Jeffrey C. Murray
Active 1984–2025
- 162
- Papers
- 27,463
- Citations
- 97
- h-index
- 154
- i10-index
Citations
Citation sources
Countries
Institutions
- Harvard University1.1%
- University of Iowa1%
- Johns Hopkins University0.6%
- University of Pittsburgh0.6%
- National Institutes of Health0.6%
- Inserm0.6%
- Other95.5%
Fields
- Biochemistry, Genetics and Molecular Biology49.5%
- Medicine37.4%
- Neuroscience4.3%
- Immunology and Microbiology2%
- Agricultural and Biological Sciences1.2%
- Dentistry0.8%
- Other4.8%
Topics
- Cleft Lip and Palate Research5.2%
- Craniofacial Disorders and Treatments3%
- Genetic Associations and Epidemiology2.3%
- dental development and anomalies2.2%
- Genomic variations and chromosomal abnormalities1.9%
- Neonatal Respiratory Health Research1.7%
- Other83.7%
Coauthors
- Mary L. Marazita40
- Kaare Christensen24
- Andrew C. Lidral23
- Terri H. Beaty21
- Elizabeth J. Leslie19
- Alexandre R. Vieira17
- Sandra Daack‐Hirsch17
- George L. Wehby16
- Seth M. Weinberg15
- Eleanor Feingold13
- Kenneth H. Buetow13
- Azeez Butali12
- Brian C. Schutte12
- Margaret E. Cooper12
- Tamara Busch12
- Ingo Ruczinski11
- Wasiu Lanre Adeyemo11
- Elena V. Semina10
- Frederic W.‐B. Deleyiannis10
- Jacqueline B. Hetmanski10
- Jacqueline T. Hecht10
- John R. Shaffer10
- Lina M. Moreno10
- Paul A. Romitti10
All papers
- Cleft lip and palate: understanding genetic and environmental influences
Authors: Michael J. Dixon, Mary L. Marazita, Terri H. Beaty, Jeffrey C. Murray - Nature Reviews Genetics 2011 cited by 1,969
- Between-Hospital Variation in Treatment and Outcomes in Extremely Preterm Infants
Authors: Matthew A. Rysavy, Lei Li, Edward F. Bell, Abhik Das, Susan R. Hintz, Barbara J. Stoll, Betty R. Vohr, Waldemar A. Carlo, Seetha Shankaran, Michele C. Walsh, Jon E. Tyson, C. Michael Cotten, P. Brian Smith, Jeffrey C. Murray, Tarah T. Colaizy, Jane E. Brumbaugh, Rosemary D. Higgins - New England Journal of Medicine 2015 cited by 658
- Detectable clonal mosaicism from birth to old age and its relationship to cancer
Authors: Cathy C. Laurie, Cecelia Laurie, Kenneth Rice, Kimberly F. Doheny, Leila R. Zelnick, Caitlin McHugh, Hua Ling, Kurt N. Hetrick, Elizabeth Pugh, Chris Amos, Qingyi Wei, Lie Wang, Jeffrey E. Lee, Kathleen C. Barnes, Nadia N. Hansel, Rasika A. Mathias, Denise Daley, Terri H. Beaty, Alan F. Scott, Ingo Ruczinski, Rob Scharpf, Laura J. Bierut, Sarah M. Hartz, Maria Teresa Landi, Neal D. Freedman, Lynn R. Goldin, David Ginsburg, Jun Li, Karl C. Desch, Sara S. Strom, William J. Blot, Lisa B. Signorello, Sue A. Ingles, Stephen J. Chanock, Sonja I. Berndt, Loı̈c Le Marchand, Brian E. Henderson, Kristine R. Monroe, John A. Heit, Mariza de Andrade, Sebastian M. Armasu, C Régnier, William L. Lowe, M. Geoffrey Hayes, Mary L. Marazita, Eleanor Feingold, Jeffrey C. Murray, Mads Melbye, Bjarke Feenstra, Jae H. Kang, Janey L. Wiggs, Gail P. Jarvik, Andrew McDavid, Venkatraman Seshan, Daniel B. Mirel, Andrew Crenshaw, Nataliya Sharopova, Anastasia L. Wise, Jess Shen, David R. Crosslin, David Levine, Xiuwen Zheng, Jenna Udren, Siiri Bennett, Sarah C. Nelson, Stephanie M. Gogarten, Matthew P. Conomos, Patrick J. Heagerty, Teri A. Manolio, Louis R. Pasquale, Christopher A. Haiman, Neil E. Caporaso, Bruce S. Weir - Nature Genetics 2012 cited by 599
