Browse by Divisions pre August 2011

Anderson, Christopher, Davies, Justin H., Lamont, Lilias and Foulds, Nicola (2011) Early pontocerebellar hypoplasia with vanishing testes: A new syndrome? American Journal of Medical Genetics Part A, 155, (4), 667-672. (doi:10.1002/ajmg.a.33897).

Baple, Emma L., Poole, Rebecca L., Mansour, Sahar, Willoughby, Catherine, Temple, I. Karen, Docherty, Louise E., Taylor, Rohan and Mackay, Deborah J.G. (2011) An atypical case of hypomethylation at multiple imprinted loci. European Journal of Human Genetics, 19, (3), 360-362. (doi:10.1038/ejhg.2010.218). (PMID:21206512).

Bianchi, F., Raponi, M., Piva, F., Viel, A., Bearzi, I., Galizia, E., Bracci, R., Belvederesi, L., Loretelli, C., Brugiati, C., Corradini, F., Baralle, D. and Cellerino, R. (2011) An intronic mutation in MLH1 associated with familial colon and breast cancer. Familial Cancer, 10, (1), 27-35. (doi:10.1007/s10689-010-9371-4). (PMID:20717847).

Bicknell, Louise S., Bongers, Ernie M.H.F., Leitch, Andrea, Brown, Stephen, Schoots, Jeroen, Harley, Margaret E., Aftimos, Salim, Al-Aama, Jumana Y., Bober, Michael, Brown, Paul A.J., van Bokhoven, Hans, Dean, John, Edrees, Alaa Y., Feingold, Murray, Fryer, Alan, Hoefsloot, Lies H., Kau, Nikolaus, Knoers, Nine V.A.M., MacKenzie, James, Opitz, John M., Sarda, Pierre, Ross, Alison, Temple, I. Karen, Toutain, Annick, Wise, Carol A., Wright, Michael and Jackson, Andrew P. (2011) Mutations in the pre-replication complex cause Meier-Gorlin syndrome. Nature Genetics, 43, (4), 356-359. (doi:10.1038/ng.775). (PMID:21358632).

Bishop, Dorothy V.M., Jacobs, Patricia A., Lachlan, Katherine, Wellesley, Diana, Barnicoat, Angela, Boyd, Patricia A., Fryer, Alan, Middlemiss, Prisca, Smithsom, Sarah, Metcalfe, Kay, Shears, Deborah, Leggett, Victoria, Natiion, Kate and Scerif, Gaia (2011) Autism, language and communication in children with sex chromosome trisomies. Archives of Disease in Childhood (doi:10.1136/adc.2009.179747).

Blyth, Moira and Baralle, Diana (2011) Anophthalmia in fronto–facial–nasal dysplasia. Clinical Dysmorphology, 20, (2), 73-74. (doi:10.1097/MCD.0b013e328343515c). (PMID:21317770).

Buratti, Emanuele, Chivers, Martin, Hwang, Gyulin and Vorechovsky, Igor (2011) DBASS3 and DBASS5: databases of aberrant 3'- and 5'-splice sites. Nucleic Acids Research, 39, (Supplement 1), D86-D91. (doi:10.1093/nar/gkq887). (PMID:20929868).

Carroll, Christopher J., Suleman, Naushaad, Davidson, Sean M., Faulkes, David J., Diss, James K., Knight, Richard, Stephanou, Anastasis, Latchman, David S. and Townsend, Paul A. (2011) Transgenic overexpression of HSP56 does not result in cardiac hypertrophy nor protect from ischaemia/reperfusion injury. International Journal of Biochemistry & Cell Biology, 43, (1), 74-79. (doi:10.1016/j.biocel.2010.09.020). (PMID:20932935).

Chase, Andrew and Cross, Nicholas C. (2011) Aberrations of EZH2 in cancer. Clinical Cancer Research, 17, (9), 2613-2618. (doi:10.1158/1078-0432.CCR-10-2156). (PMID:21367748).

