F Mone, R Y Eberhardt, R K Morris, M E Hurles, D J McMullan, E R Maher, J Lord, L S Chitty, J L Giordano, R J Wapner, M D Kilby. Ultrasound Obstet Gynecol 2021
Times Cited: 11
Times Cited: 11
Times Cited
Times Co-cited
Similarity
Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.
Jenny Lord, Dominic J McMullan, Ruth Y Eberhardt, Gabriele Rinck, Susan J Hamilton, Elizabeth Quinlan-Jones, Elena Prigmore, Rebecca Keelagher, Sunayna K Best, Georgina K Carey,[...]. Lancet 2019
Jenny Lord, Dominic J McMullan, Ruth Y Eberhardt, Gabriele Rinck, Susan J Hamilton, Elizabeth Quinlan-Jones, Elena Prigmore, Rebecca Keelagher, Sunayna K Best, Georgina K Carey,[...]. Lancet 2019
54
Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study.
Slavé Petrovski, Vimla Aggarwal, Jessica L Giordano, Melissa Stosic, Karen Wou, Louise Bier, Erica Spiegel, Kelly Brennan, Nicholas Stong, Vaidehi Jobanputra,[...]. Lancet 2019
Slavé Petrovski, Vimla Aggarwal, Jessica L Giordano, Melissa Stosic, Karen Wou, Louise Bier, Erica Spiegel, Kelly Brennan, Nicholas Stong, Vaidehi Jobanputra,[...]. Lancet 2019
54
Lessons from exome sequencing in prenatally diagnosed heart defects: A basis for prenatal testing.
Dominik S Westphal, Gloria S Leszinski, Esther Rieger-Fackeldey, Elisabeth Graf, Gregor Weirich, Thomas Meitinger, Eva Ostermayer, Renate Oberhoffer, Matias Wagner. Clin Genet 2019
Dominik S Westphal, Gloria S Leszinski, Esther Rieger-Fackeldey, Elisabeth Graf, Gregor Weirich, Thomas Meitinger, Eva Ostermayer, Renate Oberhoffer, Matias Wagner. Clin Genet 2019
45
The prevalence of genetic diagnoses in fetuses with severe congenital heart defects.
Amber E L van Nisselrooij, Malou A Lugthart, Sally-Ann Clur, Ingeborg H Linskens, Eva Pajkrt, Lukas A Rammeloo, Lieke Rozendaal, Nico A Blom, Jan M M van Lith, Alida C Knegt,[...]. Genet Med 2020
Amber E L van Nisselrooij, Malou A Lugthart, Sally-Ann Clur, Ingeborg H Linskens, Eva Pajkrt, Lukas A Rammeloo, Lieke Rozendaal, Nico A Blom, Jan M M van Lith, Alida C Knegt,[...]. Genet Med 2020
45
Whole-exome sequencing on deceased fetuses with ultrasound anomalies: expanding our knowledge of genetic disease during fetal development.
Carin L Yates, Kristin G Monaghan, Deborah Copenheaver, Kyle Retterer, Julie Scuffins, Cathlin R Kucera, Bethany Friedman, Gabriele Richard, Jane Juusola. Genet Med 2017
Carin L Yates, Kristin G Monaghan, Deborah Copenheaver, Kyle Retterer, Julie Scuffins, Cathlin R Kucera, Bethany Friedman, Gabriele Richard, Jane Juusola. Genet Med 2017
45
Prenatal exome sequencing in anomalous fetuses: new opportunities and challenges.
Neeta L Vora, Bradford Powell, Alicia Brandt, Natasha Strande, Emily Hardisty, Kelly Gilmore, Ann Katherine M Foreman, Kirk Wilhelmsen, Chris Bizon, Jason Reilly,[...]. Genet Med 2017
Neeta L Vora, Bradford Powell, Alicia Brandt, Natasha Strande, Emily Hardisty, Kelly Gilmore, Ann Katherine M Foreman, Kirk Wilhelmsen, Chris Bizon, Jason Reilly,[...]. Genet Med 2017
45
The use of fetal exome sequencing in prenatal diagnosis: a points to consider document of the American College of Medical Genetics and Genomics (ACMG).
