Klaudia Walter

ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 16

Top Venues

Nature genetics

Nature communications

PLoS genetics

Nature medicine

Wellcome Trust Sanger Institute

University of Cambridge (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Wellcome Trust Sanger Institute Aug 28 2007

United Kingdom

Senior Staff Scientist :: Human Genetics

Education History

University of Cambridge Oct 06 2003 - May 10 2008

United Kingdom

PHD :: MRC Biostatistics Unit

University of Sheffield Oct 01 2001 - Sep 30 2003

United Kingdom

MSC :: Statistics

Publications

Jing Guo, Klaudia Walter, Pedro M Quiros, Muxin Gu, E Joanna Baxter, John Danesh, Emanuele Di Angelantonio, David Roberts, Paola Guglielmelli, Claire N Harrison, Anna L Godfrey, Anthony R Green, George S Vassiliou, Dragana Vuckovic, Jyoti Nangalia, Nicole Soranzo
Inherited polygenic effects on common hematological traits influence clonal selection on JAK2 V617F and the development of myeloproliferative neoplasms. Nature genetics 56 (2) (2024)
Jing Guo, Klaudia Walter, Pedro M Quiros, Muxin Gu, E Joanna Baxter, John Danesh, Emanuele Di Angelantonio, David Roberts, Paola Guglielmelli, Claire N Harrison, Anna L Godfrey, Anthony R Green, George S Vassiliou, Dragana Vuckovic, Jyoti Nangalia, Nicole Soranzo
Inherited polygenic effects on common hematological traits influence clonal selection on JAK2 V617F and the development of myeloproliferative neoplasms. Nature genetics 56 (2) (2024)
Jing Guo, Klaudia Walter, Pedro M Quiros, Muxin Gu, E Joanna Baxter, John Danesh, Emanuele Di Angelantonio, David Roberts, Paola Guglielmelli, Claire N Harrison, Anna L Godfrey, Anthony R Green, George S Vassiliou, Dragana Vuckovic, Jyoti Nangalia, Nicole Soranzo
Inherited polygenic effects on common hematological traits influence clonal selection on JAK2 V617F and the development of myeloproliferative neoplasms. Nature genetics 56 (2) (2024)
Jing Guo, Klaudia Walter, Pedro M Quiros, Muxin Gu, E Joanna Baxter, John Danesh, Emanuele Di Angelantonio, David Roberts, Paola Guglielmelli, Claire N Harrison, Anna L Godfrey, Anthony R Green, George S Vassiliou, Dragana Vuckovic, Jyoti Nangalia, Nicole Soranzo
Inherited polygenic effects on common hematological traits influence clonal selection on JAK2 V617F and the development of myeloproliferative neoplasms. Nature genetics 56 (2) (2024)
Jing Guo, Klaudia Walter, Pedro M Quiros, Muxin Gu, E Joanna Baxter, John Danesh, Emanuele Di Angelantonio, David Roberts, Paola Guglielmelli, Claire N Harrison, Anna L Godfrey, Anthony R Green, George S Vassiliou, Dragana Vuckovic, Jyoti Nangalia, Nicole Soranzo
Inherited polygenic effects on common hematological traits influence clonal selection on JAK2 V617F and the development of myeloproliferative neoplasms. Nature genetics (2024)
Parsa Akbari, Dragana Vuckovic, Luca Stefanucci, Tao Jiang, Kousik Kundu, Roman Kreuzhuber, Erik L Bao, Janine H Collins, Kate Downes, Luigi Grassi, Jose Antonio Guerrero, Stephen Kaptoge, Julian C Knight, Stuart Meacham, Jennifer Sambrook, Denis Seyres, Oliver Stegle, Jeffrey M Verboon, Klaudia Walter, Nicholas A Watkins, John Danesh, David J Roberts, Emanuele Di Angelantonio, Vijay G Sankaran, Mattia Frontini, Stephen Burgess, Taco Kuijpers, James E Peters, Adam S Butterworth, Willem Hendrik Ouwehand, Nicole Soranzo, William John Astle
A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Nature communications 14 (1) (2023)
