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Amplification-free sequencing of cell-free DNA for prenatal non-invasive diagnosis of chromosomal aberrations
Karlsson K, Sahlin E, Iwarsson E, Westgren M, Nordenskjöld M, Linnarsson S
Genomics 2015;105(3):150-8

Costs And Cost-Effectiveness Of Non-Invasive Prenatal Diagnosis (Nipt) For Detection Of Trisomy 21 In Sweden
Davidson T, Iwarsson E, Jacobsson B, Dagerhamn J, Heibert Arnlind M
Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research 2015;18(7):A352-

Disomy 21 in spermatozoa and the paternal origin of trisomy 21 Down syndrome
Iwarsson E, Kvist U, Hultén Ma
Molecular cytogenetics 2015;8():67-

Fetal calcifications are associated with chromosomal abnormalities
Sahlin E, Sirotkina M, Marnerides A, Iwarsson E, Papadogiannakis N
PloS one 2015;10(4):e0123343-

CNS involvement in OFD1 syndrome: a clinical, molecular, and neuroimaging study
Del Giudice E, Macca M, Imperati F, D'amico A, Parent P, Pasquier L, et al
Orphanet journal of rare diseases 2014;9():74-

Identification of a duplication within the GDF9 gene and novel candidate genes for primary ovarian insufficiency (POI) by a customized high-resolution array comparative genomic hybridization platform
Norling A, Hirschberg Al, Rodriguez-wallberg Ka, Iwarsson E, Wedell A, Barbaro M
Human reproduction (Oxford, England) 2014;29(8):1818-27

Maternal Germinal Trisomy 21 in Down Syndrome
Hultén Ma, Öijerstedt L, Iwarsson E, Jonasson J
Journal of clinical medicine 2014;3(1):167-75

Molecular and Cytogenetic Analysis in Stillbirth: Results from 481 Consecutive Cases
Sahlin E, Gustavsson P, Lieden A, Papadogiannakis N, Bjareborn L, Pettersson K, et al
FETAL DIAGNOSIS AND THERAPY 2014;36(4):326-32

Mutation screening and array comparative genomic hybridization using a 180K oligonucleotide array in VACTERL association
Winberg J, Gustavsson P, Papadogiannakis N, Sahlin E, Bradley F, Nordenskjöld E, et al
PloS one 2014;9(1):e85313-

No mutations in the PSMC3IP gene identified in a Swedish cohort of women with primary ovarian insufficiency
Norling A, Hirschberg Al, Karlsson L, Rodriguez-wallberg Ka, Iwarsson E, Wedell A, et al
Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation 2014;8(4):146-50

CBX2 gene analysis in patients with 46,XY and 46,XX gonadal disorders of sex development
Norling A, Hirschberg Al, Iwarsson E, Wedell A, Barbaro M
FERTILITY AND STERILITY 2013;99(3):819-826.e3

Fetal membrane cells for treatment of steroid-refractory acute graft-versus-host disease
Ringdén O, Erkers T, Nava S, Uzunel M, Iwarsson E, Conrad R, et al
Stem cells (Dayton, Ohio) 2013;31(3):592-601

Novel candidate genes for 46,XY gonadal dysgenesis identified by a customized 1 M array-CGH platform
Norling A, Lindén Hirschberg A, Iwarsson E, Persson B, Wedell A, Barbaro M
European journal of medical genetics 2013;56(12):661-8

Trisomy 21 Mosaicism: We May All Have a Touch of Down Syndrome
Hulten Ma, Jonasson J, Iwarsson E, Uppal P, Vorsanova Sg, Yurov Yb, et al
CYTOGENETIC AND GENOME RESEARCH 2013;139(3):189-92

Comment on "Origin of trisomy: no evidence to support the ovarian mosaicism theory"
Hulten Ma, Jonasson J, Westgren M, Jonsson Am, Papadogiannakis N, Iwarsson E
PRENATAL DIAGNOSIS 2012;32(12):1221-

Fetal mediastinal tumor of neuroepithelial origin in a case of missed abortion
Sirotkina M, Iwarsson E, Marnerides A, Papadogiannakis N
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society 2012;15(6):511-3

Preimplantation genetic diagnosis: twenty years of practice
Iwarsson E, Malmgren H, Blennow E
SEMINARS IN FETAL & NEONATAL MEDICINE 2011;16(2):74-80

Chimerism Resulting From Parthenogenetic Activation and Dispermic Fertilization
Winberg J, Gustavsson P, Lagerstedt-robinson K, Blennow E, Lundin J, Iwarsson E, et al
AMERICAN JOURNAL OF MEDICAL GENETICS PART A 2010;152A(9):2277-86

Germinal and Somatic Trisomy 21 Mosaicism: How Common is it, What are the Implications for Individual Carriers and How Does it Come About?
Hulten Ma, Jonasson J, Nordgren A, Iwarsson E
CURRENT GENOMICS 2010;11(6):409-19

On the origin of the maternal age effect in trisomy 21 Down syndrome: the Oocyte Mosaicism Selection model
Hulten Ma, Patel S, Jonasson J, Iwarsson E
REPRODUCTION 2010;139(1):1-9

On the paternal origin of trisomy 21 Down syndrome
Hulten Ma, Patel Sd, Westgren M, Papadogiannakis N, Jonsson Am, Jonasson J, et al
MOLECULAR CYTOGENETICS 2010;:4-

