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1

Two rare deletions upstream of the NRXN1 gene (2p16.3) affecting the non-coding mRNA AK127244 segregate with diverse psychopathological phenotypes in a family

Duong, Linh T.T., Hoeffding, Louise K., Petersen, Kirsten B., Knudsen, Charlotte D., Thygesen, Johan H., Klitten, Laura L., Tommerup, Niels, Ingason, Andrés, Werge, Thomas

Journal:

European Journal of Medical Genetics

Year:

2015

Language:

english

File:

PDF, 579 KB

english, 2015

2

Comorbidity of migraine with ADHD in adults

Hansen, Thomas Folkmann, Hoeffding, Louise K., Kogelman, Lisette, Haspang, Thilde Marie, Ullum, Henrik, Sørensen, Erik, Erikstrup, Christian, Pedersen, Ole Birger, Nielsen, Kaspar René, Hjalgrim, Henr

Journal:

Year:

2018

Language:

english

File:

PDF, 974 KB

english, 2018

3

BREAKPOINT ANALYSIS OF NRXN1 DELETIONS IN SCHIZOPHRENIA

Louise K.E. Hoeffding, Andrés Ingason, Thomas Hansen, Thomas Werge, Dan Rujescu

Journal:

Schizophrenia Research

Year:

2010

Language:

english

File:

PDF, 73 KB

english, 2010

4

Sequence analysis of 17 NRXN1 deletions

Hoeffding, Louise Kristine Enggaard, Hansen, Thomas, Ingason, Andrés, Doung, Linh, Thygesen, Johan H., Møller, Rikke S., Tommerup, Niels, Kirov, George, Rujescu, Dan, Larsen, Lars A., Werge, Thomas

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2014

Language:

english

File:

PDF, 231 KB

english, 2014

5

Erratum: Sequence analysis of 17 NRXN1 deletions

Hoeffding, Louise K., Hansen, Thomas, Ingason, Andrés, Doung, Linh, Thygesen, Johan H., Møller, Rikke S., Tommerup, Niels, Kirov, George, Rujescu, Dan, Larsen, Lars A., Werge, Thomas

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2014

Language:

english

File:

PDF, 56 KB

english, 2014

6

Copy number variations in affective disorders and meta-analysis

Olsen, Line, Hansen, Thomas, Djurovic, Srdjan, Haastrup, Eva, Albrecthsen, Anders, Hoeffding, Louise K.E., Secher, Anna, Gustafsson, Omar, Jakobsen, Klaus D., Nielsen, Finn C., Ullum, Henrik, Morken,

Journal:

Psychiatric Genetics

Year:

2011

Language:

english

File:

PDF, 89 KB

english, 2011

7

Usefulness of the SNP microarray technology to identify rare mutations in the case of perinatal death

Hoeffding, Louise K., Kock, Kirsten F., Johnsen, Iben G., Hansen, Thomas, Werge, Thomas

Journal:

Case Reports in Perinatal Medicine

Year:

2015

Language:

english

File:

PDF, 759 KB

english, 2015

8

Identification of rare high-risk copy number variants affecting the dopamine transporter gene in mental disorders

Hoeffding, Louise K., Duong, Linh T.T., Ingason, Andrés, Rosengren, Anders, Sorbanski, Ester, Witt, Stephanie H., Djurovic, Srdjan, Andreassen, Ole A., Hansen, Thomas, Werge, Thomas, Rasmussen, Henrik

Journal:

Nordic Journal of Psychiatry

Year:

2015

Language:

english

File:

PDF, 620 KB

english, 2015

9

Schizophrenia Spectrum Disorders in a Danish 22q11.2 Deletion Syndrome Cohort Compared to the Total Danish Population—A Nationwide Register Study

Vangkilde, Anders, Olsen, Line, Hoeffding, Louise K., Pedersen, Carsten B., Mortensen, Preben B., Werge, Thomas, Trabjerg, Betina

Journal:

Schizophrenia Bulletin

Year:

2016

Language:

english

File:

PDF, 322 KB

english, 2016

10

Evaluation of shared genetic susceptibility loci between autoimmune diseases and schizophrenia based on genome-wide association studies

Hoeffding, Louise K., Rosengren, Anders, Thygesen, Johan H., Schmock, Henriette, Werge, Thomas, Hansen, Thomas

Journal:

Nordic Journal of Psychiatry

Year:

2016

Language:

english

File:

PDF, 978 KB

english, 2016

11

Risk of Psychiatric Disorders Among Individuals With the 22q11.2 Deletion or Duplication

Hoeffding, Louise K., Trabjerg, Betina B., Olsen, Line, Mazin, Wiktor, Sparsø, Thomas, Vangkilde, Anders, Mortensen, Preben B., Pedersen, Carsten B., Werge, Thomas

Journal:

JAMA Psychiatry

Year:

2017

Language:

english

File:

PDF, 336 KB

english, 2017

12

Erratum to: A manual-based vocational rehabilitation program for patients with an acquired brain injury: study protocol of a pragmatic randomized controlled trial (RCT)

Hoeffding, Louise K., Nielsen, Maria Haahr, Rasmussen, Morten A., Norup, Anne, Arango-Lasprilla, Juan Carlos, Kjær, Ulrikka K., Burgdorf, Kristoffer Sølvsten, Quas, Kirsten Jensen, Schow, Trine

Journal:

Year:

2017

Language:

english

File:

PDF, 211 KB

english, 2017

13

A manual-based vocational rehabilitation program for patients with an acquired brain injury: study protocol of a pragmatic randomized controlled trial (RCT)

Hoeffding, Louise K., Nielsen, Maria Haahr, Rasmussen, Morten A., Norup, Anne, Arango-Lasprilla, Juan Carlos, Kjær, Ulrikka K., Burgdorf, Kristoffer Sølvsten, Quas, Kirsten Jensen, Schow, Trine

Journal:

Year:

2017

Language:

english

File:

PDF, 765 KB

english, 2017

14

Prevalence of rearrangements in the 22q11.2 region and population-based risk of neuropsychiatric and developmental disorders in a Danish population: a case-cohort study

Olsen, Line, Sparsø, Thomas, Weinsheimer, Shantel M, Dos Santos, Marcelo Bertalan Quintanilha, Mazin, Wiktor, Rosengren, Anders, Sanchez, Xabier Calle, Hoeffding, Louise K, Schmock, Henriette, Baekvad

Journal:

The Lancet Psychiatry

Year:

2018

Language:

english

File:

PDF, 1.26 MB

english, 2018

15

Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorder

Hughes, Timothy, Sønderby, Ida E., Polushina, Tatiana, Hansson, Lars, Holmgren, Asbjørn, Athanasiu, Lavinia, Melbø-Jørgensen, Christian, Hassani, Sahar, Hoeffding, Louise K., Herms, Stefan, Bergen, Sa

Journal:

Translational Psychiatry

Year:

2018

Language:

english

File:

PDF, 2.65 MB

english, 2018

16

Lessons to be Learned From 22q2.11 Syndromes—Reply

Hoeffding, Louise K., Pedersen, Carsten B., Werge, Thomas

Journal:

JAMA Psychiatry

Year:

2017

Language:

english

File:

PDF, 65 KB

english, 2017

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