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Author/Creator Ritchie, Marylyn

2. A Genome-First Approach to Rare Variants in Dominant Postlingual Hearing Loss Genes in a Large Adult Population. (April 2022)

Authors:
Ahmadmehrabi, Shadi; Li, Binglan; Hui, Daniel; Park, Joseph; Ritchie, Marylyn; Rader, Daniel J.; Ruckenstein, Michael J.; Epstein, Douglas J.; Brant, Jason
Journal:
Otolaryngology--head and neck surgery
Issue:
Volume 166:Number 4(2022)
Page Start:
746
Record Type:
Journal Article
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3. A Genome‐First Approach to Rare Variants in Dominant Postlingual Hearing Loss Genes in a Large Adult Population. (20th July 2021)

Authors:
Ahmadmehrabi, Shadi; Li, Binglan; Hui, Daniel; Park, Joseph; Ritchie, Marylyn; Rader, Daniel J.; Ruckenstein, Michael J.; Epstein, Douglas J.; Brant, Jason
Journal:
Otolaryngology--head and neck surgery
Issue:
Volume 166:Number 4(2022)
Page Start:
746
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

6. Author Correction: Rare variants in drug target genes contributing to complex diseases, phenome-wide. Issue 1 (December 2018)

Authors:
Verma, Shefali; Josyula, Navya; Verma, Anurag; Zhang, Xinyuan; Veturi, Yogasudha; Dewey, Frederick; Hartzel, Dustin; Lavage, Daniel; Leader, Joe; Ritchie, Marylyn; Pendergrass, Sarah
Journal:
Scientific reports
Issue:
Volume 8:Issue 1(2018)
Page Start:
1
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

7. Concept and design of a genome-wide association genotyping array tailored for transplantation-specific studies. Issue 1 (December 2015)

Authors:
Li, Yun; van Setten, Jessica; Verma, Shefali; Lu, Yontao; Holmes, Michael; Gao, Hui; Lek, Monkol; Nair, Nikhil; Chandrupatla, Hareesh; Chang, Baoli; Karczewski, Konrad; Wong, Chanel; Mohebnasab, Maede; Mukhtar, Eyas; Phillips, Randy; Tragante, Vinicius; Hou, Cuiping; Steel, Laura; Lee, Takesha; G...
Journal:
Genome medicine
Issue:
Volume 7:Issue 1(2015)
Page Start:
1
Record Type:
Journal Article
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8. EMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants. Issue 1 (August 2016)

Authors:
Verma, Anurag; Verma, Shefali; Pendergrass, Sarah; Crawford, Dana; Crosslin, David; Kuivaniemi, Helena; Bush, William; Bradford, Yuki; Kullo, Iftikhar; Bielinski, Suzette; Li, Rongling; Denny, Joshua; Peissig, Peggy; Hebbring, Scott; De Andrade, Mariza; Ritchie, Marylyn; Tromp, Gerard
Journal:
BMC medical genomics
Issue:
Volume 9:Issue 1(2016)
Page Start:
19
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

9. EMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants. Issue 1 (August 2016)

Authors:
Verma, Anurag; Verma, Shefali; Pendergrass, Sarah; Crawford, Dana; Crosslin, David; Kuivaniemi, Helena; Bush, William; Bradford, Yuki; Kullo, Iftikhar; Bielinski, Suzette; Li, Rongling; Denny, Joshua; Peissig, Peggy; Hebbring, Scott; De Andrade, Mariza; Ritchie, Marylyn; Tromp, Gerard
Journal:
BMC medical genomics
Issue:
Volume 9:Issue 1(2016)
Page Start:
19
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

10. Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program. Issue 17 (27th October 2020)

Authors:
Klarin, Derek; Verma, Shefali Setia; Judy, Renae; Dikilitas, Ozan; Wolford, Brooke N.; Paranjpe, Ishan; Levin, Michael G.; Pan, Cuiping; Tcheandjieu, Catherine; Spin, Joshua M.; Lynch, Julie; Assimes, Themistocles L.; Åldstedt Nyrønning, Linn; Mattsson, Erney; Edwards, Todd L.; Denny, Josh; Larso...
Journal:
Circulation
Issue:
Volume 142:Issue 17(2020)
Page Start:
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