William G Newman (W G Newman, William Newman)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 47

Top Venues

Clinical genetics

The pharmacogenomics journal

European journal of human genetics : EJHG

Journal of medical genetics

University of Manchester (PHD)

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

Education History

University of Manchester Mar 01 2004

United Kingdom

PHD :: Manchester Centre for Genomic Medicine

Publications

Rabia Faridi, Pamela Stratton, Noemi Salmeri, Robert J Morell, Asma Ali Khan, Muhammad A Usmani, William G Newman, Sheikh Riazuddin, Thomas B Friedman
Homozygous novel truncating variant of CLPP associated with severe Perrault syndrome. Clinical genetics 105 (5) (2024)
John Henry McDermott, Videha Sharma, Glenda M Beaman, Jessica Keen, William G Newman, Paul Wilson, Katherine Payne, Stuart Wright
Understanding general practitioner and pharmacist preferences for pharmacogenetic testing in primary care: a discrete choice experiment. The pharmacogenomics journal 24 (5) (2024)
Videha Sharma, John Henry McDermott, Jessica Keen, Simon Foster, Pauline Whelan, William G Newman
Pharmacogenetics Clinical Decision Support Systems for Primary Care in England: Co-Design Study. Journal of medical Internet research 26 (2024)
John Henry McDermott, Videha Sharma, Glenda M Beaman, Jessica Keen, William G Newman, Paul Wilson, Katherine Payne, Stuart Wright
Understanding general practitioner and pharmacist preferences for pharmacogenetic testing in primary care: a discrete choice experiment. The pharmacogenomics journal 24 (5) (2024)
John Henry McDermott, Videha Sharma, Glenda M Beaman, Jessica Keen, William G Newman, Paul Wilson, Katherine Payne, Stuart Wright
Understanding general practitioner and pharmacist preferences for pharmacogenetic testing in primary care: a discrete choice experiment. The pharmacogenomics journal 24 (5) (2024)
Rabia Faridi, Pamela Stratton, Noemi Salmeri, Robert J Morell, Asma Ali Khan, Muhammad A Usmani, William G Newman, Sheikh Riazuddin, Thomas B Friedman
Homozygous novel truncating variant of CLPP associated with severe Perrault syndrome. Clinical genetics (2024)
Rabia Faridi, Pamela Stratton, Noemi Salmeri, Robert J Morell, Asma Ali Khan, Muhammad A Usmani, William G Newman, Sheikh Riazuddin, Thomas B Friedman
Homozygous novel truncating variant of CLPP associated with severe Perrault syndrome. Clinical genetics 105 (5) (2024)
Rabia Faridi, Pamela Stratton, Noemi Salmeri, Robert J Morell, Asma Ali Khan, Muhammad A Usmani, William G Newman, Sheikh Riazuddin, Thomas B Friedman
Homozygous novel truncating variant of CLPP associated with severe Perrault syndrome. Clinical genetics 105 (5) (2024)
Marc Leach, William G Newman, John Henry McDermott
Rapid point of care testing: the next frontier in pharmacogenomics. Pharmacogenomics (2024)
Videha Sharma, John Henry McDermott, Jessica Keen, Simon Foster, Pauline Whelan, William G Newman
Pharmacogenetics Clinical Decision Support Systems for Primary Care in England: Co-Design Study. Journal of medical Internet research 26 (2024)
Rabia Faridi, Pamela Stratton, Noemi Salmeri, Robert J Morell, Asma Ali Khan, Muhammad A Usmani, William G Newman, Sheikh Riazuddin, Thomas B Friedman
Homozygous novel truncating variant of CLPP associated with severe Perrault syndrome. Clinical genetics 105 (5) (2024)
Rabia Faridi, Pamela Stratton, Noemi Salmeri, Robert J Morell, Asma Ali Khan, Muhammad A Usmani, William G Newman, Sheikh Riazuddin, Thomas B Friedman
Homozygous novel truncating variant of CLPP associated with severe Perrault syndrome. Clinical genetics 105 (5) (2024)
Taru A Muranen, Anna Morra, Sofia Khan, Daniel R Barnes, Manjeet K Bolla, Joe G Dennis, Renske Keeman, Goska Leslie, Michael T Parsons, Qin Wang, Thomas U Ahearn, Kristiina Aittomäki, Irene L Andrulis, Banu K Arun, Sabine Behrens, Katarzyna Bialkowska, Stig E Bojesen, Nicola J Camp, Jenny Chang-Claude, Kamila Czene, Peter Devilee, null null, Susan M Domchek, Alison M Dunning, Christoph Engel, Dafydd Gareth Evans, Manuela Gago-Dominguez, Montserrat Garcia-Closas, Anne-Marie Gerdes, Gord Glendon, Pascal Guénel, Eric Hahnen, Ute Hamann, Helen Hanson, Maartje J Hooning, Reiner Hoppe, Louise Izatt, Anna Jakubowska, Paul A James, Vessela N Kristensen, Fiona Lalloo, Geoffrey J Lindeman, Arto Mannermaa, Sara Margolin, Susan L Neuhausen, William G Newman, Paolo Peterlongo, Kelly-Anne Phillips, Miquel Angel Pujana, Johanna Rantala, Karina Rønlund, Emmanouil Saloustros, Rita K Schmutzler, Andreas Schneeweiss, Christian F Singer, Maija Suvanto, Yen Yen Tan, Manuel R Teixeira, Mads Thomassen, Marc Tischkowitz, Vishakha Tripathi, Barbara Wappenschmidt, Emily Zhao, Douglas F Easton, Antonis C Antoniou, Georgia Chenevix-Trench, Paul David Peter Pharoah, Marjanka K Schmidt, Carl Blomqvist, Heli Nevanlinna
PREDICT validity for prognosis of breast cancer patients with pathogenic BRCA1/2 variants. NPJ breast cancer 9 (1) (2023)
