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Understanding the Processes that Regulate Positive Emotional Experience: Unsolved Problems and Future Directions for Theory and Research on Savoring

International journal of wellbeing, 2011-01, Vol.1 (1)

2011

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Facebook Use and the Tendency to Ruminate among College Students: Testing Mediational Hypotheses

Journal of educational computing research, 2012-01, Vol.46 (4), p.377-394

2012

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The influence of racial and crime stereotypes on jurors' representations of trial evidence and verdict decisions

Kluwe, Katharina

2015

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Decision Making in Groups and Organizations

The Wiley Blackwell Handbook of Judgment and Decision Making, 2015, p.849-874

2015

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Good and bad group performance: Same process—different outcomes

Group processes & intergroup relations, 2012-09, Vol.15 (5), p.603-618

2012

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Justice efficacy and argument strength in mock juror decision-making in a civil trial

Kluwe, Katharina

2012

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Prognostic Relevance of Circulating Tumor Cells in Blood and Disseminated Tumor Cells in Bone Marrow of Patients with Squamous Cell Carcinoma of the Oral Cavity

Clinical cancer research, 2014-01, Vol.20 (2), p.425-433

2014

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BRCA1 promoter hypermethylation on circulating tumor DNA correlates with improved survival of patients with ovarian cancer

Molecular oncology, 2021-12, Vol.15 (12), p.3615-3625

2021

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Separating Response of Tumor and non-Tumor Cells to Drug In Vitro by Quantifying a Mutation

Anticancer research, 2019-04, Vol.39 (4), p.1777-1783

2019

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Heterozygous carriage of the alpha1-antitrypsin PiZ variant increases the risk to develop liver cirrhosis

Gut, 2019-06, Vol.68 (6), p.1099-1107

2019

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Type 2 NF1 Deletions Are Highly Unusual by Virtue of the Absence of Nonallelic Homologous Recombination Hotspots and an Apparent Preference for Female Mitotic Recombination

American journal of human genetics, 2007-12, Vol.81 (6), p.1201-1220

2007

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Intrachromosomal mitotic nonallelic homologous recombination is the major molecular mechanism underlying type-2 NF1 deletions

Human mutation, 2010-10, Vol.31 (10), p.1163-1173

2010

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novel third type of recurrent NF1 microdeletion mediated by nonallelic homologous recombination between LRRC37B-containing low-copy repeats in 17q11.2

Human mutation, 2010-06, Vol.31 (6), p.742-751

2010

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Mechanisms of Loss of Heterozygosity in Neurofibromatosis Type 1-Associated Plexiform Neurofibromas

Journal of investigative dermatology, 2009-03, Vol.129 (3), p.615-621

2009

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Conservation of hotspots for recombination in low-copy repeats associated with the NF1 microdeletion

Nature genetics, 2006-12, Vol.38 (12), p.1419-1423

2006

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Tissue-specific differences in the proportion of mosaic large NF1 deletions are suggestive of a selective growth advantage of hematopoietic del(+/−) stem cells

Human mutation, 2012-03, Vol.33 (3), p.541-550

2012

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Characterization of the nonallelic homologous recombination hotspot PRS3 associated with type-3 NF1 deletions

Human mutation, 2012-02, Vol.33 (2), p.372-383

2012

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A novel third type of recurrent NF1 microdeletion mediated by non-allelic homologous recombination between LRRC37B-containing low-copy repeats in 17q11.2

Human mutation, 2010-04, Vol.31 (6)

2010

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Copy number variations in the NF1 gene region are infrequent and do not predispose to recurrent type-1 deletions

European journal of human genetics : EJHG, 2008-05, Vol.16 (5), p.572-580

2008

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Intrachromosomal mitotic non-allelic homologous recombination is the major molecular mechanism underlying type-2 NF1 deletions

Human mutation, 2010-09, Vol.31 (10)

2010

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Extended runs of homozygosity at 17q11.2: an association with type-2 NF1 deletions

Human mutation, 2010-03, Vol.31 (3), p.325-334

2010

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Type 2 NFl Deletions Are Highly Unusual by Virtue of the Absence of Nonallelic Homologous Recombination Hotspots and an Apparent Preference for Female Mitotic Recombination

American journal of human genetics, 2007-12, Vol.81 (6), p.1201

2007

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Recombination, Genetic
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Gene Deletion
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Polymorphism, Single Nucleotide
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Understanding the Processes that Regulate Positive Emotional Experience: Unsolved Problems and Future Directions for Theory and Research on Savoring

Facebook Use and the Tendency to Ruminate among College Students: Testing Mediational Hypotheses

The influence of racial and crime stereotypes on jurors' representations of trial evidence and verdict decisions

Decision Making in Groups and Organizations

Good and bad group performance: Same process—different outcomes

Justice efficacy and argument strength in mock juror decision-making in a civil trial

Prognostic Relevance of Circulating Tumor Cells in Blood and Disseminated Tumor Cells in Bone Marrow of Patients with Squamous Cell Carcinoma of the Oral Cavity

BRCA1 promoter hypermethylation on circulating tumor DNA correlates with improved survival of patients with ovarian cancer

Separating Response of Tumor and non-Tumor Cells to Drug In Vitro by Quantifying a Mutation

Heterozygous carriage of the alpha1-antitrypsin PiZ variant increases the risk to develop liver cirrhosis

Type 2 NF1 Deletions Are Highly Unusual by Virtue of the Absence of Nonallelic Homologous Recombination Hotspots and an Apparent Preference for Female Mitotic Recombination

Intrachromosomal mitotic nonallelic homologous recombination is the major molecular mechanism underlying type-2 NF1 deletions

novel third type of recurrent NF1 microdeletion mediated by nonallelic homologous recombination between LRRC37B-containing low-copy repeats in 17q11.2

Mechanisms of Loss of Heterozygosity in Neurofibromatosis Type 1-Associated Plexiform Neurofibromas

Conservation of hotspots for recombination in low-copy repeats associated with the NF1 microdeletion

Tissue-specific differences in the proportion of mosaic large NF1 deletions are suggestive of a selective growth advantage of hematopoietic del(+/−) stem cells

Characterization of the nonallelic homologous recombination hotspot PRS3 associated with type-3 NF1 deletions

A novel third type of recurrent NF1 microdeletion mediated by non-allelic homologous recombination between LRRC37B-containing low-copy repeats in 17q11.2

Copy number variations in the NF1 gene region are infrequent and do not predispose to recurrent type-1 deletions

Intrachromosomal mitotic non-allelic homologous recombination is the major molecular mechanism underlying type-2 NF1 deletions

Extended runs of homozygosity at 17q11.2: an association with type-2 NF1 deletions

Type 2 NFl Deletions Are Highly Unusual by Virtue of the Absence of Nonallelic Homologous Recombination Hotspots and an Apparent Preference for Female Mitotic Recombination

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