Intersections of Epigenetics, Twinning and Developmental Asymmetries: Insights Into Monogenic and Complex Diseases and a Role for 3D Facial Analysis

Silver-Russell patients showing a broad range of ICR1 and ICR2 hypomethylation in different tissues

(2010) M Begemann et al.   CLINICAL GENETICS

Objective 3D face recognition: Evolution, approaches and challenges

(2010) Dirk Smeets et al.   FORENSIC SCIENCE INTERNATIONAL

Epigenomics reveals a functional genome anatomy and a new approach to common disease

(2010) Andrew P Feinberg   NATURE BIOTECHNOLOGY

Phenomics: the next challenge

(2010) David Houle et al.   NATURE REVIEWS GENETICS

Familial monozygotic twinning: A report of seven pedigrees

(2009) Geoffrey Machin   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

Fluctuating Asymmetry and Developmental Instability in Sagittal Craniosynostosis

(2009) Valerie Burke DeLeon et al.   CLEFT PALATE-CRANIOFACIAL JOURNAL

Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells

(2009) Jet Bliek et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Imprinting disorders and assisted reproductive technology

(2009) Somjate Manipalviratn et al.   FERTILITY AND STERILITY

Silver-Russell and Beckwith-Wiedemann Syndromes: Opposite (Epi)Mutations in 11p15 Result in Opposite Clinical Pictures

(2009) Thomas Eggermann   Hormone Research in Paediatrics

Heterotaxy Syndrome with Mirror Image Anomalies in Identical Twins

(2009) Deepika Thacker et al.   Congenital Heart Disease

Three-dimensional morphometric analysis of craniofacial shape in the unaffected relatives of individuals with nonsyndromic orofacial clefts: A possible marker for genetic susceptibility

(2008) Seth M. Weinberg et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

GENETIC DIVERSITY REVEALED IN HUMAN FACES

(2008) Hanne C. Lie et al.   EVOLUTION

Monozygotic female twins discordant for Silver–Russell syndrome and hypomethylation of the H19-DMR

(2008) Kazuki Yamazawa et al.   JOURNAL OF HUMAN GENETICS

Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome (SRS): results from a large cohort of patients with SRS and SRS-like phenotypes

(2008) D Bartholdi et al.   JOURNAL OF MEDICAL GENETICS

Face–brain asymmetry in autism spectrum disorders

(2008) P Hammond et al.   MOLECULAR PSYCHIATRY

Inhibition of neural crest migration underlies craniofacial dysmorphology and Hirschsprung's disease in Bardet-Biedl syndrome

(2008) J. L. Tobin et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA