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Nature Communications|July 17, 2021
Discovery and prioritization of variants and genes for kidney function in >1.2 million individualsKira J Stanzick, Yong Li, Pascal Schlosser, et al.
The Journal of Rheumatology|December 25, 2009
Safety, tolerability, and clinical outcomes after intraarticular injection of a recombinant adeno-associated vector containing a tumor necrosis factor antagonist gene: results of a phase 1/2 StudyPhilip J Mease, Nathan Wei, Edward J Fudman, et al.
Canadian Urological Association Journal = Journal De L'Association Des Urologues Du Canada|December 10, 2013
Canadian guideline on genetic screening for hereditary renal cell cancersM Neil Reaume, Gail E Graham, Eva Tomiak, et al.
Nature Communications|October 24, 2020
MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture riskIda Surakka, Lars G Fritsche, Wei Zhou, et al.
The Journal of Clinical Endocrinology and Metabolism|November 24, 1999
A comparison of recombinant human thyrotropin and thyroid hormone withdrawal for the detection of thyroid remnant or cancerB R Haugen, F Pacini, C Reiners, et al.
The Journal of Allergy and Clinical Immunology|August 3, 2010
Transplantation of hematopoietic stem cells and long-term survival for primary immunodeficiencies in Europe: entering a new century, do we do better?Andrew R Gennery, Mary A Slatter, Laure Grandin, et al.
Plos Genetics|July 13, 2018
Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birthJohanna M Huusko, Minna K Karjalainen, Britney E Graham, et al.
Journal of Clinical Immunology|January 19, 2021
Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous MutationsGiuliana Giardino, Svetlana O Sharapova, Peter Ciznar, et al.
Blood Advances|February 10, 2025
Single-cell dynamics of breakthrough toxicities after anakinra prophylaxis for axicabtagene ciloleucel in lymphomaMatthew J Frigault, Ning Yao, Trisha R Berger, et al.
Plos Genetics|September 14, 2018
Correction: Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birthJohanna M Huusko, Minna K Karjalainen, Britney E Graham, et al.
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