Gisella Figlioli, Amandine Billaud, Thomas U Ahearn, Natalia N Antonenkova, Heiko Becher, Matthias W Beckmann, Sabine Behrens, Javier Benitez, Marina Bermisheva, Marinus J Blok, Natalia V Bogdanova, Bernardo Bonanni, Barbara Burwinkel, Nicola J Camp, Archie Campbell, Jose E Castelao, Melissa H Cessna, Stephen J Chanock, null null, Kamila Czene, Peter Devilee, Thilo Dörk, Christoph Engel, Mikael Eriksson, Peter Andreas Fasching, Jonine D Figueroa, Marike Gabrielson, Manuela Gago-Dominguez, Montserrat García-Closas, Anna González-Neira, Felix Grassmann, Pascal Guénel, Melanie Gündert, Andreas Hadjisavvas, Eric Hahnen, Per Hall, Ute Hamann, Patricia A Harrington, Wei He, Peter Hillemanns, Antoinette Hollestelle, Maartje J Hooning, Reiner Hoppe, Anthony Howell, Keith Humphreys, null null, Agnes Jager, Anna Jakubowska, Elza K Khusnutdinova, Yon-Dschun Ko, Vessela N Kristensen, Annika Lindblom, Jolanta Lissowska, Jan Lubiński, Arto Mannermaa, Siranoush Manoukian, Sara Margolin, Dimitrios Mavroudis, William G Newman, Nadia Obi, Mihalis I Panayiotidis, Muhammad Usman Rashid, Valerie Rhenius, Matti A Rookus, Emmanouil Saloustros, Elinor J Sawyer, Rita K Schmutzler, Mitul Shah, Reijo Sironen, Melissa C Southey, Maija Suvanto, Rob A E M Tollenaar, Ian Tomlinson, Thérèse Truong, Lizet E van der Kolk, Elke M van Veen, Barbara Wappenschmidt, Xiaohong R Yang, Manjeet K Bolla, Joe G Dennis, Alison M Dunning, Douglas F Easton, Michael Lush, Kyriaki Michailidou, Paul David Peter Pharoah, Qin Wang, Muriel A Adank, Marjanka K Schmidt, Irene L Andrulis, Jenny Chang-Claude, Heli Nevanlinna, Georgia Chenevix-Trench, D Gareth Evans, Jonathan Beesley, Paolo Radice, Paolo Peterlongo
FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women. European journal of human genetics : EJHG (2023)
Gisella Figlioli, Amandine Billaud, Thomas U Ahearn, Natalia N Antonenkova, Heiko Becher, Matthias W Beckmann, Sabine Behrens, Javier Benitez, Marina Bermisheva, Marinus J Blok, Natalia V Bogdanova, Bernardo Bonanni, Barbara Burwinkel, Nicola J Camp, Archie Campbell, Jose E Castelao, Melissa H Cessna, Stephen J Chanock, null null, Kamila Czene, Peter Devilee, Thilo Dörk, Christoph Engel, Mikael Eriksson, Peter Andreas Fasching, Jonine D Figueroa, Marike Gabrielson, Manuela Gago-Dominguez, Montserrat García-Closas, Anna González-Neira, Felix Grassmann, Pascal Guénel, Melanie Gündert, Andreas Hadjisavvas, Eric Hahnen, Per Hall, Ute Hamann, Patricia A Harrington, Wei He, Peter Hillemanns, Antoinette Hollestelle, Maartje J Hooning, Reiner Hoppe, Anthony Howell, Keith Humphreys, null null, Agnes Jager, Anna Jakubowska, Elza K Khusnutdinova, Yon-Dschun Ko, Vessela N Kristensen, Annika Lindblom, Jolanta Lissowska, Jan Lubiński, Arto Mannermaa, Siranoush Manoukian, Sara Margolin, Dimitrios Mavroudis, William G Newman, Nadia Obi, Mihalis I Panayiotidis, Muhammad Usman Rashid, Valerie Rhenius, Matti A Rookus, Emmanouil Saloustros, Elinor J Sawyer, Rita K Schmutzler, Mitul Shah, Reijo Sironen, Melissa C Southey, Maija Suvanto, Rob A E M Tollenaar, Ian Tomlinson, Thérèse Truong, Lizet E van der Kolk, Elke M van Veen, Barbara Wappenschmidt, Xiaohong R Yang, Manjeet K Bolla, Joe G Dennis, Alison M Dunning, Douglas F Easton, Michael Lush, Kyriaki Michailidou, Paul David Peter Pharoah, Qin Wang, Muriel A Adank, Marjanka K Schmidt, Irene L Andrulis, Jenny Chang-Claude, Heli Nevanlinna, Georgia Chenevix-Trench, D Gareth Evans, Jonathan Beesley, Paolo Radice, Paolo Peterlongo
FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women. European journal of human genetics : EJHG (2023)
Gisella Figlioli, Amandine Billaud, Qin Wang, Manjeet K Bolla, Joe G Dennis, Michael Lush, Anders Kvist, Muriel A Adank, Thomas U Ahearn, Natalia N Antonenkova, Päivi Auvinen, Sabine Behrens, Marina Bermisheva, Natalia V Bogdanova, Stig E Bojesen, Bernardo Bonanni, Thomas Brüning, Nicola J Camp, Archie I Campbell, Jose E Castelao, Melissa H Cessna, null Nbcs Collaborators, Kamila Czene, Peter Devilee, Thilo Dörk, Mikael Eriksson, Peter Andreas Fasching, Henrik Flyger, Marike Gabrielson, Manuela Gago-Dominguez, Montserrat García-Closas, Gord Glendon, Encarna B Gómez Garcia, Anna González-Neira, Felix Grassmann, Pascal Guénel, Eric Hahnen, Ute Hamann, Peter Hillemanns, Maartje J Hooning, Reiner Hoppe, Anthony Howell, Keith Humphreys, null kConFab Investigators, Anna Jakubowska, Elza K Khusnutdinova, Vessela N Kristensen, Annika Lindblom, Maria A Loizidou, Jan Lubiński, Arto Mannermaa, Tabea Maurer, Dimitrios Mavroudis, William G Newman, Nadia Obi, Mihalis I Panayiotidis, Paolo Radice, Muhammad Usman Rashid, Valerie Rhenius, Matthias Ruebner, Emmanouil Saloustros, Elinor J Sawyer, Marjanka K Schmidt, Rita K Schmutzler, Mitul Shah, Melissa C Southey, Ian Tomlinson, Thérèse Truong, Elke Maria van Veen, Camilla Wendt, Xiaohong R Yang, Kyriaki Michailidou, Alison M Dunning, Paul David Peter Pharoah, Douglas F Easton, Irene L Andrulis, Dafydd Gareth Evans, Antoinette Hollestelle, Jenny Chang-Claude, Roger L Milne, Paolo Peterlongo
