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Classification of non-bacterial osteitis : Retrospective study of clinical, immunological and genetic aspects in 89 patients

Rheumatology (Oxford, England), 2007, Vol.46 (1), p.154-160

2007

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Keratinocyte growth factor supports pulmonary innate immune defense through maintenance of alveolar antimicrobial protein levels and macrophage function

American journal of physiology. Lung cellular and molecular physiology, 2016-05, Vol.310 (9), p.L868-L879

2016

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Deficits in pattern separation and dentate gyrus proliferation after rodent lateral fluid percussion injury

IBRO neuroscience reports, 2021-06, Vol.10, p.31-41

2021

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The DNA sequence of human chromosome 21

Nature (London), 2000-05, Vol.405 (6784), p.311-319

2000

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Cancer Risks Associated With BRCA1 and BRCA2 Pathogenic Variants

Journal of clinical oncology, 2022-05, Vol.40 (14), p.1529-1541

2022

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Thermal injury of the skin induces G-CSF-dependent attenuation of EPO-mediated STAT signaling and erythroid differentiation arrest in mice

Experimental hematology, 2017-12, Vol.56, p.16-30

2017

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A splice site mutation in the methyltransferase gene FTSJ1 in Xp11.23 is associated with non-syndromic mental retardation in a large Belgian family (MRX9)

Journal of medical genetics, 2004-09, Vol.41 (9), p.679-683

2004

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Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores

JNCI : Journal of the National Cancer Institute, 2022-01, Vol.114 (1), p.109-122

2022

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Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

Genetics in medicine, 2020-10, Vol.22 (10), p.1653-1666

2020

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Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

Cancer research (Chicago, Ill.), 2020-02, Vol.80 (3), p.624-638

2020

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Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

Nature communications, 2019-04, Vol.10 (1), p.1741-18, Article 1741

2019

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Classification of Non-Bacterial Osteitis

Rheumatology (Oxford, England), 2007-01, Vol.46 (1), p.154-160

2007

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The DNA sequence of the human X chromosome

Nature, 2005-03, Vol.434 (7031), p.325-337

2005

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Decentralized versus collective bargaining - An experimental study

International journal of game theory, 2002, Vol.30 (3), p.437-448

2002

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Rare Missense and Synonymous Variants in UBE1 Are Associated with X-Linked Infantile Spinal Muscular Atrophy

American journal of human genetics, 2008-01, Vol.82 (1), p.188-193

2008

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Eine hohe CRYAB-Expression ist mit einer schlechten Prognose bei Patientinnen mit basalem Brustkrebs-Subtyp assoziiert und hemmt die TRAIL-induzierte Apoptose in basalen Brustkrebszellen in vitro

Geburtshilfe und Frauenheilkunde, 2014, Vol.74 (S 01)

2014

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A physical map of the human genome

Nature (London), 2001-02, Vol.409 (6822), p.934-941

2001

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Initial sequencing and analysis of the human genome

Nature (London), 2001-02, Vol.409 (6822), p.860-921

2001

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A unique exonic splice enhancer mutation in a family with X-linked mental retardation and epilepsy points to a novel role of the renin receptor

Human molecular genetics, 2005-04, Vol.14 (8), p.1019-1027

2005

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Re: Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

The Journal of urology, 2020-09, Vol.204 (3), p.619-620

Taneja, Samir S.

2020

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Hybridization of microsatellites to RAPD: a new source of polymorphic markers

Nucleic acids research, 1995-09, Vol.23 (18), p.3798-3799

1995

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Abstract P3-09-04: Beyond CHEK2 in breast cancer: Search for additional moderately penetrant risk gene variants by analyzing the oligogenic disease course in CHEK2 mutation carriers

Cancer research (Chicago, Ill.), 2017-02, Vol.77 (4_Supplement), p.P3-P3-09-04

2017

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Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers

Communications biology, 2022-10, Vol.5 (1), p.1061-1061, Article 1061

2022

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DNA sequence comparison of human and mouse retinitis pigmentosa GTPase regulator (RPGR) identifies tissue-specific exons and putative regulatory elements

Human genetics, 2001-09, Vol.109 (3), p.271-278

2001

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Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca(2+) pump

Human molecular genetics, 2000-04, Vol.9 (7), p.1131-1140

2000

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Classification of non-bacterial osteitis : Retrospective study of clinical, immunological and genetic aspects in 89 patients

Keratinocyte growth factor supports pulmonary innate immune defense through maintenance of alveolar antimicrobial protein levels and macrophage function

Deficits in pattern separation and dentate gyrus proliferation after rodent lateral fluid percussion injury

The DNA sequence of human chromosome 21

Cancer Risks Associated With BRCA1 and BRCA2 Pathogenic Variants

Thermal injury of the skin induces G-CSF-dependent attenuation of EPO-mediated STAT signaling and erythroid differentiation arrest in mice

A splice site mutation in the methyltransferase gene FTSJ1 in Xp11.23 is associated with non-syndromic mental retardation in a large Belgian family (MRX9)

Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores

Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

Classification of Non-Bacterial Osteitis

The DNA sequence of the human X chromosome

Decentralized versus collective bargaining - An experimental study

Rare Missense and Synonymous Variants in UBE1 Are Associated with X-Linked Infantile Spinal Muscular Atrophy

Eine hohe CRYAB-Expression ist mit einer schlechten Prognose bei Patientinnen mit basalem Brustkrebs-Subtyp assoziiert und hemmt die TRAIL-induzierte Apoptose in basalen Brustkrebszellen in vitro

A physical map of the human genome

Initial sequencing and analysis of the human genome

A unique exonic splice enhancer mutation in a family with X-linked mental retardation and epilepsy points to a novel role of the renin receptor

Re: Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

Hybridization of microsatellites to RAPD: a new source of polymorphic markers

Abstract P3-09-04: Beyond CHEK2 in breast cancer: Search for additional moderately penetrant risk gene variants by analyzing the oligogenic disease course in CHEK2 mutation carriers

Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers

DNA sequence comparison of human and mouse retinitis pigmentosa GTPase regulator (RPGR) identifies tissue-specific exons and putative regulatory elements

Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca(2+) pump

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