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Author/Creator Klee, Eric W.

2. A novel de novo frameshift deletion in EHMT1 in a patient with Kleefstra Syndrome results in decreased H3K9 dimethylation. Issue 2 (26th January 2017)

Authors:
Blackburn, Patrick R.; Williams, Monique; Cousin, Margot A.; Boczek, Nicole J.; Beek, Geoffrey J.; Lomberk, Gwen A.; Urrutia, Raul A.; Babovic‐Vuksanovic, Dusica; Klee, Eric W.
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 5:Issue 2(2017)
Page Start:
141
Record Type:
Journal Article
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3. Aetiology and outcomes of secondary myelofibrosis occurring in the context of inherited platelet disorders: A single institutional study of four patients. (22nd June 2020)

Authors:
Saliba, Antoine N.; Ferrer, Alejandro; Gangat, Naseema; Pruthi, Rajiv K.; Tefferi, Ayalew; Higgins, Alexandra; Bezerra, Evandro D.; Buglioni, Alessia; Salama, Mohamed E.; Klee, Eric W.; Pinto e Vairo, Filippo; Mangaonkar, Abhishek; Majerus, Julie; Chen, Dong; Patnaik, Mrinal M.
Journal:
British journal of haematology
Issue:
Volume 190:Number 5(2020)
Page Start:
e316
Record Type:
Journal Article
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4. Antiangiogenic Effects and Therapeutic Targets of Azadirachta indica Leaf Extract in Endothelial Cells. (22nd February 2012)

Authors:
Mahapatra, Saswati; Young, Charles Y. F.; Kohli, Manish; Karnes, R. Jeffrey; Klee, Eric W.; Holmes, Michael W.; Tindall, Donald J.; Donkena, Krishna Vanaja
Other Names:
Olajide Olumayokun A. Academic Editor.
Journal:
Evidence-based complementary and alternative medicine
Issue:
Volume 2012(2012)
Page Start:
Record Type:
Journal Article
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6. Case-Based Learning in Translational Biomedical Research Education: Providing Realistic and Adaptive Skills for Early-Career Scientists. (February 2019)

Authors:
Greenberg-Worisek, Alexandra J.; Campbell, Katherine A.; Klee, Eric W.; Staff, Nathan P.; Schimmenti, Lisa A.; Weavers, Karen M.; Ekker, Stephen C.; Windebank, Anthony J.
Journal:
Academic medicine
Issue:
Volume 94:Number 2(2019)
Page Start:
Record Type:
Journal Article
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7. Clinical characteristics and platelet phenotype in a family with RUNX1 mutated thrombocytopenia. Issue 8 (3rd August 2017)

Authors:
Perez Botero, Juliana; Chen, Dong; Cousin, Margot A.; Majerus, Julie A.; Coon, Lea M.; Kruisselbrink, Teresa M.; Klee, Eric W.; Lazaridis, Konstantinos N.; Pruthi, Rajiv K.; Patnaik, Mrinal M.
Journal:
Leukemia & lymphoma
Issue:
Volume 58:Issue 8(2017)
Page Start:
1963
Record Type:
Journal Article
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8. Clinical spectrum of STX1B-related epileptic disorders. (12th March 2019)

Authors:
Wolking, Stefan; May, Patrick; Mei, Davide; Møller, Rikke S.; Balestrini, Simona; Helbig, Katherine L.; Altuzarra, Cecilia Desmettre; Chatron, Nicolas; Kaiwar, Charu; Stöhr, Katharina; Widdess-Walsh, Peter; Mendelsohn, Bryce A.; Numis, Adam; Cilio, Maria R.; Van Paesschen, Wim; Svendsen, Lene L.;...
Journal:
Neurology
Issue:
Volume 92:Number 11(2019)
Page Start:
Record Type:
Journal Article
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9. Clinicoradiographic and genetic features of cerebral small vessel disease indicate variability in mode of inheritance for monoallelic HTRA1 variants. Issue 10 (12th September 2021)

Authors:
Muthusamy, Karthik; Ferrer, Alejandro; Klee, Eric W.; Wierenga, Klaas J.; Gavrilova, Ralitza H.
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 9:Issue 10(2021)
Page Start:
n/a
Record Type:
Journal Article
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10. Congenital ichthyosis in Prader–Willi syndrome associated with maternal chromosome 15 uniparental disomy: Case report and review of autosomal recessive conditions unmasked by UPD. Issue 10 (20th August 2020)

Authors:
Muthusamy, Karthik; Macke, Erica L.; Klee, Eric W.; Tebben, Peter J.; Hand, Jennifer L.; Hasadsri, Linda; Marcou, Cherisse A.; Schimmenti, Lisa A.
Journal:
American journal of medical genetics
Issue:
Volume 182:Issue 10(2020)
Page Start:
2442
Record Type:
Journal Article
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