Spectrum and Frequency of Germline FANCM Protein-Truncating Variants in 44,803 European Female Breast Cancer Cases. Cancers 15 (13) (2023)
Taru A Muranen, Anna Morra, Sofia Khan, Daniel R Barnes, Manjeet K Bolla, Joe G Dennis, Renske Keeman, Goska Leslie, Michael T Parsons, Qin Wang, Thomas U Ahearn, Kristiina Aittomäki, Irene L Andrulis, Banu K Arun, Sabine Behrens, Katarzyna Bialkowska, Stig E Bojesen, Nicola J Camp, Jenny Chang-Claude, Kamila Czene, Peter Devilee, null null, Susan M Domchek, Alison M Dunning, Christoph Engel, Dafydd Gareth Evans, Manuela Gago-Dominguez, Montserrat Garcia-Closas, Anne-Marie Gerdes, Gord Glendon, Pascal Guénel, Eric Hahnen, Ute Hamann, Helen Hanson, Maartje J Hooning, Reiner Hoppe, Louise Izatt, Anna Jakubowska, Paul A James, Vessela N Kristensen, Fiona Lalloo, Geoffrey J Lindeman, Arto Mannermaa, Sara Margolin, Susan L Neuhausen, William G Newman, Paolo Peterlongo, Kelly-Anne Phillips, Miquel Angel Pujana, Johanna Rantala, Karina Rønlund, Emmanouil Saloustros, Rita K Schmutzler, Andreas Schneeweiss, Christian F Singer, Maija Suvanto, Yen Yen Tan, Manuel R Teixeira, Mads Thomassen, Marc Tischkowitz, Vishakha Tripathi, Barbara Wappenschmidt, Emily Zhao, Douglas F Easton, Antonis C Antoniou, Georgia Chenevix-Trench, Paul David Peter Pharoah, Marjanka K Schmidt, Carl Blomqvist, Heli Nevanlinna
PREDICT validity for prognosis of breast cancer patients with pathogenic BRCA1/2 variants. NPJ breast cancer 9 (1) (2023)
Hagai Levi, Shai Carmi, Saharon Rosset, Rinat Yerushalmi, Aviad Zick, Tamar Yablonski-Peretz, null null, Qin Wang, Manjeet K Bolla, Joe Dennis, Kyriaki Michailidou, Michael Lush, Thomas Ahearn, Irene L Andrulis, Hoda Anton-Culver, Antonis C Antoniou, Volker Arndt, Annelie Augustinsson, Päivi Auvinen, Laura Beane Freeman, Matthias Beckmann, Sabine Behrens, Marina Bermisheva, Clara Bodelon, Natalia V Bogdanova, Stig E Bojesen, Hermann Brenner, Helen Byers, Nicola Camp, Jose Castelao, Jenny Chang-Claude, María-Dolores Chirlaque, Wendy Chung, Christine Clarke, null null, Margriet J Collee, Sarah Colonna, null null, Fergus Couch, Angela Cox, Simon S Cross, Kamila Czene, Mary Daly, Peter Devilee, Thilo Dork, Laure Dossus, Diana M Eccles, A Heather Eliassen, Mikael Eriksson, Gareth Evans, Peter Fasching, Olivia Fletcher, Henrik Flyger, Lin Fritschi, Marike Gabrielson, Manuela Gago-Dominguez, Montserrat García-Closas, Jose Angel Garcia-Saenz, Jeanine Genkinger, Graham G Giles, Mark Goldberg, Pascal Guénel, Per Hall, Ute Hamann, Wei He, Peter Hillemanns, Antoinette Hollestelle, Reiner Hoppe, John Hopper, null null, Simona Jakovchevska, Anna Jakubowska, Helena Jernström, Esther John, Nichola Johnson, Michael Jones, Joseph Vijai, Rudolf Kaaks, Elza Khusnutdinova, Cari Kitahara, Stella Koutros, Vessela Kristensen, Allison W Kurian, James Lacey, Diether Lambrechts, Loic Le Marchand, Flavio Lejbkowicz, Annika Lindblom, Sibylle Loibl, Adriana Lori, Jan Lubinski, Arto Mannermaa, Mehdi Manoochehri, Dimitrios Mavroudis, Usha Menon, AnnaMarie Mulligan, Rachel Murphy, Ines Nevelsteen, William G Newman, Nadia Obi, Katie O'Brien, Ken Offit, Andrew Olshan, Dijana Plaseska-Karanfilska, Janet Olson, Salvatore Panico, Tjoung-Won Park-Simon, Alpa Patel, Paolo Peterlongo, Brigitte Rack, Paolo Radice, Gad Rennert, Valerie Rhenius, Atocha Romero, Emmanouil Saloustros, Dale Sandler, Marjanka K Schmidt, Lukas Schwentner, Mitul Shah, Priyanka Sharma, Jacques Simard, Melissa Southey, Jennifer Stone, William J Tapper, Jack Taylor, Lauren Teras, Amanda E Toland, Melissa Troester, Thérèse Truong, Lizet E van der Kolk, Clarice Weinberg, Camilla Wendt, Xiaohong Rose Yang, Wei Zheng, Argyrios Ziogas, Alison M Dunning, Paul Pharoah, Douglas F Easton, Shay Ben-Sachar, Naama Elefant, Ron Shamir, Ran Elkon
Evaluation of European-based polygenic risk score for breast cancer in Ashkenazi Jewish women in Israel. Journal of medical genetics (2023)
Thomas B Smith, Alessandro Rea, Huw B Thomas, Kyle Thompson, Monika Oláhová, Reza Maroofian, Mina Zamani, Langping He, Saeid Sadeghian, Hamid Galehdari, Nava Shaul Lotan, Tal Gilboa, Kristin C Herman, Thomas J McCorvie, Wyatt W Yue, Henry Houlden, Robert W Taylor, William G Newman, Raymond T O'Keefe
Novel homozygous variants in PRORP expand the genotypic spectrum of combined oxidative phosphorylation deficiency 54. European journal of human genetics : EJHG (2023)
Dafydd Gareth Evans, George Joseph Burghel, Helene Schlecht, Elaine F Harkness, Ashu Gandhi, Sacha J Howell, Anthony Howell, Claire Forde, Fiona Lalloo, William G Newman, Miriam Jane Smith, Emma Roisin Woodward
Detection of pathogenic variants in breast cancer susceptibility genes in bilateral breast cancer. Journal of medical genetics (2023)
Kah Ying Ng, Guleycan Lutfullahoglu Bal, Uwe Richter, Omid Safronov, Lars Paulin, Cory D Dunn, Ville O Paavilainen, Julie Richer, William G Newman, Robert W Taylor, Brendan J Battersby