Clericuzio, Carol, Hingorani, Melanie, Crolla, John A., van Heyningen, Veronica and Verloes, Alain (2011) Clinical utility gene card for: WAGR syndrome. European Journal of Human Genetics, 19, (4) (doi:10.1038/ejhg.2010.220). (PMID:21224893).

Cohen, Nicola R., Hammans, Simon R., Macpherson, James and Nicoll, James A.R. (2011) New neuropathological findings in Unverrichta–Lundborg disease: neuronal intranuclear and cytoplasmic inclusions. Acta Neuropathologica, 121, (3), 421-427. (doi:10.1007/s00401-010-0738-2). (PMID:20721566).

Davies, J.H. and Shaw, N.J. (2011) Preventable but no strategy: vitamin D deficiency in the UK. Archives of Disease in Childhood, 96, (7), 614-615. (doi:10.1136/adc.2010.191627).

Dowling, James J., Lillis, Suzanne, Amburgey, Kimberley, Zhou, Haiyan, Al-Sarraj, Safa, Buk, Stefan J.A., Wraige, Elizabeth, Chow, Gabby, Abbs, Stephen, Leber, Steven, Lachlan, Katherine, Baralle, Diana, Taylor, Alexandra, Sewry, Caroline, Muntoni, Francesco and Jungbluth, Heinz (2011) King–Denborough syndrome with and without mutations in the skeletal muscle ryanodine receptor (RYR1) gene. Neuromuscular Disorders, 21, (6), 420-427. (doi:10.1016/j.nmd.2011.03.006). (PMID: 21514828).

Duhoux, Francois P., Auger, Nathalie, De Wilde, Sigrid, Wittnebel, Sebastian, Ameye, Geneviève, Bahloula, Khadija, Van den Berg, Catherine, Libouton, Jeanne-Marie, Saussoy, Pascale and Grand, Francis H. (2011) Letter to the Editor. The t(1;9)(p34;q34) fusing ABL1 with SFPQ, a pre-mRNA processing gene, is recurrent in acute lymphoblastic leukemias. Leukemia Research, 35, (7), e114-e117. (doi:10.1016/j.leukres.2011.02.011). (PMID:21388681).

Eggermann, Thomas, Buiting, Karin and Temple, I. Karen (2011) Clinical utility gene card for: Silver–Russell syndrome. European Journal of Human Genetics, 19, (3) (doi:10.1038/ejhg.2010.202). (PMID:21150879).

El-Serafi, A.T., Wilson, D.I., Roach, H.I. and Oreffo, R.O.C. (2011) Developmental plasticity of human foetal femur-derived cells in pellet culture: self assembly of an osteoid shell around a cartilaginous core. European Cells & Materials, 21, 558-567. (PMID:21710446).

Elling, Christian, Erben, Phillipp, Walz, Christoph, Frickenhaus, Marie, Schemionek, Mirle, Stehling, Martin, Serve, Hubert, Cross, Nicholas C.P., Hochhaus, Andreas, Hofmann, Wolf-Karsten, Berdel, Wolfgang E., Muller-Tidow, Carsten, Reiter, Andreas and Koschmieder, Steffen (2011) Novel imatinib-sensitive PDGFRA activating point mutations in hypereosinophilic syndrome induce growth factor independence and leukemia-like disease. Blood, 117, (10), 2935-2943. (doi:10.1182/blood-2010-05-286757). (PMID:21224473).

Ernst, Thomas, Score, Joannah, Deininger, Michael, Hidalgo-Curtis, Claire, Lackie, Peter, Ershler, William B., Goldman, John M., Cross, Nicholas C.P. and Grand, Francis H. (2011) Identification of FOXP1 and SNX2 as novel ABL1 fusion partners in acute lymphoblastic leukaemia. British Journal of Haematology, 153, (1), 43-46. (doi:10.1111/j.1365-2141.2010.08457.x).

