Francis J. Smith - Publications, H-index & Citations

Francis J. Smith

university of colorado anschutz medical campus

15H指数

36论文数

782被引数

收录论文 11

发表时间

MEMO1 Is Required for Ameloblast Maturation and Functional Enamel Formation MEMO1是成釉细胞成熟和功能性牙釉质形成所必需的

JOURNAL OF DENTAL RESEARCH

IF5.9

2023-07-20

OAAI

Kiel, M.; Wuebker, S.; Remy, M. T.; Riemondy, K. A.; Smith, F.; Carey, C. M.; Williams, T.; Van Otterloo, E.

An Alternative Splicing Program for Mouse Craniofacial Development

FRONTIERS IN PHYSIOLOGY

IF3.4

2020-09-04

OAAI

Hooper, Joan E.; Jones, Kenneth L.; Smith, Francis J.; Williams, Trevor; Li, Hong

Striate palmoplantar keratoderma resulting from a missense mutation in DSG1

BRITISH JOURNAL OF DERMATOLOGY

IF9.6

2018-05-05

OAAI

Vodo, D.; O'Toole, E. A.; Malchin, N.; Lahav, A.; Adir, N.; Sarig, O.; Green, K. J.; Smith, F. J. D.; Sprecher, E.

Developmental nonlinearity drives phenotypic robustness

NATURE COMMUNICATIONS

IF15.7

2017-12-06

OAAI

Green, Rebecca M.; Fish, Jennifer L.; Young, Nathan M.; Smith, Francis J.; Roberts, Benjamin; Dolan, Katie; Choi, Irene; Leach, Courtney L.; Gordon, Paul; Cheverud, James M.; Roseman, Charles C.; Williams, Trevor J.; Marcucio, Ralph S.; Hallgrimsson, Benedikt

Mutations in desmoglein 1 cause diverse inherited palmoplantar keratoderma phenotypes: implications for genetic screening

BRITISH JOURNAL OF DERMATOLOGY

IF9.6

2017-04-02

OAAI

Lovgren, M. -L.; McAleer, M. A.; Irvine, A. D.; Wilson, N. J.; Tavadia, S.; Schwartz, M. E.; Cole, C.; Sandilands, A.; Smith, F. J. D.; Zamiri, M.

Embryonic bauplans and the developmental origins of facial diversity and constraint

DEVELOPMENT

IF3.6

2014-03-01

112

OAAI

Young, Nathan M.; Hu, Diane; Lainoff, Alexis J.; Smith, Francis J.; Diaz, Raul; Tucker, Abigail S.; Trainor, Paul A.; Schneider, Richard A.; Hallgrimsson, Benedikt; Marcucio, Ralph S.

A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by DSP mutations

CLINICAL AND EXPERIMENTAL DERMATOLOGY

IF2.8

2013-12-17

PREAI

Vahlquist, A.; Virtanen, M.; Hellstrom-Pigg, M.; Dragomir, A.; Ryberg, K.; Wilson, N. J.; Ostman-Smith, I.; Lu, L.; McGrath, J. A.; Smith, F. J. D.

Mutations in AQP5, Encoding a Water-Channel Protein, Cause Autosomal-Dominant Diffuse Nonepidermolytic Palmoplantar Keratoderma

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2013-08-01

OAAI

Blaydon, Diana C.; Lind, Lisbet K.; Plagnol, Vincent; Linton, Kenneth J.; Smith, Francis J. D.; Wilson, Neil J.; McLean, W. H. Irwin; Munro, Colin S.; South, Andrew P.; Leigh, Irene M.; O'Toole, Edel A.; Lundstrom, Anita; Kelsell, David P.

The effect of hypoxia on facial shape variation and disease phenotypes in chicken embryos

DISEASE MODELS & MECHANISMS

IF3.3

2013-01-01

OAAI

Smith, Francis; Hu, Diane; Young, Nathan M.; Lainoff, Alexis J.; Jamniczky, Heather A.; Maltepe, Emin; Hallgrimsson, Benedikt; Marcucio, Ralph S.

Compound heterozygous mutations in desmoplakin cause skin fragility and woolly hair

BRITISH JOURNAL OF DERMATOLOGY

IF9.6

2011-12-05

PREAI

Smith, F. J. D.; Wilson, N. J.; Moss, C.; Dopping-Hepenstal, P.; McGrath, J.