日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Contribution of genetics to hematopoietic stem cell mobilization: a genome-wide association study of 564 healthy donors mobilized with granulocyte colony-stimulating factor

遗传因素对造血干细胞动员的贡献:一项针对564名接受粒细胞集落刺激因子动员的健康供者的全基因组关联研究

Stenzinger, Miriam; Beck, Susanne; Ourailidis, Iordanis; Volckmar, Anna-Lena; Paramasivam, Nagarajan; Ahadova, Aysel; Portilla, Aitzkoa Lopez de Lapuente; La Yen, Phuong; Nilsson, Bjorn; Bermejo, Justo Lorenzo; Bonig, Halvard; Budczies, Jan

Genetic variation at PPM1H predicts mobilization efficiency in stem cell donors

PPM1H基因变异可预测干细胞供体的动员效率

La, Yen Phuong; Torres Di Bello, Daniela; Mahecha Escobar, Maria Laura; Cafaro, Caterina; Wichert, Stina; Lopez de Lapuente Portilla, Aitzkoa; Nilsson, Björn

Functional dissection of the gene regulatory mechanism underlying variation in blood CD34(+) cell levels at 1p36.23/ENO1

对 1p36.23/ENO1 位点血液 CD34(+) 细胞水平变异的基因调控机制进行功能性解析

Ali, Zain; Cafaro, Caterina; Ekdahl, Ludvig; Lamarca, Antton; Lopez de Lapuente Portilla, Aitzkoa; Nilsson, Björn

Deciphering the genetics and mechanisms of predisposition to multiple myeloma

揭示多发性骨髓瘤的遗传学和易感机制

Molly Went #, Laura Duran-Lozano #, Gisli H Halldorsson, Andrea Gunnell, Nerea Ugidos-Damboriena, Philip Law, Ludvig Ekdahl, Amit Sud, Gudmar Thorleifsson, Malte Thodberg, Thorunn Olafsdottir, Antton Lamarca-Arrizabalaga, Caterina Cafaro, Abhishek Niroula, Ram Ajore, Aitzkoa Lopez de Lapuente Portil

Sequence variants influencing the regulation of serum IgG subclass levels

影响血清 IgG 亚类水平调节的序列变异

Thorunn A Olafsdottir, Gudmar Thorleifsson, Aitzkoa Lopez de Lapuente Portilla, Stefan Jonsson, Lilja Stefansdottir, Abhishek Niroula, Aslaug Jonasdottir, Hannes P Eggertsson, Gisli H Halldorsson, Gudny E Thorlacius, Asgeir O Arnthorsson, Unnur S Bjornsdottir, Folkert W Asselbergs, Arthur E H Bentla

The insertion/deletion polymorphism rs201494641 at ITGA9 influences blood CD34(+) cell levels by altering ZNF384 binding

ITGA9基因上的插入/缺失多态性rs201494641通过改变ZNF384的结合来影响血液中CD34(+)细胞的水平。

Cafaro, Caterina; Ali, Zain; Lamarca, Antton; Di Bello, Daniela Torres; Lozano, Laura Duran; Ekdahl, Ludvig; Thodberg, Malte; Pertesi, Maroulio; De Lapuente Portilla, Aitzkoa Lopez; Nilsson, Björn

Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality

出版商更正:152万个体中纯合性缺失以及隐性致死的遗传原因

Oddsson, Asmundur; Sulem, Patrick; Sveinbjornsson, Gardar; Arnadottir, Gudny A; Steinthorsdottir, Valgerdur; Halldorsson, Gisli H; Atlason, Bjarni A; Oskarsson, Gudjon R; Helgason, Hannes; Nielsen, Henriette Svarre; Westergaard, David; Karjalainen, Juha M; Katrinardottir, Hildigunnur; Fridriksdottir, Run; Jensson, Brynjar O; Tragante, Vinicius; Ferkingstad, Egil; Jonsson, Hakon; Gudjonsson, Sigurjon A; Beyter, Doruk; Moore, Kristjan H S; Thordardottir, Helga B; Kristmundsdottir, Snaedis; Stefansson, Olafur A; Rantapää-Dahlqvist, Solbritt; Sonderby, Ida Elken; Didriksen, Maria; Stridh, Pernilla; Haavik, Jan; Tryggvadottir, Laufey; Frei, Oleksandr; Walters, G Bragi; Kockum, Ingrid; Hjalgrim, Henrik; Olafsdottir, Thorunn A; Selbaek, Geir; Nyegaard, Mette; Erikstrup, Christian; Brodersen, Thorsten; Saevarsdottir, Saedis; Olsson, Tomas; Nielsen, Kaspar Rene; Haraldsson, Asgeir; Bruun, Mie Topholm; Hansen, Thomas Folkmann; Steingrimsdottir, Thora; Jacobsen, Rikke Louise; Lie, Rolv T; Djurovic, Srdjan; Alfredsson, Lars; Lopez de Lapuente Portilla, Aitzkoa; Brunak, Soren; Melsted, Pall; Halldorsson, Bjarni V; Saemundsdottir, Jona; Magnusson, Olafur Th; Padyukov, Leonid; Banasik, Karina; Rafnar, Thorunn; Askling, Johan; Klareskog, Lars; Pedersen, Ole Birger; Masson, Gisli; Havdahl, Alexandra; Nilsson, Bjorn; Andreassen, Ole A; Daly, Mark; Ostrowski, Sisse Rye; Jonsdottir, Ingileif; Stefansson, Hreinn; Holm, Hilma; Helgason, Agnar; Thorsteinsdottir, Unnur; Stefansson, Kari; Gudbjartsson, Daniel F

Genetic regulation of fetal hemoglobin across global populations

全球人口胎儿血红蛋白的遗传调控

Liam D Cato, Rick Li, Henry Y Lu, Fulong Yu, Mariel Wissman, Baraka S Mkumbe, Supachai Ekwattanakit, Patrick Deelen, Liberata Mwita, Raphael Sangeda, Thidarat Suksangpleng, Suchada Riolueang, Paola G Bronson, Dirk S Paul, Emily Kawabata, William J Astle, Francois Aguet, Kristin Ardlie, Aitzkoa Lopez

Author Correction: Functional dissection of inherited non-coding variation influencing multiple myeloma risk

作者更正:对影响多发性骨髓瘤风险的遗传性非编码变异进行功能性剖析

Ajore, Ram; Niroula, Abhishek; Pertesi, Maroulio; Cafaro, Caterina; Thodberg, Malte; Went, Molly; Bao, Erik L; Duran-Lozano, Laura; Lopez de Lapuente Portilla, Aitzkoa; Olafsdottir, Thorunn; Ugidos-Damboriena, Nerea; Magnusson, Olafur; Samur, Mehmet; Lareau, Caleb A; Halldorsson, Gisli H; Thorleifsson, Gudmar; Norddahl, Gudmundur L; Gunnarsdottir, Kristbjorg; Försti, Asta; Goldschmidt, Hartmut; Hemminki, Kari; van Rhee, Frits; Kimber, Scott; Sperling, Adam S; Kaiser, Martin; Anderson, Kenneth; Jonsdottir, Ingileif; Munshi, Nikhil; Rafnar, Thorunn; Waage, Anders; Weinhold, Niels; Thorsteinsdottir, Unnur; Sankaran, Vijay G; Stefansson, Kari; Houlston, Richard; Nilsson, Björn

Functional dissection of inherited non-coding variation influencing multiple myeloma risk

影响多发性骨髓瘤风险的遗传性非编码变异的功能解析

Ram Ajore, Abhishek Niroula, Maroulio Pertesi, Caterina Cafaro, Malte Thodberg, Molly Went, Erik L Bao, Laura Duran-Lozano, Aitzkoa Lopez de Lapuente Portilla, Thorunn Olafsdottir, Nerea Ugidos-Damboriena, Olafur Magnusson, Mehmet Samur, Caleb A Lareau, Gisli H Halldorsson, Gudmar Thorleifsson, Gudm