Garne, Ester, Dolk, Helen, Loane, Maria, Wellesley, Diana, Barisic, Ingeborg, Calzolari, Elisa and Densem, James EUROCAT Working Group (2011) Paper 5: Surveillance of multiple congenital anomalies: Implementation of a computer algorithm in European registers for classification of cases. Birth Defects Research Part A: Clinical and Molecular Teratology, 91, (S1), S44-S50. (doi:10.1002/bdra.20777). (PMID:21384529).

Gibson, Jane, Griffiths, Helen, Collins, Andrew, Yates, John R.W., Folk, James C., East, Jade S., Lotery, Andrew J. and Ennis, Sarah (2011) Letter to the editor: Genetic variants within chromosome 4q28.3 are not reproducibly associated with age-related macular degeneration (AMD). Acta Ophthalmologica, 89, (7), e603-e604. (doi:10.1111/j.1755-3768.2010.01986.x). (PMID:20738259).

Grand, F.H., Waghorn, K., Ernst, T., Ohyashiki, K. and Cross, N.C.P. (2011) Letter to the editor. The t(4;9)(q11;q33) fuses CEP110 to KIT in a case of acute myeloid leukemia. Leukemia, 25, (6), 1049-1050. (doi:10.1038/leu.2011.40). (PMID:21403647).

Greenlees, Ruth, Neville, Amanda, Addor, Marie-Claude, Amar, Emmanuelle, Arriola, Larraitz, Bakker, Marian, Barisic, Ingeborg, Boyd, Patricia A., Calzolari, Elisa, Doray, Berenice, Draper, Elizabeth, Emil Vollset, Stein, Garne, Ester, Gatt, Miriam, Haeusler, Martin, Kallen, Karin, Khoshnood, Babak, Latos-Bielenska, Anna, Martinez-Frias, Maria-Luisa, Materna-Kiryluk, Anna, Matias Dias, Carlos, McDonnell, Bob, Mullaney, Carmel, Nelen, Vera, O'Mahony, Mary, Pierini, Anna, Queisser-Luft, Annette, Randrianaivo-Ranjatoélina, Hanitra, Rankin, Judith, Rissmann, Anke, Ritvanen, Annukka, Salvador, Joaquin, Sipek, Antonin, Tucker, David, Verellen-Dumoulin, Christine, Wellesley, Diana and Wertelecki, Wladimir (2011) Paper 6: EUROCAT member registries: Organization and activities. [in special issue: EUROCRAT Supplement Issue] Birth Defects Research Part A: Clinical and Molecular Teratology, 91, supplement S1, S51-S100. (doi:10.1002/bdra.20775). (PMID:21381185).

Gronskov, Karen, Poole, Rebecca L., Hahnemann, Johanne M.D., Thomson, Jennifer, Tumer, Zeynup, Brondum-Nielsen, Karen, Murphy, Rinki, Ravn, Kirstine, Melchior, Linea, Dedic, Alma, Dolmer, Birgitte, Temple, I. Karen, Boonen, Susanne E. and Mackay, Deborah J.G. (2011) Deletions and rearrangements of the H19/IGF2 enhancer region in patients with Silver-Russell syndrome and growth retardation. Journal of Medical Genetics, 48, (5), 308-311. (doi:10.1136/jmg.2010.086504). (PMID:21278389).

Grossmann, V., Kohlmann, A., Eder, C., Haferlach, C., Kern, W., Cross, N.C.P., Haferlach, T. and Schnittger, S. (2011) Molecular profiling of chronic myelomonocytic leukemia reveals diverse mutations in >80% of patients with TET2 and EZH2 being of high prognostic relevance. Leukemia, 25, (5), 877-879. (doi:10.1038/leu.2011.10). (PMID:21339759 ).

