Genetic, environmental, and epigenetic factors involved in CAKUT
Nicolaou, Nayia, Renkema, Kirsten Y., Bongers, Ernie M. H. F., Giles, Rachel H., Knoers, Nine V. A. M.·2015·Nature Reviews Nephrology
Cited by (346)
Items 101–200 of 346
- Improving renal phenotype and evolving extra-renal features of 17q12 deletion encompassing the HNF1B geneRoxana Cleper, Adi Reches, Dana Shapira, Sharon Simchoni, Lewis Reisman, Liat Ben‐Sira, Yuval Yaron, Igal Wolman, G. Malinger, Dana Brabbing Goldstein et al. · 2021 · Translational Pediatrics
- Genetic spectrum of CAKUT and risk factors for kidney failure: a pediatric multicenter cohort studyJia-Lu Liu, Xiaowen Wang, Cuihua Liu, Duan Ma Xiao-Jie Gao, Xiaoyun Jiang, Jianhua Mao, Guanghua Zhu, Ai-Hua Zhang, Mo Wang, Xiqiang Dang et al. · 2022 · Nephrology Dialysis Transplantation
- The term CAKUT has outlived its usefulness: the case for the defenseNine V.A.M. Knoers · 2022 · Pediatric Nephrology
- Disease mechanisms of monogenic congenital anomalies of the kidney and urinary tractDervla M. Connaughton, Friedhelm Hildebrandt · 2022 · American Journal of Medical Genetics Part C Seminars in Medical Genetics
- Genetic Susceptibility to Chronic Kidney Disease: Links, Risks and ManagementHanny Sawaf, Tariku Tadele Gudura, Sylvester Dorobisz, Dianne Sandy, Xiangling Wang, Shane A. Bobart · 2023 · International Journal of Nephrology and Renovascular Disease
- Spectrum of congenital anomalies of the kidney and urinary tract (CAKUT) including renal parenchymal malformations during fetal life and the implementation of prenatal exome sequencing (WES)Josefine Theresia Königbauer, Laura Fangmann, Charlotte Reinhardt, Alexander Weichert, Wolfgang Henrich, Biskup Saskia, Heinz Gabriel · 2023 · Archives of Gynecology and Obstetrics
- Sex difference and risk factors in burden of urogenital congenital anomalies from 1990 to 2019Xiaoyu Huang, Jianming Tang, Mao Chen, Ya Xiao, Fangyi Zhu, Liying Chen, Xiaoyu Tian, Hong Li · 2023 · Scientific Reports
- Prenatal diagnosis of urinary tract anomalies, a cohort study in the Northern NetherlandsMarian K. Bakker, Jorieke E. H. Bergman, Hanneke Fleurke‐Rozema, Esther Streefland, Valentina Gracchi, Caterina Maddalena Bilardo, Hermien E. K. de Walle · 2017 · Prenatal Diagnosis
- Overview of pediatric kidney transplantationCaroline P. Lemoine, Marcos E. Pozo, Riccardo Antonio Superina · 2022 · Seminars in Pediatric Surgery
- Genetic Basis of Posterior Urethral Valves InheritanceCinzia Chiaramonte, Denisia Bommarito, Elisa Zambaiti, Vincenzo Antona, Giuseppe Li Voti · 2016 · Urology
- A Homozygous Dab1−/− Is a Potential Novel Cause of Autosomal Recessive Congenital Anomalies of the Mice Kidney and Urinary TractAnita Racetin, Natalija Filipović, Mirela Lozić, Masaki Ogata, Larissa Gudelj Ensor, Nela Kelam, Petra Kovačević, Koichiro Watanabe, Yu Katsuyama, Mirna Saraga‐Babić et al. · 2021 · Biomolecules
- Deciphering the mutation spectrum in south Indian children with congenital anomalies of the kidney and urinary tractAmbili Narikot, Varsha Chhotusing Pardeshi, A. M. Shubha, Arpana Aprameya Iyengar, Anil Vasudevan · 2022 · BMC Nephrology
- Congenital Anomalies of the Kidneys, Collecting System, Bladder, and UrethraHalima Saadia Janjua, Suet Kam Lam, Vedant Gupta, Sangeeta Krishna · 2019 · Pediatrics in Review
- Harnessing mechanobiology for kidney organoid researchZarina Nauryzgaliyeva, Iphigénie Goux Corredera, Elena Garreta, Núria Montserrat · 2023 · Frontiers in Cell and Developmental Biology
