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Multiplexed analysis of chromosome conformation at vastly improved sensitivity

Nature methods, 2016-01, Vol.13 (1), p.74

2016

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Intragenic Enhancers Act as Alternative Promoters

Molecular cell, 2012-02, Vol.45 (4), p.447-458

2012

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A biallelic mutation in IL6ST encoding the GP130 co-receptor causes immunodeficiency and craniosynostosis

The Journal of experimental medicine, 2017-09, Vol.214 (9), p.2547-2562

2017

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Ubiquitin-mediated fluctuations in MHC class II facilitate efficient germinal center B cell responses

The Journal of experimental medicine, 2016-05, Vol.213 (6), p.993-1009

2016

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Dynamic Analysis of Gene Expression and Genome-wide Transcription Factor Binding during Lineage Specification of Multipotent Progenitors

Cell stem cell, 2013-12, Vol.13 (6), p.754-768

2013

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Mutations in DPAGT1 Cause a Limb-Girdle Congenital Myasthenic Syndrome with Tubular Aggregates

American journal of human genetics, 2012-07, Vol.91 (1), p.193-201

2012

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Visualizing the origins of selfish de novo mutations in individual seminiferous tubules of human testes

Proceedings of the National Academy of Sciences - PNAS, 2016-03, Vol.113 (9), p.2454-2459

2016

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A Noncoding Expansion in EIF4A3 Causes Richieri-Costa-Pereira Syndrome, a Craniofacial Disorder Associated with Limb Defects

American journal of human genetics, 2014-01, Vol.94 (1), p.120-128

2014

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CPFP: a central proteomics facilities pipeline

Bioinformatics, 2010-04, Vol.26 (8), p.1131-1132

2010

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Cardamine hirsuta: a versatile genetic system for comparative studies

The Plant journal : for cell and molecular biology, 2014-04, Vol.78 (1), p.1-15

2014

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Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors

Nature genetics, 2009-11, Vol.41 (11), p.1247-1252

2009

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Global gene expression analysis of human erythroid progenitors

Blood, 2011-03, Vol.117 (13), p.e96-e108

2011

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Contributions of intrinsic mutation rate and selfish selection to levels of de novo HRAS mutations in the paternal germline

Proceedings of the National Academy of Sciences - PNAS, 2013-12, Vol.110 (50), p.20152-20157

2013

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Germinal Center B Cells Replace Their Antigen Receptors in Dark Zones and Fail Light Zone Entry when Immunoglobulin Gene Mutations are Damaging

Immunity (Cambridge, Mass.), 2018-09, Vol.49 (3), p.477-489.e7

2018

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Gain-of-Function Mutations in ZIC1 Are Associated with Coronal Craniosynostosis and Learning Disability

American journal of human genetics, 2015-09, Vol.97 (3), p.378-388

2015

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Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type I

Haematologica (Roma), 2013-09, Vol.98 (9), p.1383-1387

2013

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Mutations in Multidomain Protein MEGF8 Identify a Carpenter Syndrome Subtype Associated with Defective Lateralization

American journal of human genetics, 2012-11, Vol.91 (5), p.897-905

2012

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Germinal centers output clonally diverse plasma cell populations expressing high- and low-affinity antibodies

Cell, 2023-12, Vol.186 (25), p.5486-5499.e13

2023

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Cellular interference in craniofrontonasal syndrome: males mosaic for mutations in the X-linked EFNB1 gene are more severely affected than true hemizygotes

Human molecular genetics, 2013-04, Vol.22 (8), p.1654-1662

2013

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MIG: Multi-Image Genome viewer

Bioinformatics, 2013-10, Vol.29 (19), p.2477-2478

2013

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CSynth: an interactive modelling and visualization tool for 3D chromatin structure

Bioinformatics, 2021-05, Vol.37 (7), p.951-955

2021

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Diagnostic value of exome and whole genome sequencing in craniosynostosis

Journal of medical genetics, 2017-04, Vol.54 (4), p.260

2017

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Congenital myasthenic syndromes due to mutations in ALG2 and ALG14

Brain (London, England : 1878), 2013-03, Vol.136 (Pt 3), p.944-956

2013

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Genome-wide identification of TAL1's functional targets: insights into its mechanisms of action in primary erythroid cells

Genome research, 2010-08, Vol.20 (8), p.1064

2010

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The small FNR regulon of Neisseria gonorrhoeae: comparison with the larger Escherichia coli FNR regulon and interaction with the NarQ-NarP regulon

BMC genomics, 2007-01, Vol.8 (1), p.35-35, Article 35

2007

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Multiplexed analysis of chromosome conformation at vastly improved sensitivity

Intragenic Enhancers Act as Alternative Promoters

A biallelic mutation in IL6ST encoding the GP130 co-receptor causes immunodeficiency and craniosynostosis

Ubiquitin-mediated fluctuations in MHC class II facilitate efficient germinal center B cell responses

Dynamic Analysis of Gene Expression and Genome-wide Transcription Factor Binding during Lineage Specification of Multipotent Progenitors

Mutations in DPAGT1 Cause a Limb-Girdle Congenital Myasthenic Syndrome with Tubular Aggregates

Visualizing the origins of selfish de novo mutations in individual seminiferous tubules of human testes

A Noncoding Expansion in EIF4A3 Causes Richieri-Costa-Pereira Syndrome, a Craniofacial Disorder Associated with Limb Defects

CPFP: a central proteomics facilities pipeline

Cardamine hirsuta: a versatile genetic system for comparative studies

Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors

Global gene expression analysis of human erythroid progenitors

Contributions of intrinsic mutation rate and selfish selection to levels of de novo HRAS mutations in the paternal germline

Germinal Center B Cells Replace Their Antigen Receptors in Dark Zones and Fail Light Zone Entry when Immunoglobulin Gene Mutations are Damaging

Gain-of-Function Mutations in ZIC1 Are Associated with Coronal Craniosynostosis and Learning Disability

Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type I

Mutations in Multidomain Protein MEGF8 Identify a Carpenter Syndrome Subtype Associated with Defective Lateralization

Germinal centers output clonally diverse plasma cell populations expressing high- and low-affinity antibodies

Cellular interference in craniofrontonasal syndrome: males mosaic for mutations in the X-linked EFNB1 gene are more severely affected than true hemizygotes

MIG: Multi-Image Genome viewer

CSynth: an interactive modelling and visualization tool for 3D chromatin structure

Diagnostic value of exome and whole genome sequencing in craniosynostosis

Congenital myasthenic syndromes due to mutations in ALG2 and ALG14

Genome-wide identification of TAL1's functional targets: insights into its mechanisms of action in primary erythroid cells

The small FNR regulon of Neisseria gonorrhoeae: comparison with the larger Escherichia coli FNR regulon and interaction with the NarQ-NarP regulon

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