Peter Krawitz - University of Bonn - Medical Center

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Bio

I am interested in filtering human exome data of patients with rare disorders. For this purpose we develop a web-based filtering and annotation tool, called GeneTalk: www.gene-talk.de Besides, I am interested in congenital and acquired GPI anchor deficiencies such as the hyperphosphatasia with mental retardation syndrome

Research Interests

Papers共 245 篇Author StatisticsCo-AuthorSimilar Experts

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Schneller Zur Genetischen Diagnose Bei Kindern Mit Auffälliger Fazies Durch Künstliche Intelligenz

Peter M. Krawitz, Adele Ruder,Tim Niehues

Monatsschrift Kinderheilkunde（2025）

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Perspectives on the Current and Future State of Artificial Intelligence in Medical Genetics

Benjamin D Solomon, Morgan Cheatham, Thales A C de Guimarães, Dat Duong,Melissa A Haendel, Tzung-Chien Hsieh, Behnam Javanmardi, Britt Johnson,Peter Krawitz,Paul Kruszka, Tim Laurent, Ni-Chung Lee,Kirsty McWalter, Michel Michaelides,Klaus Mohnike,Nikolas Pontikos, Maria J Guillen Sacoto, Yousif J Shwetar, Vincent D Ustach, Rebekah L Waikel,William Woof

American journal of medical genetics Part App.e64118-e64118, (2025)

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GestaltGAN: Synthetic Photorealistic Portraits of Individuals with Rare Genetic Disorders

Aron Kirchhoff,Alexander Hustinx,Behnam Javanmardi,Tzung-Chien Hsieh,Fabian Brand,Fabio Hellmann,Silvan Mertes,Elisabeth André,Shahida Moosa,Thomas Schultz,Benjamin D. Solomon,Peter Krawitz

European Journal of Human Geneticspp.1-6, (2025)

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Schneller Zur Genetischen Diagnose Bei Kindern Mit Auffälliger Fazies Durch Künstliche Intelligenz, Einsatz in Der Kinderarztpraxis

Peter M. Krawitz, Adele Ruder,Tim Niehues

MONATSSCHRIFT KINDERHEILKUNDE (2025)

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Penetrance of Parkinson's Disease in GBA1 Carriers is Depending on the Variant Severity and Polygenic Background

Emadeldin Hassanin,Zied Landoulsi,Sinthuja Pachchek,Peter Krawitz,Carlo Maj,Rejko Kruger,Patrick May,Dheeraj Reddy Bobbili

medrxiv（2025）

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Leveraging Next-Generation Phenotyping for ACMG Classification from VUS to Likely Pathogenic in Mowat-Wilson Syndrome

Tzung-Chien Hsieh,Dylan Todd,Taylor Warner, Kayla Blankenship,Dimah Saade, Hannah Weiland, Meghna Ahuja Bhasin,Hannah Klinkhammer,Jing-Mei Li,Peter Krawitz, Wei-Liang Chen,Ho-Ming Luk,Moon Ley Tung,Bharatendu Chandra

medrxiv（2025）

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Penetrance of Parkinson's Disease in GBA1 Carriers Depends on Variant Severity and Polygenic Background

Emadeldin Hassanin,Zied Landoulsi, Sinthuja Pachchek, NCER-PD Consortium,Peter Krawitz,Carlo Maj,Rejko Krüger,Patrick May,Dheeraj Reddy Bobbili

NPJ Parkinson's diseaseno. 1 (2025): 162-162

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GANonymization: A GAN-based Face Anonymization Framework for Preserving Emotional Expressions

Fabio Hellmann,Silvan Mertes,Mohamed Benouis,Alexander Hustinx,Tzung-Chien Hsieh,Cristina Conati,Peter Krawitz,Elisabeth André

ACM Trans Multim Comput Commun Appl（2025）

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Identification of Novel Proteomic Biomarkers for Hypertension: a Targeted Approach for Precision Medicine

Rana S. Aldisi,Alsamman M. Alsamman,Peter Krawitz,Carlo Maj,Hatem Zayed

Clinical Proteomicsno. 1 (2025): 1-11

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Pathogenic De Novo Variants in PPP2R5C Cause a Neurodevelopmental Disorder Within the Houge-Janssens Syndrome Spectrum

Iris Verbinnen,Sofia Douzgou Houge,Tzung-Chien Hsieh,Hellen Lesmann, Aron Kirchhoff,David Geneviève,Elise Brimble,Lisa Lenaerts,Dorien Haesen, Rebecca J Levy,Julien Thevenon,Laurence Faivre,Elysa Marco,Jessica X Chong,Mike Bamshad,Karynne Patterson,Ghayda M Mirzaa,Kimberly Foss,William Dobyns,Susan M White,Lynn Pais,Emily O'Heir,Raphaela Itzikowitz,Kirsten A Donald,Celia Van der Merwe,Alessandro Mussa, Raffaela Cervini,Elisa Giorgio,Tony Roscioli,Kerith-Rae Dias,Carey-Anne Evans,Natasha J Brown,Anna Ruiz,Juan Pablo Trujillo Quintero,Rachel Rabin,John Pappas, Hai Yuan,Katherine Lachlan,Simon Thomas, Anita Devlin,Michael Wright, Richard Martin, Joanna Karwowska,Renata Posmyk,Nicolas Chatron,Zornitza Stark, Oliver Heath,Martin Delatycki,Rebecca Buchert,Georg-Christoph Korenke,Keri Ramsey,Vinodh Narayanan,Dorothy K Grange,Judith L Weisenberg,Tobias B Haack,Stephanie Karch,Patricia Kipkemoi, Moses Mangi,Karen G C B Bindels de Heus,Marie-Claire Y de Wit,Tahsin Stefan Barakat,Derek Lim,Géraldine Van Winckel,Rebecca C Spillmann,Vandana Shashi,Maureen Jacob, Antonia M Stehr,Undiagnosed Diseases Network,Peter Krawitz,Gunnar Douzgos Houge,Veerle Janssens

American journal of human geneticsno. 3 (2025): 554-571

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