- Genetics of anomalies of the kidney and urinary tract with congenital heart disease: A reviewAmin J. Barakat, Merlin G. Butler · 2024 · Clinical Genetics
- Translational strategies to uncover the etiology of congenital anomalies of the kidney and urinary tractLisanne M. Vendrig, Mayke A C Ten Hoor, Benthe H König, Iris Lekkerkerker, Kirsten Y. Renkema, Michiel F. Schreuder, Loes F.M. van der Zanden, Albertien M. van Eerde, Sander Groen in ’t Woud, Jaap Mulder et al. · 2024 · Pediatric Nephrology
- Long-term trends in the incidence of congenital anomalies in Central China from 1997 to 2019Zengli Yu, D. Li, Ledong Sun, Xin Zhao, Hui Chang, L. Cui, H Zhang, Xuanchen Liu, Xiang Qian Lao, Zhongxiao Wan et al. · 2022 · Public Health
- Neonatal acute kidney injury: recording rate, course, and outcome: one center experienceRoxana Cleper, Itay Shavit, D T Blumenthal, Lewis Reisman, Galit Pomeranz, Alon Haham, Shiran Friedman, Ilana Goldiner, Dror Mandel · 2018 · The Journal of Maternal-Fetal & Neonatal Medicine
- Implications of uremic cardiomyopathy for the practicing clinician: an educational reviewHiroaki Hiraiwa, Daisuke Kasugai, Takahiro Okumura, Toyoaki Murohara · 2023 · Heart Failure Reviews
- Acetyl-CoA is a key molecule for nephron progenitor cell pool maintenanceFabiola Diniz, Nguyen Yen Nhi Ngo, Mariel Colón-Leyva, Francesca Edgington-Giordano, Sylvia A. Hilliard, Kevin J. Zwezdaryk, Jiao Liu, Samir Sayem El-Dahr, Giovane G. Tortelote · 2023 · Nature Communications
- Signs and symptoms of developmental abnormalities of the genitourinary tractPaulo César Koch Nogueira, Isabel de Pádua Paz · 2016 · Jornal de Pediatria
- The genomic landscape of CAKUT; you gain some, you lose someNine V.A.M. Knoers, Kirsten Y. Renkema · 2019 · Kidney International
- Differential role of planar cell polarity gene Vangl2 in embryonic and adult mammalian kidneysIda Derish, Jeremy K. H. Lee, Melanie Wong-King-Cheong, Sima Babayeva, Jillian Caplan, Vicki Leung, Chloe Shahinian, Michel Gravel, Michael R. Deans, Philippe Gros et al. · 2020 · PLoS ONE
- Symptomatology and Clinic of Hydronephrosis Associated With Uretero Pelvic Junction Anomaliesİlmay Bilge · 2020 · Frontiers in Pediatrics
- Kidney and urinary tract disordersRasheda Amin, Sunyoung Ahn, Asha Moudgil · 2021 · Elsevier eBooks
- Copy-number variation analysis in familial nonsyndromic congenital anomalies of the kidney and urinary tract: Evidence for the causative role of a transposable element-associated genomic rearrangementEkaterini C. Siomou, Artemis G. Mitsioni, Vasileios I. Giapros, Ioanna Bouba, Dimitrios Noutsopoulos, Ioannis A. Georgiou · 2017 · Molecular Medicine Reports
- Frequency of polymorphic loci of GSTM1 and GSTT1 modifier genes in the genotype of children with pyelonephritis and congenital urinary malformationsN.S. Lukyanenko, Anastasiya Spaska, Evelina Lenha, Iryna Marazha · 2022 · Polish Annals of Medicine
- Chronic Kidney Disease Management in Developing CountriesDanielle A. Badro · 2023 · Springer eBooks
- Characterization of the prenatal renal phenotype associated with 17q12, HNF1B, microdeletionsCourtney P. Verscaj, Frances Velez‐Bartolomei, Ethan E. Bodle, Katie Chan, Michael J. Lyons, Willa L. Thorson, Wen‐Hann Tan, Nancy Rodig, John M. Graham, Angela Peron et al. · 2023 · Prenatal Diagnosis
