Hong Jiao

Publikationer
CV
Populärvetenskap och samverkan

Artiklar

Article: AUTISM RESEARCH. 2022;15(3):434-446

Rare variants in the outcome of social skills group training for autism.

Li D; Choque Olsson N; Becker M; Arora A; Jiao H; Norgren N; Jonsson U; Bölte S; Tammimies K
Article: JOURNAL OF INTERNAL MEDICINE. 2021;290(2):404-415

Founder effects facilitate the use of a genotyping-based approach to molecular diagnosis in Swedish patients with familial hypercholesterolaemia.

Benedek P; Jiao H; Duvefelt K; Skoog T; Linde M; Kiviluoma P; Kere J; Eriksson M; Angelin B
Article: NPJ GENOMIC MEDICINE. 2020;5(1):45

The influence of common polygenic risk and gene sets on social skills group training response in autism spectrum disorder.

Li D; Choque-Olsson N; Jiao H; Norgren N; Jonsson U; Bölte S; Tammimies K
Article: DIABETES. 2019;68(12):2235-2246

Evaluation of the Genetic Association Between Adult Obesity and Neuropsychiatric Disease.

Stahel P; Nahmias A; Sud SK; Lee SJ; Pucci A; Yousseif A; Youseff A; Jackson T; Urbach DR; Okrainec A; Allard JP; Sockalingam S; Yao T; Barua M; Jiao H; Magi R; Bassett AS; Paterson AD; Dahlman I; Batterham RL; Dash S
Article: NATURE COMMUNICATIONS. 2019;10(1):1396

Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions.

Olivé M; Engvall M; Ravenscroft G; Cabrera-Serrano M; Jiao H; Bortolotti CA; Pignataro M; Lambrughi M; Jiang H; Forrest ARR; Benseny-Cases N; Hofbauer S; Obinger C; Battistuzzi G; Bellei M; Borsari M; Di Rocco G; Viola HM; Hool LC; Cladera J; Lagerstedt-Robinson K; Xiang F; Wredenberg A; Miralles F; Baiges JJ; Malfatti E; Romero NB; Streichenberger N; Vial C; Claeys KG; Straathof CSM; Goris A; Freyer C; Lammens M; Bassez G; Kere J; Clemente P; Sejersen T; Udd B; Vidal N; Ferrer I; Edström L; Wedell A; Laing NG
Article: EBIOMEDICINE. 2018;30:248-260

Long Non-Coding RNAs Associated with Metabolic Traits in Human White Adipose Tissue.

Gao H; Kerr A; Jiao H; Hon C-C; Rydén M; Dahlman I; Arner P
Article: FRONTIERS IN ENDOCRINOLOGY. 2018;9:380

Rare Copy Number Variants in Array-Based Comparative Genomic Hybridization in Early-Onset Skeletal Fragility.

Costantini A; Skarp S; Kämpe A; Mäkitie RE; Pettersson M; Männikkö M; Jiao H; Taylan F; Lindstrand A; Mäkitie O
Article: JOURNAL OF BONE AND MINERAL RESEARCH. 2017;32(12):2394-2404

PLS3 Deletions Lead to Severe Spinal Osteoporosis and Disturbed Bone Matrix Mineralization.

Kämpe AJ; Costantini A; Levy-Shraga Y; Zeitlin L; Roschger P; Taylan F; Lindstrand A; Paschalis EP; Gamsjaeger S; Raas-Rothschild A; Hövel M; Jiao H; Klaushofer K; Grasemann C; Mäkitie O
Article: OSTEOPOROSIS INTERNATIONAL. 2017;28(10):3023-3032

PLS3 sequencing in childhood-onset primary osteoporosis identifies two novel disease-causing variants.

Kämpe AJ; Costantini A; Mäkitie RE; Jäntti N; Valta H; Mäyränpää M; Kröger H; Pekkinen M; Taylan F; Jiao H; Mäkitie O
Article: SCIENTIFIC REPORTS. 2017;7:45771

Sequence analysis of pooled bacterial samples enables identification of strain variation in group A streptococcus.

Weldatsadik RG; Wang J; Puhakainen K; Jiao H; Jalava J; Räisänen K; Datta N; Skoog T; Vuopio J; Jokiranta TS; Kere J
Article: PLOS ONE. 2017;12(12):e0189591

CELSR2 is a candidate susceptibility gene in idiopathic scoliosis.