Nonstop mRNAs generate a ground state of mitochondrial gene expression noise. Science advances 8 (46) (2022)
Shalini S Nayak, Robert Harkness, Anju Shukla, Siddharth Banka, William G Newman, Katta Mohan Girisha
Clinically diverse and perinatally lethal syndromes with urorectal septum malformation sequence. American journal of medical genetics. Part A (2022)
Faisal Albalwy, J H McDermott, William G Newman, A Brass, A Davies
A blockchain-based framework to support pharmacogenetic data sharing. The pharmacogenomics journal 22 (5-6) (2022)
Enrico Mingardo, Glenda Beaman, Phillip Grote, Agneta Nordenskjöld, William G Newman, Adrian S Woolf, Markus Eckstein, Alina C Hilger, Gabriel C Dworschak, Wolfgang Rösch, Anne-Karolin Ebert, Raimund Stein, Alfredo Brusco, Massimo Di Grazia, Ali Tamer, Federico M Torres, Jose L Hernandez, Philipp Erben, Carlo Maj, Jose M Olmos, Jose A Riancho, Carmen Valero, Isabel Charlotte Hostettler, Henry Houlden, David John Werring, Johannes Schumacher, Jan Gehlen, Ann-Sophie Giel, Benedikt C Buerfent, Samara Arkani, Elisabeth Åkesson, Emilia Rotstein, Michael Ludwig, Gundela Holmdahl, Elisa Giorgio, Alfredo Berettini, David Keene, Raimondo M Cervellione, Nina Younsi, Melissa Ortlieb, Josef Oswald, Bernhard Haid, Martin Promm, Claudia Neissner, Karin Hirsch, Maximilian Stehr, Frank-Mattias Schäfer, Eberhard Schmiedeke, Thomas M Boemers, Iris A L M van Rooij, Wouter F J Feitz, Carlo L M Marcelis, Martin Lacher, Jana Nelson, Benno Ure, Caroline Fortmann, Daniel P Gale, Melanie M Y Chan, Kerstin U Ludwig, Markus Maria Nöthen, Stefanie Heilmann-Heimbach, Nadine Zwink, Ekkehart Jenetzky, Benjamin Odermatt, Michael Knapp, Heiko Martin Reutter
A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy. Communications biology 5 (1) (2022)
Sam Hodgson, Qin Qin Huang, Neneh Sallah, null null, Chris J Griffiths, William G Newman, Richard C Trembath, John Wright, R Thomas Lumbers, Karoline B Kuchenbaecker, David A van Heel, Rohini Mathur, Hilary C Martin, Sarah Finer
Integrating polygenic risk scores in the prediction of type 2 diabetes risk and subtypes in British Pakistanis and Bangladeshis: A population-based cohort study. PLoS medicine 19 (5) (2022)
Judith Hayward, John Henry McDermott, Nadeem Qureshi, William G Newman
Pharmacogenomic testing to support prescribing in primary care: a structured review of implementation models. Pharmacogenomics 22 (12) (2021)
Hanla A Park, Sonja Neumeyer, Kyriaki Michailidou, Manjeet K Bolla, Qin Wang, Joe G Dennis, Thomas U Ahearn, Irene L Andrulis, Hoda Anton-Culver, Natalia N Antonenkova, Volker Arndt, Kristan J Aronson, Annelie Augustinsson, Adinda Baten, Laura E Beane Freeman, Heiko Becher, Matthias W Beckmann, Sabine Behrens, Javier Benitez, Marina Bermisheva, Natalia V Bogdanova, Stig E Bojesen, Hiltrud Brauch, Hermann Brenner, Sara Y Brucker, Barbara Burwinkel, Daniele Campa, Frederico Canzian, Jose E Castelao, Stephen J Chanock, Georgia Chenevix-Trench, Christine L Clarke, null null, Don M Conroy, Fergus J Couch, Angela Cox, Simon S Cross, Kamila Czene, Mary B Daly, Peter Devilee, Thilo Dörk, Isabel Dos-Santos-Silva, Miriam Dwek, Diana M Eccles, A Heather Eliassen, Christoph Engel, Mikael Eriksson, D Gareth Evans, Peter Andreas Fasching, Henrik Flyger, Lin Fritschi, Montserrat García-Closas, José A García-Sáenz, Mia M Gaudet, Graham G Giles, Gord Glendon, Mark S Goldberg, David E Goldgar, Anna González-Neira, Mervi Grip, Pascal Guénel, Eric Hahnen, Christopher A Haiman, Niclas Håkansson, Per Hall, Ute Hamann, Sileny Han, Elaine F Harkness, Steven N Hart, Wei He, Bernadette Anna Maria Heemskerk-Gerritsen, John L Hopper, David J Hunter, null null, null null, Agnes Jager, Anna Jakubowska, Esther M John, Audrey Jung, Rudolf Kaaks, Pooja Middha Kapoor, Renske Keeman, Elza Khusnutdinova, Cari M Kitahara, Linetta B Koppert, Stella Koutros, Vessela N Kristensen, Allison W Kurian, James Lacey, Diether Lambrechts, Loic Le Marchand, Wing-Yee Lo, Jan Lubiński, Arto Mannermaa, Mehdi Manoochehri, Sara Margolin, Maria Elena Martinez, Dimitrios Mavroudis, Alfons Meindl, Usha Menon, Roger L Milne, Taru A Muranen, Heli Nevanlinna, William G Newman, Børge G Nordestgaard, Kenneth Offit, Andrew F Olshan, Håkan Olsson, Tjoung-Won Park-Simon, Paolo Peterlongo, Julian Peto, Dijana Plaseska-Karanfilska, Nadege Presneau, Paolo Radice, Gad Rennert, Hedy S Rennert, Atocha Romero, Emmanouil Saloustros, Elinor J Sawyer, Marjanka K Schmidt, Rita K Schmutzler, Minouk J Schoemaker, Lukas Schwentner, Christopher G Scott, Mitul Shah, Xiao-Ou Shu, Jacques Simard, Ann Smeets, Melissa C Southey, John J Spinelli, Victoria Stevens, Anthony J Swerdlow, Rulla M Tamimi, William J Tapper, Jack A Taylor, Mary Beth Terry, Ian P M Tomlinson, Melissa A Troester, Thérèse Truong, Celine M Vachon, Elke M van Veen, Joseph Vijai, Sophia Wang, Camilla Wendt, Robert Winqvist, Alicja Wolk, Argyrios Ziogas, Alison M Dunning, Paul David Peter Pharoah, Douglas F Easton, Wei Zheng, Peter Kraft, Jenny Chang-Claude
