Dominance and interloci interactions in transcriptional activation cascades: Models explaining compensatory mutations and inheritance patterns

Digenic inheritance in medical genetics

(2013) Alejandro A Schäffer   JOURNAL OF MEDICAL GENETICS

Widespread evidence of cooperative DNA binding by transcription factors in Drosophila development

(2013) Majid Kazemian et al.   NUCLEIC ACIDS RESEARCH

Gene dosage effects: nonlinearities, genetic interactions, and dosage compensation

(2013) Reiner A. Veitia et al.   TRENDS IN GENETICS

Modeling regulatory cascades using Artificial Neural Networks: the case of transcriptional regulatory networks shaped during the yeast stress response

(2013) Maria E. Manioudaki et al.   Frontiers in Genetics

Precision of Hunchback Expression in the Drosophila Embryo

(2012) Michael W. Perry et al.   CURRENT BIOLOGY

The Molecular Genetics of Sex Determination and Sex Reversal in Mammals

(2012) Alexander Quinn et al.   SEMINARS IN REPRODUCTIVE MEDICINE

Digenic inheritance of mutations in FOXC1 and PITX2 : Correlating transcription factor function and axenfeld-rieger disease severity

(2011) Daniel Kelberman et al.   HUMAN MUTATION

The Bicoid Morphogen System

(2010) Aude Porcher et al.   CURRENT BIOLOGY

Generic binding sites, generic DNA-binding domains: where does specific promoter recognition come from?

(2009) Adrien B. Georges et al.   FASEB JOURNAL

One thousand and one ways of making functionally similar transcriptional enhancers

(2008) Reiner A. Veitia   BIOESSAYS

Identification of human haploinsufficient genes and their genomic proximity to segmental duplications

(2008) Vinh T Dang et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

The Complex Genetics of Kallmann Syndrome: KAL1, FGFR1, FGF8, PROKR2, PROK2, et al.

(2008) J.-P. Hardelin et al.   Sexual Development

A Careful Look at Binding Site Reorganization in the even-skipped Enhancers of Drosophila and Sepsids

(2008) Emily E. Hare et al.   PLoS Genetics

Sepsid even-skipped Enhancers Are Functionally Conserved in Drosophila Despite Lack of Sequence Conservation

(2008) Emily E. Hare et al.   PLoS Genetics