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human sex ratio from conception to birth

Proceedings of the National Academy of Sciences - PNAS, 2015-04, Vol.112 (16), p.E2102-E2111

2015

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Chromosomal Microarray versus Karyotyping for Prenatal Diagnosis

The New England journal of medicine, 2012-12, Vol.367 (23), p.2175-2184

2012

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BRCA1 and BRCA2 mutations in women of different ethnicities undergoing testing for hereditary breast‐ovarian cancer

Cancer, 2009-05, Vol.115 (10), p.2222-2233

2009

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Pan-ethnic carrier screening and prenatal diagnosis for spinal muscular atrophy: clinical laboratory analysis of >72 400 specimens

European journal of human genetics : EJHG, 2012-01, Vol.20 (1), p.27-32

2012

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Amniotic fluid RNA gene expression profiling provides insights into the phenotype of Turner syndrome

Human genetics, 2014-09, Vol.133 (9), p.1075-1082

2014

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Clinical Characteristics of Individuals With Germline Mutations in BRCA1 and BRCA2: Analysis of 10,000 Individuals

Journal of clinical oncology, 2002-03, Vol.20 (6), p.1480-1490

Frank, T. S.

2002

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Cystic Fibrosis Carrier Testing in an Ethnically Diverse US Population

Clinical chemistry (Baltimore, Md.), 2011-06, Vol.57 (6), p.841-848

2011

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The visual analog scale allows effective measurement of preoperative Anxiety and detection of patients' anesthetic concerns

Anesthesia and analgesia, 2000-03, Vol.90 (3), p.706-712

2000

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Supplementary delta-rod configurations provide superior stiffness and reduced rod stress compared to traditional multiple-rod configurations after pedicle subtraction osteotomy: a finite element study

European spine journal, 2019-09, Vol.28 (9), p.2198-2207

2019

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Specific Complex Formation between the Type II Bare Lymphocyte Syndrome-Associated Transactivators CIITA and RFX5

Proceedings of the National Academy of Sciences - PNAS, 1997-06, Vol.94 (12), p.6330-6334

1997

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Transactivation by CIITA, the Type II Bare Lymphocyte Syndrome-Associated Factor, Requires Participation of Multiple Regions of the TATA Box Binding Protein

Proceedings of the National Academy of Sciences - PNAS, 1997-06, Vol.94 (12), p.6324-6329

1997

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Prediction of MLH1 and MSH2 mutations in Lynch syndrome

JAMA : the journal of the American Medical Association, 2006-09, Vol.296 (12), p.1469

2006

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Genetic heterozygosity and pseudodeficiency in the Pompe disease newborn screening pilot program

Molecular genetics and metabolism, 2010-04, Vol.99 (4), p.379-383

2010

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"Psychisch Belastete können nicht unter Druck gesunden"

Zeitschrift für Sozialhilfe : ZESO, 2018, Vol.115 (2), p.24

Ihde-Scholl, Thomas

2018

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Shared Genetic Susceptibility to Breast Cancer, Brain Tumors, and Fanconi Anemia

JNCI : Journal of the National Cancer Institute, 2003-10, Vol.95 (20), p.1548-1551

2003

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Multiple Rare Nonsynonymous Variants in the Adenomatous Polyposis Coli Gene Predispose to Colorectal Adenomas

Cancer research (Chicago, Ill.), 2008-01, Vol.68 (2), p.358-363

2008

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Germline mutations in BRCA2: shared genetic susceptibility to breast cancer, early onset leukemia, and Fanconi anemia

Blood, 2004-04, Vol.103 (8), p.3226-3229

2004

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Development of a Pompe disease CRIM assay for blood samples

Molecular genetics and metabolism, 2011-02, Vol.102 (2), p.S23-S23

2011

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Late angiotensin II receptor blockade in progressive rat mesangioproliferative glomerulonephritis: new insights into mechanisms