Mendelian randomisation study of smoking exposure in relation to breast cancer risk. British journal of cancer 125 (8) (2021)
Leslie Patricia Molina-Ramírez, Emma Mm Burkitt-Wright, Haroon Saeed, John Henry McDermott, Claire Kyle, Ronnie Wright, Christopher Campbell, Sanjeev S Bhaskar, Algy Taylor, Laura Dutton, Claire Forde, Kay Metcalfe, Audrey Smith, Jill Clayton-Smith, Sofia Douzgou Houge, Kate Chandler, Tracy A Briggs, Siddharth Banka, William G Newman, David Gokhale, Iain A Bruce, Graeme C M Black
The diagnostic utility of clinical exome sequencing in 60 patients with hearing loss disorders: A single-institution experience. Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery 46 (6) (2021)
Anna Morra, Audrey Y Jung, Sabine Behrens, Renske Keeman, Thomas U Ahearn, Hoda Anton-Culver, Volker Arndt, Annelie Augustinsson, Päivi K Auvinen, Laura E Beane Freeman, Heiko Becher, Matthias W Beckmann, Carl Blomqvist, Stig E Bojesen, Manjeet K Bolla, Hermann Brenner, Ignacio Briceno, Sara Y Brucker, Nicola J Camp, Daniele Campa, Frederico Canzian, Jose E Castelao, Stephen J Chanock, Ji-Yeob Choi, Christine L Clarke, Fergus J Couch, Angela Cox, Simon S Cross, Kamila Czene, Thilo Dörk, Alison M Dunning, Miriam Dwek, Douglas F Easton, Diana M Eccles, Kathleen M Egan, Dafydd Gareth Evans, Peter Andreas Fasching, Henrik Flyger, Manuela Gago-Dominquez, Susan M Gapstur, José Angel García-Saenz, Mia M Gaudet, Graham G Giles, Mervi Grip, Pascal Guénel, Christopher A Haiman, Niclas Håkansson, Per Hall, Ute Hamann, Sileny N Han, Steven N Hart, Mikael Hartman, Jane S Heyworth, Reiner Hoppe, John L Hopper, David J Hunter, Hidemi Ito, Agnes Jager, Milena Jakimovska, Anna Jakubowska, Wolfgang Janni, Rudolf Kaaks, Daehee Kang, Pooja Middha Kapoor, Cari M Kitahara, Stella Koutros, Peter Kraft, Vessela N Kristensen, James V Lacey, Diether Lambrechts, Loic Le Marchand, Jingmei Li, Annika Lindblom, Jan Lubiński, Michael Lush, Arto Mannermaa, Mehdi Manoochehri, Sara Margolin, Shivaani Mariapun, Keitaro Matsuo, Dimitrios Mavroudis, Jonathan Beesley, Taru A Muranen, William G Newman, Dong-Young Noh, Børge G Nordestgaard, Nadia Obi, Andrew F Olshan, Håkan Olsson, Tjoung-Won Park-Simon, Christos Petridis, Paul David Peter Pharoah, Dijana Plaseska-Karanfilska, Nadege Presneau, Muhammad U Rashid, Gadi Rennert, Hedy S Rennert, Valerie Rhenius, Atocha Romero, Emmanouil Saloustros, Elinor J Sawyer, Andreas Schneeweiß, Lukas Schwentner, Christopher G Scott, Mitul Shah, Chen-Yang Shen, Xiao-Ou Shu, Melissa C Southey, Daniel O Stram, Rulla M Tamimi, William Tapper, Rob A E M Tollenaar, Ian P M Tomlinson, Diana Torres, Melissa A Troester, Thérèse Truong, Celine M Vachon, Qin Wang, Sophia S Wang, Justin A Williams, Robert Winqvist, Alicja Wolk, Anna H Wu, Keun-Young Yoo, Jyh-Cherng Yu, Wei Zheng, Argyrios Ziogas, Xiaohong R Yang, A Heather Eliassen, Michelle D Holmes, Montserrat Garcia-Closas, Soo-Hwang Teo, Marjanka K Schmidt, Jenny Chang-Claude, null null, null null
Breast Cancer Risk Factors and Survival by Tumor Subtype: Pooled Analyses from the Breast Cancer Association Consortium. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 30 (4) (2021)
Víctor Faundes, Martin D Jennings, Siobhan Crilly, Sarah Legraie, Sarah E Withers, Sara Cuvertino, Sally J Davies, Andrew G L Douglas, Andrew E Fry, Victoria Harrison, Jeanne Amiel, Daphné Lehalle, William G Newman, Patricia Newkirk, Judith Ranells, Miranda Splitt, Laura Ann Cross, Carol J Saunders, Bonnie R Sullivan, Jorge L Granadillo, Christopher T Gordon, Paul R Kasher, Graham D Pavitt, Siddharth Banka
Impaired eIF5A function causes a Mendelian disorder that is partially rescued in model systems by spermidine. Nature communications 12 (1) (2021)
Dafydd Gareth Evans, Elke Maria van Veen, Helen J Byers, Sarah J Evans, George Joseph Burghel, Emma Roisin Woodward, Elaine F Harkness, Diana M Eccles, Stephanie L Greville-Haygate, Jamie M Ellingford, Naomi L Bowers, Marta Pereira, Andrew J Wallace, Sasha J Howell, Anthony Howell, Fiona Lalloo, William G Newman, Miriam Jane Smith
High likelihood of actionable pathogenic variant detection in breast cancer genes in women with very early onset breast cancer. Journal of medical genetics (2021)
Rabia Faridi, Alessandro Rea, Cristina Fenollar-Ferrer, Raymond T O'Keefe, Shoujun Gu, Zunaira Munir, Asma Ali Khan, Sheikh Riazuddin, Michael Hoa, Sadaf Naz, William G Newman, Thomas B Friedman
New insights into Perrault syndrome, a clinically and genetically heterogeneous disorder. Human genetics (2021)
Katherine A Wood, Jamie M Ellingford, Huw B Thomas, null null, Sofia Douzgou Houge, Glenda M Beaman, Emma Hobson, Katrina Prescott, Raymond T O'Keefe, William G Newman
Expanding the genotypic spectrum of TXNL4A variants in Burn-McKeown syndrome. Clinical genetics (2021)