Hildebrand, Michael S., Morín, Matías, Meyer, Nicole C., Mayo, Fernando, Modamio-Hoybjor, Silvia, Mencía, Angeles, Olavarrieta, Leticia, Morales-Angulo, Carmelo, Nishimura, Carla J., Workman, Heather, DeLuca, Adam P., del Castillo, Ignacio, Taylor, Kyle R., Tompkins, Bruce, Goodman, Corey W., Schrauwen, Isabelle, Van Wesemael, Maarten, Lachlan, K., Shearer, A. Eliot, Braun, Terry A., Huygen, Patrick L.M., Kremer, Hannie, Van Camp, Guy, Moreno, Felipe, Casavant, Thomas L., Smith, Richard J.H. and Moreno-Pelayo, Miguel A. (2011) DFNA8/12 caused by TECTA mutations is the most identified subtype of non-syndromic autosomal dominant hearing loss. Human Mutation, 32, (7), 825-834. (doi:10.1002/humu.21512). (PMID:21520338).

Holroyd, Ailsa, Cross, Nicholas C.P. and Macdonald, Donald H. (2011) The two faces of myeloproliferative neoplasms: Molecular events underlying lymphoid transformation. Leukemia Research, 35, (10), 1279-1285. (doi:10.1016/j.leukres.2011.05.037). (PMID:21722956).

Kapustin, Yuri, Chan, Elcie, Sarkar, Rupa, Wong, Frederick, Vorechovsky, Igor, Winston, Robert M., Tatusova, Tatiana and Dibb, Nick J. (2011) Cryptic splice sites and split genes. Nucleic Acids Research, 39, (14), 5837-5844. (doi:10.1093/nar/gkr203). (PMID:21470962).

Kohler, J.A., Moon, R.J., Wright, S., Willows, E. and Davies, J.H. (2011) Increased adiposity and altered adipocyte function in female survivors of childhood acute lymphoblastic leukaemia treated without cranial radiation. Hormone Research in Paediatrics, 75, (6), 433-440. (doi:10.1159/000324412). (PMID:21464554).

Kralovicova, Jana, Hwang, Gyulin, Asplund, A. Charlotta, Churbanov, Alexander, Smith, C.I. Edvard and Vorechovsky, Igor (2011) Compensatory signals associated with the activation of human GC 5' splice sites. Nucleic Acids Research, 39, (16), 7077-7091. (doi:10.1093/nar/gkr306).

Lazzari, G., Colleoni, S., Duchi, R., Galli, A., Houghton, F.D. and Galli, C. (2011) Embryonic genotype and inbreeding affect preimplantation development in cattle. Reproduction, 141, (5), 625-632. (doi:10.1530/REP-10-0282). (PMID:21310813).

Lynch, Sally Ann, Foulds, Nicola, Thuresson, Ann-Charlotte, Collins, Amanda L., Annerén, Göran, Hedberg, Bernt-Oves, Delaney, Carol A., Iremonger, James, Murray, Caroline M., Crolla, John A., Costigan, Colm, Lam, Wayne, Fitzpatrick, David R., Regan, Regina, Ennis, Sean and Sharkey, Freddie (2011) The 12q14 microdeletion syndrome: six new cases confirming the role of HMGA2 in growth. European Journal of Human Genetics, 19, (5), 534-539. (doi:10.1038/ejhg.2010.215). (PMID:21267005).

Mant, Alexandra, Elliott, David, Eyers, Patrick A. and O'Kelly, Ita M. (2011) Protein kinase A (PKA) is central for forward transport of two pore domain potassium channels K2P3.1 and K2P9.1. Journal of Biological Chemistry, 286, (16), 14110-14119. (doi:10.1074/jbc.M110.190702). (PMID:21357689).