- Expression Profiles of ITGA8 and VANGL2 Are Altered in Congenital Anomalies of the Kidney and Urinary Tract (CAKUT)Nikola Pavlović, Nela Kelam, Anita Racetin, Natalija Filipović, Zenon Pogorelić, Ivana Kuzmiç Prusac, Katarina Vukojević · 2024 · Molecules
- Cellular and molecular determinants of normal and abnormal kidney developmentMing Shen Tham, Ian Smyth · 2018 · Wiley Interdisciplinary Reviews Developmental Biology
- Congenital Anomalies of the Kidney and Urinary Tract (CAKUT): An Emerging Relationship With Pregestational Diabetes Mellitus Among First Nations and Non-First Nations People in Saskatchewan—Results From the DIP: ORRIIGENSS ProjectRoland F Dyck, Chandima P. Karunanayake, Punam Pahwa, MaryRose Stang, Robin L. Erickson, Nathaniel David Osgood · 2020 · Canadian Journal of Diabetes
- Robo2 and Gen1 Coregulate Ureteric Budding by Activating the MAPK/ERK Signaling Pathway in MiceYaxin Li, Minghui Yu, Lihong Tan, Shanshan Xue, Xuanjin Du, Xiaohui Wu, Hong Ming Xu, Qian Shen · 2022 · Frontiers in Medicine
- Maternal risk factors for congenital anomalies of the kidney and urinary tract: A case-control studyRaíssa T Boato, Marcos B. Aguiar, ROBERT H. K. MAK, Enrico A. Colosimo, Ana Cristina Simões e Silva, Eduardo Araujo OLIVEIRA · 2022 · Journal of Pediatric Urology
- Evaluation of Renal Function in Children with Congenital Scoliosis and Congenital Anomalies of the Kidney and Urinary TractZhengchao Gao, Zhengmou Wang, Jiantao Liu, Binbin Niu, Wenlong Yang, Yibin Wang, Hui Wen Liang, Yuhuan Li, Haopeng Li, Xijing He · 2018 · Medical Science Monitor
- Is an analysis of copy number variants necessary for various types of kidney ultrasound anomalies in fetuses?Shaobin Lin, Shanshan Shi, Linhuan Huang, Ting Lei, Danlei Cai, Wenlong Hu, Yi Yuan Zhou, Yanmin Luo · 2019 · Molecular Cytogenetics
- Kongenitale Anomalien der Nieren und ableitenden Harnwege (CA KUT)Anne Kosfeld, Helge K. Martens, Imke Hennies, Dieter Haffner, Ruthild G. Weber · 2018 · Medizinische Genetik
- Estrogen Signaling Influences Nephron Segmentation of the Zebrafish Embryonic KidneyHannah M. Wesselman, Allison E. Gatz, Mairead R. Pfaff, Liana Arceri, Rebecca A. Wingert · 2023 · Cells
- (Zebra)fishing for nephrogenesis genesBrooke E. Chambers, Nicole E. Weaver, Caroline M. Lara, Thanh Khoa Nguyen, Rebecca A. Wingert · 2023 · Tissue Barriers
- Cardiovascular Disease Risk in Children With Chronic Kidney Disease: Impact of Apolipoprotein C-II and Apolipoprotein C-IIIWeiling Chen, You‐Lin Tain, Hung‐En Chen, Chien‐Ning Hsu · 2021 · Frontiers in Pediatrics
- From allergens to epigenetics: how histone acetylation shapes immune gene expression in allergic diseasesXuejun Cai, Muhammed Afthab, Shadi Hambo, Mohamed Salem, Rasika Ramesh Bhitale, Hani Harb · 2025 · Epigenomics
- Immunoexpression Pattern of Autophagy Markers in Developing and Postnatal Kidneys of Dab1−/−(yotari) MiceMirko Maglica, Nela Kelam, Ejazul Haque, Ilija Perutina, Anita Racetin, Natalija Filipović, Yu Katsuyama, Katarina Vukojević · 2023 · Biomolecules
- Advocacy for DOHaD research optimizing child kidney healthYou‐Lin Tain · 2024 · Pediatrics & Neonatology
- Responsible genes in children with primary vesicoureteral reflux: findings from the Chinese Children Genetic Kidney Disease DatabaseJia-Lu Liu, Qian Shen, Mingyan Wu, Guanghua Zhu, Yufeng Li, Xiaowen Wang, Xiaoshan Tang, Yunli Bi, Yinv Gong, Jing Chen et al. · 2021 · World Journal of Pediatrics
