Göran Annerén

A novel quantitative targeted analysis of X-chromosome Inactivation (XCI) using Nanopore sequencing

Johansson, Josefin; Lidéus, Sarah; Höijer, Ida; Ameur, Adam et al.

Ingår i Scientific Reports, 2023

• DOI för A novel quantitative targeted analysis of X-chromosome Inactivation (XCI) using Nanopore sequencing
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DNA methylation changes in Down syndrome derived neural iPSCs uncover co-dysregulation of ZNF and HOX3 families of transcription factors

Laan, Loora; Klar, Joakim; Sobol, Maria; Hoeber, Jan et al.

Ingår i Clinical Epigenetics, 2020

• DOI för DNA methylation changes in Down syndrome derived neural iPSCs uncover co-dysregulation of ZNF and HOX3 families of transcription factors
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Generation of two human iPSC lines (UUIGPi013-A and UUIPGi014-A) from cases with Down syndrome and full trisomy for chromosome 21 (T21)

Schuster, Jens; Hoeber, Jan; Sobol, Maria; Fatima, Ambrin et al.

Ingår i Stem Cell Research, 2020

• DOI för Generation of two human iPSC lines (UUIGPi013-A and UUIPGi014-A) from cases with Down syndrome and full trisomy for chromosome 21 (T21)

Exome sequencing in Crisponi/cold-induced sweating syndrome-like individuals reveals unpredicted alternative diagnoses

Angius, Andrea; Uva, Paolo; Oppo, Manuela; Buers, Insa et al.

Ingår i Clinical Genetics, s. 607-614, 2019

• DOI för Exome sequencing in Crisponi/cold-induced sweating syndrome-like individuals reveals unpredicted alternative diagnoses

TAF1, associated with intellectual disability in humans, is essential for embryogenesis and regulates neurodevelopmental processes in zebrafish

Gudmundsson, Sanna; Wilbe, Maria; Gorniok, Beata Filipek; Molin, Anna-Maja et al.

Ingår i Scientific Reports, 2019

• DOI för TAF1, associated with intellectual disability in humans, is essential for embryogenesis and regulates neurodevelopmental processes in zebrafish
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A novel quantitative targeted analysis of X-chromosome Inactivation (XCI) using Nanopore sequencing

Johansson, Josefin; Lidéus, Sarah; Höijer, Ida; Ameur, Adam et al.

Ingår i Scientific Reports, 2023

• DOI för A novel quantitative targeted analysis of X-chromosome Inactivation (XCI) using Nanopore sequencing
• Ladda ner fulltext (pdf) av A novel quantitative targeted analysis of X-chromosome Inactivation (XCI) using Nanopore sequencing

DNA methylation changes in Down syndrome derived neural iPSCs uncover co-dysregulation of ZNF and HOX3 families of transcription factors

Laan, Loora; Klar, Joakim; Sobol, Maria; Hoeber, Jan et al.

Ingår i Clinical Epigenetics, 2020

• DOI för DNA methylation changes in Down syndrome derived neural iPSCs uncover co-dysregulation of ZNF and HOX3 families of transcription factors
• Ladda ner fulltext (pdf) av DNA methylation changes in Down syndrome derived neural iPSCs uncover co-dysregulation of ZNF and HOX3 families of transcription factors

Generation of two human iPSC lines (UUIGPi013-A and UUIPGi014-A) from cases with Down syndrome and full trisomy for chromosome 21 (T21)

Schuster, Jens; Hoeber, Jan; Sobol, Maria; Fatima, Ambrin et al.

Ingår i Stem Cell Research, 2020

• DOI för Generation of two human iPSC lines (UUIGPi013-A and UUIPGi014-A) from cases with Down syndrome and full trisomy for chromosome 21 (T21)

Exome sequencing in Crisponi/cold-induced sweating syndrome-like individuals reveals unpredicted alternative diagnoses

Angius, Andrea; Uva, Paolo; Oppo, Manuela; Buers, Insa et al.