McKay, Gareth J., Silvestri, Guiliana, Chakravarthy, Usha, Dasari, Shilpa, Fritsche, Lars G., Weber, Bernhard H., Keilhauer, Claudia N., Klein, Michael L., Francis, Peter J., Klaver, Caroline C., Vingerling, Johannes R., Ho, Lintje, De Jong, Pauluus T.D.V., Dean, Michael , Sawitzke, Julie, Baird, Paul N., Guymer, Robyn H., Stambolian, Dwight, Orlin, Anton, Seddon, Johanna M., Peter, Inga, Wright, Alan F., Hayward, Caroline, Lotery, Andrew J., Ennis, Sarah, Gorin, Michael B., Weeks, Daniel E., Kuo, Chia-Ling, Hingorani, Aroon D., Sofat, Reecha, Cipriani, Valentina, Swaroop, Anand, Othman, Mohammed, Kanda, Atsuhiro, Chen, Wei, Abecasis, Goncalo R., Yates, John R., Webster, Andrew R., Moore, Anthony T., Seland, Johan H., Rahu, Mati, Soubrane, Gisele, Tomazzoli, Laura, Topouzis, Fotis, Vioque, Jesus, Young, Ian S., Fletcher, Aatrid E. and Patterson, Chris C. (2011) Variations in apolipoprotein E frequency with age in a pooled analysis of a large group of older people. American Journal of Epidemiology, 173, (12), 1357-1364. (doi:10.1093/aje/kwr015). (PMID:21498624).

Murray, Anna, Bennett, Claire E., Perry, John R.B., Weedon, Michael N., Jacobs, Patricia A., Morris, Danielle H., Orr, Nicholas, Schoemaker, Minouk J., Jones, Michael, Ashworth, Alan and Swerdlow, Anthony J. (2011) Common genetic variants are significant risk factors for early menopause: results from the breakthrough generations study. Human Molecular Genetics, 20, (1), 186-192. (doi:10.1093/hmg/ddq417). (PMID:20952801).

Naik, Swati, Riordan-Eva, Elliott, Thomas, N. Simon, Poole, Rebecca, Ashton, Mark, Crolla, John A. and Temple, I. Karen (2011) Large de novo deletion of 7p15.1 to 7p12.1 involving the imprinted gene GRB10 associated with a complex phenotype including features of Beckwith Wiedemann syndrome. European Journal of Medical Genetics, 54, (1), 89-93. (doi:10.1016/j.ejmg.2010.09.006). (PMID:20933618).

Parker, H., Rose-Zerilli, M.J.J., Parker, A., Chaplin, T., Wade, R., Gardiner, A., Griffiths, M., Collins, A., Young, B.D., Oscier, D.G. and Strefford, J.C. (2011) 13q deletion anatomy and disease progression in patients with chronic lymphocytic leukemia. Leukemia, 25, (3), 489-497. (doi:10.1038/leu.2010.288). (PMID:21151023).

Perl, Anne-Karina T., Riethmacher, Dieter and Whitsett, Jeffrey A. (2011) Conditional depletion of airway progenitor cells induces peribronchiolar fibrosis. American Journal of Respiratory and Critical Care Medicine, 183, (4), 511-521. (doi:10.1164/rccm.201005-0744OC ). (PMID:20870756).

Pohl, Hartmut B.F., Porcheri, Christina, Mueggler, Thomas, Bachmann, Lukas C., Martino, Gianvito, Riethmacher, Dieter, Franklin, Robin J. M, Rudin, Markus and Suter, Ueli (2011) Genetically induced adult oligodendrocyte cell death is associated with poor myelin clearance, reduced remyelination, and axonal damage. The Journal of Neuroscience, 31, (3), 1069-1080. (doi:10.1523/JNEUROSCI.5035-10.2011). (PMID:21248132).

Politopoulos, Ioannis, Gibson, Jane, Tapper, William, Ennis, Sarah, Eccles, Diana and Collins, Andrew (2011) Composite likelihood-based meta-analysis of breast cancer association studies. Journal of Human Genetics, 56, (5), 377-382. (doi:10.1038/jhg.2011.23).

