Search

Author/Creator Halvardson, Jonatan

2. Exome sequencing reveals NAA15 and PUF60 as candidate genes associated with intellectual disability. Issue 1 (9th October 2017)

Authors:
Zhao, Jin J.; Halvardson, Jonatan; Zander, Cecilia S.; Zaghlool, Ammar; Georgii‐Hemming, Patrik; Månsson, Else; Brandberg, Göran; Sävmarker, Helena E.; Frykholm, Carina; Kuchinskaya, Ekaterina; Thuresson, Ann‐Charlotte; Feuk, Lars
Journal:
American journal of medical genetics
Issue:
Volume 177:Issue 1(2018)
Page Start:
10
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Mosaic loss of chromosome Y in leukocytes matters. (January 2019)

Authors:
Forsberg, Lars; Halvardson, Jonatan; Rychlicka-Buniowska, Edyta; Danielsson, Marcus; Moghadam, Behrooz; Mattisson, Jonas; Rasi, Chiara; Davies, Hanna; Lind, Lars; Giedraitis, Vilmantas; Lannfelt, Lars; Kilander, Lena; Ingelsson, Martin; Dumanski, Jan
Journal:
Nature genetics
Issue:
Volume 51:Number 1(2019)
Page Start:
4
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. Mutations in HECW2 are associated with intellectual disability and epilepsy. Issue 10 (22nd June 2016)

Authors:
Halvardson, Jonatan; Zhao, Jin J; Zaghlool, Ammar; Wentzel, Christian; Georgii-Hemming, Patrik; Månsson, Else; Ederth Sävmarker, Helena; Brandberg, Göran; Soussi Zander, Cecilia; Thuresson, Ann-Charlotte; Feuk, Lars
Journal:
Journal of medical genetics
Issue:
Volume 53:Issue 10(2016)
Page Start:
697
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

6. Spatial sexual dimorphism of X and Y homolog gene expression in the human central nervous system during early male development. Issue 1 (December 2016)

Authors:
Johansson, Martin; Lundin, Elin; Qian, Xiaoyan; Mirzazadeh, Mohammadreza; Halvardson, Jonatan; Darj, Elisabeth; Feuk, Lars; Nilsson, Mats; Jazin, Elena
Journal:
Biology of sex differences
Issue:
Volume 7:Issue 1(2016)
Page Start:
1
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

7. Whole genome sequencing of consanguineous families reveals novel pathogenic variants in intellectual disability. Issue 3 (7th December 2018)

Authors:
Thuresson, Ann‐Charlotte; Soussi Zander, Cecilia; Zhao, Jin J.; Halvardson, Jonatan; Maqbool, Khurram; Månsson, Else; Stenninger, Eric; Holmlund, Ulrika; Öhrner, Ylva; Feuk, Lars
Journal:
Clinical genetics
Issue:
Volume 95:Issue 3(2019)
Page Start:
436
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