Einarsdottir E; Grauers A; Wang J; Jiao H; Escher SA; Danielsson A; Simony A; Andersen M; Christensen SB; Åkesson K; Kou I; Khanshour AM; Ohlin A; Wise C; Ikegawa S; Kere J; Gerdhem P
Article: DIABETES. 2016;65(10):2980-2989

Whole-Exome Sequencing Suggests LAMB3 as a Susceptibility Gene for Morbid Obesity.

Jiao H; Kulyté A; Näslund E; Thorell A; Gerdhem P; Kere J; Arner P; Dahlman I
Article: SCIENTIFIC REPORTS. 2016;6:33256

Investigation of rare and low-frequency variants using high-throughput sequencing with pooled DNA samples.

Wang J; Skoog T; Einarsdottir E; Kaartokallio T; Laivuori H; Grauers A; Gerdhem P; Hytönen M; Lohi H; Kere J; Jiao H
Article: SCIENTIFIC REPORTS. 2016;6:29085

Exome sequencing in pooled DNA samples to identify maternal pre-eclampsia risk variants.

Kaartokallio T; Wang J; Heinonen S; Kajantie E; Kivinen K; Pouta A; Gerdhem P; Jiao H; Kere J; Laivuori H
Article: JOURNAL OF NEURODEVELOPMENTAL DISORDERS. 2016;8:4

Genomic sequencing of a dyslexia susceptibility haplotype encompassing ROBO1.

Massinen S; Wang J; Laivuori K; Bieder A; Tapia Paez I; Jiao H; Kere J
Article: PLOS ONE. 2016;11(7):e0160197

Identification of Novel Transcribed Regions in Zebrafish (Danio rerio) Using RNA-Sequencing.

Wang J; Vesterlund L; Kere J; Jiao H
Article: SPINE JOURNAL. 2015;15(10):2239-2246

Candidate gene analysis and exome sequencing confirm LBX1 as a susceptibility gene for idiopathic scoliosis.

Grauers A; Wang J; Einarsdottir E; Simony A; Danielsson A; Åkesson K; Ohlin A; Halldin K; Grabowski P; Tenne M; Laivuori H; Dahlman I; Andersen M; Christensen SB; Karlsson MK; Jiao H; Kere J; Gerdhem P
Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2015;23(9):1216-1222

Exome sequencing followed by genotyping suggests SYPL2 as a susceptibility gene for morbid obesity.

Jiao H; Arner P; Gerdhem P; Strawbridge RJ; Näslund E; Thorell A; Hamsten A; Kere J; Dahlman I
Article: PLOS ONE. 2013;8(2):e56225

Genetic susceptibility to non-necrotizing erysipelas/cellulitis.

Hannula-Jouppi K; Massinen S; Siljander T; Mäkelä S; Kivinen K; Leinonen R; Jiao H; Aitos P; Karppelin M; Vuopio J; Syrjänen J; Kere J
Article: PLOS ONE. 2013;8(5):e61920

Ultra-rare mutation in long-range enhancer predisposes to thyroid carcinoma with high penetrance.

He H; Li W; Wu D; Nagy R; Liyanarachchi S; Akagi K; Jendrzejewski J; Jiao H; Hoag K; Wen B; Srinivas M; Waidyaratne G; Wang R; Wojcicka A; Lattimer IR; Stachlewska E; Czetwertynska M; Dlugosinska J; Gierlikowski W; Ploski R; Krawczyk M; Jazdzewski K; Kere J; Symer DE; Jin V; Wang Q; de la Chapelle A
Article: BMC MEDICAL GENOMICS. 2011;4:51

Genome wide association study identifies KCNMA1 contributing to human obesity.

Jiao H; Arner P; Hoffstedt J; Brodin D; Dubern B; Czernichow S; van't Hooft F; Axelsson T; Pedersen O; Hansen T; Sørensen TIA; Hebebrand J; Kere J; Dahlman-Wright K; Hamsten A; Clement K; Dahlman I
Article: JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM. 2011;96(6):E962-E966

Genetic association and gene expression analysis identify FGFR1 as a new susceptibility gene for human obesity.

