| Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a comprehensive update MK Herlin, MB Petersen, M Brännström Orphanet Journal of Rare Diseases 15, 1-16, 2020 | 242 | 2020 |
| 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 | 162 | 2016 |
| 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 | 93 | 2014 |
| 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 | 58 | 2019 |
| 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 | 50 | 2021 |
| 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 | 47 | 2018 |
| 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 | 39 | 2016 |
| 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 | 21 | 2022 |
| 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 | 20 | 2017 |
| 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 | 13 | 2023 |
| Update on genetic susceptibility and pathogenesis in juvenile idiopathic arthritis M Herlin, MB Petersen, T Herlin EMJ Rheumatol 1, 73-83, 2014 | 12 | 2014 |
| 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 | 8 | 2021 |
| 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 | 6 | 2022 |
| 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 | 6 | 2018 |
| Mayer-Rokitansky-Küster-Hauser syndrome M Herlin, MB Petersen Ugeskrift for laeger 179 (13), V10160744-V10160744, 2017 | 6 | 2017 |
| 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 | 3 | 2024 |
| 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 | 3 | 2023 |
| 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 | 2 | 2022 |
| Clinical presentation and genetics of tricho-rhino-phalangeal syndrome (TRPS) type 1: A single-center case series of 15 patients and seven novel TRPS1 variants LK Herlin, MK Herlin, J Blechingberg, K Rønholt, L Graversen, ... European Journal of Medical Genetics 69, 104937, 2024 | 1 | 2024 |
| Genetics of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: advancements and implications MK Herlin Frontiers in Endocrinology 15, 1368990, 2024 | 1 | 2024 |
