Kurth, Ingo

Severe COVID-19 Is Marked by a Dysregulated Myeloid Cell Compartment

Schulte-Schrepping, J., Reusch, N., Paclik, D., Baßler, K., Schlickeiser, S., Zhang, B., Krämer, B., Krammer, T., Brumhard, S., Bonaguro, L., et al. (2020) · Cell

COVID-19 Clinical Research StudiesSARS-CoV-2 and COVID-19 Research

Cited by 1,461

Regulation of endoplasmic reticulum turnover by selective autophagy

Khaminets, A., Heinrich, T., Mari, M., Grumati, P., Huebner, A. K., Akutsu, M., Liebmann, L., Stolz, A., Nietzsche, S., Koch, N., et al. (2015) · Nature

Autophagy in Disease and TherapyEndoplasmic Reticulum Stress and Disease

Cited by 956

Swarm Learning for decentralized and confidential clinical machine learning

Warnat-Herresthal, S., Schultze, H., Shastry, K. L., Manamohan, S., Mukherjee, S., Garg, V., Sarveswara, R., Händler, K., Pickkers, P., Aziz, N. A., et al. (2021) · Nature

Privacy-Preserving Technologies in DataBlockchain Technology Applications and Security

Cited by 884

Formation of new chromatin domains determines pathogenicity of genomic duplications

Franke, M., Ibrahim, D. M., Andrey, G., Schwarzer, W., Heinrich, V., Schöpflin, R., Kraft, K., Kempfer, R., Jerković, I., Chan, W.-L., et al. (2016) · Nature

Genomics and Chromatin DynamicsGenomic variations and chromosomal abnormalities

Cited by 673

Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome

Kim, H.-G., Kurth, I., Lan, F., Meliciani, I., Wenzel, W., Eom, S. H., Kang, G. B., Rosenberger, G., Tekin, M., Ozata, M., et al. (2008) · The American Journal of Human Genetics

Congenital Ear and Nasal AnomaliesHypothalamic control of reproductive hormones

Cited by 338

Mutations in FAM134B, encoding a newly identified Golgi protein, cause severe sensory and autonomic neuropathy

Kurth, I., Pamminger, T., Hennings, J. C., Soehendra, D., Huebner, A. K., Rotthier, A., Baets, J., Senderek, J., Topaloglu, H., Farrell, S. A., et al. (2009) · Nature Genetics

Hereditary Neurological DisordersPain Mechanisms and Treatments

Cited by 260

WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome

Kim, H.-G., Ahn, J.-W., Kurth, I., Ullmann, R., Kim, H.-T., Kulharya, A., Ha, K.-S., Itokawa, Y., Meliciani, I., Wenzel, W., et al. (2010) · The American Journal of Human Genetics

Hypothalamic control of reproductive hormonesGenetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Cited by 195

Sensory neuropathy with bone destruction due to a mutation in the membrane-shaping atlastin GTPase 3

Kornak, U., Mademan, I., Schinke, M., Voigt, M., Krawitz, P., Hecht, J., Barvencik, F., Schinke, T., Gießelmann, S., Beil, F. T., et al. (2014) · Brain

Hereditary Neurological DisordersCellular transport and secretion

Cited by 109

Diagnosing small fiber neuropathy in clinical practice: a deep phenotyping study

Egenolf, N., Altenschildesche, C. M. Z., Kreß, L., Eggermann, K., Namer, B., Gross, F., Klitsch, A., Malzacher, T., Kampik, D., Malik, R. A., et al. (2021) · Therapeutic Advances in Neurological Disorders

Hereditary Neurological DisordersPain Mechanisms and Treatments

Cited by 72

Rdh12 activity and effects on retinoid processing in the murine retina

Chrispell, J. D., Feathers, K. L., Kane, M. A., Kim, C. Y., Brooks, M., Khanna, R., Kurth, I., Hübner, C. A., Gal, A., Mears, A. J., et al. (2009) · Journal of Biological Chemistry

Retinal Development and DisordersRetinoids in leukemia and cellular processes

Cited by 56

A disease causing ATLASTIN 3 mutation affects multiple endoplasmic reticulum-related pathways

Behrendt, L., Kurth, I., & Kaether, C. (2019) · Cellular and Molecular Life Sciences

Hereditary Neurological DisordersCellular transport and secretion

Cited by 48

ADGRL1 haploinsufficiency causes a variable spectrum of neurodevelopmental disorders in humans and alters synaptic activity and behavior in a mouse model

Vitobello, A., Mazel, B., Lelianova, V. G., Zangrandi, A., Petitto, E., Suckling, J., Salpietro, V., Meyer, R., Elbracht, M., Kurth, I., et al. (2022) · The American Journal of Human Genetics

Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research

Cited by 46

Sensory neuropathy-causing mutations in ATL3 affect ER–mitochondria contact sites and impair axonal mitochondrial distribution

Krols, M., Asselbergh, B., De Rycke, R., De Winter, V., Seyer, A., Müller, F.-J., Kurth, I., Bultynck, G., Timmerman, V., & Janssens, S. (2019) · Human Molecular Genetics

Hereditary Neurological DisordersMitochondrial Function and Pathology

Cited by 40

Label-free single-cell RNA multiplexing leveraging genetic variability

Hoeft, K., Bleckwehl, T., Schumacher, D., Kim, H., Meyer, R., Long, Q., Zhang, L., Möller, C., Clahsen-van Groningen, M. C., Babler, A., et al. (2024) · Nature Communications

Single-cell and spatial transcriptomicsGenomics and Phylogenetic Studies

Cited by 3

Utilizing protein structure graph embeddings to predict the pathogenicity of missense variants

Danner, M., Begemann, M., Elbracht, M., Kurth, I., & Krause, J. (2025) · NAR Genomics and Bioinformatics

Genomics and Rare DiseasesProtein Structure and Dynamics

Cited by 2