Kristin G Monaghan, Natalia T Leach, Dawn Pekarek, Priya Prasad, Nancy C Rose. Genet Med 2020
Kristin G Monaghan, Natalia T Leach, Dawn Pekarek, Priya Prasad, Nancy C Rose. Genet Med 2020
45
Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder.
Elizabeth A Normand, Alicia Braxton, Salma Nassef, Patricia A Ward, Francesco Vetrini, Weimin He, Vipulkumar Patel, Chunjing Qu, Lauren E Westerfield, Samantha Stover,[...]. Genome Med 2018
Elizabeth A Normand, Alicia Braxton, Salma Nassef, Patricia A Ward, Francesco Vetrini, Weimin He, Vipulkumar Patel, Chunjing Qu, Lauren E Westerfield, Samantha Stover,[...]. Genome Med 2018
45
Reproductive genetic counseling challenges associated with diagnostic exome sequencing in a large academic private reproductive genetic counseling practice.
Lauren E Westerfield, Samantha R Stover, Veena S Mathur, Salma A Nassef, Tiffiney G Carter, Yaping Yang, Christine M Eng, Ignatia B Van den Veyver. Prenat Diagn 2015
Lauren E Westerfield, Samantha R Stover, Veena S Mathur, Salma A Nassef, Tiffiney G Carter, Yaping Yang, Christine M Eng, Ignatia B Van den Veyver. Prenat Diagn 2015
36
Contribution of single-gene defects to congenital cardiac left-sided lesions in the prenatal setting.
H Sun, T Yi, X Hao, H Yan, J Wang, Q Li, X Gu, X Zhou, S Wang, X Wang,[...]. Ultrasound Obstet Gynecol 2020
H Sun, T Yi, X Hao, H Yan, J Wang, Q Li, X Gu, X Zhou, S Wang, X Wang,[...]. Ultrasound Obstet Gynecol 2020
36
From diagnostic yield to clinical impact: a pilot study on the implementation of prenatal exome sequencing in routine care.
Maayke A de Koning, Monique C Haak, Phebe N Adama van Scheltema, Cacha M P C D Peeters-Scholte, Tamara T Koopmann, Esther A R Nibbeling, Emmelien Aten, Nicolette S den Hollander, Claudia A L Ruivenkamp, Mariëtte J V Hoffer,[...]. Genet Med 2019
Maayke A de Koning, Monique C Haak, Phebe N Adama van Scheltema, Cacha M P C D Peeters-Scholte, Tamara T Koopmann, Esther A R Nibbeling, Emmelien Aten, Nicolette S den Hollander, Claudia A L Ruivenkamp, Mariëtte J V Hoffer,[...]. Genet Med 2019
36
Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesis.
Sarah Boissel, Catherine Fallet-Bianco, David Chitayat, Valérie Kremer, Christina Nassif, Françoise Rypens, Marie-Ange Delrue, Dorothée Dal Soglio, Luc L Oligny, Natalie Patey,[...]. Genet Med 2018
Sarah Boissel, Catherine Fallet-Bianco, David Chitayat, Valérie Kremer, Christina Nassif, Françoise Rypens, Marie-Ange Delrue, Dorothée Dal Soglio, Luc L Oligny, Natalie Patey,[...]. Genet Med 2018
36
Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
36
Diagnosis of lethal or prenatal-onset autosomal recessive disorders by parental exome sequencing.
