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Specific features to differentiate Giant cell arteritis aortitis from aortic atheroma using FDG-PET/CT

Scientific reports, 2021-08, Vol.11 (1), p.17389-17389, Article 17389

2021

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ADAR1 mediated regulation of neural crest derived melanocytes and Schwann cell development

Nature communications, 2020-01, Vol.11 (1), p.198-14, Article 198

2020

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Germline deletion of the miR-17∼92 cluster causes skeletal and growth defects in humans

Nature genetics, 2011-10, Vol.43 (10), p.1026-1030

2011

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Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome

Nature genetics, 2003-04, Vol.33 (4), p.459-461

2003

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A prospective cohort study of postpartum glucose metabolic disorders in early versus standard diagnosed gestational diabetes mellitus

Scientific reports, 2021-05, Vol.11 (1), p.10430-10430, Article 10430

2021

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Early skin-to-skin contact and risk of late-onset-sepsis in very and extremely preterm infants

Pediatric research, 2023-06, Vol.93 (7), p.2091-2100

2023

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Adjuvant dendritic cell therapy in stage IIIB/C melanoma: the MIND-DC randomized phase III trial

Nature communications, 2024-02, Vol.15 (1), p.1632-1632

2024

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Mediator contributes to IgH locus VDJ rearrangements by promoting usage of most distal V segments

Cellular & molecular immunology, 2020-04, Vol.17 (4), p.407-409

2020

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WNT pathway and mammary carcinogenesis: Loss of expression of candidate tumor suppressor gene SFRP1 in most invasive carcinomas except of the medullary type

Oncogene, 2001-09, Vol.20 (41), p.5810-5817

2001

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Mapping female bodily features of attractiveness

Scientific reports, 2016-01, Vol.6 (1), p.18551-18551, Article 18551

2016

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Uncovering the genetic architecture of broad antisocial behavior through a genome-wide association study meta-analysis

Molecular psychiatry, 2022-11, Vol.27 (11), p.4453-4463

2022

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IgH locus suicide recombination does not depend on NHEJ in contrast to CSR in B cells

Cellular & molecular immunology, 2019-02, Vol.16 (2), p.201-202

2019

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Stimulation of the β3-Adrenoceptor as a Novel Treatment Strategy for Anxiety and Depressive Disorders

Neuropsychopharmacology (New York, N.Y.), 2007-04, Vol.33 (3), p.574-587

2007

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Dissection of the MYCN locus in Feingold syndrome and isolated oesophageal atresia

European journal of human genetics : EJHG, 2011-05, Vol.19 (5), p.602-606

2011

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Delineation of Late Onset Hypoventilation Associated with Hypothalamic Dysfunction Syndrome

Pediatric research, 2008-12, Vol.64 (6), p.689-694

2008

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SOX10 mutations in patients with Waardenburg-Hirschsprung disease

Nature genetics, 1998-02, Vol.18 (2), p.171-173

1998

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PAX2 mutations in renal-coloboma syndrome: mutational hotspot and germline mosaicism

European journal of human genetics : EJHG, 2000-11, Vol.8 (11), p.820-826

2000

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Genetics and early disturbances of breathing control

Pediatric research, 2004-05, Vol.55 (5), p.729-733

2004

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Germline deletion of the miR-1792 cluster causes skeletal and growth defects in humans

Nature genetics, 2011-10, Vol.43 (10), p.1026-1030

2011

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Germline deletion of the miR-17-92 cluster causes growth and skeletal defects in humans

Nature genetics, 2011-09, Vol.43 (10), p.1026-1030

2011

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Early inhaled nitric oxide improves oxidative balance in very preterm infants

Pediatric research, 2005-05, Vol.57 (5), p.637-643

2005

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Specific features to differentiate Giant cell arteritis aortitis from aortic atheroma using FDG-PET/CT

ADAR1 mediated regulation of neural crest derived melanocytes and Schwann cell development

Germline deletion of the miR-17∼92 cluster causes skeletal and growth defects in humans

Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome

A prospective cohort study of postpartum glucose metabolic disorders in early versus standard diagnosed gestational diabetes mellitus

Risk factors for placenta accreta spectrum disorders in women with any prior cesarean and a placenta previa or low lying: a prospective population-based study

Neurochemical, Electrophysiological and Pharmacological Profiles of the Selective Inhibitor of the Glycine Transporter-1 SSR504734, a Potential New Type of Antipsychotic

Early skin-to-skin contact and risk of late-onset-sepsis in very and extremely preterm infants

Adjuvant dendritic cell therapy in stage IIIB/C melanoma: the MIND-DC randomized phase III trial

TMPRSS2 is a functional receptor for human coronavirus HKU1

Mediator contributes to IgH locus VDJ rearrangements by promoting usage of most distal V segments

WNT pathway and mammary carcinogenesis: Loss of expression of candidate tumor suppressor gene SFRP1 in most invasive carcinomas except of the medullary type

Mapping female bodily features of attractiveness

Uncovering the genetic architecture of broad antisocial behavior through a genome-wide association study meta-analysis

IgH locus suicide recombination does not depend on NHEJ in contrast to CSR in B cells

Stimulation of the β3-Adrenoceptor as a Novel Treatment Strategy for Anxiety and Depressive Disorders

Neurochemical, electrophysiological and pharmacological profiles of the selective inhibitor of the glycine transporter-I SSR504734, a potential new type of antipsychotic

Dissection of the MYCN locus in Feingold syndrome and isolated oesophageal atresia

Delineation of Late Onset Hypoventilation Associated with Hypothalamic Dysfunction Syndrome

SOX10 mutations in patients with Waardenburg-Hirschsprung disease

PAX2 mutations in renal-coloboma syndrome: mutational hotspot and germline mosaicism

Genetics and early disturbances of breathing control

Germline deletion of the miR-1792 cluster causes skeletal and growth defects in humans

Germline deletion of the miR-17-92 cluster causes growth and skeletal defects in humans

Early inhaled nitric oxide improves oxidative balance in very preterm infants

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