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Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database

Thompson, B.A. (author)
Spurdle, A.B. (author)
Plazzer, J.P. (author)
show more...
Greenblatt, M.S. (author)
Akagi, K. (author)
Al-Mulla, F. (author)
Bapat, B.V. (author)
Bernstein, I.T. (author)
Capellá, G.M. (author)
Den Dunnen, J.T. (author)
Du Sart, D. (author)
Fabre, A.J. (author)
Farrell, M.P. (author)
Farrington, S.M. (author)
Frayling, I.M. (author)
Frébourg, T.H. (author)
Goldgar, D.E.J. (author)
Cummings, C. (author)
Holinski-Feder, E. (author)
Kohonen-Corish, M.R.J. (author)
Robinson, K.L. (author)
Karolinska Institutet
Leung, S.Y. (author)
Martins, A. (author)
Möller, P. (author)
Morak, M. (author)
Nyström, M. (author)
Peltomäki, P.T. (author)
Pineda, M. (author)
Qi, M. (author)
Ramesar, R. (author)
Rasmussen, L.J. (author)
Royer-Pokora, B. (author)
Scott, R.J. (author)
Sijmons, R.H. (author)
Tavtigian, S.V.S.V. (author)
Tops, C.M.J. (author)
Weber, T.K. (author)
Wijnen, J.T.H. (author)
Woods, M.O. (author)
Macrae, F.A. (author)
Genuardi, M. (author)
Castillejo, A. (author)
Sexton, A.C. (author)
Chan, A.K.W. (author)
Viel, A.G.M. (author)
Blanco, A.M. (author)
French, A.J. (author)
Laner, A. (author)
Wagner, A. (author)
Van Den Ouweland, A.M.W. (author)
Mensenkamp, A.R. (author)
Payá, A. (author)
Betz, B. (author)
Redeker, B.J.W. (author)
Smith, B.G. (author)
Espenschied, C.R. (author)
Cummings, C. (author)
Engel, C. (author)
Fornes, C. (author)
Valenzuela, C. (author)
Alenda, C. (author)
Buchanan, D.D. (author)
Barana, D. (author)
Konstantinova, D.V. (author)
Cairns, D. (author)
Glaser, E. (author)
Silva, F. (author)
Lalloo, F.I. (author)
Crucianelli, F. (author)
Hogervorst, F.B.L. (author)
Casey, G.R. (author)
Tomlinson, I.P.M. (author)
Blanco, I.B.S.I. (author)
Villar, I.L. (author)
García-Planells, J. (author)
Bigler, J. (author)
Shia, J. (author)
Martínez-López, J.J. (author)
Gille, J.J.P. (author)
Hopper, J.L. (author)
Potter, J.D. (author)
Soto, J.L. (author)
Kantelinen, J. (author)
Ellis, K. (author)
Mann, K. (author)
Varesco, L. (author)
Zhang, L. (author)
Marchand, L.L. (author)
Marafie, M.J. (author)
Nordling, Margareta, 1962 (author)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för medicinsk genetik och klinisk genetik,Institute of Biomedicine, Department of Medical and Clinical Genetics
Tibiletti, M.G. (author)
Kahan, M.A. (author)
Ligtenberg, M.J.L. (author)
Clendenning, M. (author)
Jenkins, M.A. (author)
Dominguez, Mev (author)
Lund University,Lunds universitet,Bröstcancer-genetik,Sektion I,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Breastcancer-genetics,Section I,Department of Clinical Sciences, Lund,Faculty of Medicine
Digweed, M. (author)
Kloor, M. (author)
Hitchins, M.P. (author)
Myers, M. (author)
Aronson, M.D. (author)
Valentin, M.D. (author)
Kutsche, M. (author)
Parsons, M.T. (author)
Walsh, M.D. (author)
Kansikas, M. (author)
Zahary, M.N. (author)
Pedroni, M. (author)
Heider, N. (author)
Poplawski, N.K. (author)
Rahner, N. (author)
Lindor, N.M. (author)
Sala, P. (author)
Nan, P. (author)
Propping, P. (author)
Newcomb, P. (author)
Sarin, R. (author)
Haile, R.W.C. (author)
Hofstra, R.M.W. (author)
Ward, R.L. (author)
Tricarico, R. (author)
Bacares, R. (author)
Young, S. (author)
Chialina, S.G. (author)
Kovalenko, S.P. (author)
Gunawardena, S.R. (author)
Moreno, S. (author)
Ho, S. (author)
Yuen, S.T. (author)
Thibodeau, S.N. (author)
Gallinger, S.S. (author)
Burnett, T.S. (author)
Teitsch, T. (author)
Chan, T.L. (author)
Smyrk, T.C. (author)
Cranston, T. (author)
Psofaki, V. (author)
Steinke-Lange, V. (author)
Barberá, V.M. (author)
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 (creator_code:org_t)
2013-12-22
2014
English.
In: Nature Genetics. - : Springer Science and Business Media LLC. - 1061-4036 .- 1546-1718. ; 46:2, s. 107-115
  • Journal article (peer-reviewed)
Abstract Subject headings
Close  
  • The clinical classification of hereditary sequence variants identified in disease-related genes directly affects clinical management of patients and their relatives. The International Society for Gastrointestinal Hereditary Tumours (InSiGHT) undertook a collaborative effort to develop, test and apply a standardized classification scheme to constitutional variants in the Lynch syndrome-associated genes MLH1, MSH2, MSH6 and PMS2. Unpublished data submission was encouraged to assist in variant classification and was recognized through microattribution. The scheme was refined by multidisciplinary expert committee review of the clinical and functional data available for variants, applied to 2,360 sequence alterations, and disseminated online. Assessment using validated criteria altered classifications for 66% of 12,006 database entries. Clinical recommendations based on transparent evaluation are now possible for 1,370 variants that were not obviously protein truncating from nomenclature. This large-scale endeavor will facilitate the consistent management of families suspected to have Lynch syndrome and demonstrates the value of multidisciplinary collaboration in the curation and classification of variants in public locus-specific databases. © 2014 Nature America, Inc.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Medicinsk genetik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Medical Genetics (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