- Siglec-5 and Siglec-14 are polymorphic paired receptors that modulate neutrophil and amnion signaling responses to group B Streptococcus
Authors: Syed R. Ali, Jerry J. Fong, Aaron F. Carlin, Tamara Busch, Rebecka Linden, Takashi Angata, Thomas Areschoug, Mana M. Parast, Nissi Varki, Jeffrey C. Murray, Victor Nizet, Ajit Varki - The Journal of Experimental Medicine 2014 cited by 195
- Dissecting maternal and fetal genetic effects underlying the associations between maternal phenotypes, birth outcomes, and adult phenotypes: A mendelian-randomization and haplotype-based genetic score analysis in 10,734 mother–infant pairs
Authors: Jing Chen, Jonas Bačelis, Pol Solé-Navais, Amit Kumar Srivastava, Julius Juodakis, Amy Rouse, Mikko Hallman, Kari Teramo, Mads Melbye, Bjarke Feenstra, Rachel M. Freathy, George Davey Smith, Debbie A. Lawlor, Jeffrey C. Murray, Scott M. Williams, Bo Jacobsson, Louis J. Muglia, Ge Zhang - PLoS Medicine 2020 cited by 88
- Multiomics Characterization of Preterm Birth in Low- and Middle-Income Countries
Authors: Fyezah Jehan, Sunil Sazawal, Abdullah H Baqui, Muhammad Imran Nisar, Usha Dhingra, Rasheda Khanam, Muhammad Ilyas, Arup Dutta, Dipak Kumar Mitra, Usma Mehmood, Saikat Deb, Arif Mahmud, Aneeta Hotwani, Said M. Ali, Sayedur Rahman, Ambreen Nizar, Shaali Makame, Mamun Ibne Moin, Muhammad Sajid, Aishwarya Chauhan, Nazma Begum, Waqasuddin Khan, Sayan Das, Salahuddin Ahmed, Tarik Hasan, Javairia Khalid, Syed Jafar Raza Rizvi, Mohammed Hamad Juma, Nabidul Haque Chowdhury, Furqan Kabir, Fahad Aftab, Abdul Quaiyum, Alexander Manu, Sachiyo Yoshida, Rajiv Bahl, Anisur Rahman, Jesmin Pervin, Jennifer Winston, Patrick Musonda, Jeffrey S. A. Stringer, James A. Litch, Mohammad Sajjad Ghaemi, Mira N. Moufarrej, Kévin Contrepois, Songjie Chen, Ina A. Stelzer, Natalie Stanley, Alan L. Chang, Ghaith Bany Hammad, Ronald J. Wong, Candace Liu, Cecele C. Quaintance, Anthony Culos, Camilo Espinosa, Maria Xenochristou, Martin Becker, Ramin Fallahzadeh, Edward A. Ganio, Amy S. Tsai, Dyani Gaudillière, Eileen S. Tsai, Xiaoyuan Han, Kazuo Ando, Martha Tingle, Ivana Marić, Paul H. Wise, Virginia D. Winn, Maurice L. Druzin, Ronald S. Gibbs, Gary L. Darmstadt, Jeffrey C. Murray, Gary M. Shaw, David K. Stevenson, M Snyder, Stephen R. Quake, Martin S. Angst, Brice Gaudillière, Nima Aghaeepour - JAMA Network Open 2020 cited by 105
- Abnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 (Irf6)
