Szot, Justin O.; Cuny, Hartmut; Martin, Ella M. M. A.; Sheng, Delicia Z.; Iyer, Kavitha; Portelli, Stephanie; Nguyen, Vivien; Gereis, Jessica M.; Alankarage, Dimuthu; Chitayat, David; Chong, Karen; Wentzensen, Ingrid M.; Vincent-Delorme, Catherine; Lermine, Alban; Burkitt-Wright, Emma; Ji, Weizhen; Jeffries, Lauren; Pais, Lynn S.; Tan, Tiong Y.; Pitt, James; Wise, Cheryl A.; Wright, Helen; Andrews, Israel D.; Pruniski, Brianna; Grebe, Theresa A.; Corsten-Janssen, Nicole; Bouman, Katelijne; Poulton, Cathryn; Prakash, Supraja; Keren, Boris; Brown, Natasha J.; Hunter, Matthew F.; Heath, Oliver; Lakhani, Saquib A.; McDermott, John H.; Ascher, David B.; Chapman, Gavin; Bozon, Kayleigh; Dunwoodie, Sally L.

Nicotinamide Adenine Dinucleotide Deficiency and Its Impact on Mammalian Development

ANTIOXIDANTS & REDOX SIGNALING

IF6.1

2023-12-015

PRE

Myeloid-CITED2 Deficiency Exacerbates Diet-Induced Obesity and Pro-Inflammatory Macrophage Response

CELLS

IF5.2

2023-08-243

OAAI

Quantitative trait and transcriptome analysis of genetic complexity underpinning cardiac interatrial septation in mice using an advanced intercross line

ELIFE

IF0

2023-06-053

Edd, the murine hyperplastic disc gene, is essential for yolk sac vascularization and chorioallantoic fusion

MOLECULAR AND CELLULAR BIOLOGY

IF2.7

2023-03-2776

OAAI

Edd, the murine ortholog of the hyperplastic discs (hyd) gene, is essential for yolk sac vascularization and chorioallantoic fusion (vol 24, pg 7225, 2004)

MOLECULAR AND CELLULAR BIOLOGY

IF2.7

2023-03-270

OAAI

Cited1 is required in trophoblasts for placental development and for embryo growth and survival

MOLECULAR AND CELLULAR BIOLOGY

IF2.7

2023-03-2783

OAAI

Australian Genomics: Outcomes of a 5-year national program to accelerate the integration of genomics in healthcare

澳大利亚基因组学: 一项为期5年的国家计划的成果，以加速基因组学在医疗保健中的整合

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2023-03-0130

OAAI

Stark, Zornitza; Boughtwood, Tiffany; Haas, Matilda; Braithwaite, Jeffrey; Gaff, Clara L.; Goranitis, Ilias; Spurdle, Amanda B.; Hansen, David P.; Hofmann, Oliver; Laing, Nigel; Metcalfe, Sylvia; Newson, Ainsley J.; Scott, Hamish S.; Thorne, Natalie; Ward, Robyn L.; Dinger, Marcel E.; Best, Stephanie; Long, Janet C.; Grimmond, Sean M.; Pearson, John; Waddell, Nicola; Barnett, Christopher P.; Cook, Matthew; Field, Michael; Fielding, David; Fox, Stephen B.; Gecz, Jozef; Jaffe, Adam; Leventer, Richard J.; Lockhart, Paul J.; Lunke, Sebastian; Mallett, Andrew J.; McGaughran, Julie; Mileshkin, Linda; Nones, Katia; Roscioli, Tony; Scheffer, Ingrid E.; Semsarian, Christopher; Simons, Cas; Thomas, David M.; Thorburn, David R.; Tothill, Richard; White, Deborah; Dunwoodie, Sally; Simpson, Peter T.; Phillips, Peta; Brion, Marie-Jo; Finlay, Keri; Quinn, Michael CJ.; Mattiske, Tessa; Tudini, Emma; Boggs, Kirsten; Murray, Sean; Wells, Kathy; Cannings, John; Sinclair, Andrew H.; Christodoulou, John; North, Kathryn N.

Insights into the genetic architecture underlying complex, critical congenital heart disease.

深入了解复杂的关键先天性心脏病的遗传结构。

AMERICAN HEART JOURNAL

IF3.5

2022-12-013

PRE

Maternal heterozygosity of Slc6a19 causes metabolic perturbation and congenital NAD deficiency disorder in mice

DISEASE MODELS & MECHANISMS

IF3.3

2022-11-1421

OAAI

Exploring the Genetic Architecture of Spontaneous Coronary Artery Dissection Using Whole-Genome Sequencing