Wolfgang Berger - Publications, H-index & Citations

Wolfgang Berger

university of zurich

56H指数

280论文数

1.1W被引数

收录论文 96

发表时间

European Heart Journal

IF35.6

2026-03-05

PREAI

Zenghui Meng; Boldizsar Kovacs; Chen Yan; Christina Hölscher; Saltanat Zhazykbayeva; Oliver Jarkas; Chendan Zou; Lukas Cyganek; Esther Zorio; Aitana Braza-Boils; Juan Pablo Ochoa; Niels Rehbehn; Xuehui Fan; Xinhao Lei; Rui Liu; Siyuan Tong; Feng Liu; Zongqian Xue; Sara L Bober; Binyi Zhao; Firat Duru; Assem Aweimer; Alexandra Köppel; Karin Burau; Andreas Mügge; Wolfgang Berger; Nazha Hamdani; Xiaobo Zhou; Ardan M Saguner; Ibrahim Akin; Michael H Gollob; Ibrahim El-Battrawy

The Phenotypic and Genotypic Features of ADAMTSL4-Related Ocular Disease ADAMTSL4相关眼病的表型和基因型特征

Clinical Genetics

IF2.3

2025-11-01

OAAI

Williams, Katie M.; Berger, Wolfgang; Koller, Samuel; Pfiffner, Fatma Kivrak; Maspoli, Alessandro; Gloggnitzer, Jiradet; Bruhwiler, Britta V. T.; Stathopoulos, Christina; Munier, Francis; Allen, Louise; Iosifidis, Christos; Black, Graeme C.; Sergouniotis, Panagiotis I.; Lloyd, Ian Christopher; Gerth-kahlert, Christina

Genetic Landscape of Congenital Cataracts in a Swiss Cohort: Addressing Diagnostic Oversights in Nance–Horan Syndrome 瑞士队列中先天性白内障的遗传景观：解决Nance-Horan综合征的诊断遗漏问题

Biomedicines 2025, Vol. 13, Page 1883

IF3.9

2025-08-21

PREAI

Flora Delas; Jiradet Gloggnitzer; Alessandro Maspoli; Lisa Kurmann; Beatrice E. Frueh; Ivanka Dacheva; Darius Hildebrand; Wolfgang Berger; Christina Gerth-Kahlert

Rescue of cochlear vascular pathology prevents sensory hair cell loss in Norrie disease

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

IF9.1

2024-11-25

OAAI

Patel, Aara; Pauzuolyte, Valda; Ingham, Neil J.; Leong, Yeh Chwan; Berger, Wolfgang; Steel, Karen P.; Sowden, Jane C.

Identification and Characterization of ATOH7-Regulated Target Genes and Pathways in Human Neuroretinal Development

CELLS

IF5.2

2024-07-03

OAAI

Atac, David; Maggi, Kevin; Feil, Silke; Maggi, Jordi; Cuevas, Elisa; Sowden, Jane C.; Koller, Samuel; Berger, Wolfgang

SwissGenVar: A Platform for Clinical-Grade Interpretation of Genetic Variants to Foster Personalized Healthcare in Switzerland SwissGenVar: 一个用于遗传变异临床级解释的平台，以促进瑞士的个性化医疗保健

JOURNAL OF PERSONALIZED MEDICINE

IF3

2024-06-17

OAAI

Kraemer, Dennis; Terumalai, Dillenn; Famiglietti, Maria Livia; Filges, Isabel; Joset, Pascal; Koller, Samuel; Maurer, Fabienne; Meier, Stephanie; Nouspikel, Thierry; Sanz, Javier; Zweier, Christiane; Abramowicz, Marc; Berger, Wolfgang; Cichon, Sven; Schaller, Andre; Superti-Furga, Andrea; Barbie, Valerie; Rauch, Anita

Systemic gene therapy rescues retinal dysfunction and hearing loss in a model of Norrie disease

EMBO MOLECULAR MEDICINE

IF8.3

2023-08-29

OAAI

Pauzuolyte, Valda; Patel, Aara; Wawrzynski, James R.; Ingham, Neil J.; Leong, Yeh Chwan; Karda, Rajvinder; Bitner-Glindzicz, Maria; Berger, Wolfgang; Waddington, Simon N.; Steel, Karen P.; Sowden, Jane C.

