Publications by authors named "Rustem Yilmaz"

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Somatic gene mutations in the motor cortex of patients with sporadic amyotrophic lateral sclerosis.
Óscar González-Velasco, Rosanna Parlato, Rüstem Yilmaz, Lorena Decker, Sonja Menge

Brain· December 2025

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Changes in VA Intervals With Bundle Branch Block Aberration During Supraventricular Tachycardia: Wenckebach or Coumel Phenomenon?
Meryem Kara, Ozcan Ozeke, Muhammet Genes, Rustem Yilmaz, Mehmet Tolga Dogru

Pacing Clin Electrophysiol· December 2025

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Deep clinical, genetic, and serum biomarker profiling indicates glial and neuronal pathology in primary brain calcification.
Janine Schwahn, Sophie Hebestreit, Olivia Kosche, Petra Steinacker, Vesile Sandikci, Rüstem Yilmaz

Brain Commun· November 2025

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Derivation and validation of a simple prognostic risk score to predict short-term mortality in acute cardiogenic pulmonary edema: the SABIHA score.
Kenan Toprak, Mustafa Kaplangöray, Mesut Karataş, Zuhal Fatma Cellat, Yakup Arğa

Clin Exp Emerg Med· September 2025

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Predictors of Length of Stay in Hospital After Transcatheter Aortic Valve Replacement: Impact of Naples Prognostic Score.
Faruk Boyacı, Murat Akcay, Mustafa Kursat Sahin, Mustafa Yenercag, Ahmet Karagoz, Rustem Yilmaz, Emre Kasim Yilmaz

Medicina (Kaunas)· September 2025

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Identifying similar populations across independent single cell studies without data integration.
Oscar González-Velasco, Malte Simon, Rüstem Yilmaz, Rosanna Parlato, Jochen Weishaupt

NAR Genom Bioinform· June 2025

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Prognostic Value of Non-Traditional Lipid Indices for In-Hospital Mortality in Patients with Acute Coronary Syndromes.
Rustem Yilmaz, Kenan Toprak, Ahmet Karagoz, Osman Can Yontar, Melisa Ucar, Mustafa Yilmaz

Medicina (Kaunas)· May 2025

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Comparison of the effect of uric acid/albumin ratio on coronary colleteral circulation with other inflammation-based markers in stable coronary artery disease patients.
Kenan Toprak, Rüstem Yılmaz, Mustafa Kaplangoray, Tolga Memioğlu, Mehmet İnanır

Perfusion· October 2024

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Investigation of the Usefulness of HALP Score in Predicting Short-Term Mortality in Patients with Acute Decompensated Heart Failure in a Coronary Care Unit.
Rustem Yilmaz, Kenan Toprak, Mustafa Yilmaz, Ahmet Karagoz, Ersoy Öz

Medicina (Kaunas)· August 2024

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Corrigendum: Analysis of hematological indicators via explainable artificial intelligence in the diagnosis of acute heart failure: a retrospective study.
Rustem Yilmaz, Fatma Hilal Yagin, Cemil Colak, Kenan Toprak, Nagwan Abdel Samee

Front Med (Lausanne)· June 2024

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A TBK1 variant causes autophagolysosomal and motoneuron pathology without neuroinflammation in mice.
David Brenner, Kirsten Sieverding, Jahnavi Srinidhi, Susanne Zellner, Christopher Secker, Rüstem Yilmaz, Deniz Yilmazer-Hanke

J Exp Med· May 2024

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Analysis of hematological indicators via explainable artificial intelligence in the diagnosis of acute heart failure: a retrospective study.
Rustem Yilmaz, Fatma Hilal Yagin, Cemil Colak, Kenan Toprak, Nagwan Abdel Samee

Front Med (Lausanne)· March 2024

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Comparison of Electrocardiographic Parameters by Gender in Heart Failure Patients with Preserved Ejection Fraction via Artificial Intelligence.
Rustem Yilmaz, Ersoy Öz

Diagnostics (Basel)· October 2023

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Frequency of and mutations in 302 sporadic ALS patients from three German ALS centers.
Rüstem Yilmaz, Torsten Grehl, Lukas Eckrich, Ines Marschalkowski, Kanchi Weishaupt

Amyotroph Lateral Scler Frontotemporal Degener· August 2023

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PSEN1/SLC20A2 double mutation causes early-onset Alzheimer's disease and primary familial brain calcification co-morbidity.
Sophie Hebestreit, Janine Schwahn, Vesile Sandikci, Mate E Maros, Ivan Valkadinov, Rüstem Yilmaz

Neurogenetics· July 2023

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ALS-linked KIF5A ΔExon27 mutant causes neuronal toxicity through gain-of-function.
Devesh C Pant, Janani Parameswaran, Lu Rao, Isabel Loss, Ganesh Chilukuri, Rüstem Yilmaz

EMBO Rep· August 2022

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Quadruple genetic variants in a sporadic ALS patient.
Rüstem Yilmaz, Kanchi Weishaupt, Ivan Valkadinov, Antje Knehr, David Brenner

Mol Genet Genomic Med· July 2022

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FUS mutations dominate TBK1 mutations in FUS/TBK1 double-mutant ALS/FTD pedigrees.
David Brenner, Kathrin Müller, Serena Lattante, Rüstem Yilmaz, Antje Knehr

Neurogenetics· January 2022

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Targeted Ablation of Primary Cilia in Differentiated Dopaminergic Neurons Reduces Striatal Dopamine and Responsiveness to Metabolic Stress.
Rasem Mustafa, Chahinaz Rawas, Nadja Mannal, Grzegorz Kreiner, Björn Spittau, Rüstem Yilmaz

Antioxidants (Basel)· August 2021

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The murine ortholog of Kaufman oculocerebrofacial syndrome protein Ube3b regulates synapse number by ubiquitinating Ppp3cc.
Mateusz C Ambrozkiewicz, Ekaterina Borisova, Manuela Schwark, Silvia Ripamonti, Theres Schaub, Rüstem Yilmaz

Mol Psychiatry· June 2021

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A novel nonsense variant in SLC24A4 causing a rare form of amelogenesis imperfecta in a Pakistani family.
Sher Alam Khan, Muhammad Adnan Khan, Nazif Muhammad, Hina Bashir, Niamat Khan, Rüstem Yilmaz

BMC Med Genet· May 2020

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SQSTM1/p62 variants in 486 patients with familial ALS from Germany and Sweden.
Rüstem Yilmaz, Kathrin Müller, David Brenner, Alexander E Volk, Guntram Borck

Neurobiol Aging· March 2020

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Reply: Adult-onset distal spinal muscular atrophy: a new phenotype associated with KIF5A mutations.
David Brenner, Angela Rosenbohm, Rüstem Yilmaz, Kathrin Müller, Torsten Grehl

Brain· December 2019

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Hot-spot KIF5A mutations cause familial ALS.
David Brenner, Rüstem Yilmaz, Kathrin Müller, Torsten Grehl, Susanne Petri

Brain· March 2018

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Kaufman oculocerebrofacial syndrome: Novel UBE3B mutations and clinical features in four unrelated patients.
Rüstem Yilmaz, Katalin Szakszon, Anna Altmann, Umut Altunoglu, Leyli Senturk

Am J Med Genet A· January 2018

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