 Connection
Co-Authors
This is a "connection" page, showing publications co-authored by Mohammed Orloff and Wendy Nembhard.
|
|
| |
Connection Strength |
|
 |
|
 |
| |
0.342 |
|
|
|
-
Mukherjee N, Bolin EH, Qasim A, Orloff MS, Lupo PJ, Nembhard WN. DNA methylation of the Lamin A/C gene is associated with congenital heart disease. Birth Defects Res. 2024 Jul; 116(7):e2381.
Score: 0.234
-
Carter TC, Kay DM, Pangilinan F, Almli LM, Jenkins MM, Blue EE, Sok P, White JJ, Cunniff CM, Agopian AJ, Bamshad MJ, Botto LD, Brody LC, Gucsavas-Calikoglu M, Chong JX, Gomez-Acevedo H, Lupo PJ, Moore CA, Nembhard WN, Olney RS, Olshan AF, Orloff MS, Reefhuis J, Romitti PA, Shaw GM, Werler MM, Yazdy MM, Browne ML, Howley MM. Exome Sequencing to Identify Novel Susceptibility Genes for Nonsyndromic Split-Hand/Ft Malformation: A Report From the National Birth Defects Prevention Study. Birth Defects Res. 2025 May; 117(5):e2472.
Score: 0.062
-
Patel J, Bircan E, Tang X, Orloff M, Hobbs CA, Browne ML, Botto LD, Finnell RH, Jenkins MM, Olshan A, Romitti PA, Shaw GM, Werler MM, Li J, Nembhard WN. Paternal genetic variants and risk of obstructive heart defects: A parent-of-origin approach. PLoS Genet. 2021 03; 17(3):e1009413.
Score: 0.046
|
Connection Strength
The connection strength for concepts is the sum of the scores for each matching publication.
Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.
|