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Reassessing the association: Evaluation of a polyalanine deletion variant of RUNX2 in non‐syndromic sagittal and metopic craniosynostosis.
Published in:
Journal of Anatomy, 2024, v. 245, n. 6, p. 874, doi. 10.1111/joa.14052
By:
- Walton, Isaac S.;
- McCann, Emma;
- Weber, Astrid;
- Morton, Jenny E. V.;
- Noons, Peter;
- Wilson, Louise C.;
- Ching, Rosanna C.;
- Cilliers, Deirdre;
- Johnson, David;
- Phipps, Julie M.;
- Shears, Deborah J.;
- Thomas, Gregory P. L.;
- Wall, Steven A.;
- Twigg, Stephen R. F.;
- Wilkie, Andrew O. M.
Publication type:
Article
A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosis.
Published in:
Human Genetics, 2020, v. 139, n. 8, p. 1077, doi. 10.1007/s00439-020-02157-z
By:
- Justice, Cristina M.;
- Cuellar, Araceli;
- Bala, Krithi;
- Sabourin, Jeremy A.;
- Cunningham, Michael L.;
- Crawford, Karen;
- Phipps, Julie M.;
- Zhou, Yan;
- Cilliers, Deirdre;
- Byren, Jo C.;
- Johnson, David;
- Wall, Steven A.;
- Morton, Jenny E. V.;
- Noons, Peter;
- Sweeney, Elizabeth;
- Weber, Astrid;
- Rees, Katie E. M.;
- Wilson, Louise C.;
- Simeonov, Emil;
- Kaneva, Radka
Publication type:
Article
Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis.
Published in:
Nature Genetics, 2013, v. 45, n. 10, p. 1261, doi. 10.1038/ng1013-1261a
By:
- Sharma, Vikram P;
- Fenwick, Aimée L;
- Brockop, Mia S;
- McGowan, Simon J;
- Goos, Jacqueline A C;
- Hoogeboom, A Jeannette M;
- Brady, Angela F;
- Jeelani, Nu Owase;
- Lynch, Sally Ann;
- Mulliken, John B;
- Murray, Dylan J;
- Phipps, Julie M;
- Sweeney, Elizabeth;
- Tomkins, Susan E;
- Wilson, Louise C;
- Bennett, Sophia;
- Cornall, Richard J;
- Broxholme, John;
- Kanapin, Alexander;
- Johnson, David
Publication type:
Article
Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis.
Published in:
Nature Genetics, 2013, v. 45, n. 3, p. 304, doi. 10.1038/ng.2531
By:
- Sharma, Vikram P;
- Fenwick, Aimée L;
- Brockop, Mia S;
- McGowan, Simon J;
- Goos, Jacqueline A C;
- Hoogeboom, A Jeannette M;
- Brady, Angela F;
- Jeelani, Nu Owase;
- Lynch, Sally Ann;
- Mulliken, John B;
- Murray, Dylan J;
- Phipps, Julie M;
- Sweeney, Elizabeth;
- Tomkins, Susan E;
- Wilson, Louise C;
- Bennett, Sophia;
- Cornall, Richard J;
- Broxholme, John;
- Kanapin, Alexander;
- Johnson, David
Publication type:
Article

Found: 4

Reassessing the association: Evaluation of a polyalanine deletion variant of RUNX2 in non‐syndromic sagittal and metopic craniosynostosis.

A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosis.

Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis.

Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis.