Philipp Mayer‐Kuckuk

Hospital for Special Surgery — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

23h-index2.0kcitations69works0.02yr avg
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Research Topics

Virus-based gene therapy research(22), bioluminescence and chemiluminescence research(16), Cancer Research and Treatments(16), Bone Metabolism and Diseases(8), Cell Adhesion Molecules Research(6)

Publications69 total

Data from Integrin α<sub>v</sub>β<sub>3</sub>-Targeted IRDye 800CW Near-Infrared Imaging of Glioblastoma
2023Open Access
Data from Integrin α<sub>v</sub>β<sub>3</sub>-Targeted IRDye 800CW Near-Infrared Imaging of Glioblastoma
2023Open Access
Supplementary Methods from Integrin α<sub>v</sub>β<sub>3</sub>-Targeted IRDye 800CW Near-Infrared Imaging of Glioblastoma
2023Open Access
Supplementary Methods from Integrin α<sub>v</sub>β<sub>3</sub>-Targeted IRDye 800CW Near-Infrared Imaging of Glioblastoma
2023Open Access
Supplementary Figure 2 from Imaging Transgene Activity <i>In vivo</i>
2023Open Access
Supplementary Figure Legends 1-4 from Imaging Transgene Activity <i>In vivo</i>
2023Open Access
Supplementary Figure Legends 1-4 from Imaging Transgene Activity <i>In vivo</i>
2023Open Access
Data from Imaging Transgene Activity <i>In vivo</i>
2023Open Access
Supplementary Figure 1 from Imaging Transgene Activity <i>In vivo</i>
2023Open Access
Supplementary Figure 3 from Imaging Transgene Activity <i>In vivo</i>
2023Open Access
Supplementary Figure 4 from Imaging Transgene Activity <i>In vivo</i>
2023Open Access
Supplementary Figure 2 from Imaging Transgene Activity <i>In vivo</i>
2023Open Access
Supplementary Figure 4 from Imaging Transgene Activity <i>In vivo</i>
2023Open Access
Data from Imaging Transgene Activity <i>In vivo</i>
2023Open Access
Supplementary Figure 1 from Imaging Transgene Activity <i>In vivo</i>
2023Open Access
Supplementary Figure 3 from Imaging Transgene Activity <i>In vivo</i>
2023Open Access
Publisher Correction: Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy
Nature Cardiovascular Research·2022· 4 citedOpen Access
Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy
Nature Cardiovascular Research·2022· 66 citedOpen Access
Characterising a homozygous two‐exon deletion in <i>UQCRH</i> : comparing human and mouse phenotypes
EMBO Molecular Medicine·2021· 14 citedOpen Access
Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density
PLoS Genetics·2020· 30 citedOpen Access
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Frequent Co-authors

Adele L. Boskey(12), Ronald G. Blasberg(10), Debabrata Banerjee(9), Joseph R. Bertino(9), Marie K. Reumann(8), Jan Rozman(8), Juan Antonio Aguilar‐Pimentel(8), Lore Becker(8), Mikhail Doubrovin(7), Birgit Rathkolb(7), Lillian Garrett(7), Sabine M. Hölter(7), Oana V. Amarie(7), Julia Calzada‐Wack(7), Rüdiger von Eisenhart‐Rothe(6), Nadine Spielmann(6), Helmut Fuchs(6), Valérie Gailus‐Durner(6), Martin Hrabě de Angelis(6), Jeremy Mason(5)