日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Clinical and Genetic Characteristics of Congenital Hyperinsulinism in Norway: A Nationwide Cohort Study

挪威先天性高胰岛素血症的临床和遗传特征:一项全国性队列研究

Velde, Christoffer Drabløs; Molnes, Janne; Berland, Siren; Njølstad, Pål Rasmus; Molven, Anders

The Use of Proton Pump Inhibitors Among Adults in Norway-A Nationwide Drug Utilization Study

挪威成年人使用质子泵抑制剂情况——一项全国性药物利用研究

Fossmark, Reidar; Molnes, Sveinung; Sagatun, Liv; Salvesen, Øyvind; Spigset, Olav

Molecular mechanism of HNF-1A-mediated HNF4A gene regulation and promoter-driven HNF4A-MODY diabetes

HNF-1A介导的HNF4A基因调控及启动子驱动的HNF4A-MODY糖尿病的分子机制

Kind, Laura; Molnes, Janne; Tjora, Erling; Raasakka, Arne; Myllykoski, Matti; Colclough, Kevin; Saint-Martin, Cécile; Adelfalk, Caroline; Dusatkova, Petra; Pruhova, Stepanka; Valtonen-André, Camilla; Bellanné-Chantelot, Christine; Arnesen, Thomas; Kursula, Petri; Njølstad, Pål Rasmus

Functional characterization of HNF4A gene variants identify promoter and cell line specific transactivation effects

HNF4A 基因变异的功能表征可识别启动子和细胞系特异性转录激活效应

Alba Kaci, Marie Holm Solheim, Trine Silgjerd, Jorunn Hjaltadottir, Lorentze Hope Hornnes, Janne Molnes, Andre Madsen, Gry Sjøholt, Christine Bellanné-Chantelot, Richard Caswell, Jørn V Sagen, Pål R Njølstad, Ingvild Aukrust, Lise Bjørkhaug

Bioinformatics pipeline for the systematic mining genomic and proteomic variation linked to rare diseases: The example of monogenic diabetes

用于系统挖掘与罕见病相关的基因组和蛋白质组变异的生物信息学流程:以单基因糖尿病为例

Kuznetsova, Ksenia G; Vašíček, Jakub; Skiadopoulou, Dafni; Molnes, Janne; Udler, Miriam; Johansson, Stefan; Njølstad, Pål Rasmus; Manning, Alisa; Vaudel, Marc

Second international consensus report on gaps and opportunities for the clinical translation of precision diabetes medicine