Jiao H; Arner P; Dickson SL; Vidal H; Mejhert N; Henegar C; Taube M; Hansson C; Hinney A; Galan P; Simon C; Silveira A; Benrick A; Jansson J-O; Bouloumié A; Langin D; Laville M; Debard C; Axelsson T; Rydén M; Kere J; Dahlman-Wright K; Hamsten A; Clement K; Dahlman I
Article: BMC DEVELOPMENTAL BIOLOGY. 2011;11:30

The zebrafish transcriptome during early development.

Vesterlund L; Jiao H; Unneberg P; Hovatta O; Kere J
Article: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY. 2010;36(3):198-210

Molecular genetic and epigenetic analysis of NCX2/SLC8A2 at 19q13.3 in human gliomas.

Qu M; Jiao H; Zhao J; Ren Z-P; Smits A; Kere J; Nistér M
Article: MOLECULAR HUMAN REPRODUCTION. 2009;15(7):443-449

ROCK2 allelic variants are not associated with pre-eclampsia susceptibility in the Finnish population.

Peterson H; Laivuori H; Kerkelä E; Jiao H; Hiltunen L; Heino S; Tiala I; Knuutila S; Rasi V; Kere J; Kivinen K
Article: JOURNAL OF BONE AND MINERAL RESEARCH. 2009;24(6):1066-1074

Genetic regulation of bone traits is influenced by sex and reciprocal cross in F(2) progeny from GK and F344 rats.

Lagerholm S; Li L-S; Jiao H; Park H-B; Ohlsson C; Akesson K; Luthman H
Article: CANCER RESEARCH. 2009;69(2):625-631

A susceptibility locus for papillary thyroid carcinoma on chromosome 8q24.

He H; Nagy R; Liyanarachchi S; Jiao H; Li W; Suster S; Kere J; de la Chapelle A
Article: MOLECULAR IMMUNOLOGY. 2008;46(1):202-206

Novel and recurrent STAT3 mutations in hyper-IgE syndrome patients from different ethnic groups.

Jiao H; Tóth B; Erdos M; Fransson I; Rákóczi E; Balogh I; Magyarics Z; Dérfalvi B; Csorba G; Szaflarska A; Megarbane A; Akatcherian C; Dbaibo G; Rajnavölgyi E; Hammarström L; Kere J; Lefranc G; Maródi L
Article: INTERNATIONAL JOURNAL OF OBESITY. 2008;32(5):816-825

Association analysis of positional obesity candidate genes based on integrated data from transcriptomics and linkage analysis.

Jiao H; Kaaman M; Dungner E; Kere J; Arner P; Dahlman I
Article: HORMONE RESEARCH IN PAEDIATRICS. 2008;69(1):31-36

Association of ADRB1 and UCP3 gene polymorphisms with insulin sensitivity but not obesity.

Mottagui-Tabar S; Hoffstedt J; Brookes AJ; Jiao H; Arner P; Dahlman I
Article: BMC MEDICAL GENETICS. 2007;8:73

Impact of estrogen receptor gene polymorphisms and mRNA levels on obesity and lipolysis--a cohort study.

Nilsson M; Dahlman I; Jiao H; Gustafsson J-A; Arner P; Dahlman-Wright K
Article: AMERICAN JOURNAL OF HUMAN GENETICS. 2007;81(3):467-474

Physical exercise-induced hypoglycemia caused by failed silencing of monocarboxylate transporter 1 in pancreatic beta cells.

Otonkoski T; Jiao H; Kaminen-Ahola N; Tapia-Paez I; Ullah MS; Parton LE; Schuit F; Quintens R; Sipilä I; Mayatepek E; Meissner T; Halestrap AP; Rutter GA; Kere J
Article: MOLECULAR VISION. 2007;13:1154-1160

Two Chinese families with pulverulent congenital cataracts and deltaG91 CRYBA1 mutations.

Lu S; Zhao C; Jiao H; Kere J; Tang X; Zhao F; Zhang X; Zhao K; Larsson C
Article: AMERICAN JOURNAL OF HUMAN GENETICS. 2007;80(6):1115-1124

A common haplotype in the G-protein-coupled receptor gene GPR74 is associated with leanness and increased lipolysis.

Dahlman I; Dicker A; Jiao H; Kere J; Blomqvist L; van Harmelen V; Hoffstedt J; Borch-Johnsen K; Jorgensen T; Hansen T; Pedersen O; Laakso M; Arner P
Article: JOURNAL OF MOLECULAR MEDICINE-JMM. 2007;85(6):589-601

The CCHCR1 (HCR) gene is relevant for skin steroidogenesis and downregulated in cultured psoriatic keratinocytes.