Authors: Christopher R. Ingraham, Akira Kinoshita, Shinji Kondo, Baoli Yang, Samin A. Sajan, Kurt J Trout, Margaret Malik, Martine Dunnwald, Stephen L Goudy, Michael Lovett, Jeffrey C. Murray, Brian C. Schutte - Nature Genetics 2006 cited by 363
- Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis
Authors: Lavinia Paternoster, Marie Standl, Chih‐Mei Chen, Adaikalavan Ramasamy, Klaus Bønnelykke, Liesbeth Duijts, Manuel A. R. Ferreira, Alexessander Couto Alves, Jacob P. Thyssen, Eva Albrecht, Hansjörg Baurecht, Bjarke Feenstra, Patrick Sleiman, Pirro G. Hysi, Nicole M. Warrington, Ivan Curjuric, Ronny Myhre, John A. Curtin, Maria M. Groen‐Blokhuis, Marjan Kerkhof, Annika Sääf, André Franke, David Ellinghaus, Regina Fölster‐Holst, Emmanouil T. Dermitzakis, Stephen B. Montgomery, Holger Prokisch, Katharina Heim, Anna‐Liisa Hartikainen, Anneli Pouta, Juha Pekkanen, Alexandra I. F. Blakemore, Jessica L. Buxton, Marika Kaakinen, David L Duffy, Pamela A. F. Madden, Andrew C. Heath, Grant W. Montgomery, Philip J. Thompson, Melanie C. Matheson, Peter N. Le Souëf, Beaté St Pourcain, George Davey Smith, John Henderson, John P. Kemp, Nicholas J. Timpson, Panos Deloukas, Susan M. Ring, H‐Erich Wichmann, Martina Müller‐Nurasyid, Natalija Novak, Norman Klopp, Elke Rodríguez, Wendy L. McArdle, Allan Linneberg, Torkil Menné, Ellen A. Nøhr, Albert Hofman, André G. Uitterlinden, Cornelia M. van Duijn, Fernando Rivadeneira, Johan C. de Jongste, Ralf J.P. van der Valk, Matthias Wjst, Rain Jögi, Frank Geller, Heather A. Boyd, Jeffrey C. Murray, Cecilia Kim, Frank Mentch, Michael March, Massimo Mangino, Tim D. Spector, Véronique Bataille, Craig E. Pennell, Patrick G. Holt, Peter D. Sly, Carla M. T. Tiesler, Elisabeth Thiering, Thomas Illig, Medea Imboden, Wenche Nystad, Angela Simpson, Jouke‐Jan Hottenga, Dirkje S. Postma, Gerard H. Koppelman, Henriëtte A. Smit, Cilla Söderhäll, Bo Chawes, Eskil Kreiner‐Møller, Hans Bisgaard, Erik Melén, Dorret I. Boomsma, Adnan Čustović, Bo Jacobsson, Nicole Probst‐Hensch, Lyle J. Palmer, Daniel Glass, Håkon Håkonarson, Mads Melbye and 8 more - Nature Genetics 2011 cited by 351
- Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight
Authors: Jessica Tyrrell, Rebecca C. Richmond, Tom Palmer, Bjarke Feenstra, Janani Rangarajan, Sarah Metrustry, Alana Cavadino, Lavinia Paternoster, Loren L. Armstrong, N. Maneka G. De Silva, Andrew R. Wood, Momoko Horikoshi, Frank Geller, Ronny Myhre, Jonathan P. Bradfield, Eskil Kreiner‐Møller, Ville Huikari, Jodie N. Painter, Jouke‐Jan Hottenga, Catherine Allard, Diane J. Berry, Luigi Bouchard, Shikta Das, David M. Evans, Håkon Håkonarson, M. Geoffrey Hayes, Jani Heikkinen, Albert Hofman, Bridget Knight, Penelope A. Lind, Mark I. McCarthy, George McMahon, Sarah E. Medland, Mads Melbye, Andrew P. Morris, Michael Nodzenski, Christoph Reichetzeder, Susan M. Ring, Sylvain Sebért, Verena Sengpiel, Thorkild I. A. Sørensen, Gonneke Willemsen, Eco J. C. de Geus, Nicholas G. Martin, Tim D. Spector, Christopher Power, Marjo‐Riitta Järvelin, Hans Bisgaard, Struan F.A. Grant, Ellen A. Nøhr, Vincent W. V. Jaddoe, Bo Jacobsson, Jeffrey C. Murray, Berthold Hocher, Andrew T. Hattersley, Denise Scholtens, George Davey Smith, Marie‐France Hivert, Janine F. Felix, Elina Hyppönen, William L. Lowe, Timothy M. Frayling, Debbie A. Lawlor, Rachel M. Freathy - JAMA 2016 cited by 290
