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Author/Creator Wheeler, Marsha M.

1. An FBN1 deep intronic variant is associated with pseudoexon formation and a variable Marfan phenotype in a five generation family. Issue 6 (7th March 2023)

Authors:
Guo, Dong‐chuan; Duan, Xueyan; Mimnagh, Kathleen; Cecchi, Alana C.; Marin, Isabella C.; Yu, Yang; Velasco, Walter V.; Lee, Kwanghyuk; Zhu, Xue; Murdock, David R.; Leal, Suzanne M.; Wheeler, Marsha M.; Smith, Josh; Bamshad, Michael J.; Milewicz, Dianna M.
Journal:
Clinical genetics
Issue:
Volume 103:Issue 6(2023)
Page Start:
704
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Coagulation factor VIII: Relationship to cardiovascular disease risk and whole genome sequence and epigenome‐wide analysis in African Americans. (20th February 2020)

Authors:
Raffield, Laura M.; Lu, Ake T.; Szeto, Mindy D.; Little, Amarise; Grinde, Kelsey E.; Shaw, Jessica; Auer, Paul L.; Cushman, Mary; Horvath, Steve; Irvin, Marguerite R.; Lange, Ethan M.; Lange, Leslie A.; Nickerson, Deborah A.; Thornton, Timothy A.; Wilson, James G.; Wheeler, Marsha M.; Zakai, Neil...
Journal:
Journal of thrombosis and haemostasis
Issue:
Volume 18:Number 6(2020)
Page Start:
1335
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

4. Diversity of variant alleles encoding Kidd, Duffy, and Kell antigens in individuals with sickle cell disease using whole genome sequencing data from the NHLBI TOPMed Program. Issue 2 (24th November 2020)

Authors:
Dinardo, Carla L.; Oliveira, Theo G. M.; Kelly, Shannon; Ashley‐Koch, Allison; Telen, Marilyn; Schmidt, Luciana C.; Castilho, Shirley; Melo, Karla; Dezan, Marcia R.; Wheeler, Marsha M.; Johnsen, Jill M.; Nickerson, Deborah A.; Jain, Deepti; Custer, Brian; Pereira, Alexandre C.; Sabino, Ester C.
Journal:
Transfusion
Issue:
Volume 61:Issue 2(2021)
Page Start:
603
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