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Author/Creator Wand, Hannah

1. ClinVar database of global familial hypercholesterolemia‐associated DNA variants. Issue 11 (11th October 2018)

Authors:
Iacocca, Michael A.; Chora, Joana R.; Carrié, Alain; Freiberger, Tomáš; Leigh, Sarah E.; Defesche, Joep C.; Kurtz, C. Lisa; DiStefano, Marina T.; Santos, Raul D.; Humphries, Steve E.; Mata, Pedro; Jannes, Cinthia E.; Hooper, Amanda J.; Wilemon, Katherine A.; Benlian, Pascale; O'Connor, Robert; Ga...
Other Names:
Rehm Heidi L. guestEditor.; Berg Jonathan S. guestEditor.; Plon Sharon E. guestEditor.
Journal:
Human mutation
Issue:
Volume 39:Issue 11(2018)
Page Start:
1631
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. The clinical imperative for inclusivity: Race, ethnicity, and ancestry (REA) in genomics. Issue 11 (11th October 2018)

Authors:
Popejoy, Alice B.; Ritter, Deborah I.; Crooks, Kristy; Currey, Erin; Fullerton, Stephanie M.; Hindorff, Lucia A.; Koenig, Barbara; Ramos, Erin M.; Sorokin, Elena P.; Wand, Hannah; Wright, Mathew W.; Zou, James; Gignoux, Christopher R.; Bonham, Vence L.; Plon, Sharon E.; Bustamante, Carlos D.
Other Names:
Rehm Heidi L. guestEditor.; Berg Jonathan S. guestEditor.; Plon Sharon E. guestEditor.
Journal:
Human mutation
Issue:
Volume 39:Issue 11(2018)
Page Start:
1713
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