Ingår i Clinical Genetics, s. 607-614, 2019

• DOI för Exome sequencing in Crisponi/cold-induced sweating syndrome-like individuals reveals unpredicted alternative diagnoses

TAF1, associated with intellectual disability in humans, is essential for embryogenesis and regulates neurodevelopmental processes in zebrafish

Gudmundsson, Sanna; Wilbe, Maria; Gorniok, Beata Filipek; Molin, Anna-Maja et al.

Ingår i Scientific Reports, 2019

• DOI för TAF1, associated with intellectual disability in humans, is essential for embryogenesis and regulates neurodevelopmental processes in zebrafish
• Ladda ner fulltext (pdf) av TAF1, associated with intellectual disability in humans, is essential for embryogenesis and regulates neurodevelopmental processes in zebrafish

A novel RAD21 p.(Gln592del) variant expands the clinical description of Cornelia de Lange syndrome type 4: Review of the literature

Gudmundsson, Sanna; Annerén, Göran; Marcos-Alcalde, Íñigo; Wilbe, Maria et al.

Ingår i European Journal of Medical Genetics, 2019

• DOI för A novel RAD21 p.(Gln592del) variant expands the clinical description of Cornelia de Lange syndrome type 4: Review of the literature

Autism needs to be considered in children with Down syndrome

Wester Oxelgren, Ulrika; Åberg, Marie; Myrelid, Åsa; Annerén, Göran et al.

Ingår i Acta Paediatrica, s. 2019-2026, 2019

• DOI för Autism needs to be considered in children with Down syndrome

Transcriptome and Proteome Profiling of Neural Induced Pluripotent Stem Cells from Individuals with Down Syndrome Disclose Dynamic Dysregulations of Key Pathways and Cellular Functions

Sobol, Maria; Klar, Joakim; Laan, Loora; Shahsavani, Mansoureh et al.

Ingår i Molecular Neurobiology, s. 7113-7127, 2019

• DOI för Transcriptome and Proteome Profiling of Neural Induced Pluripotent Stem Cells from Individuals with Down Syndrome Disclose Dynamic Dysregulations of Key Pathways and Cellular Functions
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An intervention targeting social, communication and daily activity skills in children and adolescents with Down syndrome and autism: a pilot study

Wester Oxelgren, Ulrika; Westerlund, Joakim; Myrelid, Åsa; Annerén, Göran et al.

Ingår i Neuropsychiatric Disease and Treatment, s. 2049-2056, 2019

• DOI för An intervention targeting social, communication and daily activity skills in children and adolescents with Down syndrome and autism: a pilot study
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Early activating somatic PIK3CA mutations promote ectopic muscle development and upper limb overgrowth

Frisk, Sofia; Taylan, Fulya; Blaszczyk, Izabela; Nennesmo, Inger et al.

Ingår i Clinical Genetics, s. 118-125, 2019

• DOI för Early activating somatic PIK3CA mutations promote ectopic muscle development and upper limb overgrowth
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More severe intellectual disability found in teenagers compared to younger children with Down syndrome.

Wester Oxelgren, Ulrika; Myrelid, Åsa; Annerén, Göran; Westerlund, Joakim et al.

Ingår i Acta Paediatrica, s. 961-966, 2019

• DOI för More severe intellectual disability found in teenagers compared to younger children with Down syndrome.

A novel approach using long-read sequencing and ddPCR to investigate gonadal mosaicism and estimate recurrence risk in two families with developmental disorders

Wilbe, Maria; Gudmundsson, Sanna; Johansson, Josefin; Ameur, Adam et al.

Ingår i Prenatal Diagnosis, s. 1146-1154, 2017

• DOI för A novel approach using long-read sequencing and ddPCR to investigate gonadal mosaicism and estimate recurrence risk in two families with developmental disorders
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Prevalence of autism and attention-deficit-hyperactivity disorder in Down syndrome: a population-based study

Wester Oxelgren, Ulrika; Myrelid, Åsa; Annerén, Göran; Ekstam, Bodil et al.

Ingår i Developmental Medicine & Child Neurology, s. 276-283, 2017

• DOI för Prevalence of autism and attention-deficit-hyperactivity disorder in Down syndrome: a population-based study

Why do pregnant women accept or decline prenatal diagnosis for Down syndrome?