- Pregnancy Outcomes in Wilson’s Disease Women: Single-Center Case SeriesMarcela Chagas Lima Mussi, Mateus Jorge Nardelli, Bruno Campos Santos, Eliabe Silva de Abreu, Fernanda Maria Farage Osório, Guilherme Grossi Lopes Cançado, Teresa Cristina Abreu Ferrari, Luciana Costa Faria, Cláudia Alves Couto · 2021 · Fetal and Pediatric Pathology
- Modeling Podocyte Ontogeny and Podocytopathies with the ZebrafishBridgette E. Drummond, Wesley S. Ercanbrack, Rebecca A. Wingert · 2023 · Journal of Developmental Biology
- Isthmin-1 (Ism1) modulates renal branching morphogenesis and mesenchyme condensation during early kidney developmentGe Gao, Xiaoping Li, Zhixin Jiang, Liliana Osório, Ying Tang, Xueqing Yu, Guoxiang Jin, Zhongjun Zhou · 2023 · Nature Communications
- Transcriptome-driven integrative exploration of functional state of ureter tissue affected by CAKUTIvan B. Jovanović, Maja Živković, Mirjana Kostic, Zoran D. Krstic, Tamara Djurić, Danilo Licastro, Germana Meroni, Dragan Alavantić, Aleksandra Stanković · 2018 · Life Sciences
- Three Optimized Methods for In Situ Quantification of Progenitor Cell Proliferation in Embryonic Kidneys Using BrdU, EdU, and PCNARosalie E. O’Hara, Michel G. Arsenault, Blanca P. Esparza Gonzalez, Ashley Patriquen, Sunny Hartwig · 2019 · Canadian Journal of Kidney Health and Disease
- Programmed Adult Kidney Disease: Importance of Fetal EnvironmentRogério Argeri, Fernanda Thomazini, Débora Conte Kimura, Karina Thieme, Maria do Carmo Franco, Guiomar Nascimento Gomes · 2020 · Frontiers in Physiology
- Towards Modelling Genetic Kidney Diseases with Human Pluripotent Stem CellsKirsty M. Rooney, Adrian S. Woolf, Susan J. Kimber · 2021 · The Nephron journals/Nephron journals
- Overlap of vitamin A and vitamin D target genes with CAKUT-related processesOzan Özışık, Friederike Ehrhart, Chris T. Evelo, Alberto Mantovani, Anaı̈s Baudot · 2021 · F1000Research
- Homozygous WNT9B variants in two families with bilateral renal agenesis/hypoplasia/dysplasiaGabrielle Lemire, Bixia Zheng, Grace Uwaila Ediae, Ruobing Zou, Priya T. Bhola, Caitlin Chisholm, Joseph de Nanassy, Bryan Lo, Chunyan Wang, Shirlee Shril et al. · 2021 · American Journal of Medical Genetics Part A
- Congenital Anomalies of the Kidney and Urinary Tract: A Continuum of CareBärbel Lange-Sperandio, Hans‐Joachim Anders, Maximilian Stehr, Robert L. Chevalier, Richard Klaus · 2023 · Seminars in Nephrology
- Gestational Exposure to Maternal Systemic Glucocorticoids and Childhood Risk of CKDYou‐Lin Tain, Lung‐Chih Li, Hsiao‐Ching Kuo, Chien‐Ning Hsu · 2024 · American Journal of Kidney Diseases
- Gen1 Modulates Metanephric Morphology Through Retinoic Acid SignalingYa Zhang, Xin Zhang, Xiaowen Wang, Herui Wang, Xiaohui Wu, Hong Ming Xu, Qian Shen · 2019 · DNA and Cell Biology
- Hedgehog-GLI mediated control of renal formation and malformationDina Greenberg, Robert D’Cruz, Jon L. Lacanlale, Christopher J. Rowan, Norman D. Rosenblum · 2023 · Frontiers in Nephrology
- Disturbances in Switching between Canonical and Non-Canonical Wnt Signaling Characterize Developing and Postnatal Kidneys of Dab1−/− (yotari) MiceIlija Perutina, Nela Kelam, Mirko Maglica, Anita Racetin, Marin Ogorevc, Natalija Filipović, Yu Katsuyama, Josip Mišković, Katarina Vukojević · 2023 · Biomedicines
- Epigenetics of Renal Development and Disease.Sylvia A. Hilliard, Samir Sayem El-Dahr · 2016 · Europe PMC (PubMed Central)
