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Morten Krogh Herlin
Morten Krogh Herlin
MD, PhD, Department of Clinical Genetics
在 rm.dk 的电子邮件经过验证 - 首页
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引用次数
引用次数
年份
Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a comprehensive update
MK Herlin, MB Petersen, M Brännström
Orphanet Journal of Rare Diseases 15, 1-16, 2020
2392020
Prevalence and patient characteristics of Mayer–Rokitansky–Küster–Hauser syndrome: a nationwide registry-based study
M Herlin, AMB Bjørn, M Rasmussen, B Trolle, MB Petersen
Human reproduction 31 (10), 2384-2390, 2016
1612016
Familial occurrence of Mayer–Rokitansky–Küster–Hauser syndrome: a case report and review of the literature
M Herlin, AT Højland, MB Petersen
American Journal of Medical Genetics Part A 164 (9), 2276-2286, 2014
932014
Whole-exome sequencing identifies a GREB1L variant in a three-generation family with Müllerian and renal agenesis: a novel candidate gene in Mayer …
MK Herlin, VQ Le, AT Højland, A Ernst, H Okkels, AC Petersen, ...
Human Reproduction 34 (9), 1838-1846, 2019
572019
Genomic characterization of relapsed acute myeloid leukemia reveals novel putative therapeutic targets
S Stratmann, SA Yones, M Mayrhofer, N Norgren, A Skaftason, J Sun, ...
Blood advances 5 (3), 900-912, 2021
502021
Treatment of vaginal agenesis in Mayer-Rokitansky-Küster-Hauser syndrome in Denmark: a nationwide comparative study of anatomical outcome and complications
M Herlin, AMB Bjørn, LK Jørgensen, B Trolle, MB Petersen
Fertility and sterility 110 (4), 746-753, 2018
452018
Vertebral defect, anal atresia, cardiac defect, tracheoesophageal fistula/esophageal atresia, renal defect, and limb defect association with Mayer-Rokitansky-Küster-Hauser …
T Bjørsum-Meyer, M Herlin, N Qvist, MB Petersen
Journal of medical case reports 10, 1-10, 2016
392016
Transcriptomic analysis reveals proinflammatory signatures associated with acute myeloid leukemia progression
S Stratmann, SA Yones, M Garbulowski, J Sun, A Skaftason, M Mayrhofer, ...
Blood advances 6 (1), 152-164, 2022
212022
Accelerometer-assessed daily physical activity in relation to pain cognition in juvenile idiopathic arthritis
M Nørgaard, JJ Lomholt, M Thastum, M Herlin, M Twilt, T Herlin
Scandinavian Journal of Rheumatology 46 (1), 22-26, 2017
192017
Proteogenomic analysis of acute myeloid leukemia associates relapsed disease with reprogrammed energy metabolism both in adults and children
S Stratmann, M Vesterlund, HM Umer, S Eshtad, A Skaftason, MK Herlin, ...
Leukemia 37 (3), 550-559, 2023
132023
Update on genetic susceptibility and pathogenesis in juvenile idiopathic arthritis
M Herlin, MB Petersen, T Herlin
EMJ Rheumatol 1, 73-83, 2014
122014
What Is Abnormal in Normal Karyotype Acute Myeloid Leukemia in Children? Analysis of the Mutational Landscape and Prognosis of the TARGET-AML Cohort
MK Herlin, SA Yones, E Kjeldsen, L Holmfeldt, H Hasle
Genes 12 (6), 792, 2021
72021
Autosomal dominant sleep-related hypermotor epilepsy caused by a previously unreported CHRNA4 variant
TØ Nielsen, MK Herlin, KM Linnet, S Beniczky, M Sommerlund, ...
European journal of medical genetics 65 (3), 104444, 2022
62022
A.-M.; Jørgensen, LK; Trolle, B.; Petersen, MB Treatment of Vaginal Agenesis in Mayer-Rokitansky-Küster-Hauser Syndrome in Denmark: A Nationwide Comparative Study of Anatomical …
M Herlin, B Bjørn
Fertil. Steril 110, 746-753, 2018
62018
Mayer-Rokitansky-Küster-Hauser syndrome
M Herlin, MB Petersen
Ugeskrift for laeger 179 (13), V10160744-V10160744, 2017
62017
A life course perspective on Mayer-Rokitansky-Küster-Hauser syndrome: women’s experiences and negotiations of living with an underdeveloped uterus and vagina
AH Jensen, MK Herlin, I Vogel, S Lou
Disability and Rehabilitation 46 (6), 1130-1140, 2024
32024
Description of a novel subtype of acute myeloid leukemia defined by recurrent CBFB insertions
GL Ryland, M Umeda, L Holmfeldt, S Lehmann, MK Herlin, J Ma, ...
Blood 141 (7), 800-805, 2023
32023
Novel homozygous CD46 variant with C‐isoform expression affects C3b inactivation in atypical hemolytic uremic syndrome
VR Schack, MK Herlin, H Pedersen, JMB Jensen, M Færch, B Bundgaard, ...
European Journal of Immunology 52 (10), 1610-1619, 2022
22022
Understanding the Diagnostic Odyssey of Women with Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrome in Denmark: A Qualitative Interview Study
S Lou, AH Jensen, I Vogel, B Trolle, MK Herlin
Journal of pediatric and adolescent gynecology, 2024
12024
Congenital mirror movements are associated with defective polymerisation of RAD51
O Trouillard, P Dupaigne, M Dunoyer, M Doulazmi, MK Herlin, S Frismand, ...
Journal of Medical Genetics 60 (11), 1116-1126, 2023
12023
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