Ternby, Ellen; Axelsson, Ove; Annerén, Göran; Lindgren, Peter et al.

Ingår i Journal of community genetics, s. 237-242, 2016

• DOI för Why do pregnant women accept or decline prenatal diagnosis for Down syndrome?

1p13.2 deletion displays clinical features overlapping Noonan syndrome, likely related to NRAS gene haploinsufficiency

Linhares, Natalia Duarte; Menezes Freire, Maira Cristina; do Carmo Lisboa Cardenas, Raony Guimaraes Correa; Pena, Heloisa Barbosa et al.

Ingår i Genetics and Molecular Biology, s. 349-357, 2016

• DOI för 1p13.2 deletion displays clinical features overlapping Noonan syndrome, likely related to NRAS gene haploinsufficiency
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X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes

Hu, H.; Haas, S. A.; Chelly, J.; Van Esch, H. et al.

Ingår i Molecular Psychiatry, s. 133-148, 2016

• DOI för X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes

Midwives and information on prenatal testing with focus on Down syndrome

Ternby, Ellen; Ingvoldstad, Charlotta; Annerén, Göran; Axelsson, Ove

Ingår i Prenatal Diagnosis, s. 1202-1207, 2015

• DOI för Midwives and information on prenatal testing with focus on Down syndrome

Information and knowledge about Down syndrome among women and partners after first trimester combined testing

Ternby, Ellen; Ingvoldstad, Charlotta; Annerén, Göran; Lindgren, Peter et al.

Ingår i Acta Obstetricia et Gynecologica Scandinavica, s. 329-32, 2015

• DOI för Information and knowledge about Down syndrome among women and partners after first trimester combined testing

Mutation in NRAS in familial Noonan syndrome: case report and review of the literature

Ekvall, Sara; Wilbe, Maria; Dahlgren, Jovanna; Legius, Eric et al.

Ingår i BMC Medical Genetics, 2015

• DOI för Mutation in NRAS in familial Noonan syndrome: case report and review of the literature

A Study of the Clinical and Radiological Features in a Cohort of 93 Patients with a COL2A1 Mutation Causing Spondyloepiphyseal Dysplasia Congenita or a Related Phenotype

Terhal, Paulien A.; Nievelstein, Rutger Jan A. J.; Verver, Eva J. J.; Topsakal, Vedat et al.

Ingår i American Journal of Medical Genetics. Part A, s. 461-475, 2015

• DOI för A Study of the Clinical and Radiological Features in a Cohort of 93 Patients with a COL2A1 Mutation Causing Spondyloepiphyseal Dysplasia Congenita or a Related Phenotype

MuSK: a new target for lethal fetal akinesia deformation sequence (FADS).

Wilbe, Maria; Ekvall, Sara; Eurenius, Karin; Ericson, Katharina et al.

Ingår i Journal of Medical Genetics, s. 195-202, 2015

• DOI för MuSK: a new target for lethal fetal akinesia deformation sequence (FADS).

Transcriptome Profiling Reveals Degree of Variability in Induced Pluripotent Stem Cell Lines: Impact for Human Disease Modeling

Schuster, Jens; Halvardson, Jonatan; Lorenzo, Laureanne Pilar; Ameur, Adam et al.

Ingår i Cellular Reprogramming, s. 327-337, 2015

• DOI för Transcriptome Profiling Reveals Degree of Variability in Induced Pluripotent Stem Cell Lines: Impact for Human Disease Modeling

A maternal de novo non-reciprocal translocation results in a 6q13-q16 deletion in one offspring and a 6q13-q16 duplication in another

Wentzel, Christian; Annerén, Göran; Thuresson, Ann-Charlotte

Ingår i European Journal of Medical Genetics, s. 259-263, 2014

• DOI för A maternal de novo non-reciprocal translocation results in a 6q13-q16 deletion in one offspring and a 6q13-q16 duplication in another

Novel association of neurofibromatosis type 1-causing mutations in families with neurofibromatosis-Noonan syndrome

Ekvall, Sara; Sjörs, Kerstin; Jonzon, Anders; Vihinen, Mauno et al.