Karen L Stals, Matthew Wakeling, Júlia Baptista, Richard Caswell, Andrew Parrish, Julia Rankin, Carolyn Tysoe, Garan Jones, Adam C Gunning, Hana Lango Allen,[...]. Prenat Diagn 2018
Karen L Stals, Matthew Wakeling, Júlia Baptista, Richard Caswell, Andrew Parrish, Julia Rankin, Carolyn Tysoe, Garan Jones, Adam C Gunning, Hana Lango Allen,[...]. Prenat Diagn 2018
36
Prenatal exome sequencing in fetuses with congenital heart defects.
Ru Li, Fang Fu, Qiuxia Yu, Dan Wang, Xiangyi Jing, Yongling Zhang, Fucheng Li, Fatao Li, Jin Han, Min Pan,[...]. Clin Genet 2020
Ru Li, Fang Fu, Qiuxia Yu, Dan Wang, Xiangyi Jing, Yongling Zhang, Fucheng Li, Fatao Li, Jin Han, Min Pan,[...]. Clin Genet 2020
66
Whole exome sequencing as a diagnostic adjunct to clinical testing in fetuses with structural abnormalities.
F Fu, R Li, Y Li, Z-Q Nie, T Lei, D Wang, X Yang, J Han, M Pan, L Zhen,[...]. Ultrasound Obstet Gynecol 2018
F Fu, R Li, Y Li, Z-Q Nie, T Lei, D Wang, X Yang, J Han, M Pan, L Zhen,[...]. Ultrasound Obstet Gynecol 2018
36
Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis.
Teresa N Sparks, Billie R Lianoglou, Rebecca R Adami, Ilina D Pluym, Kerry Holliman, Jennifer Duffy, Sarah L Downum, Sachi Patel, Amanda Faubel, Nina M Boe,[...]. N Engl J Med 2020
Teresa N Sparks, Billie R Lianoglou, Rebecca R Adami, Ilina D Pluym, Kerry Holliman, Jennifer Duffy, Sarah L Downum, Sachi Patel, Amanda Faubel, Nina M Boe,[...]. N Engl J Med 2020
36
Rapid prenatal diagnosis using targeted exome sequencing: a cohort study to assess feasibility and potential impact on prenatal counseling and pregnancy management.
Natalie Chandler, Sunayna Best, Jane Hayward, Francesca Faravelli, Sahar Mansour, Emma Kivuva, Dagmar Tapon, Alison Male, Catherine DeVile, Lyn S Chitty. Genet Med 2018
Natalie Chandler, Sunayna Best, Jane Hayward, Francesca Faravelli, Sahar Mansour, Emma Kivuva, Dagmar Tapon, Alison Male, Catherine DeVile, Lyn S Chitty. Genet Med 2018
36
Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES).
Gordon K C Leung, Christopher C Y Mak, Jasmine L F Fung, Wilfred H S Wong, Mandy H Y Tsang, Mullin H C Yu, Steven L C Pei, K S Yeung, Gary T K Mok, C P Lee,[...]. BMC Med Genomics 2018
Gordon K C Leung, Christopher C Y Mak, Jasmine L F Fung, Wilfred H S Wong, Mandy H Y Tsang, Mullin H C Yu, Steven L C Pei, K S Yeung, Gary T K Mok, C P Lee,[...]. BMC Med Genomics 2018
27
Array comparative genomic hybridization and fetal congenital heart defects: a systematic review and meta-analysis.
F A R Jansen, Y J Blumenfeld, A Fisher, J M Cobben, A O Odibo, A Borrell, M C Haak. Ultrasound Obstet Gynecol 2015
F A R Jansen, Y J Blumenfeld, A Fisher, J M Cobben, A O Odibo, A Borrell, M C Haak. Ultrasound Obstet Gynecol 2015
27
Fetal exome sequencing: yield and limitations in a tertiary referral center.
H Daum, V Meiner, O Elpeleg, T Harel. Ultrasound Obstet Gynecol 2019
H Daum, V Meiner, O Elpeleg, T Harel. Ultrasound Obstet Gynecol 2019
27
Importance of complete phenotyping in prenatal whole exome sequencing.