Politopoulos, Ioannis, Gibson, Jane, Tapper, William, Ennis, Sarah, Eccles, Diana and Collins, Andrew (2011) Genome-wide association of breast cancer: composite likelihood with imputed genotypes. European Journal of Human Genetics, 19, (2), 194-199. (doi:10.1038/ejhg.2010.157). (PMID:20959865).

Raponi, Michela, Kralovicova, Jana, Copson, Ellen, Divina, Petr, Eccles, Diana, Johnson, Peter, Baralle, Diana and Vorechovsky, Igor (2011) Prediction of single-nucleotide substitutions that result in exon skipping: identification of a splicing silencer in BRCA1 exon 6. Human Mutation, 32, (4), 436-444. (doi:10.1002/humu.21458). (PMID:21309043).

Richardson, Cassandra, Hogan, Alexandra M., Bucks, Romola S., Baya, Ana, Virues-Ortega, Javier, Holloway, John W., Rose-Zerilli, Matthew, Palmer, Lyle J., Webster, Rebecca J., Kirkham, Fenella J. and Baldeweg, Torsten (2011) Neurophysiological evidence for cognitive and brain functional adaptation in adolescents living at high altitude. Clinical Neurophysiology, 122, (9), 1726-1734. (doi:10.1016/j.clinph.2011.02.001). (PMID:21377415).

Robinson, David O., Hilton-Jones, David, Mansfield, David, Hildebrand, Göran Darius, Marks, Sophie, Mechan, Dorothy and Ramsay, Joanne (2011) Two cases of oculopharyngeal muscular dystrophy (OPMD) with the rare PABPN1 c.35G>C; p.Gly12Ala point mutation. Neuromuscular Disorders, 21, (11), 809-811. (doi:10.1016/j.nmd.2011.06.003). (PMID:21742497).

Shaheen, Seif O., Jameson, Karen A., Robinson, Sian M., Boucher, Barbara J., Syddall, Holly E., Aihie Sayer, Avan, Cooper, Cyrus, Holloway, John W. and Dennison, Elaine M. (2011) Relationship of vitamin D status to adult lung function and COPD. Thorax, 66, (8), 692-698. (doi:10.1136/thx.2010.155234). (PMID:21653927).

Shaheen, Seif O., Newson, Roger B., Ring, Susan M., Rose-Zerilli, Matthew J., Holloway, John W. and Henderson, A. John (2011) Prenatal and infant acetaminophen exposure, antioxidant gene polymorphisms, and childhood asthma. Journal of Allergy and Clinical Immunology, 126, (6), 1141-1148.e7. (doi:10.1016/j.jaci.2010.08.047). (PMID:21051083).

Shuttleworth, Stephen, Townsend, Paul, Silva, Franck, Cecil, Alexander, Hill, Thomas, Tomassi, Cyrille, Rogers, Helen and Harrison, Rebecca (2011) Progress in the development of small molecule therapeutics targeting Th17 cell function for the treatment of immune-inflammatory diseases. In, Lawton, G. (ed.) Progress in Medicinal Chemistry. New York, US, Elsevier, 109-133. (doi:10.1016/B978-0-12-381290-2.00003-3).

Silver, Richard T., Vandris, Katherine, Wang, Y.Lynn, Adriano, Fernando, Jones, Amy V., Christos, Paul J. and Cross, Nicholas C.P. (2011) JAK2(V617F) allele burden in polycythemia vera correlates with grade of myelofibrosis, but is not substantially affected by therapy. Leukemia Research, 35, (2), 177-182. (doi:10.1016/j.leukres.2010.06.017). (PMID:20650526).

Soverini, S., Score, J., Iacobucci, I., Poerio, A., Lonetti, A., Gnani, A., Colarossi, S., Ferrari, A., Castagnetti, F., Rosti, G., Cervantes, F., Hochhaus, A., Delledonne, M., Ferrarini, A., Sazzini, M., Luiselli, D., Baccarani, M., Cross, N.C.P. and Martinelli, G. (2011) IDH2 somatic mutations in chronic myeloid leukemia patients in blast crisis. Leukemia, 25, (1), 178-181. (doi:10.1038/leu.2010.236).