Ingår i American Journal of Medical Genetics. Part A, s. 579-587, 2014

• DOI för Novel association of neurofibromatosis type 1-causing mutations in families with neurofibromatosis-Noonan syndrome

Mutation Screening and Array Comparative Genomic Hybridization Using a 180K Oligonucleotide Array in VACTERL Association

Winberg, Johanna; Gustavsson, Peter; Papadogiannakis, Nikos; Sahlin, Ellika et al.

Ingår i PLOS ONE, 2014

• DOI för Mutation Screening and Array Comparative Genomic Hybridization Using a 180K Oligonucleotide Array in VACTERL Association
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Altered Expression of Autoimmune Regulator in Infant Down Syndrome Thymus, a Possible Contributor to an Autoimmune Phenotype

Skogberg, Gabriel; Lundberg, Vanja; Lindgren, Susanne; Gudmundsdottir, Judith et al.

Ingår i Journal of Immunology, s. 2187-2195, 2014

• DOI för Altered Expression of Autoimmune Regulator in Infant Down Syndrome Thymus, a Possible Contributor to an Autoimmune Phenotype

A novel microdeletion syndrome at 9q21.13 characterised by mental retardation, speech delay, epilepsy and characteristic facial features

Boudry-Labis, Elise; Demeer, Benedicte; Le Caignec, Cedric; Isidor, Bertrand et al.

Ingår i European Journal of Medical Genetics, s. 163-170, 2013

• DOI för A novel microdeletion syndrome at 9q21.13 characterised by mental retardation, speech delay, epilepsy and characteristic facial features

Changes in mortality and causes of death in the Swedish Down syndrome population

Englund, Annika; Jonsson, Björn; Zander, Cecilia Soussi; Gustafsson, Jan et al.

Ingår i American Journal of Medical Genetics. Part A, s. 642-649, 2013

• DOI för Changes in mortality and causes of death in the Swedish Down syndrome population

Genotype-phenotype analysis of 18q12.1-q12.2 copy number variation in autism

Wang, Peter; Carrion, Prescilla; Qiao, Ying; Tyson, Christine et al.

Ingår i European Journal of Medical Genetics, s. 420-425, 2013

• DOI för Genotype-phenotype analysis of 18q12.1-q12.2 copy number variation in autism

A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial features

Molin, Anna-Maja; Andrieux, J.; Koolen, D. A.; Malan, V. et al.

Ingår i Journal of Medical Genetics, s. 104-109, 2012

• DOI för A novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial features

De novo microdeletions of chromosome 6q14.1-q14.3 and 6q12.1-q14.1 in two patients with intellectual disability: further delineation of the 6q14 microdeletion syndrome and review of the literature

Becker, Kerstin; Di Donato, Nataliya; Holder-Espinasse, Muriel; Andrieux, Joris et al.

Ingår i European Journal of Medical Genetics, s. 490-497, 2012

• DOI för De novo microdeletions of chromosome 6q14.1-q14.3 and 6q12.1-q14.1 in two patients with intellectual disability: further delineation of the 6q14 microdeletion syndrome and review of the literature

Unbalanced translocation 9;16 in two children with dysmorphic features, and severe developmental delay: Evidence of cross-over within derivative chromosome 9 in patient #1

Zambrano, Regina M.; Wohler, Elizabeth; Annerén, Göran; Thuresson, Ann-Charlotte et al.

Ingår i European Journal of Medical Genetics, s. 189-193, 2011

• DOI för Unbalanced translocation 9;16 in two children with dysmorphic features, and severe developmental delay: Evidence of cross-over within derivative chromosome 9 in patient #1

Co-Occurring SHOC2 and PTPN11 Mutations in a Patient With Severe/Complex Noonan Syndrome-Like Phenotype

Ekvall, Sara; Hagenäs, Lars; Allanson, Judith; Annerén, Göran et al.

Ingår i American Journal of Medical Genetics Part A, s. 1217-1224, 2011

• DOI för Co-Occurring SHOC2 and PTPN11 Mutations in a Patient With Severe/Complex Noonan Syndrome-Like Phenotype

Cardio-Facio-Cutaneous Syndrome: Does Genotype Predict Phenotype?