Mahmoud Aarabi, Olivia Sniezek, Huaiyang Jiang, Devereux N Saller, Daniel Bellissimo, Svetlana A Yatsenko, Aleksandar Rajkovic. Hum Genet 2018
Mahmoud Aarabi, Olivia Sniezek, Huaiyang Jiang, Devereux N Saller, Daniel Bellissimo, Svetlana A Yatsenko, Aleksandar Rajkovic. Hum Genet 2018
27
Exome sequencing in the assessment of congenital malformations in the fetus and neonate.
Fionnuala Mone, Elizabeth Quinlan-Jones, Andrew K Ewer, Mark D Kilby. Arch Dis Child Fetal Neonatal Ed 2019
Fionnuala Mone, Elizabeth Quinlan-Jones, Andrew K Ewer, Mark D Kilby. Arch Dis Child Fetal Neonatal Ed 2019
33
Implementation of exome sequencing in fetal diagnostics-Data and experiences from a tertiary center in Denmark.
Naja Becher, Lotte Andreasen, Puk Sandager, Stina Lou, Olav Bjørn Petersen, Rikke Christensen, Ida Vogel. Acta Obstet Gynecol Scand 2020
Naja Becher, Lotte Andreasen, Puk Sandager, Stina Lou, Olav Bjørn Petersen, Rikke Christensen, Ida Vogel. Acta Obstet Gynecol Scand 2020
27
The Human Phenotype Ontology in 2021.
Sebastian Köhler, Michael Gargano, Nicolas Matentzoglu, Leigh C Carmody, David Lewis-Smith, Nicole A Vasilevsky, Daniel Danis, Ganna Balagura, Gareth Baynam, Amy M Brower,[...]. Nucleic Acids Res 2021
Sebastian Köhler, Michael Gargano, Nicolas Matentzoglu, Leigh C Carmody, David Lewis-Smith, Nicole A Vasilevsky, Daniel Danis, Ganna Balagura, Gareth Baynam, Amy M Brower,[...]. Nucleic Acids Res 2021
27
Molecular autopsy by trio exome sequencing (ES) and postmortem examination in fetuses and neonates with prenatally identified structural anomalies.
Elizabeth Quinlan-Jones, Jenny Lord, Denise Williams, Sue Hamilton, Tamas Marton, Ruth Y Eberhardt, Gabriele Rinck, Elena Prigmore, Rebecca Keelagher, Dominic J McMullan,[...]. Genet Med 2019
Elizabeth Quinlan-Jones, Jenny Lord, Denise Williams, Sue Hamilton, Tamas Marton, Ruth Y Eberhardt, Gabriele Rinck, Elena Prigmore, Rebecca Keelagher, Dominic J McMullan,[...]. Genet Med 2019
27
Promises, pitfalls and practicalities of prenatal whole exome sequencing.
Sunayna Best, Karen Wou, Neeta Vora, Ignatia B Van der Veyver, Ronald Wapner, Lyn S Chitty. Prenat Diagn 2018
Sunayna Best, Karen Wou, Neeta Vora, Ignatia B Van der Veyver, Ronald Wapner, Lyn S Chitty. Prenat Diagn 2018
27
An approach to integrating exome sequencing for fetal structural anomalies into clinical practice.
Neeta L Vora, Kelly Gilmore, Alicia Brandt, Chelsea Gustafson, Natasha Strande, Lori Ramkissoon, Emily Hardisty, Ann Katherine M Foreman, Kirk Wilhelmsen, Phillips Owen,[...]. Genet Med 2020
Neeta L Vora, Kelly Gilmore, Alicia Brandt, Chelsea Gustafson, Natasha Strande, Lori Ramkissoon, Emily Hardisty, Ann Katherine M Foreman, Kirk Wilhelmsen, Phillips Owen,[...]. Genet Med 2020
27
Exome sequencing improves genetic diagnosis of fetal increased nuchal translucency.
