin, Serkan; Williamson, Kathleen A; Rainger, Joe; Stortchevoi, Alexei; Samocha, Kaitlin; Currall, Benjamin B; Dunican, Donncha S; Collins, Ryan L; Willer, Jason R; Lek, Angela; Lek, Monkol; Nassan, Malik; Pereira, Shahrin; Kammin, Tammy; Lucente, Diane; Silva, Alexandra; Seabra, Catarina M; Chiang, Colby; An, Yu; Ansari, Morad; Rainger, Jacqueline K; Joss, Shelagh; Smith, Jill Clayton; Lippincott, Margaret F; et al (2017). Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome. Nature Genetics, 49(6):969.

Shaw, Natalie D; Brand, Harrison; Kupchinsky, Zachary A; Bengani, Hemant; Plummer, Lacey; Jones, Takako I; Erdin, Serkan; Williamson, Kathleen A; Rainger, Joe; Stortchevoi, Alexei; Samocha, Kaitlin; Currall, Benjamin B; Dunican, Donncha S; Collins, Ryan L; Willer, Jason R; Lek, Angela; Lek, Monkol; Nassan, Malik; Pereira, Shahrin; Kammin, Tammy; Lucente, Diane; Silva, Alexandra; Seabra, Catarina M; Chiang, Colby; An, Yu; Ansari, Morad; Rainger, Jacqueline K; Joss, Shelagh; Smith, Jill Clayton; Lippincott, Margaret F; et al (2017). SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome. Nature Genetics, 49(2):238-248.

Marquardt, L; Lacour, M; Hoernes, M; Opitz, L; Lecca, R; Volkmer, B; Reichenbach, J; Hohl, D; Ansari, M; Ozsahin, H; Güngör, T; Pachlopnik Schmid, J (2017). Unusual dermatological presentation and immune phenotype in SCID due to an IL7R mutation: the value of whole-exome sequencing and the potential benefit of newborn screening. Journal of the European Academy of Dermatology and Venerology, 31(3):e147-e148.

2016

Bartelink, Imke H; Lalmohamed, Arief; van Reij, Elisabeth M L; Dvorak, Christopher C; Savic, Rada M; Zwaveling, Juliette; Bredius, Robbert G M; Egberts, Antoine C G; Bierings, Marc; Kletzel, Morris; Shaw, Peter J; Nath, Christa E; Hempel, George; Ansari, Marc; Krajinovic, Maja; Théorêt, Yves; Duval, Michel; Keizer, Ron J; Bittencourt, Henrique; Hassan, Moustapha; Güngör, Tayfun; Wynn, Robert F; Veys, Paul; Cuvelier, Geoff D E; Marktel, Sarah; Chiesa, Robert; Cowan, Morton J; Slatter, Mary A; Stricherz, Melisa K; Jennissen, Cathryn; et al (2016). Association of busulfan exposure with survival and toxicity after haemopoietic cell transplantation in children and young adults: a multicentre, retrospective cohort analysis. The Lancet Haematology, 3(11):526-536.

Ruhe, Katharina Maria; Wangmo, Tenzin; De Clercq, Eva; Badarau, Domnita Oana; Ansari, Marc; Kühne, Thomas; Niggli, Felix; Elger, Bernice Simone; Swiss Pediatric Oncology Group (SPOG) (2016). Putting patient participation into practice in pediatrics-results from a qualitative study in pediatric oncology. European Journal of Pediatrics, 175(9):1147-1155.

Mader, Luzius; Rueegg, Corina S; Vetsch, Janine; Rischewski, Johannes; Ansari, Marc; Kuehni, Claudia E; Michel, Gisela; Swiss Paediatric Oncology Group (SPOG) (2016). Employment Situation of Parents of Long-Term Childhood Cancer Survivors. PLoS ONE, 11(3):e0151966.

2014

Marek, A; Stern, M; Chalandon, Y; Ansari, M; Ozsahin, H; Güngör, T; Gerber, B; Kühne, T; Passweg, J R; Gratwohl, A; Tichelli, A; Seger, R; Schanz, U; Halter, J; Stussi, G (2014). The impact of T-cell depletion techniques on the outcome after haploidentical hematopoietic SCT. Bone Marrow Transplantation, 49(1):55-61.

2013

Gerth-Kahlert, C; Williamson, K; Ansari, M; Rainger, J K; Hingst, V; Zimmermann, T; Tech, S; Guthoff, R F; van Heyningen, V; FitzPatrick, D R (2013). Clinical and mutation analysis of 51 probands with anophthalmia and/or severe microphthalmia from a single center. Molecular Genetics & Genomic Medicine, 1(1):15-31.

This list was generated on Sat Nov 18 02:42:01 2017 CET.