Allanson, Judith E.; Annerén, Göran; Aoki, Yoki; Armour, Christine M. et al.

Ingår i American Journal of Medical Genetics, Part C: Seminars in Medical Genetics, s. 129-135, 2011

• DOI för Cardio-Facio-Cutaneous Syndrome: Does Genotype Predict Phenotype?

Ultrasonographic findings in spontaneous miscarriage: relation to euploidy and aneuploidy

Ljunger, Elisabeth; Stavreus-Evers, Anneli; Cnattingius, Sven; Ekbom, Anders et al.

Ingår i Fertility and Sterility, s. 221-224, 2011

• DOI för Ultrasonographic findings in spontaneous miscarriage: relation to euploidy and aneuploidy

The 12q14 microdeletion syndrome: six new cases confirming the role of HMGA2 in growth

Lynch, Sally Ann; Foulds, Nicola; Thuresson, Ann-Charlotte; Collins, Amanda L. et al.

Ingår i European Journal of Human Genetics, s. 534-539, 2011

• DOI för The 12q14 microdeletion syndrome: six new cases confirming the role of HMGA2 in growth

Characterization of a 8q21.11 Microdeletion Syndrome Associated with Intellectual Disability and a Recognizable Phenotype

Palomares, Maria; Delicado, Alicia; Mansilla, Elena; Luisa de Torres, Maria et al.

Ingår i American Journal of Human Genetics, s. 295-301, 2011

• DOI för Characterization of a 8q21.11 Microdeletion Syndrome Associated with Intellectual Disability and a Recognizable Phenotype

Genomic and clinical characteristics of six patients with partially overlapping interstitial deletions at 10p12p11

Wentzel, Christian; Rajcan-Separovic, Evica; Ruivenkamp, Claudia A. L.; Chantot-Bastaraud, Sandra et al.

Ingår i European Journal of Human Genetics, s. 959-964, 2011

• DOI för Genomic and clinical characteristics of six patients with partially overlapping interstitial deletions at 10p12p11

Investigation of gene dosage imbalances in patients with Noonan syndrome using multiplex ligation-dependent probe amplification analysis

Nyström, Anna-Maja; Ekvall, Sara; Thuresson, Ann-Charlotte; Kamali-Moghaddam, Masood et al.

Ingår i European Journal of Medical Genetics, s. 117-121, 2010

• DOI för Investigation of gene dosage imbalances in patients with Noonan syndrome using multiplex ligation-dependent probe amplification analysis

The 12q14 microdeletion syndrome, 6 new cases confirming the role of HMGA2 in growth

Sharkey, Freddie H.; Foulds, N.; Thuresson, Ann-Charlotte; Collins, A. L. et al.

Ingår i Journal of Medical Genetics, 2010

International Trends of Down Syndrome 1993-2004: Births in Relation to Maternal Age and Terminations of Pregnancies

Cocchi, Guido; Gualdi, Silvia; Bower, Caroline; Halliday, Jane et al.

Ingår i Birth defects research. Clinical and molecular teratology, s. 474-479, 2010

• DOI för International Trends of Down Syndrome 1993-2004: Births in Relation to Maternal Age and Terminations of Pregnancies

How Valid Are the Rates of Down Syndrome Internationally?: Findings from the International Clearinghouse for Birth Defects Surveillance and Research

Leoncini, Emanuele; Botto, Lorenzo D.; Cocchi, Guido; Annerén, Göran et al.

Ingår i American Journal of Medical Genetics, Part A, s. 1670-1680, 2010

• DOI för How Valid Are the Rates of Down Syndrome Internationally?: Findings from the International Clearinghouse for Birth Defects Surveillance and Research

Late effects of early growth hormone treatment in Down syndrome

Myrelid, Åsa; Bergman, Sara; Elfvik Strömberg, Maria; Jonsson, Björn et al.

Ingår i Acta Paediatrica, s. 763-769, 2010

• DOI för Late effects of early growth hormone treatment in Down syndrome

Normal growth hormone secretion in overweight young adults with Down syndrome

Myrelid, Åsa; Frisk, Per; Stridsberg, Mats; Annerén, Göran et al.