The Spectrum of MORC2-Related Disorders: A Potential Link to Cockayne Syndrome MORC2-Related障碍的范围: 与Cockayne综合征的潜在联系

PEDIATRIC NEUROLOGY

IF2.1

2023-04-01

OAAI

Stafki, Seth A.; Turner, Johnnie; Littel, Hannah R.; Bruels, Christine C.; Truong, Don; Knirsch, Ursula; Stettner, Georg M.; Graf, Urs; Berger, Wolfgang; Kinali, Maria; Jungbluth, Heinz; Pacak, Christina A.; Hughes, Jayne; Mirchi, Amytice; Derksen, Alexa; Vincent-Delorme, Catherine; Theil, Arjan F.; Bernard, Genevieve; Ellis, David; Fassihi, Hiva; Lehmann, Alan R.; Laugel, Vincent; Mohammed, Shehla; Kang, Peter B.

Whole genome sequencing for USH2A-associated disease reveals several pathogenic deep-intronic variants that are amenable to splice correction

HUMAN GENETICS AND GENOMICS ADVANCES

IF3.6

2023-04-01

OAAI

Reurink, Janine; Weisschuh, Nicole; Garanto, Alejandro; Dockery, Adrian; van den Born, L. Ingeborgh; Fajardy, Isabelle; Haer-Wigman, Lonneke; Kohl, Susanne; Wissinger, Bernd; Farrar, G. Jane; Ben-Yosef, Tamar; Pfiffner, Fatma Kivrak; Berger, Wolfgang; Weener, Marianna E.; Dudakova, Lubica; Liskova, Petra; Sharon, Dror; Salameh, Manar; Offenheim, Ashley; Heon, Elise; Girotto, Giorgia; Gasparini, Paolo; Morgan, Anna; Bergen, Arthur A.; ten Brink, Jacoline B.; Klaver, Caroline C. W.; Tranebjaerg, Lisbeth; Rendtorff, Nanna D.; Vermeer, Sascha; Smits, Jeroen J.; Pennings, Ronald J. E.; Aben, Marco; Oostrik, Jaap; Astuti, Galuh D. N.; Galbany, Jordi Corominas; Kroes, Hester Y.; Phan, Milan; Zelst-Stams, Wendy A. G. van; Thiadens, Alberta A. H. J.; Verheij, Joke B. G. M.; Schooneveld, Mary J. van; Bruijn, Suzanne E. de; Li, Catherina H. Z.; Hoyng, Carel B.; Gilissen, Christian; Vissers, Lisenka E. L. M.; Cremers, Frans P. M.; Kremer, Hannie; van Wijk, Erwin; Roosing, Susanne

Optical genome mapping and revisiting short-read genome sequencing data reveal previously overlooked structural variants disrupting retinal disease- associated genes 光学基因组图谱和重新审视短读基因组测序数据揭示了先前被忽视的破坏视网膜疾病相关基因的结构变异

GENETICS IN MEDICINE

IF6.2

2023-03-01

OAAI

Bruijn, Suzanne E. de; Rodenburg, Kim; Corominas, Jordi; Ben-Yosef, Tamar; Reurink, Janine; Kremer, Hannie; Whelan, Laura; Plomp, Astrid S.; Berger, Wolfgang; Farrar, G. Jane; Kovaecs, Arpaed Ferenc; Fajardy, Isabelle; Hitti-Malin, Rebekkah J.; Weisschuh, Nicole; Weener, Marianna E.; Sharon, Dror; Pennings, Ronald J. E.; Haer-Wigman, Lonneke; Hoyng, Carel B.; Nelen, Marcel R.; Vissers, Lisenka E. L. M.; van den Born, L. Ingeborgh; Gilissen, Christian; Cremers, Frans P. M.; Hoischen, Alexander; Neveling, Kornelia; Roosing, Susanne

The timing of auditory sensory deficits in Norrie disease has implications for intervention

JCI INSIGHT

IF6.1

2022-02-08

OAAI

Bryant, Dale; Pauzuolyte, Valda; Ingham, Neil J.; Patel, Aara; Pagarkar, Waheeda; Anderson, Lucy A.; Smith, Katie E.; Moulding, Dale A.; Leong, Yeh C.; Jafree, Daniyal J.; Long, David A.; Al-Yassin, Amina; Steel, Karen P.; Jagger, Daniel J.; Forge, Andrew; Berger, Wolfgang; Sowden, Jane C.; Bitner-Glindzicz, Maria

Impact of Genetic Variant Reassessment on the Diagnosis of Arrhythmogenic Right Ventricular Cardiomyopathy Based on the 2010 Task Force Criteria

CIRCULATION-GENOMIC AND PRECISION MEDICINE

IF5.5

2021-02-01

OAAI

Costa, Sarah; Medeiros-Domingo, Argelia; Gasperetti, Alessio; Akdis, Deniz; Berger, Wolfgang; James, Cynthia A.; Ruschitzka, Frank; Brunckhorst, Corinna B.; Duru, Firat; Saguner, Ardan M.