Elke Maria van Veen, Dafydd Gareth Evans, Elaine F Harkness, Helen J Byers, Jamie M Ellingford, Emma R Woodward, Naomi L Bowers, Andrew J Wallace, Sacha J Howell, Anthony Howell, Fiona Lalloo, William G Newman, Miriam Jane Smith
Extended gene panel testing in lobular breast cancer. Familial cancer (2021)
Silvia Vidali, Raffaele Gerlini, Kyle Thompson, Jill E Urquhart, Jana Meisterknecht, Juan Antonio Aguilar-Pimentel, Oana V Amarie, Lore Becker, Catherine Breen, Julia Calzada-Wack, Nirav F Chhabra, Yi-Li Cho, Patricia da Silva-Buttkus, René Günther Feichtinger, Kristine Gampe, Lillian Garrett, Kai P Hoefig, Sabine Maria Hölter, Elisabeth Jameson, Tanja Klein-Rodewald, Stefanie Leuchtenberger, Susan Marschall, Philipp Mayer-Kuckuk, Gregor Miller, Manuela A Oestereicher, Kristina Pfannes, Birgit Rathkolb, Jan Rozman, Charlotte Sanders, Nadine Spielmann, Claudia Stoeger, Marten Szibor, Irina Treise, John H Walter, Wolfgang Wurst, Johannes Adalbert Mayr, Helmut Fuchs, Ulrich Gärtner, Ilka Wittig, Robert W Taylor, William G Newman, Holger Prokisch, Valérie Gailus-Durner, Martin Hrabě de Angelis
Characterising a homozygous two-exon deletion in UQCRH: comparing human and mouse phenotypes. EMBO molecular medicine 13 (12) (2021)
William G Newman
Genetic testing in the acute setting: a round table discussion. Journal of medical ethics 46 (8) (2020)
Huw B Thomas, Katherine A Wood, Weronika A Buczek, Christopher T Gordon, Véronique Pingault, Tania Attie-Bitach, Kathryn E Hentges, Vinod C Varghese, Jeanne Amiel, William G Newman, Raymond T O'Keefe
EFTUD2 missense variants disrupt protein function and splicing in mandibulofacial dysostosis Guion-Almeida type. Human mutation 41 (8) (2020)
Anneke M Lucassen, John Henry McDermott, William G Newman
Using a biomarker acutely to identify babies at risk of serious adverse effects from antibiotics: where is the 'Terrible Moral and Medical Dilemma'? Journal of medical ethics 47 (2) (2020)
Stuart James Wright, William G Newman, Katherine Payne
Accounting for Capacity Constraints in Economic Evaluations of Precision Medicine: A Systematic Review. PharmacoEconomics 37 (8) (2020)
Damilola Olubando, Claire Hopton, James Eden, Richard C Caswell, N Lowri Thomas, Stephen A Roberts, Deborah Morris-Rosendahl, Luigi Venetucci, William G Newman
Classification and correlation of RYR2 missense variants in individuals with catecholaminergic polymorphic ventricular tachycardia reveals phenotypic relationships. Journal of human genetics 65 (6) (2020)
Haoyu Zhang, Thomas U Ahearn, Julie Lecarpentier, Daniel R Barnes, Jonathan Beesley, Guanghao Qi, Xia Jiang, Tracy A O'Mara, Ni Zhao, Manjeet K Bolla, Alison M Dunning, Joe G Dennis, Qin Wang, Zumuruda Abu Ful, Kristiina Aittomäki, Irene L Andrulis, Hoda Anton-Culver, Volker Arndt, Kristan J Aronson, Banu K Arun, Paul L Auer, Jacopo Azzollini, Daniel Barrowdale, Heiko Becher, Matthias W Beckmann, Sabine Behrens, Javier Benitez, Marina Bermisheva, Katarzyna Bialkowska, Ana Blanco, Carl Blomqvist, Natalia V Bogdanova, Stig Egil Bojesen, Bernardo Bonanni, Davide Bondavalli, Ake Borg, Hiltrud B Brauch, Hermann Brenner, Ignacio Briceno, Annegien Broeks, Sara Y Brucker, Thomas Brüning, Barbara Burwinkel, Saundra S Buys, Helen Byers, Trinidad Caldés, Maria A Caligo, Mariarosaria Calvello, Daniele Campa, Jose E Castelao, Jenny Chang-Claude, Stephen J Chanock, Melissa Christiaens, Hans Christiansen, Wendy K Chung, Kathleen B M Claes, Christine L Clarke, Sten Cornelissen, Fergus J Couch, Angela Cox, Simon S Cross, Kamila Czene, Mary B Daly, Peter Devilee, Orland Diez, Susan M Domchek, Thilo Dörk, Miriam V Dwek, Diana M Eccles, Arif Bülent Ekici, D Gareth Evans, Peter Andreas Fasching, Jonine Figueroa, Lenka Foretova, Florentia Fostira, Eitan Friedman, Debra Frost, Manuela Gago-Dominguez, Susan M Gapstur, Judy Garber, José Angel García-Saenz, Mia M Gaudet, Simon A Gayther, Graham G Giles, Andrew K Godwin, Mark S Goldberg, David E Goldgar, Anna González-Neira, Mark H Greene, Jacek Gronwald, Pascal Guénel, Lothar Häberle, Eric Hahnen, Christopher A Haiman, Christopher R Hake, Per Hall, Ute Hamann, Elaine F Harkness, Bernadette Anna Maria Heemskerk-Gerritsen, Peter Hillemanns, Frans B L Hogervorst, Bernd Holleczek, Antoinette Hollestelle, Maartje J Hooning, Robert N Hoover, John L Hopper, Anthony Howell, Hanna Huebner, Peter J Hulick, Evgeny N Imyanitov, null null, null null, Claudine Isaacs, Louise Izatt, Agnes Jager, Milena Jakimovska Özdemir, Anna Jakubowska, Paul A James, Ramunas Janavicius, Wolfgang Janni, Esther M John, Michael E Jones, Audrey Jung, Rudolf Kaaks, Pooja Middha Kapoor, Beth Y Karlan, Renske Keeman, Sofia Khan, Elza Khusnutdinova, Cari M Kitahara, Yon-Dschun Ko, Irene Konstantopoulou, Linetta B Koppert, Stella Koutros, Vessela N Kristensen, Anne-Vibeke Laenkholm, Diether Lambrechts, Susanna C Larsson, Pierre Laurent-Puig, Conxi Lazaro, Emilija Lazarova, Flavio Lejbkowicz, Goska Leslie, Fabienne