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Negative spin Hall magnetoresistance of Pt on the bulk easy-plane antiferromagnet NiO

Applied physics letters, 2017-07, Vol.111 (5)

2017

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Nonlocal spin Seebeck effect in the bulk easy-plane antiferromagnet NiO

Physical review. B, 2020-12, Vol.102 (21), p.1, Article 214415

2020

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A novel chronic lymphocytic leukemia subset expressing mutated IGHV3-7-encoded rheumatoid factor B-cell receptors that are functionally proficient

Leukemia, 2013-03, Vol.27 (3), p.738-740

2013

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In vitro induction of antibody secretion of primary B-cell chronic lymphocytic leukaemia cells

Leukemia, 2015-01, Vol.29 (1), p.244-247

2015

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Magnetic order of Dy3+ and Fe3+ moments in antiferromagnetic DyFeO3 probed by spin Hall magnetoresistance and spin Seebeck effect

Physical review. B, 2021-04, Vol.103 (13)

2021

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Role of NiO in the nonlocal spin transport through thin NiO films on Y3Fe5O12

Physical review. B, 2021-04, Vol.103 (14)

2021

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Antiferromagnetic Ordering and Uncoupled Spins in CaFe 2 O 4 Thin Films Probed by Spin Hall Magnetoresistance

Advanced electronic materials, 2022-06, Vol.8 (6)

2022

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Antiferromagnetic Ordering and Uncoupled Spins in CaFe2O4 Thin Films Probed by Spin Hall Magnetoresistance

Advanced electronic materials, 2022-06, Vol.8 (6), p.n/a

2022

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Magnetic order of Dy 3 + and Fe 3 + moments in antiferromagnetic Dy Fe O 3 probed by spin Hall magnetoresistance and spin Seebeck effect

Physical review. B, 2021-04, Vol.103 (13), Article 134406

2021

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Role of NiO in the nonlocal spin transport through thin NiO films on Y 3 Fe 5 O 12

Physical review. B, 2021-04, Vol.103 (14), Article 144406

2021

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Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome

Nature genetics, 2011-01, Vol.43 (1), p.20-22

2011

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Frontorhiny, a Distinctive Presentation of Frontonasal Dysplasia Caused by Recessive Mutations in the ALX3 Homeobox Gene

American journal of human genetics, 2009-05, Vol.84 (5), p.698-705

2009

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Design and Analysis of Compressed Sensing Radar Detectors

IEEE transactions on signal processing, 2013-02, Vol.61 (4), p.813-827

2013

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Evidence base for exercise prehabilitation suggests favourable outcomes for patients undergoing surgery for non-small cell lung cancer despite being of low therapeutic quality: a systematic review and meta-analysis

European journal of surgical oncology, 2023-05, Vol.49 (5), p.879-894

2023

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Genetic basis of alpha-aminoadipic and alpha-ketoadipic aciduria

Journal of inherited metabolic disease, 2015-09, Vol.38 (5), p.873-879

2015

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Development and internal validation of a machine learning prediction model for low back pain non-recovery in patients with an acute episode consulting a physiotherapist in primary care

BMC musculoskeletal disorders, 2022-09, Vol.23 (1), p.1-834, Article 834

2022

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How Well Do Randomized Controlled Trials Reflect Standard Care: A Comparison between Scientific Research Data and Standard Care Data in Patients with Intermittent Claudication undergoing Supervised Exercise Therapy

PloS one, 2016-06, Vol.11 (6), p.e0157921-e0157921

2016

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Cellular interference in craniofrontonasal syndrome: males mosaic for mutations in the X-linked EFNB1 gene are more severely affected than true hemizygotes

Human molecular genetics, 2013-04, Vol.22 (8), p.1654-1662

2013

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Current Prehabilitation Programs Do Not Improve the Postoperative Outcomes of Patients Scheduled for Lumbar Spine Surgery: A Systematic Review With Meta-analysis

The journal of orthopaedic and sports physical therapy, 2021-03, Vol.51 (3), p.103-114

2021

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NGS panel analysis in 24 ectopia lentis patients; a clinically relevant test with a high diagnostic yield