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By the author/editor
Thompson, B.A.
Spurdle, A.B.
Plazzer, J.P.
Greenblatt, M.S.
Akagi, K.
Al-Mulla, F.
show more...
Bapat, B.V.
Bernstein, I.T.
Capellá, G.M.
Den Dunnen, J.T.
Du Sart, D.
Fabre, A.J.
Farrell, M.P.
Farrington, S.M.
Frayling, I.M.
Frébourg, T.H.
Goldgar, D.E.J.
Cummings, C.
Holinski-Feder, ...
Kohonen-Corish, ...
Robinson, K.L.
Leung, S.Y.
Martins, A.
Möller, P.
Morak, M.
Nyström, M.
Peltomäki, P.T.
Pineda, M.
Qi, M.
Ramesar, R.
Rasmussen, L.J.
Royer-Pokora, B.
Scott, R.J.
Sijmons, R.H.
Tavtigian, S.V.S ...
Tops, C.M.J.
Weber, T.K.
Wijnen, J.T.H.
Woods, M.O.
Macrae, F.A.
Genuardi, M.
Castillejo, A.
Sexton, A.C.
Chan, A.K.W.
Viel, A.G.M.
Blanco, A.M.
French, A.J.
Laner, A.
Wagner, A.
Van Den Ouweland ...
Mensenkamp, A.R.
Payá, A.
Betz, B.
Redeker, B.J.W.
Smith, B.G.
Espenschied, C.R ...
Engel, C.
Fornes, C.
Valenzuela, C.
Alenda, C.
Buchanan, D.D.
Barana, D.
Konstantinova, D ...
Cairns, D.
Glaser, E.
Silva, F.
Lalloo, F.I.
Crucianelli, F.
Hogervorst, F.B. ...
Casey, G.R.
Tomlinson, I.P.M ...
Blanco, I.B.S.I.
Villar, I.L.
García-Planells, ...
Bigler, J.
Shia, J.
Martínez-López, ...
Gille, J.J.P.
Hopper, J.L.
Potter, J.D.
Soto, J.L.
Kantelinen, J.
Ellis, K.
Mann, K.
Varesco, L.
Zhang, L.
Marchand, L.L.
Marafie, M.J.
Nordling, Margar ...
Tibiletti, M.G.
Kahan, M.A.
Ligtenberg, M.J. ...
Clendenning, M.
Jenkins, M.A.
Dominguez, Mev
Digweed, M.
Kloor, M.
Hitchins, M.P.
Myers, M.
Aronson, M.D.
Valentin, M.D.
Kutsche, M.
Parsons, M.T.
Walsh, M.D.
Kansikas, M.
Zahary, M.N.
Pedroni, M.
Heider, N.
Poplawski, N.K.
Rahner, N.
Lindor, N.M.
Sala, P.
Nan, P.
Propping, P.
Newcomb, P.
Sarin, R.
Haile, R.W.C.
Hofstra, R.M.W.
Ward, R.L.
Tricarico, R.
Bacares, R.
Young, S.
Chialina, S.G.
Kovalenko, S.P.
Gunawardena, S.R ...
Moreno, S.
Ho, S.
Yuen, S.T.
Thibodeau, S.N.
Gallinger, S.S.
Burnett, T.S.
Teitsch, T.
Chan, T.L.
Smyrk, T.C.
Cranston, T.
Psofaki, V.
Steinke-Lange, V ...
Barberá, V.M.
show less...
About the subject
MEDICAL AND HEALTH SCIENCES
MEDICAL AND HEAL ...
and Basic Medicine
and Medical Genetics
MEDICAL AND HEALTH SCIENCES
MEDICAL AND HEAL ...
and Clinical Medicin ...
and Cancer and Oncol ...
Articles in the publication
Nature Genetics
By the university
University of Gothenburg
Lund University
Karolinska Institutet

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