Jumping Translocation in a Phenotypically Normal Male: A Study of Mosaicism in Spermatozoa, Lymphocytes, and Fibroblasts
Iwarsson E, Sahlen S, Nordgren A
AMERICAN JOURNAL OF MEDICAL GENETICS PART A 2009;149A(8):1706-11

On the origin of constitutional aneuploidy
Hulten M, Iwarsson E
CHROMOSOME RESEARCH 2009;:108-109

On the origin of trisomy 21-the evidence from oocyte and polar body analysis
Hulten M, Iwarsson E
JOURNAL OF MEDICAL GENETICS 2009;:S97-S97

Expanded HSAN4 phenotype associated with two novel mutations in NTRK1
Wieczorek S, Bergstrom J, Saaf M, Kotting J, Iwarsson E
NEUROMUSCULAR DISORDERS 2008;18(8):681-4

Lack of aneuploidy for chromosomes 15, 16, and 18 in placentas from small-for-gestational-age liveborn infants
Papadogiannakis N, Iwarsson E, Taimi T, Zaphiropoulos Pg, Westgren M
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY 2008;198(2):-

Lack of aneuploidy for chromosomes 15, 16, and 18 in placentas from small-for-gestational-age liveborn infants
Papadogiannakis N, Iwarsson E, Taimi T, Zaphiropoulos Pg, Westgren M
American journal of obstetrics and gynecology 2008;198(2):231.e1-7

Mutational Spectrum of the Oral-Facial-Digital Type I Syndrome: A Study on a Large Collection of Patients
Oral Facial Digital Type I Ofdi Co, Prattichizzo C, Macca M, Novelli V, Giorgio G, Barra A, et al
HUMAN MUTATION 2008;29(10):1237-46

On the origin of trisomy 21 Down syndrome
Hulten Ma, Patel Sd, Tankimanova M, Westgren M, Papadogiannakis N, Jonsson Am, et al
MOLECULAR CYTOGENETICS 2008;:21-

Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy
Nicot As, Toussaint A, Tosch V, Kretz C, Wallgren-pettersson C, Iwarsson E, et al
NATURE GENETICS 2007;39(9):1134-9

Update on congenital muscular dystrophies and congenital myopathies: Oral presentations
Nicot A, Toussaint A, Tosch V, Kretz C, Wallgren-pettersson C, Iwarsson E, et al
NEUROMUSCULAR DISORDERS 2007;17(9-10):833-833

PGD for dystrophin gene deletions using fluorescence in situ hybridization
Malmgren H, White I, Johansson S, Levkov L, Iwarsson E, Fridstrom M, et al
MOLECULAR HUMAN REPRODUCTION 2006;12(5):353-6

Clinical outcome of treatment cycles using preimplantation genetic diagnosis for structural chromosomal abnormalities
Fridstrom M, Ahrlund-richter L, Iwarsson E, Malmgren H, Inzunza J, Rosenlund B, et al
PRENATAL DIAGNOSIS 2001;21(9):781-7

Highly abnormal cleavage divisions in preimplantation embryos from translocation carriers
Iwarsson E, Malmgren H, Inzunza J, Ahrlund-richter L, Sjoblom P, Rosenlund B, et al
PRENATAL DIAGNOSIS 2000;20(13):1038-47

A high degree of aneuploidy in frozen-thawed human preimplantation embryos
Iwarsson E, Lundqvist M, Inzunza J, Ahrlund-richter L, Sjoblom P, Lundkvist O, et al
HUMAN GENETICS 1999;104(5):376-82

A high degree of mosaicism in preimplantation embryos from a carrier of a reciprocal translocation t(11;22)(q23;q11).
Iwarsson E, Malmgren H, Inzunza J, Ahrlund-richter L, Rosenlund B, Fridstrom M, et al
AMERICAN JOURNAL OF HUMAN GENETICS 1999;65(4):A165-A165

Application of single-needle blastomere biopsy in human preimplantation genetic diagnosis
Inzunza J, Iwarsson E, Fridstrom M, Rosenlund B, Sjoblom P, Hillensjo T, et al
PRENATAL DIAGNOSIS 1998;18(13):1381-8

Birth of healthy twins after preimplantation genetic diagnosis of a pericentric inversion of chromosome 5
Iwarsson E, Ahrlund-richter L, Inzunza J, Rosenlund B, Fridstrom M, Sjoblom P, et al
HUMAN REPRODUCTION 1998;:81-82

Numerical chromosomal abnormalities in tripronuclear preimplantation embryos fertilized in vitro
Iwarsson E, Lundquist M, Inzunza J, Ahrlund-richter L, Nordenskjold M, Sjoblom P, et al
HUMAN REPRODUCTION 1998;:330-331

Preimplantation genetic diagnosis of a large pericentric inversion of chromosome 5
Iwarsson E, Ahrlund-richter L, Inzunza J, Rosenlund B, Fridstrom M, Hillensjo T, et al
MOLECULAR HUMAN REPRODUCTION 1998;4(7):719-23

Preimplantation genetic diagnosis of DiGeorge syndrome
Iwarsson E, Ahrlund-richter L, Inzunza J, Fridstrom M, Rosenlund B, Hillensjo T, et al
MOLECULAR HUMAN REPRODUCTION 1998;4(9):871-5

[Preimplantation genetic diagnosis. An alternative to traditional prenatal diagnosis]
Iwarsson E, Blennow Es, Anvret M, Nordenskjöld M, Inzunza J, Ahrlund-richter L, et al
Lakartidningen 1997;94(35):2919-22

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