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Welche Determinanten beeinflussen den Studienerfolg?: Eine empirische Analyse zum Studienerfolg der ersten Kohorte der Bachelorstudenten in der Assessmentphase am Fachbereich Wirtschaftswissenschaften der Friedrich-Alexander-Universität Erlangen-Nürnberg

Erdel, Barbara

2010

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Are incentive effects on response rates and nonresponse bias in large-scale, face-to-face surveys generalizable to Germany?: Evidence from ten experiments

Public opinion quarterly, 2015, Vol.79 (3), p.740-768

2015

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Lebenslanges Lernen und Trends in der Weiterbildung: Ergebnisse der Erwachsenenbefragung des Nationalen Bildungspanels (NEPS)

Wirtschaftsdienst (Hamburg), 2013-07, Vol.93 (7), p.496-498

2013

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Life-long learning and trends in continuing education: results from the a survey of the National Education Panel (NEPS)

Wirtschaftsdienst (Hamburg), 2013-01, Vol.93 (1)

2013

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SIRT6 Recruits SNF2H to DNA Break Sites, Preventing Genomic Instability through Chromatin Remodeling

Molecular cell, 2013-08, Vol.51 (4), p.454-468

2013

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Isolation and characterization of CD133+CD34+VEGFR-2+CD45− fetal endothelial cells from human term placenta

Microvascular research, 2012-07, Vol.84 (1), p.65-73

2012

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Mutations in the Δ7-sterol reductase gene in patients with the Smith–Lemli–Opitz syndrome

Proceedings of the National Academy of Sciences - PNAS, 1998-07, Vol.95 (14), p.8181-8186

1998

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Mutations in the Δ 7-sterol Reductase Gene in Patients with the Smith--Lemli--Opitz Syndrome

Proceedings of the National Academy of Sciences - PNAS, 1998-07, Vol.95 (14), p.8181-8186

1998

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Single-Nucleotide Polymorphism Array-Based Characterization of Ring Chromosome 18

The Journal of pediatrics, 2013-10, Vol.163 (4), p.1174-1178.e3

2013

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Disruption of the ARID1B and ADAMTS6 loci due to a t(5;6)(q12.3;q25.3) in a patient with developmental delay

American journal of medical genetics. Part A, 2014-12, Vol.164A (12), p.3126-3131

2014

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Unravelling the parental origin and mechanism of formation of the 47,XY,i(X)(q10) Klinefelter karyotype variant

Fertility and sterility, 2008-11, Vol.90 (5), p.2009.e13-2009.e17

2008

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Molecular characterization of a de novo ring chromosome 6 in a growth retarded but otherwise healthy woman

American journal of medical genetics. Part A, 2008-04, Vol.146A (7), p.925-929

2008

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SIRT6 recruits SNF2H to sites of DNA breaks, preventing genomic instability through chromatin remodeling

Molecular cell, 2013-08, Vol.51 (4), p.454-468

2013

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Effects of deletion and duplication in a patient with a 46,XX,der(7)t(7;17)(q36;p13)mat karyotype

American journal of medical genetics. Part A, 2012-09, Vol.158A (9), p.2239-2244

2012

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Analysis of Pharmacist Interventions Used to Resolve Safety Target of Polypharmacy (STOP) Drug Interactions

Federal practitioner, 2020-06, Vol.37 (6), p.268-275

2020

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Pre- and postnatal findings in trisomy 17 mosaicism

American journal of medical genetics. Part A, 2006-08, Vol.140A (15), p.1628-1636

2006

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Detection of a de novo duplication of 1q32-qter by fluorescence in situ hybridisation in a boy with multiple malformations: further delineation of the trisomy 1q syndrome

Journal of medical genetics, 1997-04, Vol.34 (4), p.309-313

1997

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Muellerian aplasia associated with ring chromosome 8p12q12 mosaicism

American journal of medical genetics. Part A, 2003-01, Vol.116A (3), p.290-294

2003

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Comparative genomic hybridization reveals a partial de novo trisomy 6q23-qter in an infant with congenital malformations : delineation of the phenotype

Human genetics, 1997-05, Vol.99 (5), p.596-601

1997

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Routine screening for microdeletions by FISH in 77 patients suspected of having Prader-Willi or Angelman syndromes using YAC clone 273A2 (D15S10)