Ingår i Growth Hormone & IGF Research, s. 174-178, 2010

• DOI för Normal growth hormone secretion in overweight young adults with Down syndrome

Interstitial Deletions at 6q14.1-q15 Associated with Obesity, Developmental Delay and a Distinct Clinical Phenotype

Wentzel, Christian; Lynch, S. A.; Stattin, E.-L.; Sharkey, F. H. et al.

Ingår i Molecular Syndromology, s. 75-81, 2010

• DOI för Interstitial Deletions at 6q14.1-q15 Associated with Obesity, Developmental Delay and a Distinct Clinical Phenotype

Bättre stöd åt nyblivna föräldrar till barn med livslångt funktionshinder: Förslag till nya riktlinjer

Hedov, Gerth; Annerén, Göran

Ingår i Läkartidningen, s. 1477-1479, 2010

A severe form of Noonan syndrome and autosomal dominant café-au-lait spots: evidence for different genetic origins

Nyström, Anna-Maja; Ekvall, Sara; Strömberg, Bo; Holmström, Gerd et al.

Ingår i Acta Paediatrica, s. 693-698, 2009

• DOI för A severe form of Noonan syndrome and autosomal dominant café-au-lait spots: evidence for different genetic origins

Increased neonatal thyrotropin in Down syndrome

Myrelid, Åsa; Jonsson, Björn; Guthenberg, Claes; Döbeln, von et al.

Ingår i Acta Paediatrica, s. 1010-1013, 2009

• DOI för Increased neonatal thyrotropin in Down syndrome

The Swedish Birth Defects Registry: ascertainment and incidence of spina bifida and cleft lip/palate

Amini, Hashem; Axelsson, Ove; Ollars, Birgitta; Annerén, Göran

Ingår i Acta Obstetricia et Gynecologica Scandinavica, s. 654-659, 2009

• DOI för The Swedish Birth Defects Registry: ascertainment and incidence of spina bifida and cleft lip/palate

Noonan syndrome and Neurofibromatosis type I in a family with a novel mutation in NF1

Nyström, Anna-Maja; Ekvall, Sara; Allanson, Judith; Edeby, Christina et al.

Ingår i Clinical Genetics, s. 524-534, 2009

• DOI för Noonan syndrome and Neurofibromatosis type I in a family with a novel mutation in NF1

Noonan and cardio-facio-cutanenous syndromes: two clinically and genetically overlapping disorders

Nyström, Anna-Maja; Ekvall, Sara; Berglund, Erna; Björkqvist, Maria et al.

Ingår i Journal of Medical Genetics, s. 500-506, 2008

• DOI för Noonan and cardio-facio-cutanenous syndromes: two clinically and genetically overlapping disorders

Clinical variability of the 22q11.2 duplication syndrome

Wentzel, Christian; Fernström, Maria; Öhrner, Ylva; Annerén, Göran et al.

Ingår i European Journal of Medical Genetics, s. 501-510, 2008

• DOI för Clinical variability of the 22q11.2 duplication syndrome
• Ladda ner fulltext (pdf) av Clinical variability of the 22q11.2 duplication syndrome

Frequency of holoprosencephaly in the International Clearinghouse Birth Defects Surveillance Systems: Searching for population variations.

Leoncini, Emanuele; Baranello, Giovanni; Orioli, Iêda M; Annerén, Göran et al.

Ingår i Birth defects research. Clinical and molecular teratology, s. 585-591, 2008

• DOI för Frequency of holoprosencephaly in the International Clearinghouse Birth Defects Surveillance Systems: Searching for population variations.

Gastroschisis and associated defects: an international study

Mastroiacovo, Pierpaolo; Lisi, Alessandra; Castilla, Eduardo E.; Martínez-Frías, María-Luisa et al.

Ingår i American Journal of Medical Genetics, Part A, s. 660-671, 2007

• DOI för Gastroschisis and associated defects: an international study

Duplication 16q12.1-q22.1 characterized by array CGH in a girl with spina bifida

Gustavsson, Peter; Schoumans, Jacqueline; Staaf, Johan; Borg, Åke et al.