- Screening for Renal and Urinary Tract Anomalies in Asymptomatic First Degree Relatives of Children with Congenital Anomalies of the Kidney and Urinary Tract (CAKUT)Aravindhan Manoharan, Sriram Krishnamurthy, Palanisamy Sivamurukan, Ramesh Ananthakrishnan, Bibekanand Jindal · 2020 · The Indian Journal of Pediatrics
- Altered Expression of Candidate Genes in Mayer–Rokitansky–Küster–Hauser Syndrome May Influence Vaginal Keratinocytes Biology: A Focus on Protein Kinase XPaola Pontecorvi, Francesca Megiorni, Simona Camero, Simona Ceccarelli, Laura Bernardini, Anna Capalbo, Eleni Anastasiadou, Giulia Gerini, Elena Messina, Giorgia Perniola et al. · 2021 · Biology
- Mapping of the amniotic fluid proteome of fetuses with congenital anomalies of the kidney and urinary tract identifies plastin 3 as a protein involved in glomerular integrityCamille Fédou, Mylène Camus, Ophélie Lescat, Guylène Feuillet, Ilka Mueller, Bryony Ross, Marie Buléon, Eric Neau, Mélinda Alvès, Dominique Goudounèche et al. · 2021 · The Journal of Pathology
- CAKUT-SYNDROME IN THE ETIOLOGICAL STRUCTURE OF CHRONIC KIDNEY DISEASE IN CHILDREN AND ADOLESCENTSЕ. В. Лысова, Н. Д. Савенкова · 2017 · Nephrology (Saint-Petersburg)
- Noncoding rare variants of TBX6 in congenital anomalies of the kidney and urinary tractShuangshuang Dong, Chunyan Wang, Xueping Li, Qian Shen, Xiaoyi Fu, Mingyan Wu, Chengcheng Song, Nan Yang, Yanhua Wu, Hongyan Wang et al. · 2019 · Molecular Genetics and Genomics
- Fetal urinary tract dilation: What to tell the parentsKatrien Nulens, Armando José Lorenzo, Joana Dos Santos, Katie Ellul, Mandy Rickard · 2023 · Prenatal Diagnosis
- ASH2L Controls Ureteric Bud Morphogenesis through the Regulation of RET/GFRA1 Signaling Activity in a Mouse ModelZiyi Zhao, Xuantong Dai, Gengru Jiang, Fujun Fiona Lin · 2023 · Journal of the American Society of Nephrology
- Increased incidence of renal and urinary tract anomalies among individuals with fetal alcohol spectrum disorders (FASD)Katarzyna Anna Dyląg, Paulina Dumnicka, Katarzyna Kowalska, Agata Migas‐Majoch, Katarzyna Przybyszewska, Dorota Drożdż · 2023 · Birth Defects Research
- Potential and pitfalls in the genetic diagnosis of kidney diseasesAnne Kesselheim, Emma Ashton, Detlef Böckenhauer · 2017 · Clinical Kidney Journal
- A Presumed Synonymous Mutation of PKD2 Caused Autosomal Dominant Polycystic Kidney Disease in a Chinese FamilyLinxia Deng, Yuan Yang, Jing Yang, Luowen Zhou, Kang Wang, Jianhua Zhou · 2021 · Current Medical Science
- Whole Exome Sequencing in a Population With Severe Congenital Anomalies of Kidney and Urinary TractMeredith Harris, Meredith Posner Schuh, David Nelson McKinney, Kenneth M. Kaufman, Elif Erkan · 2022 · Frontiers in Pediatrics
- Cardiovascular Risks of Hypertension: Lessons from Children with Chronic Kidney DiseaseYou‐Lin Tain, Chien‐Ning Hsu · 2022 · Children
- The association between gestational use of personal care products and neonatal urological abnormality at birth: The Japan Environment and Children’s StudyYukiko Nishihama, Nozomi Tatsuta, Miyuki Iwai‐Shimada, Kunihiko Nakai, Takahiro Arima, Ikuma Fujiwara, Nobuo Yaegashi, Ayano Takeuchi, Shoji F. Nakayama · 2020 · Reproductive Toxicology
- Mutational analysis of genes with ureteric progenitor cell‐specific expression in branching morphogenesis of the mouse kidneyElisabeth A. Rutledge, Andrew P. McMahon · 2020 · Developmental Dynamics
