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Author/Creator Hoffmann, Per

1. A common microdeletion affecting a hippocampus‐ and amygdala‐specific isoform of tryptophan hydroxylase 2 is not associated with affective disorders. (23rd April 2014)

Authors:
Hammer, Christian; Degenhardt, Franziska; Priebe, Lutz; Stütz, Adrian M; Heilmann, Stefanie; Waszak, Sebastian M; Schlattl, Andreas; Mangold, Elisabeth; Hoffmann, Per; MooDS Consortium; Nöthen, Markus M; Rietschel, Marcella; Rappold, Gudrun; Korbel, Jan; Cichon, Sven; Niesler, Beate
Journal:
Bipolar disorders
Issue:
Volume 16:Number 7(2014)
Page Start:
764
Record Type:
Journal Article
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2. A genome-wide association study identifies nucleotide variants at SIGLEC5 and DEFA1A3 as risk loci for periodontitis. (16th January 2018)

Authors:
Munz, Matthias; Willenborg, Christina; Richter, Gesa M; Jockel-Schneider, Yvonne; Graetz, Christian; Staufenbiel, Ingmar; Wellmann, Jürgen; Berger, Klaus; Krone, Bastian; Hoffmann, Per; van der Velde, Nathalie; Uitterlinden, André G; de Groot, Lisette C P G M; Sawalha, Amr H; Direskeneli, Haner; ...
Journal:
Human molecular genetics
Issue:
Volume 27:Number 5(2018:Mar. 01)
Page Start:
941
Record Type:
Journal Article
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4. Association between neuropeptide Y receptor Y2 promoter variant rs6857715 and major depressive disorder. (February 2017)

Authors:
Treutlein, Jens; Strohmaier, Jana; Frank, Josef; Witt, Stephanie H.; Rietschel, Liz; Forstner, Andreas J.; Lang, Maren; Degenhardt, Franziska; Dukal, Helene; Herms, Stefan; Streit, Fabian; Hoffmann, Per; Cichon, Sven; Nöthen, Markus M.; Rietschel, Marcella
Journal:
Psychiatric genetics
Issue:
Volume 27:Number 1(2017:Feb.)
Page Start:
Record Type:
Journal Article
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6. Common obesity risk alleles in childhood attention‐deficit/hyperactivity disorder1. Issue 4 (26th March 2013)

Authors:
Albayrak, Özgür; Pütter, Carolin; Volckmar, Anna‐Lena; Cichon, Sven; Hoffmann, Per; Nöthen, Markus M.; Jöckel, Karl‐Heinz; Schreiber, Stefan; Wichmann, H‐Erich; Faraone, Stephen V.; Neale, Benjamin M.; Herpertz‐Dahlmann, Beate; Lehmkuhl, Gerd; Sinzig, Judith; Renner, Tobias J.; Romanos, Marcel; W...
Journal:
American journal of medical genetics
Issue:
Volume 162:Issue 4(2013)
Page Start:
295
Record Type:
Journal Article
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7. Complete homozygous deletion of CTSC in an Iranian family with Papillon–Lefèvre syndrome. (4th April 2013)

Authors:
Schackert, Hans K.; Agha‐Hosseini, Farzaneh; Görgens, Heike; Jatzwauk, Maria; von Kannen, Stephanie; Noack, Barbara; Eckelt, Uwe; Hoffmann, Per; Shabestari, Samira B.; Mehdipour, Parvin
Journal:
International journal of dermatology
Issue:
Volume 53:Number 7(2014:Jul.)
Page Start:
885
Record Type:
Journal Article
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8. Compound heterozygous SZT2 mutations in two siblings with early-onset epilepsy, intellectual disability and macrocephaly. (March 2019)

Authors:
Domingues, Francisco S.; König, Eva; Schwienbacher, Christine; Volpato, Claudia B.; Picard, Anne; Cantaloni, Chiara; Mascalzoni, Deborah; Lackner, Peter; Heimbach, André; Hoffmann, Per; Stanzial, Franco; Hicks, Andrew A.; Parmeggiani, Lucio; Benedicenti, Francesco; Pellegrin, Serena; Casara, Gian...
Journal:
Seizure
Issue:
Volume 66(2019)
Page Start:
81
Record Type:
Journal Article
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9. Copy number variation analysis and targeted NGS in 77 families with suspected Lynch syndrome reveals novel potential causative genes. Issue 11 (3rd October 2018)

Authors:
Kayser, Katrin; Degenhardt, Franziska; Holzapfel, Stefanie; Horpaopan, Sukanya; Peters, Sophia; Spier, Isabel; Morak, Monika; Vangala, Deepak; Rahner, Nils; von Knebel‐Doeberitz, Magnus; Schackert, Hans K.; Engel, Christoph; Büttner, Reinhard; Wijnen, Juul; Doerks, Tobias; Bork, Peer; Moebus, Sus...
Journal:
International journal of cancer
Issue:
Volume 143:Issue 11(2018)
Page Start:
2800
Record Type:
Journal Article
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