Aitzkoa Portilla-Lapuente

Lund, M 22184, Sweden

Last Updated: 09/26/2026

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Found 13 publications

Genome-wide association study in 21,271 individuals identifies 9 novel loci associated with circulating CD34+ hematopoietic stem and progenitor cell levels.

Genome-wide association study in 21,271 individuals identifies 9 novel loci associated with circulating CD34+ hematopoietic stem and progenitor cell levels.

Journal: HemaSphere
Published: December 05, 2025

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

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

Journal: Scientific reports
Published: March 31, 2025

Genetic variation at PPM1H predicts mobilization efficiency in stem cell donors.

Genetic variation at PPM1H predicts mobilization efficiency in stem cell donors.

Journal: Blood advances
Published: November 05, 2024

Deciphering the genetics and mechanisms of predisposition to multiple myeloma.

Deciphering the genetics and mechanisms of predisposition to multiple myeloma.

Journal: Nature communications
Published: January 03, 2024

Sequence variants influencing the regulation of serum IgG subclass levels.

Sequence variants influencing the regulation of serum IgG subclass levels.

Journal: Nature communications
Published: December 01, 2023

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

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

Journal: Nature communications
Published: July 03, 2023

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

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

Journal: Nature communications
Published: December 13, 2022

Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality.

Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality.

Journal: Nature communications
Published: July 14, 2022

Author Correction: Germline variants at SOHLH2 influence multiple myeloma risk.

Author Correction: Germline variants at SOHLH2 influence multiple myeloma risk.

Journal: Blood cancer journal
Published: November 16, 2021

Genome-wide association study on 13 167 individuals identifies regulators of blood CD34+cell levels.

Genome-wide association study on 13 167 individuals identifies regulators of blood CD34+cell levels.

Journal: Blood
Published: July 06, 2021

Germline variants at SOHLH2 influence multiple myeloma risk.

Germline variants at SOHLH2 influence multiple myeloma risk.

Journal: Blood cancer journal
Published: January 21, 2021

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

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

Journal: Nature communications
Published: November 05, 2020
Showing 1-12 of 13

Last Updated: 09/26/2026