European journal of medical genetics, 2017-09, Vol.60 (9), p.465-473

2017

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Identification of Intragenic Exon Deletions and Duplication of TCF12 by Whole Genome or Targeted Sequencing as a Cause of TCF12-Related Craniosynostosis

Human mutation, 2016-08, Vol.37 (8), p.732-736

2016

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Gain-of-Function Mutations in ZIC1 Are Associated with Coronal Craniosynostosis and Learning Disability

American journal of human genetics, 2015-09, Vol.97 (3), p.378-388

2015

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Preaxial polydactyly of the foot: Clinical and genetic implications for the orthopedic practice based on a literature review and 76 patients

Acta orthopaedica, 2018-01, Vol.89 (1), p.113-118

2018

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Longitudinal impact of joint pain comorbidity on quality of life and activity levels in knee osteoarthritis: data from the Osteoarthritis Initiative

Rheumatology (Oxford, England), 2013-03, Vol.52 (3), p.543-546

2013

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Negative spin Hall magnetoresistance of Pt on the bulk easy-plane antiferromagnet NiO

Nonlocal spin Seebeck effect in the bulk easy-plane antiferromagnet NiO

A novel chronic lymphocytic leukemia subset expressing mutated IGHV3-7-encoded rheumatoid factor B-cell receptors that are functionally proficient

In vitro induction of antibody secretion of primary B-cell chronic lymphocytic leukaemia cells

Magnetic order of Dy3+ and Fe3+ moments in antiferromagnetic DyFeO3 probed by spin Hall magnetoresistance and spin Seebeck effect

Role of NiO in the nonlocal spin transport through thin NiO films on Y3Fe5O12

Antiferromagnetic Ordering and Uncoupled Spins in CaFe 2 O 4 Thin Films Probed by Spin Hall Magnetoresistance

Antiferromagnetic Ordering and Uncoupled Spins in CaFe2O4 Thin Films Probed by Spin Hall Magnetoresistance

Magnetic order of Dy 3 + and Fe 3 + moments in antiferromagnetic Dy Fe O 3 probed by spin Hall magnetoresistance and spin Seebeck effect

Role of NiO in the nonlocal spin transport through thin NiO films on Y 3 Fe 5 O 12

Mutations in genes encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome

Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis

Frontorhiny, a Distinctive Presentation of Frontonasal Dysplasia Caused by Recessive Mutations in the ALX3 Homeobox Gene

Design and Analysis of Compressed Sensing Radar Detectors

Evidence base for exercise prehabilitation suggests favourable outcomes for patients undergoing surgery for non-small cell lung cancer despite being of low therapeutic quality: a systematic review and meta-analysis

Genetic basis of alpha-aminoadipic and alpha-ketoadipic aciduria

Development and internal validation of a machine learning prediction model for low back pain non-recovery in patients with an acute episode consulting a physiotherapist in primary care

How Well Do Randomized Controlled Trials Reflect Standard Care: A Comparison between Scientific Research Data and Standard Care Data in Patients with Intermittent Claudication undergoing Supervised Exercise Therapy

Cellular interference in craniofrontonasal syndrome: males mosaic for mutations in the X-linked EFNB1 gene are more severely affected than true hemizygotes

Current Prehabilitation Programs Do Not Improve the Postoperative Outcomes of Patients Scheduled for Lumbar Spine Surgery: A Systematic Review With Meta-analysis

NGS panel analysis in 24 ectopia lentis patients; a clinically relevant test with a high diagnostic yield

Identification of Intragenic Exon Deletions and Duplication of TCF12 by Whole Genome or Targeted Sequencing as a Cause of TCF12-Related Craniosynostosis

Gain-of-Function Mutations in ZIC1 Are Associated with Coronal Craniosynostosis and Learning Disability

Preaxial polydactyly of the foot: Clinical and genetic implications for the orthopedic practice based on a literature review and 76 patients

Longitudinal impact of joint pain comorbidity on quality of life and activity levels in knee osteoarthritis: data from the Osteoarthritis Initiative

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