Ingår i European Journal of Medical Genetics, s. 237-241, 2007

• DOI för Duplication 16q12.1-q22.1 characterized by array CGH in a girl with spina bifida

Whole-genome array-CGH for detection of submicroscopic chromosomal imbalances in children with mental retardation

Thuresson, Ann-Charlotte; Bondeson, Marie-Louise; Edeby, Christina; Ellis, P. et al.

Ingår i Cytogenetic and Genome Research, s. 1-7, 2007

• DOI för Whole-genome array-CGH for detection of submicroscopic chromosomal imbalances in children with mental retardation

Increase in beta-Amyloid Levels in Cerebrospinal Fluid of Children with Down Syndrome

Englund, Hillevi; Annerén, Göran; Gustafsson, Jan; Wester, Ulrika et al.

Ingår i Dementia and Geriatric Cognitive Disorders, s. 369-374, 2007

• DOI för Increase in beta-Amyloid Levels in Cerebrospinal Fluid of Children with Down Syndrome

Clinical and molecular characterization of individuals with 18p deletion: a genotype-phenotype correlation

Wester, Ulrika; Bondeson, Marie-Louise; Edeby, Christina; Annerén, Göran

Ingår i American Journal of Medical Genetics. Part A, s. 1164-1171, 2006

• DOI för Clinical and molecular characterization of individuals with 18p deletion: a genotype-phenotype correlation

Autoantibodies linked to autoimmune polyendocrine syndrome type I are prevalent in Down syndrome

Söderbergh, Annika; Gustafsson, Jan; Ekwall, Olov; Hallgren, Åsa et al.

Ingår i Acta Paediatrica, s. 1657-1660, 2006

• DOI för Autoantibodies linked to autoimmune polyendocrine syndrome type I are prevalent in Down syndrome

Molecular genetic analysis of a de novo balanced translocation t(6;17) (p21.31;q11.2) associated with hypospadias and anorectal malformation

Mansouri, Mahmoud Reza; Carlsson, Birgit; Davey, Edward; Nordenskjöld, Agneta et al.

Ingår i Human Genetics, s. 162-168, 2006

• DOI för Molecular genetic analysis of a de novo balanced translocation t(6;17) (p21.31;q11.2) associated with hypospadias and anorectal malformation

Environmental tobacco smoke and risk of spontaneous abortion

George, Lena; Granath, Fredrik; Johansson, Anna L. V.; Annerén, Göran et al.

Ingår i Epidemiology, s. 500-505, 2006

• DOI för Environmental tobacco smoke and risk of spontaneous abortion

Genome-wide screening using array-CGH does not reveal microdeletions/microduplications in children with Kabuki syndrome.

Schoumans, Jacqueline; Nordgren, Ann; Ruivenkamp, Claudia; Bröndum-Nielsen, Karen et al.

Ingår i Eur J Hum Genet, s. 260-3, 2005

RAR-related orphan receptor A isoform 1 (RORa1) is disrupted by a balanced translocation t(4;15)(q22.3;q21.3) associated with severe obesity.

Klar, Joakim; Åsling, Bengt; Carlsson, Birgit; Ulvsbäck, Magnus et al.

Ingår i Eur J Hum Genet, 2005

Fetal Mesenchymal Stem-Cell Engraftment in Bone after In Utero Transplantation in a Patient with Severe Osteogenesis Imperfecta

Le Blanc, Katarina; Götherström, Cecilia; Ringdeén, Olle; Hassan, Moustapha et al.

Ingår i Transplantation, s. 1607-14, 2005

Chromosomal anomalies in first-trimester miscarriages.

Ljunger, Elisabeth; Cnattingius, Sven; Lundin, Catarina; Anneren, Göran

Ingår i Acta Obstet Gynecol Scand, s. 1103-7, 2005

Antitissue transglutaminase and antithyroid autoantibodies in children with Down syndrome and celiac disease.

Hansson, Tony; Dahlbom, Ingrid; Rogberg, Siv; Nyberg, Britt-Inger et al.

Ingår i J Pediatr Gastroenterol Nutr, s. 170-4; discussion 125, 2005

A novel nonsense mutation of the mineralocorticoid receptor gene in a Swedish family with pseudohypoaldosteronism type I (PHA1).

