Al Turki, Saeed; Manickaraj, Ashok K.; Mercer, Catherine L.; Gerety, Sebastian S.; Hitz, Marc-Phillip; Lindsay, Sarah; D'Alessandro, Lisa C. A.; Swaminathan, G. Jawahar; Bentham, Jamie; Arndt, Anne-Karin; Louw, Jacoba; Breckpot, Jeroen; Gewillig, Marc; Thienpont, Bernard; Abdul-Khaliq, Hashim; Harnack, Christine; Hoff, Kirstin; Kramer, Hans-Heiner; Schubert, Stephan; Siebert, Reiner; Toka, Okan; Cosgrove, Catherine; Watkins, Hugh; Lucassen, Anneke M.; O'Kelly, Ita M.; Salmon, Anthony P.; Bu'Lock, Frances A.; Granados-Riveron, Javier; Setchfield, Kerry; Thornborough, Chris; Brook, J. David; Mulder, Barbara; Klaassen, Sabine; Bhattacharya, Shoumo; Devriendt, Koen; FitzPatrick, David R.; Wilson, David I.; Mital, Seema; Hurles, Matthew E.

Human endothelial and foetal femur-derived stem cell co-cultures modulate osteogenesis and angiogenesis

STEM CELL RESEARCH & THERAPY

IF7.3

2016-01-1823

OAAI

Regionally-derived cell populations and skeletal stem cells from human foetal femora exhibit specific osteochondral and multi-lineage differentiation capacity in vitro and ex vivo

STEM CELL RESEARCH & THERAPY

IF7.3

2015-12-1811

OAAI

Long-range evolutionary constraints reveal cis-regulatory interactions on the human X chromosome

NATURE COMMUNICATIONS

IF15.7

2015-04-2427

OAAI

Evidence for centriolar satellite localization of CDK1 and cyclin B2

CELL CYCLE

IF3.4

2014-11-038

RBFOX2 protein domains and cellular activities

BIOCHEMICAL SOCIETY TRANSACTIONS

IF4.3

2014-08-1123

PREAI

Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans (vol 94, pg 574, 2014)

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2014-07-010

OAAI

Al Turki, Saeed; Manickaraj, Ashok K.; Mercer, Catherine L.; Gerety, Sebastian S.; Hitz, Marc-Phillip; Lindsay, Sarah; D'Alessandro, Lisa C. A.; Swaminathan, G. Jawahar; Bentham, Jamie; Arndt, Anne-Karin; Low, Jacoba; Breckpot, Jeroen; Gewillig, Marc; Thienpont, Bernard; Abdul-Khaliq, Hashim; Harnack, Christine; Hoff, Kirstin; Kramer, Hans-Heiner; Schubert, Stephan; Siebert, Reiner; Toka, Okan; Cosgrove, Catherine; Watkins, Hugh; Lucassen, Anneke M.; O'Kelly, Ita M.; Salmon, Anthony P.; Bu'Lock, Frances A.; Granados-Riveron, Javier; Setchfield, Kerry; Thornborough, Chris; Brook, J. David; Mulder, Barbara; Klaassen, Sabine; Bhattacharya, Shoumo; Devriendt, Koen; FitzPatrick, David R.; Wilson, David I.; Mital, Seema; Hurles, Matthew E.

FRA2A Is a CGG Repeat Expansion Associated with Silencing of AFF3

PLOS GENETICS

IF3.7

2014-04-2440

OAAI

Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans

NR2F2的罕见变异导致人类先天性心脏缺陷

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2014-04-01138

Al Turki, Saeed; Manickaraj, Ashok K.; Mercer, Catherine L.; Gerety, Sebastian S.; Hitz, Marc-Phillip; Lindsay, Sarah; D'Alessandro, Lisa C. A.; Swaminathan, G. Jawahar; Bentham, Jamie; Arndt, Anne-Karin; Low, Jacoba; Breckpot, Jeroen; Gewillig, Marc; Thienpont, Bernard; Abdul-Khaliq, Hashim; Harnack, Christine; Hoff, Kirstin; Kramer, Hans-Heiner; Schubert, Stephan; Siebert, Reiner; Toka, Okan; Cosgrove, Catherine; Watkins, Hugh; Lucassen, Anneke M.; O'Kelly, Ita M.; Salmon, Anthony P.; Bu'Lock, Frances A.; Granados-Riveron, Javier; Setchfield, Kerry; Thornborough, Chris; Brook, J. David; Mulder, Barbara; Klaassen, Sabine; Bhattacharya, Shoumo; Devriendt, Koen; FitzPatrick, David F.; Wilson, David I.; Mital, Seema; Hurles, Matthew E.

Genome-wide DNA methylation analysis of patients with imprinting disorders identifies differentially methylated regions associated with novel candidate imprinted genes

印迹疾病患者的全基因组DNA甲基化分析确定与新候选印迹基因相关的差异甲基化区域

JOURNAL OF MEDICAL GENETICS

IF3.7

2014-02-0576

OAAI

EPIGENETIC REGULATION DURING FETAL FEMUR DEVELOPMENT: DNA METHYLATION MATTERS

OSTEOARTHRITIS AND CARTILAGE

IF9

2013-04-010