Xin Yang, Lv-Yin Huang, Min Pan, Li-Li Xu, Li Zhen, Jin Han, Dong-Zhi Li. Prenat Diagn 2020
Xin Yang, Lv-Yin Huang, Min Pan, Li-Li Xu, Li Zhen, Jin Han, Dong-Zhi Li. Prenat Diagn 2020
27
Whole-exome sequencing in the evaluation of fetal congenital anomalies of the kidney and urinary tract detected by ultrasonography.
Ting-Ying Lei, Fang Fu, Ru Li, Qiu-Xia Yu, Kun Du, Wen-Wen Zhang, Qiong Deng, Lu-Shan Li, Dan Wang, Xin Yang,[...]. Prenat Diagn 2020
Ting-Ying Lei, Fang Fu, Ru Li, Qiu-Xia Yu, Kun Du, Wen-Wen Zhang, Qiong Deng, Lu-Shan Li, Dan Wang, Xin Yang,[...]. Prenat Diagn 2020
60
Prenatal diagnosis by chromosomal microarray analysis.
Brynn Levy, Ronald Wapner. Fertil Steril 2018
Brynn Levy, Ronald Wapner. Fertil Steril 2018
27
Evaluation of Diagnostic Yield in Fetal Whole-Exome Sequencing: A Report on 45 Consecutive Families.
Lior Greenbaum, Ben Pode-Shakked, Shlomit Eisenberg-Barzilai, Michal Dicastro-Keidar, Anat Bar-Ziv, Nurit Goldstein, Haike Reznik-Wolf, Hana Poran, Amihai Rigbi, Ortal Barel,[...]. Front Genet 2019
Lior Greenbaum, Ben Pode-Shakked, Shlomit Eisenberg-Barzilai, Michal Dicastro-Keidar, Anat Bar-Ziv, Nurit Goldstein, Haike Reznik-Wolf, Hana Poran, Amihai Rigbi, Ortal Barel,[...]. Front Genet 2019
27
Clinical aspects of prenatally detected congenital heart malformations and the yield of chromosomal microarray analysis.
Rivka Sukenik-Halevy, Shay Sukenik, Arie Koifman, Yoav Alpert, Reli Hershkovitz, Alex Levi, Tal Biron-Shental. Prenat Diagn 2016
Rivka Sukenik-Halevy, Shay Sukenik, Arie Koifman, Yoav Alpert, Reli Hershkovitz, Alex Levi, Tal Biron-Shental. Prenat Diagn 2016
18
Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing.
Alejandro Sifrim, Marc-Phillip Hitz, Anna Wilsdon, Jeroen Breckpot, Saeed H Al Turki, Bernard Thienpont, Jeremy McRae, Tomas W Fitzgerald, Tarjinder Singh, Ganesh Jawahar Swaminathan,[...]. Nat Genet 2016
Alejandro Sifrim, Marc-Phillip Hitz, Anna Wilsdon, Jeroen Breckpot, Saeed H Al Turki, Bernard Thienpont, Jeremy McRae, Tomas W Fitzgerald, Tarjinder Singh, Ganesh Jawahar Swaminathan,[...]. Nat Genet 2016
18
Identification of copy number variations associated with congenital heart disease by chromosomal microarray analysis and next-generation sequencing.
Xiangyu Zhu, Jie Li, Tong Ru, Yaping Wang, Yan Xu, Ying Yang, Xing Wu, David S Cram, Yali Hu. Prenat Diagn 2016
Xiangyu Zhu, Jie Li, Tong Ru, Yaping Wang, Yan Xu, Ying Yang, Xing Wu, David S Cram, Yali Hu. Prenat Diagn 2016
18
Clinical application of targeted next-generation sequencing in fetuses with congenital heart defect.
