Search

Author/Creator Becker, Kerstin

1. Author Correction: Variants in exons 5 and 6 of ACTB cause syndromic thrombocytopenia. Issue 1 (December 2018)

Authors:
Latham, Sharissa; Ehmke, Nadja; Reinke, Patrick; Taft, Manuel; Eicke, Dorothee; Reindl, Theresia; Stenzel, Werner; Lyons, Michael; Friez, Michael; Lee, Jennifer; Hecker, Ramona; Frühwald, Michael; Becker, Kerstin; Neuhann, Teresa; Horn, Denise; Schrock, Evelin; Niehaus, Indra; Sarnow, Katharina; ...
Journal:
Nature communications
Issue:
Volume 9:Issue 1(2018)
Page Start:
1
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Deep ion sequencing of amplicon adapter ligated libraries: a novel tool in molecular diagnostics of formalin fixed and paraffin embedded tissues. Issue 9 (25th April 2013)

Authors:
Becker, Kerstin; Vollbrecht, Claudia; Koitzsch, Ulrike; Koenig, Katharina; Fassunke, Jana; Huss, Sebastian; Nuernberg, Peter; Heukamp, Lukas C; Buettner, Reinhard; Odenthal, Margarete; Altmueller, Janine; Merkelbach-Bruse, Sabine
Journal:
Journal of clinical pathology
Issue:
Volume 66:Issue 9(2013)
Page Start:
803
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Genetic Landscape of Congenital Myasthenic Syndromes From Turkey: Novel Mutations and Clinical Insights. (July 2017)

Authors:
Yiş, Uluç; Becker, Kerstin; Kurul, Semra Hız; Uyanik, Gökhan; Bayram, Erhan; Haliloğlu, Göknur; Polat, Ayşe İpek; Ayanoğlu, Müge; Okur, Derya; Tosun, Ayşe Fahriye; Serdaroğlu, Gül; Yilmaz, Sanem; Topaloğlu, Haluk; Anlar, Banu; Cirak, Sebahattin; Engel, Andrew G.
Journal:
Journal of child neurology
Issue:
Volume 32:Number 8(2017:Aug.)
Page Start:
759
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. Genotype–phenotype correlation in seven motor neuron disease families with novel ALS2 mutations. Issue 2 (5th November 2020)

Authors:
Sprute, Rosanne; Jergas, Hannah; Ölmez, Akgün; Alawbathani, Salem; Karasoy, Hatice; Dafsari, Hormos Salimi; Becker, Kerstin; Daimagüler, Hülya‐Sevcan; Nürnberg, Peter; Muntoni, Francesco; Topaloglu, Haluk; Uyanik, Gökhan; Cirak, Sebahattin
Journal:
American journal of medical genetics
Issue:
Volume 185:Issue 2(2021)
Page Start:
344
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

6. Implementation of Amplicon Parallel Sequencing Leads to Improvement of Diagnosis and Therapy of Lung Cancer Patients. Issue 7 (July 2015)

Authors:
König, Katharina; Peifer, Martin; Fassunke, Jana; Ihle, Michaela A.; Künstlinger, Helen; Heydt, Carina; Stamm, Katrin; Ueckeroth, Frank; Vollbrecht, Claudia; Bos, Marc; Gardizi, Masyar; Scheffler, Matthias; Nogova, Lucia; Leenders, Frauke; Albus, Kerstin; Meder, Lydia; Becker, Kerstin; Florin, Al...
Journal:
Journal of thoracic oncology
Issue:
Volume 10:Issue 7(2015)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

7. Implementation of Amplicon Parallel Sequencing Leads to Improvement of Diagnosis and Therapy of Lung Cancer Patients. Issue 7 (July 2015)

Authors:
König, Katharina; Peifer, Martin; Fassunke, Jana; Ihle, Michaela A.; Künstlinger, Helen; Heydt, Carina; Stamm, Katrin; Ueckeroth, Frank; Vollbrecht, Claudia; Bos, Marc; Gardizi, Masyar; Scheffler, Matthias; Nogova, Lucia; Leenders, Frauke; Albus, Kerstin; Meder, Lydia; Becker, Kerstin; Florin, Al...
Journal:
Journal of thoracic oncology
Issue:
Volume 10:Issue 7(2015)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

9. Missense mutations in CASK, coding for the calcium‐/calmodulin‐dependent serine protein kinase, interfere with neurexin binding and neurexin‐induced oligomerization. Issue 4 (4th November 2020)

Authors:
Pan, Yingzhou Edward; Tibbe, Debora; Harms, Frederike Leonie; Reißner, Carsten; Becker, Kerstin; Dingmann, Bri; Mirzaa, Ghayda; Kattentidt‐Mouravieva, Anja A.; Shoukier, Moneef; Aggarwal, Shagun; Missler, Markus; Kutsche, Kerstin; Kreienkamp, Hans‐Jürgen
Journal:
Journal of neurochemistry
Issue:
Volume 157:Issue 4(2021)
Page Start:
1331
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

10. Mutations in plasmalemma vesicle-associated protein cause severe syndromic protein-losing enteropathy. Issue 9 (16th April 2018)

Authors:
Broekaert, Ilse Julia; Becker, Kerstin; Gottschalk, Ingo; Körber, Friederike; Dötsch, Jörg; Thiele, Holger; Altmüller, Janine; Nürnberg, Peter; Hünseler, Christoph; Cirak, Sebahattin
Journal:
Journal of medical genetics
Issue:
Volume 55:Issue 9(2018)
Page Start:
637
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