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Bromberg, Kirstin [Editor]; Hoff, Walburga [Editor]; Miethe, Ingrid [Editor]

Forschungstraditionen der sozialen Arbeit : Materialien, Zugänge, Methoden

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Opladen; Berlin; Toronto: Verlag Barbara Budrich, 2012

Published in: Rekonstruktive Forschung in der sozialen Arbeit ; 1000
Hoff, Kirstin [Author] ; Schulenburg, Hinrich [Degree supervisor]; Kramer, Hans-Heiner [Other]

Molekulare Mechanismen des hypoplastischen Linksherzsyndroms

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https://d-nb.info/1214241565/34

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Kiel: Universitätsbibliothek Kiel, 2016
Bromberg, Kirstin [Editor]; Hoff, Walburga [Editor]; Miethe, Ingrid [Editor]

Forschungstraditionen der Sozialen Arbeit

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https://elibrary.utb.de/doi/book/10.3224/9783847403890

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Opladen; Berlin; Toronto: Verlag Barbara Budrich, 2012

Published in: Rekonstruktive Forschung in der sozialen Arbeit ; Band 10
Hoff, Kirstin [Author]; Hitz, Marc-Phillip [Author]; Kramer, Hans-Heiner [Author] ; Klinik für Angeborene Herzfehler und Kinderkardiologie Kiel

Projekttitel: Molecular mechanisms of hypoplastic left heart syndrome : Abschlussbericht : Standortprojekt: NCCR 3.3, HF, Partner Site Hamburg/Kiel/Lübeck : Laufzeit des Projektes: 2015 bis einschließlich 2018

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Kiel: Universitätsklinikum Schleswig-Holstein, [29.03.19]
Audain, Enrique [Author]; Wilsdon, Anna [Author]; Breckpot, Jeroen [Author]; Izarzugaza, Jose M. G. [Author]; Fitzgerald, Tomas W. [Author]; Kahlert, Anne-Karin [Author]; Sifrim, Alejandro [Author]; Wünnemann, Florian [Author]; Perez-Riverol, Yasset [Author]; Abdul-Khaliq, Hashim [Author]; Bak, Mads [Author]; Bassett, Anne S. [Author]; Benson, Woodrow D. [Author]; Berger, Felix [Author]; Daehnert, Ingo [Author]; Devriendt, Koenraad [Author]; Dittrich, Sven [Author]; Daubeney, Piers E. F. [Author]; Garg, Vidu [Author]; Hackmann, Karl [Author]; Hoff, Kirstin [Author]; Hofmann, Philipp [Author]; Dombrowsky, Gregor [Author]; Pickardt, Thomas [Author]; [...]

Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease

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2021

Published in: Public Library of Science: PLoS Genetics ; 17(2021), 7, Artikel-ID 1009679, Seite 1-24
Kahlert, Anne-Karin; Hoff, Kirstin; Hitz, Marc-Phillip

Genetik der angeborenen Herzfehler

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Walter de Gruyter GmbH, 2017

Published in: Medizinische Genetik
Seth, Sebastian; Oberdörfer, Linda; Hyde, Rebecca; Hoff, Kirstin; Thies, Verena; Worbs, Tim; Schmitz, Susanne; Förster, Reinhold

CCR7 Essentially Contributes to the Homing of Plasmacytoid Dendritic Cells to Lymph Nodes under Steady-State As Well As Inflammatory Conditions

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The American Association of Immunologists, 2011

Published in: The Journal of Immunology
Hoff, Kirstin; Lemme, Marta; Kahlert, Anne-Karin; Runde, Kerstin; Audain, Enrique; Schuster, Dorit; Scheewe, Jens; Attmann, Tim; Pickardt, Thomas; Caliebe, Almuth; Siebert, Reiner; Kramer, Hans-Heiner; Milting, Hendrik; Hansen, Arne; Ammerpohl, Ole; Hitz, Marc-Phillip

DNA methylation profiling allows for characterization of atrial and ventricular cardiac tissues and hiPSC-CMs

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Springer Science and Business Media LLC, 2019

Published in: Clinical Epigenetics
Ehmke, Nadja; Caliebe, Almuth; Koenig, Rainer; Kant, Sarina G.; Stark, Zornitza; Cormier-Daire, Valérie; Wieczorek, Dagmar; Gillessen-Kaesbach, Gabriele; Hoff, Kirstin; Kawalia, Amit; Thiele, Holger; Altmüller, Janine; Fischer-Zirnsak, Björn; Knaus, Alexej; Zhu, Na; Heinrich, Verena; Huber, Celine; Harabula, Izabela; Spielmann, Malte; Horn, Denise; Kornak, Uwe; Hecht, Jochen; Krawitz, Peter M.; Nürnberg, Peter; [...]

Homozygous and Compound-Heterozygous Mutations in TGDS Cause Catel-Manzke Syndrome

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Elsevier BV, 2014

Published in: The American Journal of Human Genetics
Wünnemann, Florian; Ta-Shma, Asaf; Preuss, Christoph; Leclerc, Severine; van Vliet, Patrick Piet; Oneglia, Andrea; Thibeault, Maryse; Nordquist, Emily; Lincoln, Joy; Scharfenberg, Franka; Becker-Pauly, Christoph; Hofmann, Philipp; Hoff, Kirstin; Audain, Enrique; Kramer, Hans-Heiner; Makalowski, Wojciech; Nir, Amiram; Gerety, Sebastian S.; Hurles, Matthew; Comes, Johanna; Fournier, Anne; Osinska, Hanna; Robins, Jeffrey; Pucéat, Michel; [...]