P Hu, F Qiao, Y Wang, L Meng, X Ji, C Luo, T Xu, R Zhou, J Zhang, B Yu,[...]. Ultrasound Obstet Gynecol 2018
P Hu, F Qiao, Y Wang, L Meng, X Ji, C Luo, T Xu, R Zhou, J Zhang, B Yu,[...]. Ultrasound Obstet Gynecol 2018
18
Fetal right aortic arch: associated anomalies, genetic anomalies with chromosomal microarray analysis, and postnatal outcome.
Ruan Peng, Hong-Ning Xie, Ju Zheng, Yi Zhou, Mei-Fang Lin. Prenat Diagn 2017
Ruan Peng, Hong-Ning Xie, Ju Zheng, Yi Zhou, Mei-Fang Lin. Prenat Diagn 2017
18
Prenatal chromosomal microarray analysis in fetuses with congenital heart disease: a prospective cohort study.
Yan Wang, Li Cao, Dong Liang, Lulu Meng, Yun Wu, Fengchang Qiao, Xiuqing Ji, Chunyu Luo, Jingjing Zhang, Tianhui Xu,[...]. Am J Obstet Gynecol 2018
Yan Wang, Li Cao, Dong Liang, Lulu Meng, Yun Wu, Fengchang Qiao, Xiuqing Ji, Chunyu Luo, Jingjing Zhang, Tianhui Xu,[...]. Am J Obstet Gynecol 2018
18
Clinical utility of exome sequencing in the prenatal diagnosis of congenital anomalies: A Review.
Fionnuala Mone, Elizabeth Quinlan-Jones, Mark D Kilby. Eur J Obstet Gynecol Reprod Biol 2018
Fionnuala Mone, Elizabeth Quinlan-Jones, Mark D Kilby. Eur J Obstet Gynecol Reprod Biol 2018
18
Diagnostic power and clinical impact of exome sequencing in a cohort of 500 patients with rare diseases.
Caio Robledo D'Angioli Costa Quaio, Caroline Monaco Moreira, Gil Monteiro Novo-Filho, Patricia Rossi Sacramento-Bobotis, Michele Groenner Penna, Sandro Felix Perazzio, Aurelio Pimenta Dutra, Rafael Alves da Silva, Monize Nakamoto Provisor Santos, Vanessa Yurie Nozaki de Arruda,[...]. Am J Med Genet C Semin Med Genet 2020
Caio Robledo D'Angioli Costa Quaio, Caroline Monaco Moreira, Gil Monteiro Novo-Filho, Patricia Rossi Sacramento-Bobotis, Michele Groenner Penna, Sandro Felix Perazzio, Aurelio Pimenta Dutra, Rafael Alves da Silva, Monize Nakamoto Provisor Santos, Vanessa Yurie Nozaki de Arruda,[...]. Am J Med Genet C Semin Med Genet 2020
20
Prenatal whole exome sequencing: the views of clinicians, scientists, genetic counsellors and patient representatives.
Elizabeth Quinlan-Jones, Mark D Kilby, Sheila Greenfield, Michael Parker, Dominic McMullan, Matthew E Hurles, Sarah C Hillman. Prenat Diagn 2016
Elizabeth Quinlan-Jones, Mark D Kilby, Sheila Greenfield, Michael Parker, Dominic McMullan, Matthew E Hurles, Sarah C Hillman. Prenat Diagn 2016
18
Novel and recurrent variants identified in fetuses with central nervous system abnormalities by trios-medical exome sequencing.
Hu Tan, Yinong Xie, Fei Chen, Min Chen, Li Yu, Dunjin Chen, Jingsi Chen. Clin Chim Acta 2020
Hu Tan, Yinong Xie, Fei Chen, Min Chen, Li Yu, Dunjin Chen, Jingsi Chen. Clin Chim Acta 2020
50
Prenatal diagnosis of skeletal dysplasias using whole exome sequencing in China.