Lesueur, Annika Lindblom, Jolanta Lissowska, Wing-Yee Lo, Jennifer T Loud, Jan Lubinski, Alicja Lukomska, Robert J MacInnis, Arto Mannermaa, Mehdi Manoochehri, Siranoush Manoukian, Sara Margolin, Maria Elena Martinez, Laura Matricardi, Lesley McGuffog, Catriona A Mclean, Noura Mebirouk, Alfons Meindl, Usha Menon, Austin Miller, Elvira Mingazheva, Marco Montagna, Anna Marie Mulligan, Claire Mulot, Taru A Muranen, Katherine L Nathanson, Susan L Neuhausen, Heli Nevanlinna, Patrick Neven, William G Newman, Finn C Nielsen, Liene Nikitina-Zake, Jesse Nodora, Kenneth Offit, Edith Olah, Olufunmilayo I Olopade, Håkan Olsson, Nicholas Orr, Laura Papi, Janos Papp, Tjoung-Won Park-Simon, Michael T Parsons, Bernard Peissel, Ana Peixoto, Beth N Peshkin, Paolo Peterlongo, Julian Peto, Kelly-Anne Phillips, Marion Piedmonte, Dijana Plaseska-Karanfilska, Karolina Prajzendanc, Ross Prentice, Darya Prokofyeva, Brigitte Rack, Paolo Radice, Susan J Ramus, Johanna Rantala, Muhammad U Rashid, Gadi Rennert, Hedy S Rennert, Harvey A Risch, Atocha Romero, Matti A Rookus, Matthias Rübner, Thomas Rüdiger, Emmanouil Saloustros, Sarah Sampson, Dale P Sandler, Elinor J Sawyer, Maren T Scheuner, Rita K Schmutzler, Andreas Schneeweiss, Minouk J Schoemaker, Ben Schöttker, Peter Schürmann, Leigha Senter, Priyanka Sharma, Mark E Sherman, Xiao-Ou Shu, Christian F Singer, Snezhana Smichkoska, Penny Soucy, Melissa C Southey, John J Spinelli, Jennifer Stone, Dominique Stoppa-Lyonnet, null null, null null, Anthony J Swerdlow, Csilla I Szabo, Rulla M Tamimi, William J Tapper, Jack A Taylor, Manuel R Teixeira, MaryBeth Terry, Mads Thomassen, Darcy L Thull, Marc Tischkowitz, Amanda Ewart Toland, Rob A E M Tollenaar, Ian P M Tomlinson, Diana Torres, Melissa A Troester, Thérèse Truong, Nadine Tung, Michael Untch, Celine M Vachon, Ans M W van den Ouweland, Lizet E van der Kolk, Elke Maria van Veen, Elizabeth J vanRensburg, Ana Vega, Barbara Wappenschmidt, Clarice R Weinberg, Jeffrey N Weitzel, Hans Wildiers, Robert Winqvist, Alicja Wolk, Xiaohong R Yang, Drakoulis Yannoukakos, Quan Long, Kristin K Zorn, Jonathan Beesley, Peter Kraft, Jacques Simard, Paul David Peter Pharoah, Kyriaki Michailidou, Antonis C Antoniou, Marjanka K Schmidt, Georgia Chenevix-Trench, Douglas F Easton, Nilanjan Chatterjee, Montserrat Garcia-Closas
Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses. Nature genetics 52 (6) (2020)
Maria Escala-Garcia, Jean Abraham, Irene L Andrulis, Hoda Anton-Culver, Volker Arndt, Alan Ashworth, Paul L Auer, Päivi Auvinen, Matthias W Beckmann, Jonathan Beesley, Sabine Behrens, Javier Benitez, Marina Bermisheva, Carl Blomqvist, William Blot, Natalia V Bogdanova, Stig Egil Bojesen, Manjeet K Bolla, Anne-Lise Børresen-Dale, Hiltrud B Brauch, Hermann Brenner, Sara Y Brucker, Barbara Burwinkel, Carlos Caldas, Frederico Canzian, Jenny Chang-Claude, Stephen J Chanock, Suet-Feung Chin, Christine L Clarke, Fergus J Couch, Angela Cox, Simon S Cross, Kamila Czene, Mary B Daly, Joe G Dennis, Peter Devilee, Janet A Dunn, Alison M Dunning, Miriam V Dwek, Helena M Earl, Diana M Eccles, A Heather Eliassen, Carolina Ellberg, D Gareth Evans, Peter Andreas Fasching, Jonine Figueroa, Henrik Flyger, Manuela Gago-Dominguez, Susan M Gapstur, Montserrat Garcia-Closas, José Angel García-Saenz, Mia M Gaudet, Angela George, Graham G Giles, David E Goldgar, Anna González-Neira, Mervi Grip, Pascal Guénel, Qi Guo, Christopher A Haiman, Niclas Håkansson, Ute Hamann, Patricia A Harrington, Louise Hiller, Maartje J Hooning, John L Hopper, Anthony Howell, Chiun-Sheng Huang, Guanmengqian Huang, David J Hunter, Anna Jakubowska, Esther M John, Rudolf Kaaks, Pooja Middha Kapoor, Renske Keeman, Cari M Kitahara, Linetta B Koppert, Peter Kraft, Vessela N Kristensen, Diether Lambrechts, Loic Le Marchand, Flavio Lejbkowicz, Annika Lindblom, Jan Lubiński, Arto Mannermaa, Mehdi Manoochehri, Siranoush Manoukian, Sara Margolin, Maria Elena Martinez, Tabea Maurer, Dimitrios Mavroudis, Alfons Meindl, Jonathan Beesley, Anna Marie Mulligan, Susan L Neuhausen, Heli Nevanlinna, William G Newman, Andrew F Olshan, Janet E Olson, Håkan Olsson, Nicholas Orr, Paolo Peterlongo, Christos Petridis, Ross L Prentice, Nadege Presneau, Kevin Punie, Dhanya Ramachandran, Gadi Rennert, Atocha Romero, Mythily Sachchithananthan, Emmanouil Saloustros, Elinor J Sawyer, Rita K Schmutzler, Lukas Schwentner, Christopher G Scott, Jacques Simard, Christof Sohn, Melissa C Southey, Anthony J Swerdlow, Rulla M Tamimi, William J Tapper, Manuel R Teixeira, Mary Beth Terry, Heather Thorne, Rob A E M Tollenaar, Ian P M Tomlinson, Melissa A Troester, Thérèse Truong, Clare Turnbull, Celine M Vachon, Lizet E van der Kolk, Qin Wang, Robert Winqvist, Alicja Wolk, Xiaohong R Yang, Argyrios Ziogas, Paul David Peter Pharoah, Per Hall, Lodewyk F A Wessels, Georgia Chenevix-Trench, Gary D Baider, Thilo Dörk, Douglas F Easton, Sander Canisius, Marjanka K Schmidt