Genotype-phenotype spectrum in isolated and syndromic nanophthalmos

ACTA OPHTHALMOLOGICA

IF2.8

2020-09-30

OAAI

Lang, Elena; Koller, Samuel; Atac, David; Pfaeffli, Oliver A.; Hanson, James V. M.; Feil, Silke; Baehr, Luzy; Bahr, Angela; Kottke, Raimund; Joset, Pascal; Fasler, Katrin; Barthelmes, Daniel; Steindl, Katharina; Konrad, Daniel; Wille, David-Alexander; Berger, Wolfgang; Gerth-Kahlert, Christina

Integrin-linked kinase controls retinal angiogenesis and is linked to Wnt signaling and exudative vitreoretinopathy

NATURE COMMUNICATIONS

IF15.7

2019-11-20

OAAI

Park, Hongryeol; Yamamoto, Hiroyuki; Mohn, Lucas; Ambuhl, Lea; Kanai, Kenichi; Schmidt, Inga; Kim, Kee-Pyo; Fraccaroli, Alessia; Feil, Silke; Junge, Harald J.; Montanez, Eloi; Berger, Wolfgang; Adams, Ralf H.

Atonal homolog 7 (ATOH7) loss-of-function mutations in predominant bilateral optic nerve hypoplasia

HUMAN MOLECULAR GENETICS

IF3.2

2019-11-07

OAAI

Atac, David; Koller, Samuel; Hanson, James V. M.; Feil, Silke; Tiwari, Amit; Bahr, Angela; Baehr, Luzy; Magyar, Istvan; Kottke, Raimund; Gerth-Kahlert, Christina; Berger, Wolfgang

Genotype-Phenotype Analysis of a Novel Recessive and a Recurrent Dominant SNRNP200 Variant Causing Retinitis Pigmentosa

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE

IF4.7

2019-07-01

OAAI

Gerth-Kahlert, Christina; Koller, Samuel; Hanson, James V. M.; Baehr, Luzy; Tiwari, Amit; Kivrak-Pfiffner, Fatma; Bahr, Angela; Berger, Wolfgang

Dysfunctional LAT2 Amino Acid Transporter Is Associated With Cataract in Mouse and Humans

FRONTIERS IN PHYSIOLOGY

IF3.4

2019-06-04

OAAI

Knopfel, Emilia Boiadjieva; Vilches, Clara; Camargo, Simone M. R.; Errasti-Murugarren, Ekaitz; Staubli, Andrina; Mayayo, Clara; Munier, Francis L.; Miroshnikova, Nataliya; Poncet, Nadege; Junza, Alexandra; Bhattacharya, Shomi S.; Prat, Esther; Berry, Vanita; Berger, Wolfgang; Heon, Elise; Moore, Anthony T.; Yanes, Oscar; Nunes, Virginia; Palacin, Manuel; Verrey, Francois; Kloeckener-Gruissem, Barbara

Cystoid edema, neovascularization and inflammatory processes in the murine Norrin-deficient retina

SCIENTIFIC REPORTS

IF3.9

2018-04-13

OAAI

Beck, Susanne C.; Karlstetter, Marcus; Garrido, Marina Garcia; Feng, Yuxi; Dannhausen, Katharina; Muehlfriedel, Regine; Sothilingam, Vithiyanjali; Seebauer, Britta; Berger, Wolfgang; Hammes, Hans-Peter; Seeliger, Mathias W.; Langmann, Thomas

Genotype-dependent deterioration of sustained attention by the COMT inhibitor tolcapone after sleep deprivation

EUROPEAN NEUROPSYCHOPHARMACOLOGY

IF6.7

2018-03-01

PREAI

Holst, S. C.; Valomon, A.; Borrello, A.; Weigend, S.; Mueller, T.; Berger, W.; Sommerauer, M.; Baumann, C. R.; Landolt, H. P.

Effects of COMT genotype and tolcapone on lapses of sustained attention after sleep deprivation in healthy young men

NEUROPSYCHOPHARMACOLOGY

IF7.1

2018-02-05

OAAI

Valomon, Amandine; Holst, Sebastian C.; Borrello, Alessandro; Weigend, Susanne; Mueller, Thomas; Berger, Wolfgang; Sommerauer, Michael; Baumann, Christian R.; Landolt, Hans-Peter

研究方向