Jia Tang, Chenglong Zhou, Haihong Shi, Yuying Mo, Weilan Tan, Tielan Sun, Jinling Zhu, Qing Li, Hui Li, Yuping Li,[...]. Clin Chim Acta 2020
Jia Tang, Chenglong Zhou, Haihong Shi, Yuying Mo, Weilan Tan, Tielan Sun, Jinling Zhu, Qing Li, Hui Li, Yuping Li,[...]. Clin Chim Acta 2020
28
Simultaneous Detection of CNVs and SNVs Improves the Diagnostic Yield of Fetuses with Ultrasound Anomalies and Normal Karyotypes.
Qingwei Qi, Yulin Jiang, Xiya Zhou, Hua Meng, Na Hao, Jiazhen Chang, Junjie Bai, Chunli Wang, Mingming Wang, Jiangshan Guo,[...]. Genes (Basel) 2020
Qingwei Qi, Yulin Jiang, Xiya Zhou, Hua Meng, Na Hao, Jiazhen Chang, Junjie Bai, Chunli Wang, Mingming Wang, Jiangshan Guo,[...]. Genes (Basel) 2020
33
Genomic medicine for undiagnosed diseases.
Anastasia L Wise, Teri A Manolio, George A Mensah, Josh F Peterson, Dan M Roden, Cecelia Tamburro, Marc S Williams, Eric D Green. Lancet 2019
Anastasia L Wise, Teri A Manolio, George A Mensah, Josh F Peterson, Dan M Roden, Cecelia Tamburro, Marc S Williams, Eric D Green. Lancet 2019
18
Targeted gene sequencing and whole-exome sequencing in autopsied fetuses with prenatally diagnosed kidney anomalies.
M Rasmussen, L Sunde, M L Nielsen, M Ramsing, A Petersen, T D Hjortshøj, T E Olsen, A Tabor, J M Hertz, I Johnsen,[...]. Clin Genet 2018
M Rasmussen, L Sunde, M L Nielsen, M Ramsing, A Petersen, T D Hjortshøj, T E Olsen, A Tabor, J M Hertz, I Johnsen,[...]. Clin Genet 2018
18
Fetal Exome Sequencing on the Horizon.
Karen Wou, Isabelle DeBie, June Carroll, Jo-Ann Brock, R Douglas Wilson. J Obstet Gynaecol Can 2019
Karen Wou, Isabelle DeBie, June Carroll, Jo-Ann Brock, R Douglas Wilson. J Obstet Gynaecol Can 2019
33
Mutations in GREB1L Cause Bilateral Kidney Agenesis in Humans and Mice.
Lara De Tomasi, Pierre David, Camille Humbert, Flora Silbermann, Christelle Arrondel, Frédéric Tores, Stéphane Fouquet, Audrey Desgrange, Olivier Niel, Christine Bole-Feysot,[...]. Am J Hum Genet 2017
Lara De Tomasi, Pierre David, Camille Humbert, Flora Silbermann, Christelle Arrondel, Frédéric Tores, Stéphane Fouquet, Audrey Desgrange, Olivier Niel, Christine Bole-Feysot,[...]. Am J Hum Genet 2017
18
Next-generation sequencing and prenatal 'omics: advanced diagnostics and new insights into human development.
Neeta L Vora, Lisa Hui. Genet Med 2018
Neeta L Vora, Lisa Hui. Genet Med 2018
18
Molecular autopsy in maternal-fetal medicine.
Hanan E Shamseldin, Wesam Kurdi, Fatima Almusafri, Maha Alnemer, Alya Alkaff, Zeneb Babay, Amal Alhashem, Maha Tulbah, Nada Alsahan, Rubina Khan,[...]. Genet Med 2018
Hanan E Shamseldin, Wesam Kurdi, Fatima Almusafri, Maha Alnemer, Alya Alkaff, Zeneb Babay, Amal Alhashem, Maha Tulbah, Nada Alsahan, Rubina Khan,[...]. Genet Med 2018
18
Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.