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Abstract
Authors
Eamonn R. Maher, Wolf Reik
Total citations by year
Citation information
Citations to this article in year 2009 (8)
| Title and authors | Publication | Year |
|---|---|---|
|
Germline mutation in NLRP2 (NALP2) in a familial imprinting disorder (Beckwith-Wiedemann Syndrome)
E Meyer, D Lim, S Pasha, LJ Tee, F Rahman, JR Yates, CG Woods, W Reik, ER Maher |
PLoS genetics | 2009 |
|
The interval between Ins2 and Ascl2 is dispensable for imprinting centre function in the murine Beckwith-Wiedemann region
L Lefebvre, L Mar, A Bogutz, R Oh-McGinnis, MA Mandegar, J Paderova, M Gertsenstein, JA Squire, A Nagy |
Human Molecular Genetics | 2009 |
|
Human imprinting syndromes
DH Lim, ER Maher |
Epigenomics | 2009 |
|
Insights into the role of genetic alterations in adrenocortical tumorigenesis
M Herbet, JJ Feige, M Thomas |
Molecular and Cellular Endocrinology | 2009 |
|
Surgical Management of Nonmultiple Endocrine Neoplasia Endocrinopathies: State-of-the-Art Review
CS Landry, SG Waguespack, ND Perrier |
Surgical Clinics of North America | 2009 |
|
Isolated fetal omphalocele, Beckwith-Wiedemann syndrome, and assisted reproductive technologies
L Wilkins-Haug, A Porter, P Hawley, CB Benson |
Birth Defects Research Part A: Clinical and Molecular Teratology | 2009 |
|
Manifestation of alveolar rhabdomyosarcoma as primary cutaneous lesions in a neonate with Beckwith-Wiedemann syndrome
M Kuroiwa, J Sakamoto, A Shimada, N Suzuki, J Hirato, MJ Park, M Sotomatsu, Y Hayashi |
Journal of Pediatric Surgery | 2009 |
|
Germline Mutation in NLRP2 (NALP2) in a Familial Imprinting Disorder (Beckwith-Wiedemann Syndrome)
E Meyer, D Lim, S Pasha, LJ Tee, F Rahman, JR Yates, CG Woods, W Reik, ER Maher, GS Barsh |
PLoS genetics | 2009 |
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