Bibliografia UJ CM



Zapytanie: EUROPEAN JOURNAL OF HUMAN GENETICS
Liczba odnalezionych rekordów: 10



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Federico Canzian, Chiara Piredda, Angelica Macauda, Daria Zawirska, Niels Frost Andersen, Arnon Nagler, Jan Maciej Zaucha, Grzegorz Mazur, Charles Dumontet, Marzena Wątek, Krzysztof Jamroziak, Juan Sainz, Judit Varkonyi, Aleksandra Butrym, Katia Beider, Niels Abildgaard, Fabienne Lesueur, Marek Dudziński, Annette Juul Vangsted, Matteo Pelosini, Edyta Subocz, Mario Petrini, Gabriele Buda, Małgorzata Raźny, Federica Gemignani, Herlander Marques, Enrico Orciuolo, Katalin Kadar, Artur Jurczyszyn, Agnieszka Druzd-Sitek, Ulla Vogel, Vibeke Andersen, Rui Manuel Reis, Anna Suska, Herve Avet-Loiseau, Marcin Kruszewski, Waldemar Tomczak, Marcin Rymko, Stephane Minvielle, Daniele Campa.
A polygenic risk score for multiple myeloma risk prediction.
European Journal of Human Genetics
2022 : Vol. 30, nr 4, s. 474-479, bibliogr. 32 poz.
Autor korespondencyjny: Federico Canzian.
Open Access Creative Commons Attribution License CC-BY 4.0.
p-ISSN: 1018-4813
e-ISSN: 1476-5438
AZ
ORG
AIF
IF: 5.200
Adres url:
Streszczenie w PubMed:
2/10
A[rtur] Dobosz, M[irosław] Bik-Multanowski.
Expression of COX7A1 as a potential marker of congenital heart defects.
European Journal of Human Genetics
2016 : Vol. 24, Suppl. 1, s. 121, abstr. P05.24.
European Human Genetics Conference, Barcelona, Spain, May 21-24, 2016.
p-ISSN: 1018-4813
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3/10
M[irosław] Bik-Multanowski, J[acek] J. Pietrzyk, A. Midro, B. Stasiewicz-Jarocka, A[rtur] Dobosz.
MTRNR2L12: A candidate blood marker of early Alzheimer's diseaselike dementia.
European Journal of Human Genetics
2015 : Vol. 23, Suppl. 1, s. 154, abstr. PM08.16.
European Human Genetics Conference, Glasgow, Scotland, United Kingdom, June 6-9, 2015.
p-ISSN: 1018-4813
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4/10
Marcin Waligora.
Is a requirement of personalised assent realistic? A case from the GABRIEL project.
European Journal of Human Genetics
2014 : Vol. 22, nr 7, s. 855, bibliogr. 3 poz.
p-ISSN: 1018-4813
LR
AIF
IF: 4.349
5/10
Oliver W. Quarrell, Olivia Handley, Kirsty O'Donovan, Christine Dumoulin, Maria Ramos-Arroyo, Ida Biunno, Peter Bauer, Margaret Kline, G. Bernhard Landwehrmeyer, European Huntington's Disease Network.
Discrepancies in reporting the CAG repeat lengths for Huntington's disease.
European Journal of Human Genetics
2012 : Vol. 20, nr 1, s. 20-26, il., bibliogr. 14 poz.
p-ISSN: 1018-4813
AZ
ORG
AIF
IF: 4.319
6/10
Simon Cronin, Barbara Tomik, Daniel G. Bradley, Agnieszka Slowik, Orla Hardiman.
Screening for replication of genome-wide SNP associations in sporadic ALS.
European Journal of Human Genetics
2009 : Vol. 17, nr 2, s. 213-218, bibliogr. 26 poz.
p-ISSN: 1018-4813
AZ
ORG
AIF
IF: 3.564
7/10
R. Ugenskiene, W[ojciech] Polak, O. Veselov, J. Lekki, Z. Stachura, M[onika] Zazula, W[ojciech] Dabros, J[erzy] Stachura.
Living cell irradiation and double-strand breaks.
European Journal of Human Genetics
2006 : Vol. 14 suppl. 1, s. 361, abstr. P1193
European Human Genetics Conference 2006, Amsterdam, The Netherlands, May 6-9, 2006.
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Z. Helias-Rodziewicz, E. Bocian, P. Stankiewicz, E. Obersztyn, E[wa] Kostyk, K. Jakubow-Durska, A[nna] Kutkowska-Kazmierczak, T. Mazurczak.
Results of subtelomeric screening in 52 families with unspecific mental retardation.
European Journal of Human Genetics
2002 : Vol. 10 suppl. 1, s. 224, abstr. P0712
European Human Genetics Conference 2002 in conjunction with the European Meeting on Psychosocial Aspects of Genetics 2002, Strasbourg, France, May 25-29, 2002.
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Marek Sanak, A[ndrzej] Szczeklik.
Disequilibrium between two common non-linked genetic polymorphisms in bronchial asthma.
European Journal of Human Genetics
1999 : Vol. 7 suppl. 1, s. 137 abstr. P-559
31st Annual Meeting of the European Society of Human Genetics. Geneva, Switzerland, 29 May - 1 June 1999.
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Jacek J. Pietrzyk, E[wa] Kostyk, P. Sucharski, M[arek] Sanak, A[nna] Kruczek.
Molecular studies in osteogenesis imperfecta (OI). (Badania molekularne we wrodzonej łamliwości kości).
European Journal of Human Genetics
1999 : Vol. 7 suppl. 1, s. 125, abstr. P-506.
31st Annual Meeting Of Human Genetics, Geneva, Switzerland, 29 May-1 June, 1999.
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