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Author/Creator Lee, Jennifer A.

1. 'In-Format' screening of a novel bispecific antibody format reveals significant potency improvements relative to unformatted molecules. Issue 1 (2nd January 2017)

Authors:
Scott, Martin J.; Lee, Jennifer A.; Wake, Matthew S.; Batt, Kelly V.; Wattam, Trevor A.; Hiles, Ian D.; Batuwangala, Thil D.; Ashman, Claire I.; Steward, Michael
Journal:
MAbs
Issue:
Volume 9:Issue 1(2017)
Page Start:
85
Record Type:
Journal Article
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2. Assessing the gene–disease association of 19 genes with the RASopathies using the ClinGen gene curation framework. Issue 11 (11th October 2018)

Authors:
Grant, Andrew R.; Cushman, Brandon J.; Cavé, Hélène; Dillon, Mitchell W.; Gelb, Bruce D.; Gripp, Karen W.; Lee, Jennifer A.; Mason‐Suares, Heather; Rauen, Katherine A.; Tartaglia, Marco; Vincent, Lisa M.; Zenker, Martin
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:
1485
Record Type:
Journal Article
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4. CSNK2B: A broad spectrum of neurodevelopmental disability and epilepsy severity. (26th May 2021)

Authors:
Ernst, Michelle E.; Baugh, Evan H.; Thomas, Amanda; Bier, Louise; Lippa, Natalie; Stong, Nicholas; Mulhern, Maureen S.; Kushary, Sulagna; Akman, Cigdem I.; Heinzen, Erin L.; Yeh, Raymond; Bi, Weimin; Hanchard, Neil A.; Burrage, Lindsay C.; Leduc, Magalie S.; Chong, Josephine S. C.; Bend, Renee; L...
Journal:
Epilepsia
Issue:
Volume 62:issue 7(2021)
Page Start:
e103
Record Type:
Journal Article
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7. Functional correlation of genome‐wide DNA methylation profiles in genetic neurodevelopmental disorders. Issue 11 (21st August 2022)

Authors:
Levy, Michael A.; Relator, Raissa; McConkey, Haley; Pranckeviciene, Erinija; Kerkhof, Jennifer; Barat‐Houari, Mouna; Bargiacchi, Sara; Biamino, Elisa; Palomares Bralo, María; Cappuccio, Gerarda; Ciolfi, Andrea; Clarke, Angus; DuPont, Barbara R.; Elting, Mariet W.; Faivre, Laurence; Fee, Timothy; ...
Other Names:
Scott Stuart A. guestEditor.; Wang Kai guestEditor.; Spinner Nancy B. guestEditor.
Journal:
Human mutation
Issue:
Volume 43:Issue 11(2022)
Page Start:
1609
Record Type:
Journal Article
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8. Genome‐wide DNA methylation profiling confirms a case of low‐level mosaic Kabuki syndrome 1. Issue 7 (6th April 2022)

Authors:
Montano, Carolina; Britton, Jacquelyn F.; Harris, Jacqueline R.; Kerkhof, Jennifer; Barnes, Benjamin T.; Lee, Jennifer A.; Sadikovic, Bekim; Sobreira, Nara; Fahrner, Jill A.
Journal:
American journal of medical genetics
Issue:
Volume 188:Issue 7(2022)
Page Start:
2217
Record Type:
Journal Article
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