Human genetics, 1996-06, Vol.97 (6), p.784-793

1996

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Nail patella syndrome in a cytogenetically balanced t(9;17)(q34.1;q25) carrier

European journal of human genetics : EJHG, 1998-01, Vol.6 (1), p.75-79

1998

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Mutations in the Delta7-sterol reductase gene in patients with the Smith-Lemli-Opitz syndrome

Proceedings of the National Academy of Sciences - PNAS, 1998-07, Vol.95 (14), p.8181

1998

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Effects of deletion and duplication in a patient with a 46,XX,der(7)t(7;17)(q36;p13)mat karyotype

American Journal of Medical Genetics Part A, 2012, Vol.158A (9), p.2239-2244

2012

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Molecular characterization of a de novo ring chromosome 6 in a growth retarded but otherwise healthy woman

American Journal of Medical Genetics Part A, 2008, Vol.146A (7), p.925-929

2008

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Muellerian aplasia associated with ring chromosome 8p12q12 mosaicism

American journal of medical genetics, 2003, Vol.116A (3), p.290-294

2003

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Welche Determinanten beeinflussen den Studienerfolg?: Eine empirische Analyse zum Studienerfolg der ersten Kohorte der Bachelorstudenten in der Assessmentphase am Fachbereich Wirtschaftswissenschaften der Friedrich-Alexander-Universität Erlangen-Nürnberg

Are incentive effects on response rates and nonresponse bias in large-scale, face-to-face surveys generalizable to Germany?: Evidence from ten experiments

Lebenslanges Lernen und Trends in der Weiterbildung: Ergebnisse der Erwachsenenbefragung des Nationalen Bildungspanels (NEPS)

Life-long learning and trends in continuing education: results from the a survey of the National Education Panel (NEPS)

SIRT6 Recruits SNF2H to DNA Break Sites, Preventing Genomic Instability through Chromatin Remodeling

Isolation and characterization of CD133+CD34+VEGFR-2+CD45− fetal endothelial cells from human term placenta

Mutations in the Δ7-sterol reductase gene in patients with the Smith–Lemli–Opitz syndrome

Mutations in the Δ 7-sterol Reductase Gene in Patients with the Smith--Lemli--Opitz Syndrome

Single-Nucleotide Polymorphism Array-Based Characterization of Ring Chromosome 18

Disruption of the ARID1B and ADAMTS6 loci due to a t(5;6)(q12.3;q25.3) in a patient with developmental delay

Unravelling the parental origin and mechanism of formation of the 47,XY,i(X)(q10) Klinefelter karyotype variant

Molecular characterization of a de novo ring chromosome 6 in a growth retarded but otherwise healthy woman

SIRT6 recruits SNF2H to sites of DNA breaks, preventing genomic instability through chromatin remodeling

Effects of deletion and duplication in a patient with a 46,XX,der(7)t(7;17)(q36;p13)mat karyotype

Analysis of Pharmacist Interventions Used to Resolve Safety Target of Polypharmacy (STOP) Drug Interactions

Pre- and postnatal findings in trisomy 17 mosaicism

Detection of a de novo duplication of 1q32-qter by fluorescence in situ hybridisation in a boy with multiple malformations: further delineation of the trisomy 1q syndrome

Muellerian aplasia associated with ring chromosome 8p12q12 mosaicism

Comparative genomic hybridization reveals a partial de novo trisomy 6q23-qter in an infant with congenital malformations : delineation of the phenotype

Routine screening for microdeletions by FISH in 77 patients suspected of having Prader-Willi or Angelman syndromes using YAC clone 273A2 (D15S10)

Nail patella syndrome in a cytogenetically balanced t(9;17)(q34.1;q25) carrier

Mutations in the Delta7-sterol reductase gene in patients with the Smith-Lemli-Opitz syndrome

Effects of deletion and duplication in a patient with a 46,XX,der(7)t(7;17)(q36;p13)mat karyotype

Molecular characterization of a de novo ring chromosome 6 in a growth retarded but otherwise healthy woman

Muellerian aplasia associated with ring chromosome 8p12q12 mosaicism

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