Kousik Kundu, Manuel Tardaguila, Alice L Mann, Stephen Watt, Hannes Ponstingl, Louella Vasquez, Dominique Von Schiller, Nicholas W Morrell, Oliver Stegle, Tomi Pastinen, Stephen J Sawcer, Carl A Anderson, Klaudia Walter, Nicole Soranzo
Genetic associations at regulatory phenotypes improve fine-mapping of causal variants for 12 immune-mediated diseases. Nature genetics 54 (3) (2022)
Guillaume Butler-Laporte, Gundula Povysil, Jack A Kosmicki, Elizabeth T Cirulli, Theodore G Drivas, Simone Furini, Chadi Saad, Axel Schmidt, Pawel Olszewski, Urszula Korotko, Mathieu Quinodoz, Elifnaz Celik, Kousik Kundu, Klaudia Walter, Junghyun Jung, Amy D Stockwell, Laura G Sloofman G Sloofman, Daniel M Jordan, Ryan C Thompson, Diane M Del Valle, Nicole W Simons, Esther Cheng, Robert Sebra, Eric E Schadt, Seunghee Kim-Schulze, Sacha Gnjatic, Miriam Merad, Joseph D Buxbaum, Noam D Beckmann, Alexander W Charney, Bartlomiej Przychodzen, Timothy S Chang, Tess D Pottinger, Ning Shang, Fabian Brand, Francesca Fava, Francesca Mari, Karolina Chwialkowska, Magdalena Niemira, Szymon Pula, J Kenneth Baillie, Alex Stuckey, Antonio Salas, Xabier Bello, Jacobo Pardo-Seco, Alberto Gómez-Carballa, Irene Rivero-Calle, Federico Martinón-Torres, Andrea Ganna, Konrad J Karczewski, Kumar Veerapen, Mathieu Bourgey, Guillaume Bourque, Robert Jm Eveleigh, Vincenzo Forgetta, David R Morrison, David Langlais, Mark Lathrop, Vincent Mooser, Tomoko Nakanishi, Robert Frithiof, Michael Hultström, Miklos Lipcsey, Yanara Marincevic-Zuniga, Jessica Nordlund, Kelly M Schiabor Barrett, William Lee, Alexandre Bolze, Simon White, Stephen Riffle, Francisco Tanudjaja, Efren Sandoval, Iva Neveux, Shaun Dabe, Nicolas Casadei, Susanne Motameny, Manal Alaamery, Salam Massadeh, Nora Aljawini, Mansour S Almutairi, Yaseen M Arabi, Saleh A Alqahtani, Fawz S Al Harthi, Amal Almutairi, Fatima Alqubaishi, Sarah Alotaibi, Albandari Binowayn, Ebtehal A Alsolm, Hadeel El Bardisy, Mohammad Fawzy, Fang Cai, Nicole Soranzo, Adam Butterworth, null null, null null, null null, null null, null null, null null, null null, null null, Daniel H Geschwind, Stephanie A Arteaga, Alexis Stephens, Manish J Butte, Paul C Boutros, Takafumi N Yamaguchi, Shu Tao, Stefan E Eng, Timothy Sanders, Paul J Tung, Michael E Broudy, Yu Pan, Alfredo E Gonzalez, Nikhil Chavan, Ruth Johnson, Bogdan Pasaniuc, Brian L Yaspan, Christos M Polymeropoulos, Carlo Rivolta, Stephanie Bibert, Pierre-Yves Bochud, Maciej Dąbrowski, Pawel Zawadzki, Mateusz Sypniewski, Elżbieta Kaja, Pajaree Chariyavilaskul, Voraphoj Nilaratanakul, Nattiya Hirankarn, Vorasuk Shotelersuk, Monnat Pongpanich, Chureerat Phokaew, Wanna Chetruengchai, Katsushi Tokunaga, Masaya Sugiyama, Yosuke Kawai, Takanori Hasegawa, Tatsuhiko Naito, Ho Namkoong, Ryuya Edahiro, Akinori Kimura, Seishi Ogawa, Takanori Kanai, Koichi Fukunaga, Yukinori Okada, Seiya Imoto, Satoru Miyano, Serghei Mangul, Malak S Abedalthagafi, Hugo Zeberg, Joseph J Grzymski, Nicole L Washington, Stephan Ossowski, Kerstin U Ludwig, Eva C Schulte, Olaf Riess, Marcin Moniuszko, Miroslaw Kwasniewski, Hamdi Mbarek, Said I Ismail, Anurag Verma, David B Goldstein, Krzysztof Kiryluk, Alessandra Renieri, Manuel A R Ferreira, John Brent Richards
Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative. PLoS genetics 18 (11) (2022)
Lucy J Goudswaard, Joshua A Bell, David A Hughes, Laura J Corbin, Klaudia Walter, George Davey Smith, Nicole Soranzo, John Danesh, Emanuele Di Angelantonio, Willem Hendrik Ouwehand, Nicholas A Watkins, David J Roberts, Adam S Butterworth, Ingeborg Hers, Nicholas John Timpson