- Comprehensive Human Genetic Maps: Individual and Sex-Specific Variation in Recombination
Authors: Karl W. Broman, Jeffrey C. Murray, Val C. Sheffield, R. White, James L. Weber - The American Journal of Human Genetics 1998 cited by 1,097
- Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies
Authors: Cathy E. Elks, John R. B. Perry, Patrick Sulem, Daniel I. Chasman, Nora Franceschini, Chunyan He, Kathryn L. Lunetta, Jenny A. Visser, Enda M. Byrne, Diana L. Cousminer, Daníel F. Guðbjartsson, Tõnu Esko, Bjarke Feenstra, Jouke‐Jan Hottenga, Daniel L. Koller, Zoltán Kutalik, Peng Lin, Massimo Mangino, Mara Marongiu, Patrick F. McArdle, Albert V. Smith, Lisette Stolk, Sophie H van Wingerden, Jing Hua Zhao, Eva Albrecht, Tanguy Corre, Erik Ingelsson, Caroline Hayward, Patrik K. E. Magnusson, Erin N. Smith, Shelia Ulivi, Nicole M. Warrington, Lina Zgaga, Helen Alavere, Najaf Amin, Thor Aspelund, Stefania Bandinelli, Inês Barroso, Gerald S. Berenson, Sven Bergmann, Hannah Blackburn, Eric Boerwinkle, Julie E. Buring, Fabio Busonero, Harry Campbell, Stephen J. Chanock, Wei Chen, Marilyn C. Cornelis, David Couper, Andrea D. Coviello, Pio D’Adamo, Ulf dé Fairé, Eco J. C. de Geus, Panos Deloukas, Angela Döring, George Davey Smith, Douglas F. Easton, Guðný Eiríksdóttir, Valur Emilsson, Johan G. Eriksson, Luigi Ferrucci, Aaron R. Folsom, Tatiana Foroud, Melissa Garcia, Paolo Gasparini, Frank Geller, Christian Gieger, Vilmundur Guðnason, Per Hall, Susan E. Hankinson, Liana Ferreli, Andrew C. Heath, Dena G. Hernandez, Albert Hofman, Frank B. Hu, Thomas Illig, Marjo‐Riitta Järvelin, Andrew D. Johnson, David Karasik, Kay‐Tee Khaw, Douglas P. Kiel, Tuomas O. Kilpeläinen, Ivana Kolčić, Peter Kraft, Lenore J. Launer, Joop S.E. Laven, Shengxu Li, Jianjun Liu, Daniel Levy, Nicholas G. Martin, Wendy L. McArdle, Mads Melbye, Vincent Mooser, Jeffrey C. Murray, Sarah S. Murray, Michael A. Nalls, Pau Navarro, Mari Nelis, Andrew R Ness, Kate Northstone and 74 more - Nature Genetics 2010 cited by 511
- Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes
Authors: Shinji Kondo, Brian C. Schutte, Rebecca J. Richardson, Bryan C. Bjork, Alexandra S. Knight, Yoriko Watanabe, Emma Howard, Renata Lúcia Leite Ferreira de Lima, Sandra Daack‐Hirsch, Achim Sander, Donna M. McDonald‐McGinn, Elaine H. Zackai, Edward J. Lammer, Arthur S. Aylsworth, Holly H Ardinger, Andrew C. Lidral, Barbara R. Pober, Lina M. Moreno, Mauricio Arcos‐Burgos, Consuelo Valencia, Claude Houdayer, Michel Bahuau, Danilo Moretti‐Ferreira, Antônio Richieri‐Costa, Michael J. Dixon, Jeffrey C. Murray - Nature Genetics 2002 cited by 901
- Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios
Authors: Madison R. Bishop, Kimberly K. Diaz Perez, Miranda Sun, Samantha Ho, Pankaj Chopra, Nandita Mukhopadhyay, Jacqueline B. Hetmanski, Margaret A. Taub, Lina Moreno‐Uribe, Luz Consuelo Valencia‐Ramirez, Claudia P. Restrepo Muñeton, George L. Wehby, Jacqueline T. Hecht, Frederic W.‐B. Deleyiannis, Seth M. Weinberg, Yah Huei Wu‐Chou, Philip K. Chen, Harrison Brand, Michael P. Epstein, Ingo Ruczinski, Jeffrey C. Murray, Terri H. Beaty, Eleanor Feingold, Robert J. Lipinski, David J. Cutler, Mary L. Marazita, Elizabeth J. Leslie - The American Journal of Human Genetics 2020 cited by 96
- The heritability of hemolysis in stored human red blood cells
Authors: Thomas J. van ‘t Erve, Brett A. Wagner, Sean M. Martin, C. Michael Knudson, Robyn Blendowski, Mignon Keaton, Tracy Holt, John R. Hess, Garry R. Buettner, Kelli K. Ryckman, Benjamin W. Darbro, Jeffrey C. Murray, Thomas J. Raife - Transfusion 2015 cited by 82
- Noninvasive Whole-Genome Sequencing of a Human Fetus
Authors: Jacob O. Kitzman, Matthew W. Snyder, Mario Ventura, Alexandra P. Lewis, Ruolan Qiu, LaVone E. Simmons, Hilary S. Gammill, Craig E. Rubens, Donna A. Santillan, Jeffrey C. Murray, Holly K. Tabor, Michael J. Bamshad, Evan E. Eichler, Jay Shendure - Science Translational Medicine 2012 cited by 413
- The 3D Facial Norms Database: Part 1. A Web-Based Craniofacial Anthropometric and Image Repository for the Clinical and Research Community
Authors: Seth M. Weinberg, Zachary D. Raffensperger, Matthew J. Kesterke, Carrie L. Heike, Michael L. Cunningham, Jacqueline T. Hecht, Chung How Kau, Jeffrey C. Murray, George L. Wehby, Lina M. Moreno, Mary L. Marazita - The Cleft Palate-Craniofacial Journal 2015 cited by 110
- Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic trios
Authors: Debashree Ray, Sowmya Venkataraghavan, Wanying Zhang, Elizabeth J. Leslie, Jacqueline B. Hetmanski, Seth M. Weinberg, Jeffrey C. Murray, Mary L. Marazita, Ingo Ruczinski, Margaret A. Taub, Terri H. Beaty - PLoS Genetics 2021 cited by 52
- Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci
Authors: Kerstin U. Ludwig, Elisabeth Mangold, Stefan Herms, Stefanie Nowak, Heiko Reutter, Anna Paul, Jessica Becker, Ruth Herberz, Taofik AlChawa, Entessar Nasser, Anne C. Böhmer, Manuel Mattheisen, Margrieta A Alblas, Sandra Barth, Nadine Kluck, Carola Lauster, Bert Braumann, Rudolf H. Reich, Alexander Hemprich, Simone Pötzsch, Bettina Blaumeiser, Nikolaos Daratsianos, Thomas Kreusch, Jeffrey C. Murray, Mary L. Marazita, Ingo Ruczinski, Alan F. Scott, Terri H. Beaty, Franz-Josef Kramer, Thomas F. Wienker, Régine P.M. Steegers‐Theunissen, Michele Rubini, Peter Mossey, Per Hoffmann, Christoph Lange, Sven Cichon, Peter Propping, Michael Knapp, Markus M. Nöthen - Nature Genetics 2012 cited by 361
- Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics
Authors: Robin N. Beaumont, Nicole M. Warrington, Alana Cavadino, Jessica Tyrrell, Michael Nodzenski, Momoko Horikoshi, Frank Geller, Ronny Myhre, Rebecca C. Richmond, Lavinia Paternoster, Jonathan P. Bradfield, Eskil Kreiner‐Møller, Ville Huikari, Sarah Metrustry, Kathryn L. Lunetta, Jodie N. Painter, Jouke‐Jan Hottenga, Catherine Allard, Sheila J. Barton, Ana Espinosa, Julie Marsh, Catherine Potter, Ge Zhang, Wei Ang, Diane J. Berry, Luigi Bouchard, Shikta Das, Håkon Håkonarson, Jani Heikkinen, Øyvind Helgeland, Berthold Hocher, Albert Hofman, Hazel Inskip, Samuel E. Jones, Manolis Kogevinas, Penelope A. Lind, Letizia Marullo, Sarah E. Medland, Anna Murray, Jeffrey C. Murray, Pål R. Njølstad, Ellen A. Nøhr, Christoph Reichetzeder, Susan M. Ring, Katherine S. Ruth, Loreto Santa‐Marina, Denise Scholtens, Sylvain Sebért, Verena Sengpiel, Marcus A. Tuke, Marc Vaudel, Michael N. Weedon, Gonneke Willemsen, Andrew R. Wood, Hanieh Yaghootkar, Louis J. Muglia, Meike Bartels, Caroline L. Relton, Craig E. Pennell, Leda Chatzi, Xavier Estivill, John W. Holloway, Dorret I. Boomsma, Grant W. Montgomery, Joanne M. Murabito, Tim D. Spector, Christine Power, Marjo‐Riitta Järvelin, Hans Bisgaard, Struan F.A. Grant, Thorkild I. A. Sørensen, Vincent W.V. Jaddoe, Bo Jacobsson, Mads Melbye, Mark I. McCarthy, Andrew T. Hattersley, M. Geoffrey Hayes, Timothy M. Frayling, Marie‐France Hivert, Janine F. Felix, Elina Hyppönen, William L. Lowe, David M. Evans, Debbie A. Lawlor, Bjarke Feenstra, Rachel M. Freathy - Human Molecular Genetics 2018 cited by 198
- Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration
Authors: Xueping Liu, Dorte Helenius, Line Skotte, Robin N. Beaumont, Matthias Wielscher, Frank Geller, Julius Juodakis, Anubha Mahajan, Jonathan P. Bradfield, Frederick T. J. Lin, Suzanne Vogelezang, Mariona Bustamante, Tarunveer S. Ahluwalia, Niina Pitkänen, Carol A. Wang, Jonas Bačelis, Maria Carolina Borges, Ge Zhang, Bruce Bedell, Robert M. Rossi, Kristin Skogstrand, Shouneng Peng, Wesley K. Thompson, Vivek Appadurai, Debbie A. Lawlor, Ilkka Kalliala, Christine Power, Mark I. McCarthy, Heather A. Boyd, Mary L. Marazita, Håkon Håkonarson, M. Geoffrey Hayes, Denise Scholtens, Fernando Rivadeneira, Vincent W. V. Jaddoe, Rebecca Vinding, Hans Bisgaard, Bridget Knight, Katja Pahkala, Olli T. Raitakari, Øyvind Helgeland, Stefan Johansson, Pål R. Njølstad, João Fadista, Andrew J. Schork, Ron Nudel, Daniel E. Miller, Xiaoting Chen, Matthew T. Weirauch, Preben Bo Mortensen, Anders D. Børglum, Merete Nordentoft, Ole Mors, Ke Hao, Kelli K. Ryckman, David M. Hougaard, Leah C. Kottyan, Craig E. Pennell, Leo‐Pekka Lyytikäinen, Klaus Bønnelykke, Martine Vrijheid, Janine F. Felix, William L. Lowe, Struan F.A. Grant, Elina Hyppönen, Bo Jacobsson, Marjo‐Riitta Järvelin, Louis J. Muglia, Jeffrey C. Murray, Rachel M. Freathy, Thomas Werge, Mads Melbye, Alfonso Buil, Bjarke Feenstra - Nature Communications 2019 cited by 103