Soverini, Simona, Hochhaus, Andreas, Nicolini, Franck E., Gruber, Franz, Lange, Thoralf, Saglio, Giuseppe, Pane, Fabrizio, Muller, Martin C., Ernst, Thomas, Rosti, Gianantonio, Porkka, Kimmo, Baccarani, Michele, Cross, Nicholas C.P. and Martinelli, Giovanni (2011) Bcr-Abl kinase domain mutation analysis in chronic myeloid leukemia patients treated with tyrosine kinase inhibitors: recommendations from an expert panel on behalf of European LeukemiaNet. Blood, 118, (5), 1208-1215. (doi:10.1182/blood-2010-12-326405). (PMID:21562040).

Spolverini, Ambra, Jones, Amy V., Hochhaus, Andreas, Pieri, Lisa, Cross, Nicholas C.P. and Vannucchi, Alessandro M. (2011) The myeloproliferative neoplasm-associated JAK2 46/1 haplotype is not overrepresented in chronic myelogenous leukemia. Annals of Hematology, 90, (3), 365-366. (doi:10.1007/s00277-010-1009-y). (PMID:20556390).

Townson, Julia K., Gregory, John W., Cohen, David, Channon, Sue, Harman, Nicola, Davies, Justin H., Warner, Justin, Trevelyan, Nicola, Playle, Rebecca, Robling, Michael, Hood, Kerenza and Lowes, Lesley (2011) Delivering early care in diabetes evaluation (DECIDE): a protocol for a randomised controlled trial to assess hospital versus home management at diagnosis in childhood diabetes. BMC Pediatrics, 11, (1), 7. (doi:10.1186/1471-2431-11-7). (PMID:21247461).

Walz, Christoph, Erben, Philipp, Ritter, Michael, Bloor, Adrian, Metzgeroth, Georgia, Telford, Nick, Haferlach, Claudia, Haferlach, Torsten, Gesk, Stefan, Score, Joannah, Hofmann, Wolf-Karsten, Hochhaus, Andreas, Cross, Nicholas C.P. and Reiter, Andreas (2011) Response of ETV6-FLT3 positive myeloid/lymphoid neoplasm with eosinophilia to inhibitors of FMS-like tyrosine kinase 3. Blood, 118, (8), 2239-2242. (doi:10.1182/blood-2011-03-343426). (PMID:21705501).

Wan, Yize I., Strachan, David P., Evans, David M., Henderson, John, McKeever, Tricia, Holloway, John W., Hall, Ian P. and Sayers, Ian (2011) A genome-wide association study to identify genetic determinants of atopy in subjects from the United Kingdom. Journal of Allergy and Clinical Immunology, 127, (1), 223-231. (doi:10.1016/j.jaci.2010.10.006). (PMID:21094521).

Willemsen, Marjolein H., de Leeuw, Nicole, Mercer, Catherine, Eisenhauer, Helen, Morris, Joanne, Collinson, Morag N., Barber, John C.K., Lam, Stephen T.S., Lo, Ivan F.M., Rensen, Hanneke, Ferwerda, Annemarie, Hamel, Ben C.J. and Kleefstra, Tjitske (2011) Further molecular and clinical delineation of the Wisconsin syndrome phenotype associated with interstitial 3q24q25 deletions. American Journal of Medical Genetics. Part A, 155, (1), 106-112. (doi:10.1002/ajmg.a.33715). (PMID:21162103).

Wiskin, A.E., Davies, J.H., Wootton, S.A. and Beattie, R.M. (2011) Energy expenditure, nutrition and growth. Archives of Disease in Childhood, 96, (6), 567-572. (doi:10.1136/adc.2009.158303).