Tiala I; Suomela S; Huuhtanen J; Wakkinen J; Hölttä-Vuori M; Kainu K; Ranta S; Turpeinen U; Hämäläinen E; Jiao H; Karvonen S-L; Ikonen E; Kere J; Saarialho-Kere U; Elomaa O
Article: PHARMACOGENETICS AND GENOMICS. 2006;16(12):881-889

Liver X receptor gene polymorphisms and adipose tissue expression levels in obesity.

Dahlman I; Nilsson M; Jiao H; Hoffstedt J; Lindgren CM; Humphreys K; Kere J; Gustafsson J-A; Arner P; Dahlman-Wright K
Article: OBESITY. 2005;13(10):1645-1650

A common beta2-adrenoceptor gene haplotype protects against obesity in Swedish women.

Jiao H; Dahlman I; Eriksson P; Kere J; Arner P
Article: DIABETES. 2005;54(10):3032-3034

The CIDEA gene V115F polymorphism is associated with obesity in Swedish subjects.

Dahlman I; Kaaman M; Jiao H; Kere J; Laakso M; Arner P
Article: DIABETOLOGIA. 2004;47(11):1974-1979

alpha2-Heremans-Schmid glycoprotein gene polymorphisms are associated with adipocyte insulin action.

Dahlman I; Eriksson P; Kaaman M; Jiao H; Lindgren CM; Kere J; Arner P
Article: HUMAN MOLECULAR GENETICS. 2004;13(15):1551-1561

Transgenic mouse models support HCR as an effector gene in the PSORS1 locus.

Elomaa O; Majuri I; Suomela S; Asumalahti K; Jiao H; Mirzaei Z; Rozell B; Dahlman-Wright K; Pispa J; Kere J; Saarialho-Kere U
Article: JOURNAL OF NEUROIMMUNOLOGY. 2001;119(2):166-174

Polygenic control of autoimmune peripheral nerve inflammation in rat.

Dahlman I; Wallström E; Jiao H; Luthman H; Olsson T; Weissert R
Article: MAMMALIAN GENOME. 1999;10(11):1102-1105

A rat genetic linkage map including 67 new microsatellite markers.

Fakhrai-Rad H; Jiao H; Li LS; Glaser A; Koike G; Jacob HJ; Luthman H; Galli J
Article: NATURE GENETICS. 1996;12(1):31-37

Genetic analysis of non-insulin dependent diabetes mellitus in the GK rat.

Galli J; Li LS; Glaser A; Ostenson CG; Jiao H; Fakhrai-Rad H; Jacob HJ; Lander ES; Luthman H
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Corrigendum: DIABETES. 2020;69(4):798

Erratum. Evaluation of the Genetic Association Between Adult Obesity and Neuropsychiatric Disease. Diabetes 2019;68:2235-2246.

Stahel P; Nahmias A; Sud SK; Lee SJ; Pucci A; Yousseif A; Youseff A; Jackson T; Urbach DR; Okrainec A; Allard JP; Sockalingam S; Yao T; Barua M; Jiao H; Magi R; Bassett AS; Paterson AD; Dahlman I; Batterham RL; Dash S
Letter: JOURNAL OF INTERNAL MEDICINE. 2018;283(6):604-606

Unique case of cerebrotendinous xanthomatosis revisited: All the mutations responsible for this disease are present in the CYP27A1 gene.

Jiao H; Olin M; Hansson M; Eggertsen G; Eriksson M; Angelin B; Björkhem I
Letter: AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2017;173(3):806-808

CRTAP variants in early-onset osteoporosis and recurrent fractures.

Costantini A; Vuorimies I; Mäkitie R; Mäyränpää MK; Becker J; Pekkinen M; Valta H; Netzer C; Kämpe A; Taylan F; Jiao H; Mäkitie O

Anställningar

Anknuten till Forskning, Medicin, Huddinge, Karolinska Institutet, 2024-2024
Anknuten till Forskning, Biovetenskaper och näringslära, Karolinska Institutet, 2023-2024

Examina och utbildning

MEDICINE DOKTORSEXAMEN, Institutionen för molekylär medicin och kirurgi, Karolinska Institutet, 2002

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