- Axenfeld-Rieger syndrome: more than meets the eye
Authors: Linda M. Reis, Mohit Maheshwari, Jenina Capasso, Hüban Atilla, Ľubica Ďuďáková, Samuel Thompson, Lia Zitano, Guillermo Lay‐Son, R. Brian Lowry, Jennifer D. Black, Joseph Lee, Ann Shue, Radka Kremlíková Pourová, Manuela Vaněčková, Pavlína Skalická, Jana Jedličková, Marie Trková, Bradley A. Williams, Gabriele Richard, Kristine Bachman, Andrea Seeley, Deborah M. Costakos, Thomas Gläser, Alex V. Levin, Petra Lišková, Jeffrey C. Murray, Elena V. Semina - Journal of Medical Genetics 2022 cited by 78
- Multiomic signals associated with maternal epidemiological factors contributing to preterm birth in low- and middle-income countries
Authors: Camilo Espinosa, Waqasuddin Khan, Rasheda Khanam, Sayan Das, Javairia Khalid, Jesmin Pervin, Margaret P. Kasaro, Kévin Contrepois, Alan L. Chang, Thanaphong Phongpreecha, Basil Michael, Mathew Ellenberger, Usma Mehmood, Aneeta Hotwani, Ambreen Nizar, Furqan Kabir, Ronald J. Wong, Martin Becker, Eloïse Berson, Anthony Culos, Davide De Francesco, Samson Mataraso, Neal G. Ravindra, Melan Thuraiappah, Maria Xenochristou, Ina A. Stelzer, Ivana Marić, Arup Dutta, Rubhana Raqib, Salahuddin Ahmed, Sayedur Rahman, A. S. M. Tarik Hasan, Said M. Ali, Mohamed Hamad Juma, Monjur Rahman, Shaki Aktar, Saikat Deb, Joan T. Price, Paul H. Wise, Virginia D. Winn, Maurice L. Druzin, Ronald S. Gibbs, Gary L. Darmstadt, Jeffrey C. Murray, Jeffrey S. A. Stringer, Brice Gaudillière, M Snyder, Martin S. Angst, Anisur Rahman, Abdullah H Baqui, Fyezah Jehan, Muhammad Imran Nisar, Bellington Vwalika, Sunil Sazawal, Gary M. Shaw, David K. Stevenson, Nima Aghaeepour - Science Advances 2023 cited by 34
- Disruption of an AP-2α binding site in an IRF6 enhancer is associated with cleft lip
Authors: NISC Comparative Sequencing Program, Fedik Rahimov, Mary L. Marazita, Axel Visel, Margaret E. Cooper, Michael J. Hitchler, Michele Rubini, Frederick E. Domann, Manika Govil, Kaare Christensen, Camille Bille, Mads Melbye, Astanand Jugessur, Rolv T. Lie, Allen J. Wilcox, David Fitzpatrick, Eric D. Green, Peter Mossey, Julian Little, Régine P.M. Steegers‐Theunissen, L Pennacchio, Brian C. Schutte, Jeffrey C. Murray - Nature Genetics 2008 cited by 427
- Dominant Mutations in GRHL3 Cause Van der Woude Syndrome and Disrupt Oral Periderm Development
Authors: Myriam Peyrard‐Janvid, Elizabeth J. Leslie, Youssef A. Kousa, Tiffany L. Smith, Martine Dunnwald, Måns Magnusson, Brian Lentz, Per Unneberg, Ingegerd Fransson, Hannele Koillinen, Jorma Rautio, Marie Pegelow, Agneta Karsten, Lina Basel‐Vanagaite, William Gordon, Bogi Andersen, Thomas Svensson, Jeffrey C. Murray, Robert A. Cornell, Juha Kere, Brian C. Schutte - The American Journal of Human Genetics 2013 cited by 230