Nyström, A-M; Bondeson, M-L; Skanke, N; Mårtensson, J et al.

Ingår i J Clin Endocrinol Metab, s. 227-31, 2004

Rapp-Hodgkin and AEC syndromes due to a new frameshift mutation in the TP63 gene

Dianzani, Irma; Garelli, E.; Gustavsson, P.; Carando, A. et al.

Ingår i Journal of Medical Genetics, 2003

• DOI för Rapp-Hodgkin and AEC syndromes due to a new frameshift mutation in the TP63 gene

Chondrodysplasia punctata (CDP) with features of the tibia-metacarpal type and maternal phenytoin treatment during pregnancy

Wester, Ulrika; Brandberg, Göran; Larsson, M; Lönnerholm, Torsten et al.

Ingår i Prenatal Diagnosis, s. 663-668, 2002

• DOI för Chondrodysplasia punctata (CDP) with features of the tibia-metacarpal type and maternal phenytoin treatment during pregnancy

A balanced reciprocal translocation t(5;7)(q14;q32) associated with autistic disorder: molecular analysis of the chromosome 7 breakpoint

Tentler, Dmitry; Brandberg, Göran; Betancur, Catalina; Gillberg, Christopher et al.

Ingår i American Journal of Medical Genetics, s. 729-36, 2001

• DOI för A balanced reciprocal translocation t(5;7)(q14;q32) associated with autistic disorder: molecular analysis of the chromosome 7 breakpoint

Downs syndrom: ny kunskap ställer höga krav på medicinsk vård och habilitering

Annerén, Göran; Hedov, Gerth; Wester, Ulrika

Ingår i Socialmedicinsk Tidskrift, s. 71-79, 1999

Deletion including the oligophrenin-1 gene associated with enlarged cerebral ventricles, cerebellar hypoplasia, seizures and ataxia

Tentler, D.; Gustavsson, P.; Leisti, J.; Schueler, M. et al.

Ingår i European Journal of Human Genetics, s. 541-8, 1999

The genetics of primary nocturnal enuresis: inheritance and suggestion of a second major gene on chromosome 12q

Arnell, Henrik; Hjalmas, Kelm; Jagervall, Martin; Läckgren, Göran et al.

Ingår i Journal of Medical Genetics, s. 360-5, 1997

• DOI för The genetics of primary nocturnal enuresis: inheritance and suggestion of a second major gene on chromosome 12q

Progressive familial intrahepatic cholestasis (PFIC): evidence for genetic heterogeneity by exclusion of linkage to chromosome 18q21-q22

Arnell, Henrik; Nemeth, Antal; Annerén, Göran; Dahl, Niklas

Ingår i Human Genetics, s. 378-381, 1997

• DOI för Progressive familial intrahepatic cholestasis (PFIC): evidence for genetic heterogeneity by exclusion of linkage to chromosome 18q21-q22

Molecular analysis of chromosome 21 in a patient with a phenotype of down syndrome and apparently normal karyotype

Edman Ahlbom, Bodil; Goetz, P; Korenberg, JR; Pettersson, Ulf et al.

Ingår i American Journal of Medical Genetics. Part A, s. 566-572, 1996

• DOI för Molecular analysis of chromosome 21 in a patient with a phenotype of down syndrome and apparently normal karyotype

Asperger syndrome in a boy with a balanced de novo translocation: t(17;19)(p13.3;p11)

Annerén, Göran; Dahl, Niklas; Uddenfeldt, Ulrika; Janols, Lars-Olof

Ingår i American Journal of Medical Genetics, s. 330-1, 1995

• DOI för Asperger syndrome in a boy with a balanced de novo translocation: t(17;19)(p13.3;p11)

What do pregnant women know about Downs syndrome when they come for prenatal diagnosis?

Ternby, Ellen; Annerén, Göran; Ingvoldstad, Charlotta; Lindgren, Peter et al.

s. 134-134, 2012

Unbalanced de novo translocation in mother resulting in one child with a 6q13-q16 deletion and one child with a 6q13-q16 duplication

Wentzel, Christian; Annerén, Göran; Thuresson, Ann-Charlotte