Valerie K. Jordan

发表

RERE deficiency contributes to the development of orofacial clefts in humans and mice.

J. Carmichael, D. Scott, T. Scott, 2021, Human molecular genetics.

Genotype–phenotype correlations in individuals with pathogenic RERE variants

Donna M. Martin, J. Rosenfeld, N. Boddaert, 2018, Human mutation.

RERE deficiency leads to decreased expression of GATA4 and the development of ventricular septal defects

R. Schwartz, Wei Yu, D. Scott, 2018, Disease Models & Mechanisms.

De Novo Mutations of RERE Cause a Genetic Syndrome with Features that Overlap Those Associated with Proximal 1p36 Deletions.

J. Rosenfeld, B. D. de Vries, E. Zackai, 2016, American journal of human genetics.

Ryanodine Receptor–Mediated Calcium Leak Drives Progressive Development of an Atrial Fibrillation Substrate in a Transgenic Mouse Model

S. Nattel, X. Wehrens, D. Dobrev, 2014, Circulation.

Atrial Fibrillation Substrate in a Transgenic Mouse Model Mediated Calcium Leak Drives Progressive Development of an − Ryanodine Receptor

S. Nattel, D. Dobrev, F. Müller, 2014 .

FBN1 contributing to familial congenital diaphragmatic hernia

Alexander Hanbo Li, J. Lupski, R. Gibbs, 2015, American journal of medical genetics. Part A.

1p36 deletion syndrome: an update

D. Scott, H. P. Zaveri, Valerie K. Jordan, 2015, The application of clinical genetics.

The role of FREM2 and FRAS1 in the development of congenital diaphragmatic hernia

Alexander Hanbo Li, J. Lupski, R. Gibbs, 2018, Human molecular genetics.

Congenital heart defects and left ventricular non-compaction in males with loss-of-function variants in NONO

Mahshid S. Azamian, J. Rosenfeld, A. Breman, 2016, Journal of Medical Genetics.

SOX7 deficiency causes ventricular septal defects through its effects on endocardial-to-mesenchymal transition and the expression of Wnt4 and Bmp2

R. Lanz, Yumei Li, Rui Chen, 2020, bioRxiv.

The Application of Clinical Genetics Dovepress 1p36 Deletion Syndrome: an Update

D. Scott, H. P. Zaveri, Valerie K. Jordan, 2022 .

1 p 36 deletion syndrome : an update

D. Scott, H. P. Zaveri, Valerie K. Jordan, 2015 .

Duplication of HEY2 in cardiac and neurologic development

J. Rosenfeld, S. Lalani, D. Scott, 2015, American journal of medical genetics. Part A.

1 p 36 deletion syndrome : an update

D. Scott, H. P. Zaveri, Valerie K. Jordan, 2015 .