The Journal of pathology, 2013-04, Vol.229 (5), p.672-684

2013

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Towards an Automated Safety Suit for Industrial Service

Mobile Web Information Systems, p.137-144

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A GC-Wave Correction Algorithm that Improves the Analytical Performance of aCGH

The Journal of molecular diagnostics : JMD, 2012-11, Vol.14 (6), p.550-559

2012

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Application of embryonic lethal or other obvious phenotypes to characterize the clinical significance of genetic variants found in trans with known deleterious mutations

Cancer research (Chicago, Ill.), 2005-11, Vol.65 (21), p.10096-10103

2005

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Abstract LB-274: Clinical significance of MUC1, MUC2 and CK17 expression patterns in the diagnosis of pancreatic carcinoma

Cancer research (Chicago, Ill.), 2010-04, Vol.70 (8_Supplement), p.LB-274-LB-274

2010

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Cytoplasmic Immunoglobulin Fluorescence In Situ Hybridization (cIg FISH) Enhances the Quantitative Detection of Chromosome Abnormalities In Plasma Cell Neoplasms Compared to Conventional FISH

Blood, 2010-11, Vol.116 (21), p.1198-1198

2010

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human sex ratio from conception to birth

Chromosomal Microarray versus Karyotyping for Prenatal Diagnosis

BRCA1 and BRCA2 mutations in women of different ethnicities undergoing testing for hereditary breast‐ovarian cancer

Pan-ethnic carrier screening and prenatal diagnosis for spinal muscular atrophy: clinical laboratory analysis of >72 400 specimens

Amniotic fluid RNA gene expression profiling provides insights into the phenotype of Turner syndrome

Clinical Characteristics of Individuals With Germline Mutations in BRCA1 and BRCA2: Analysis of 10,000 Individuals

Cystic Fibrosis Carrier Testing in an Ethnically Diverse US Population

The visual analog scale allows effective measurement of preoperative Anxiety and detection of patients' anesthetic concerns

Supplementary delta-rod configurations provide superior stiffness and reduced rod stress compared to traditional multiple-rod configurations after pedicle subtraction osteotomy: a finite element study

Specific Complex Formation between the Type II Bare Lymphocyte Syndrome-Associated Transactivators CIITA and RFX5

Transactivation by CIITA, the Type II Bare Lymphocyte Syndrome-Associated Factor, Requires Participation of Multiple Regions of the TATA Box Binding Protein

Prediction of MLH1 and MSH2 mutations in Lynch syndrome

Genetic heterozygosity and pseudodeficiency in the Pompe disease newborn screening pilot program

"Psychisch Belastete können nicht unter Druck gesunden"

Shared Genetic Susceptibility to Breast Cancer, Brain Tumors, and Fanconi Anemia

Multiple Rare Nonsynonymous Variants in the Adenomatous Polyposis Coli Gene Predispose to Colorectal Adenomas

Germline mutations in BRCA2: shared genetic susceptibility to breast cancer, early onset leukemia, and Fanconi anemia

Genetics of low spinal muscular atrophy carrier frequency in sub-Saharan Africa

Development of a Pompe disease CRIM assay for blood samples

Late angiotensin II receptor blockade in progressive rat mesangioproliferative glomerulonephritis: new insights into mechanisms

Towards an Automated Safety Suit for Industrial Service

A GC-Wave Correction Algorithm that Improves the Analytical Performance of aCGH

Application of embryonic lethal or other obvious phenotypes to characterize the clinical significance of genetic variants found in trans with known deleterious mutations

Abstract LB-274: Clinical significance of MUC1, MUC2 and CK17 expression patterns in the diagnosis of pancreatic carcinoma

Cytoplasmic Immunoglobulin Fluorescence In Situ Hybridization (cIg FISH) Enhances the Quantitative Detection of Chromosome Abnormalities In Plasma Cell Neoplasms Compared to Conventional FISH

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