Loss of ADAMTS19 causes progressive non-syndromic heart valve disease

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Springer Science and Business Media LLC, 2020

Published in: Nature Genetics
Al Turki, Saeed; Manickaraj, Ashok K.; Mercer, Catherine L.; Gerety, Sebastian S.; Hitz, Marc-Phillip; Lindsay, Sarah; D’Alessandro, Lisa C.A.; Swaminathan, G. Jawahar; Bentham, Jamie; Arndt, Anne-Karin; Louw, Jacoba; Breckpot, Jeroen; Gewillig, Marc; Thienpont, Bernard; Abdul-Khaliq, Hashim; Harnack, Christine; Hoff, Kirstin; Kramer, Hans-Heiner; Schubert, Stephan; Siebert, Reiner; Toka, Okan; Cosgrove, Catherine; Watkins, Hugh; Lucassen, Anneke M.; [...]

Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans

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Elsevier BV, 2016

Published in: The American Journal of Human Genetics
Al Turki, Saeed; Manickaraj, Ashok K.; Mercer, Catherine L.; Gerety, Sebastian S.; Hitz, Marc-Phillip; Lindsay, Sarah; D’Alessandro, Lisa C.A.; Swaminathan, G. Jawahar; Bentham, Jamie; Arndt, Anne-Karin; Louw, Jacoba; Breckpot, Jeroen; Gewillig, Marc; Thienpont, Bernard; Abdul-Khaliq, Hashim; Harnack, Christine; Hoff, Kirstin; Kramer, Hans-Heiner; Schubert, Stephan; Siebert, Reiner; Toka, Okan; Cosgrove, Catherine; Watkins, Hugh; Lucassen, Anneke M.; [...]

Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans

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Elsevier BV, 2014

Published in: The American Journal of Human Genetics
Al Turki, Saeed; Manickaraj, Ashok K.; Mercer, Catherine L.; Gerety, Sebastian S.; Hitz, Marc-Phillip; Lindsay, Sarah; D’Alessandro, Lisa C.A.; Swaminathan, G. Jawahar; Bentham, Jamie; Arndt, Anne-Karin; Low, Jacoba; Breckpot, Jeroen; Gewillig, Marc; Thienpont, Bernard; Abdul-Khaliq, Hashim; Harnack, Christine; Hoff, Kirstin; Kramer, Hans-Heiner; Schubert, Stephan; Siebert, Reiner; Toka, Okan; Cosgrove, Catherine; Watkins, Hugh; Lucassen, Anneke M.; [...]

Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans

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Elsevier BV, 2014

Published in: The American Journal of Human Genetics
Audain, Enrique; Wilsdon, Anna; Breckpot, Jeroen; Izarzugaza, Jose M. G.; Fitzgerald, Tomas W.; Kahlert, Anne-Karin; Sifrim, Alejandro; Wünnemann, Florian; Perez-Riverol, Yasset; Abdul-Khaliq, Hashim; Bak, Mads; Bassett, Anne S.; Benson, D. Woodrow; Berger, Felix; Daehnert, Ingo; Devriendt, Koenraad; Dittrich, Sven; Daubeney, Piers EF; Garg, Vidu; Hackmann, Karl; Hoff, Kirstin; Hofmann, Philipp; Dombrowsky, Gregor; Pickardt, Thomas; [...]

Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease

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Public Library of Science (PLoS), 2021

Published in: PLOS Genetics
Audain, Enrique; Wilsdon, Anna; Breckpot, Jeroen; Izarzugaza, Jose M. G.; Fitzgerald, Tomas W.; Kahlert, Anne-Karin; Sifrim, Alejandro; Wünnemann, Florian; Perez-Riverol, Yasset; Abdul-Khaliq, Hashim; Bak, Mads; Bassett, Anne S.; Benson, Woodrow D.; Berger, Felix; Daehnert, Ingo; Devriendt, Koenraad; Dittrich, Sven; Daubeney, Piers EF; Garg, Vidu; Hackmann, Karl; Hoff, Kirstin; Hofmann, Philipp; Dombrowsky, Gregor; Pickardt, Thomas; [...]

Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease

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Public Library of Science (PLoS), 2021

Published in: PLOS Genetics
Sifrim, Alejandro; Hitz, Marc-Phillip; Wilsdon, Anna; Breckpot, Jeroen; Turki, Saeed H Al; Thienpont, Bernard; McRae, Jeremy; Fitzgerald, Tomas W; Singh, Tarjinder; Swaminathan, Ganesh Jawahar; Prigmore, Elena; Rajan, Diana; Abdul-Khaliq, Hashim; Banka, Siddharth; Bauer, Ulrike M M; Bentham, Jamie; Berger, Felix; Bhattacharya, Shoumo; Bu'Lock, Frances; Canham, Natalie; Colgiu, Irina-Gabriela; Cosgrove, Catherine; Cox, Helen; Daehnert, Ingo; [...]

Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing

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Springer Science and Business Media LLC, 2016

Published in: Nature Genetics

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