A network analysis to identify mediators of germline-driven differences in breast cancer prognosis. Nature communications 11 (1) (2020)
Wei Wei, Salih Tuna, Michael J Keogh, Katherine R Smith, Timothy J Aitman, Philip L Beales, David L H Bennett, Daniel P Gale, Maria A K Bitner-Glindzicz, Graeme C Black, Paul Brennan, Perry Mark Elliott, Frances A Flinter, R Andres Floto, Henry Houlden, Melita Irving, Ania Koziell, Eamonn R Maher, Hugh Stephen Markus, Nicholas W Morrell, William G Newman, Irene Roberts, John Andrew Sayer, Kenneth G C Smith, Jenny C Taylor, Hugh C Watkins, Andrew R Webster, Andrew O M Wilkie, Catherine Williamson, null null, null null, Sofie Ashford, Christopher J Penkett, Kathleen E Stirrups, Augusto Rendon, Willem H Ouwehand, John R Bradley, F Lucy Raymond, Mark Caulfield, Ernest Turro, Patrick F Chinnery
Germline selection shapes human mitochondrial DNA diversity. Science (New York, N.Y.) 364 (6442) (2019)
William G Newman, Gabriella Galatà, Keng W Teik, Jill E Urquhart, Ali Aishah, James O'Sullivan, Sanjeev S Bhaskar, Katherine A Wood, Huw B Thomas, Raymond T O'Keefe, Adrian S Woolf, Helen M Stuart, William G Newman
A homozygous missense variant in CHRM3 associated with familial urinary bladder disease. Clinical genetics 96 (6) (2019)
Thilo Dörk, Paolo Peterlongo, Arto Mannermaa, Manjeet K Bolla, Qin Wang, Joe Dennis, Thomas Ahearn, Irene L Andrulis, Hoda Anton-Culver, Volker Arndt, Kristan J Aronson, Annelie Augustinsson, Laura E Beane Freeman, Matthias W Beckmann, Alicia Beeghly-Fadiel, Sabine Behrens, Marina Bermisheva, Carl Blomqvist, Natalia V Bogdanova, Stig E Bojesen, Hiltrud B Brauch, Hermann Brenner, Barbara Burwinkel, Federico Canzian, Tsun L Chan, Jenny Chang-Claude, Stephen J Chanock, Ji-Yeob Choi, Hans Christiansen, Christine L Clarke, Fergus J Couch, Kamila Czene, Mary B Daly, Isabel Dos-Santos-Silva, Miriam V Dwek, Diana M Eccles, Arif Bülent Ekici, Mikael Eriksson, D Gareth Evans, Peter Andreas Fasching, Jonine D Figueroa, Henrik Flyger, Lin Fritschi, Marike Gabrielson, Manuela Gago-Dominguez, Chi Gao, Susan M Gapstur, Montserrat García-Closas, José A García-Sáenz, Mia M Gaudet, Graham G Giles, Mark S Goldberg, David E Goldgar, Pascal Guénel, Lothar Haeberle, Christopher A Haiman, Niclas Håkansson, Per Hall, Ute Hamann, Mikael Hartman, Jan Hauke, Alexander Hein, Peter Hillemanns, Frans B L Hogervorst, Maartje J Hooning, John L Hopper, Tony Howell, Dezheng Huo, Hidemi Ito, Motoki Iwasaki, Anna Jakubowska, Wolfgang Janni, Esther M John, Audrey Jung, Rudolf Kaaks, Daehee Kang, Pooja Middha Kapoor, Elza Khusnutdinova, Sung-Won Kim, Cari M Kitahara, Stella Koutros, Peter Kraft, Vessela N Kristensen, Ava Kwong, Diether Lambrechts, Loic Le Marchand, Jingmei Li, Sara Lindström, Martha Linet, Wing-Yee Lo, Jirong Long, Artitaya Lophatananon, Jan Lubiński, Mehdi Manoochehri, Siranoush Manoukian, Sara Margolin, Elena Martinez, Keitaro Matsuo, Dimitris Mavroudis, Alfons Meindl, Usha Menon, Jonathan Beesley, Nur Aishah Mohd Taib, Kenneth Ross Muir, Anna Marie Mulligan, Susan L Neuhausen, Heli Nevanlinna, Patrick Neven, William G Newman, Kenneth Offit, Olufunmilayo I Olopade, Andrew F Olshan, Janet E Olson, Håkan Olsson, Sue K Park, Tjoung-Won Park-Simon, Julian Peto, Dijana Plaseska-Karanfilska, Esther Pohl-Rescigno, Nadege Presneau, Brigitte Rack, Paolo Radice, Muhammad U Rashid, Gadi Rennert, Hedy S Rennert, Atocha Romero, Matthias Ruebner, Emmanouil Saloustros, Marjanka K Schmidt, Rita K Schmutzler, Michael O Schneider, Minouk J Schoemaker, Christopher G Scott, Chen-Yang Shen, Xiao-Ou Shu, Jacques Simard, Susan Slager, Snezhana Smichkoska, Melissa C Southey, John J Spinelli, Jennifer Stone, Harald Surowy, Anthony J Swerdlow, Rulla M Tamimi, William J Tapper, Soo H Teo, Mary Beth Terry, Amanda E Toland, Rob A E M Tollenaar, Diana Torres, Gabriela Torres-Mejía, Melissa A Troester, Thérèse Truong, Shoichiro Tsugane, Michael Untch, Celine M Vachon, Ans M W van den Ouweland, Elke M van Veen, Joseph Vijai, Camilla Wendt, Alicja Wolk, Jyh-Cherng Yu, Wei Zheng, Argyrios Ziogas, Elad Ziv, null null, null null, Alison M Dunning, Paul David Peter Pharoah, Detlev Schindler, Peter Devilee, Douglas F Easton
Two truncating variants in FANCC and breast cancer risk. Scientific reports 9 (1) (2019)
Leigh A M Demain, Erica H Gerkes, Richard J H Smith, Leslie P Molina-Ramirez, Raymond T O'Keefe, William G Newman
A recurrent missense variant in HARS2 results in variable sensorineural hearing loss in three unrelated families. Journal of human genetics 65 (3) (2019)
Víctor Faundes, Geraldine Malone, William G Newman, Siddharth Banka
A comparative analysis of KMT2D missense variants in Kabuki syndrome, cancers and the general population. Journal of human genetics 64 (2) (2018)

William G Newman.css-eqlu8i{font-size:small;padding-left:4px;} (W G Newman, William Newman)

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William G Newman (W G Newman, William Newman)