Effects of adiposity on the human plasma proteome: observational and Mendelian randomisation estimates. International journal of obesity (2005) 45 (10) (2021)
Stephen Watt, Louella Vasquez, Klaudia Walter, Alice L Mann, Kousik Kundu, Lu Chen, Ying Sims, Simone Ecker, Frances Burden, Samantha Farrow, Ben Farr, Valentina Iotchkova, Heather Elding, Daniel Mead, Manuel Tardaguila, Hannes Ponstingl, David Richardson, Avik Datta, Paul Flicek, Laura Clarke, Kate Downes, Tomi Pastinen, Peter Fraser, Mattia Frontini, Biola-Maria Javierre, Mikhail Spivakov, Nicole Soranzo
Genetic perturbation of PU.1 binding and chromatin looping at neutrophil enhancers associates with autoimmune disease. Nature communications 12 (1) (2021)
Na Cai, Aurora Gomez-Duran, Ekaterina Yonova-Doing, Kousik Kundu, Annette I Burgess, Zoe J Golder, Claudia Calabrese, Marc J Bonder, Marta Camacho, Rachael A Lawson, Lixin Li, Caroline H Williams-Gray, null null, Emanuele Di Angelantonio, David J Roberts, Nick A Watkins, Willem H Ouwehand, Adam S Butterworth, Isobel D Stewart, Maik Pietzner, Nicholas J Wareham, Claudia Langenberg, John Danesh, Klaudia Walter, Peter M Rothwell, Joanna M M Howson, Oliver Stegle, Patrick F Chinnery, Nicole Soranzo
Mitochondrial DNA variants modulate N-formylmethionine, proteostasis and risk of late-onset human diseases. Nature medicine 27 (9) (2021)
Fernando Riveros-McKay, Clare Oliver-Williams, Savita Karthikeyan, Klaudia Walter, Kousik Kundu, Willem Hendrik Ouwehand, David Roberts, Emanuele Di Angelantonio, Nicole Soranzo, John Danesh, null null, Eleanor Wheeler, Eleftheria Zeggini, Adam S Butterworth, Inês A Barroso
The influence of rare variants in circulating metabolic biomarkers. PLoS genetics 16 (3) (2020)
Valentina Iotchkova, Graham R S Ritchie, Matthias Geihs, Sandro Morganella, Josine L Min, Klaudia Walter, Nicholas John Timpson, null null, Ian Dunham, Ewan Birney, Nicole Soranzo
GARFIELD classifies disease-relevant genomic features through integration of functional annotations with association signals. Nature genetics 51 (2) (2019)
Arthur Gilly, Daniel Suveges, Karoline Kuchenbaecker, Martin O Pollard, Lorraine Southam, Konstantinos Hatzikotoulas, Aliki-Eleni Farmaki, Thea Bjornland, Ryan Waples, Emil Vincent R Appel, Elisabetta Casalone, Giorgio E M Melloni, Britt Kilian, Nigel W Rayner, Ioanna Ntalla, Kousik Kundu, Klaudia Walter, John Danesh, Adam S Butterworth, Inês A Barroso, Emmanouil Tsafantakis, George Dedoussis, Ida Moltke, Eleftheria Zeggini
Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits. Nature communications 9 (1) (2018)
Arthur Gilly, Daniel Suveges, Karoline Kuchenbaecker, Martin O Pollard, Lorraine Southam, Konstantinos Hatzikotoulas, Aliki-Eleni Farmaki, Thea Bjornland, Ryan Waples, Emil Vincent R Appel, Elisabetta Casalone, Giorgio E M Melloni, Britt Kilian, Nigel W Rayner, Ioanna Ntalla, Kousik Kundu, Klaudia Walter, John Danesh, Adam S Butterworth, Inês A Barroso, Emmanouil Tsafantakis, George Dedoussis, Ida Moltke, Eleftheria Zeggini
Author Correction: Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits. Nature communications 9 (1) (2018)
Himanshu Chheda, Priit Palta, Matti Pirinen, Shane A McCarthy, Klaudia Walter, Seppo Koskinen, Veikko Salomaa, Mark Daly, Richard Durbin, Aarno Palotie, Tero Aittokallio, Samuli Ripatti
Whole-genome view of the consequences of a population bottleneck using 2926 genome sequences from Finland and United Kingdom. European journal of human genetics : EJHG 25 (4) (2017)

Klaudia Walter.css-eqlu8i{font-size:small;padding-left:4px;}

Publication Activity (10 Years)

Top Topics

Top Venues

Klaudia Walter