第二份关于精准糖尿病医学临床转化差距和机遇的国际共识报告

Tobias, Deirdre K; Merino, Jordi; Ahmad, Abrar; Aiken, Catherine; Benham, Jamie L; Bodhini, Dhanasekaran; Clark, Amy L; Colclough, Kevin; Corcoy, Rosa; Cromer, Sara J; Duan, Daisy; Felton, Jamie L; Francis, Ellen C; Gillard, Pieter; Gingras, Véronique; Gaillard, Romy; Haider, Eram; Hughes, Alice; Ikle, Jennifer M; Jacobsen, Laura M; Kahkoska, Anna R; Kettunen, Jarno L T; Kreienkamp, Raymond J; Lim, Lee-Ling; Männistö, Jonna M E; Massey, Robert; Mclennan, Niamh-Maire; Miller, Rachel G; Morieri, Mario Luca; Most, Jasper; Naylor, Rochelle N; Ozkan, Bige; Patel, Kashyap Amratlal; Pilla, Scott J; Prystupa, Katsiaryna; Raghavan, Sridharan; Rooney, Mary R; Schön, Martin; Semnani-Azad, Zhila; Sevilla-Gonzalez, Magdalena; Svalastoga, Pernille; Takele, Wubet Worku; Tam, Claudia Ha-Ting; Thuesen, Anne Cathrine B; Tosur, Mustafa; Wallace, Amelia S; Wang, Caroline C; Wong, Jessie J; Yamamoto, Jennifer M; Young, Katherine; Amouyal, Chloé; Andersen, Mette K; Bonham, Maxine P; Chen, Mingling; Cheng, Feifei; Chikowore, Tinashe; Chivers, Sian C; Clemmensen, Christoffer; Dabelea, Dana; Dawed, Adem Y; Deutsch, Aaron J; Dickens, Laura T; DiMeglio, Linda A; Dudenhöffer-Pfeifer, Monika; Evans-Molina, Carmella; Fernández-Balsells, María Mercè; Fitipaldi, Hugo; Fitzpatrick, Stephanie L; Gitelman, Stephen E; Goodarzi, Mark O; Grieger, Jessica A; Guasch-Ferré, Marta; Habibi, Nahal; Hansen, Torben; Huang, Chuiguo; Harris-Kawano, Arianna; Ismail, Heba M; Hoag, Benjamin; Johnson, Randi K; Jones, Angus G; Koivula, Robert W; Leong, Aaron; Leung, Gloria K W; Libman, Ingrid M; Liu, Kai; Long, S Alice; Lowe, William L Jr; Morton, Robert W; Motala, Ayesha A; Onengut-Gumuscu, Suna; Pankow, James S; Pathirana, Maleesa; Pazmino, Sofia; Perez, Dianna; Petrie, John R; Powe, Camille E; Quinteros, Alejandra; Jain, Rashmi; Ray, Debashree; Ried-Larsen, Mathias; Saeed, Zeb; Santhakumar, Vanessa; Kanbour, Sarah; Sarkar, Sudipa; Monaco, Gabriela S F; Scholtens, Denise M; Selvin, Elizabeth; Sheu, Wayne Huey-Herng; Speake, Cate; Stanislawski, Maggie A; Steenackers, Nele; Steck, Andrea K; Stefan, Norbert; Støy, Julie; Taylor, Rachael; Tye, Sok Cin; Ukke, Gebresilasea Gendisha; Urazbayeva, Marzhan; Van der Schueren, Bart; Vatier, Camille; Wentworth, John M; Hannah, Wesley; White, Sara L; Yu, Gechang; Zhang, Yingchai; Zhou, Shao J; Beltrand, Jacques; Polak, Michel; Aukrust, Ingvild; de Franco, Elisa; Flanagan, Sarah E; Maloney, Kristin A; McGovern, Andrew; Molnes, Janne; Nakabuye, Mariam; Njølstad, Pål Rasmus; Pomares-Millan, Hugo; Provenzano, Michele; Saint-Martin, Cécile; Zhang, Cuilin; Zhu, Yeyi; Auh, Sungyoung; de Souza, Russell; Fawcett, Andrea J; Gruber, Chandra; Mekonnen, Eskedar Getie; Mixter, Emily; Sherifali, Diana; Eckel, Robert H; Nolan, John J; Philipson, Louis H; Brown, Rebecca J; Billings, Liana K; Boyle, Kristen; Costacou, Tina; Dennis, John M; Florez, Jose C; Gloyn, Anna L; Gomez, Maria F; Gottlieb, Peter A; Greeley, Siri Atma W; Griffin, Kurt; Hattersley, Andrew T; Hirsch, Irl B; Hivert, Marie-France; Hood, Korey K; Josefson, Jami L; Kwak, Soo Heon; Laffel, Lori M; Lim, Siew S; Loos, Ruth J F; Ma, Ronald C W; Mathieu, Chantal; Mathioudakis, Nestoras; Meigs, James B; Misra, Shivani; Mohan, Viswanathan; Murphy, Rinki; Oram, Richard; Owen, Katharine R; Ozanne, Susan E; Pearson, Ewan R; Perng, Wei; Pollin, Toni I; Pop-Busui, Rodica; Pratley, Richard E; Redman, Leanne M; Redondo, Maria J; Reynolds, Rebecca M; Semple, Robert K; Sherr, Jennifer L; Sims, Emily K; Sweeting, Arianne; Tuomi, Tiinamaija; Udler, Miriam S; Vesco, Kimberly K; Vilsbøll, Tina; Wagner, Robert; Rich, Stephen S; Franks, Paul W

Characterisation of HNF1A variants in paediatric diabetes in Norway using functional and clinical investigations to unmask phenotype and monogenic diabetes

利用功能和临床研究来鉴定挪威儿童糖尿病中的 HNF1A 变异,以揭示表型和单基因糖尿病

Pernille Svalastoga #, Alba Kaci #, Janne Molnes, Marie H Solheim, Bente B Johansson, Lars Krogvold, Torild Skrivarhaug, Eivind Valen, Stefan Johansson, Anders Molven, Jørn V Sagen, Eirik Søfteland, Lise Bjørkhaug, Erling Tjora, Ingvild Aukrust, Pål R Njølstad

A Systematic Review of the use of Precision Diagnostics in Monogenic Diabetes

单基因糖尿病精准诊断应用系统评价

Murphy, Rinki; Colclough, Kevin; Pollin, Toni I; Ikle, Jennifer M; Svalastoga, Pernille; Maloney, Kristin A; Saint-Martin, Cécile; Molnes, Janne; Misra, Shivani; Aukrust, Ingvild; de Franco, aiElisa; Flanagan, Sarah E; Njølstad, Pål R; Billings, Liana K; Owen, Katharine R; Gloyn, Anna L

The use of precision diagnostics for monogenic diabetes: a systematic review and expert opinion

单基因糖尿病精准诊断的应用:系统评价和专家意见

Murphy, Rinki; Colclough, Kevin; Pollin, Toni I; Ikle, Jennifer M; Svalastoga, Pernille; Maloney, Kristin A; Saint-Martin, Cécile; Molnes, Janne; Misra, Shivani; Aukrust, Ingvild; de Franco, Elisa; Flanagan, Sarah E; Njølstad, Pål R; Billings, Liana K; Owen, Katharine R; Gloyn, Anna L

Two New Mutations in the CEL Gene Causing Diabetes and Hereditary Pancreatitis: How to Correctly Identify MODY8 Cases

CEL基因的两种新突变导致糖尿病和遗传性胰腺炎:如何正确识别MODY8病例

Khadija El Jellas,Petra Dušátková,Ingfrid S Haldorsen,Janne Molnes,Erling Tjora,Bente B Johansson,Karianne Fjeld,Stefan Johansson,Štěpánka Průhová,Leif Groop,J Matthias Löhr,Pål R Njølstad,Anders Molven