- Could the interaction between LMX1B and PAX2 influence the severity of renal symptoms?Susanna Negrisolo, Andrea Carraro, Giulia Fregonese, Elisa Benetti, Franz S. Schaefer, Marta Alberti, Salvatore Melchionda, Rita Fischetto, Mario Giordano, Luisa Murer · 2018 · European Journal of Human Genetics
- Inhibition of MAPK/ERK pathway activation rescues congenital anomalies of the kidney and urinary tract (CAKUT) in Robo2PB/+ Gen1PB/+ miceXuanjin Du, Minghui Yu, Haixin Ju, Shanshan Xue, Yaxin Li, Xiaohui Wu, Hong Ming Xu, Qian Shen · 2023 · Biochemical and Biophysical Research Communications
- Risk factors of congenital nomalies of the kidney and urinary tract (CAKUT): Exposureto mobile phones during pregnancyKübra Çeleğen, Esra Özgül, Zeynep YEŞİLDAĞ, Erdem Yusuf ÇAMIRCI, Mehmet Çeleğen, Ayşegül Bükülmez · 2024 · TURKISH JOURNAL OF MEDICAL SCIENCES
- Kidney development at a glance: metabolic regulation of renal progenitor cellsKristen Kurtzeborn, Samir Sayem El-Dahr, Niklas A. Pakkasjärvi, Giovane G. Tortelote, Satu Kuure · 2024 · Current topics in developmental biology/Current Topics in Developmental Biology
- Deletion in the Cobalamin Synthetase W Domain–Containing Protein 1 Gene Is associated with Congenital Anomalies of the Kidney and Urinary TractShoichiro Kanda, Masaki Ohmuraya, Hiroyuki Akagawa, Shigeru Horita, Yasuhiro Yoshida, Naoto Kaneko, Noriko Sugawara, Kiyonobu Ishizuka, Kenichiro Miura, Yutaka Harita et al. · 2019 · Journal of the American Society of Nephrology
- Evaluation and fetal intervention in severe fetal hydronephrosisAdnan Safdar, Kristianna Singh, Raphael C. Sun, Ahmed Abobakr Nassr · 2021 · Current Opinion in Pediatrics
- Development of the metanephric kidneyIan Smyth · 2021 · Current topics in developmental biology/Current Topics in Developmental Biology
- Evaluation of normal and abnormal fetal renal microvascular flow characteristics of three-dimensional MV-flow imagingC. Y. Huang, Lihe Zhang, Yuting Jiang, Qiao Zheng, Ting Lei, Liu Du, Hongning Xie · 2024 · Early Human Development
- Risk factors for perinatal and neonatal mortality in cases with congenital anomalies of the kidney and urinary tract: a nested cohort studyRodrigo Rezende Arantes, Marcos B. Aguiar, Keyla Christy Christine Mendes Sampaio Cunha, Arthur Aguiar Amaral, José Renato O. Melo, Beatriz Chaves Coelho Vieira, Enrico A. Colosimo, Eduardo Araujo OLIVEIRA, Ana Cristina Simões e Silva · 2025 · Pediatric Nephrology
- Molecular pathways of kidney development and their applications to clinical researchFriederike Ehrhart, Helge Martens, Norman D. Rosenblum, Andreas Schedl, Thorben A. Schlesinger, Ann Christin Gjerstad, Dieter Haffner, Jacqueline Ho, Chris T. Evelo, Adrian S. Woolf et al. · 2025 · Kidney International
- Assessment of antenatal risk factors for the formation of congenital defects of the development of the urinary system in childrenE. V. Sergeeva, A. Nее, Шуматова Татьяна Александровна, О. Г. Быкова, Н. Г. Приходченко, Зернова Екатерина Сергеевна · 2022 · Meditsinskiy sovet = Medical Council
- GEN1 as a risk factor for human congenital anomalies of the kidney and urinary tractXuanjin Du, Chunyan Wang, Jialu Liu, Minghui Yu, Haixin Ju, Shanshan Xue, Yaxin Li, Jiaojiao Liu, Rufeng Dai, Jing Chen et al. · 2024 · Human Genomics
- Clinical exome sequencing efficacy and phenotypic expansions involving non-isolated congenital anomalies of kidney and urinary tract (CAKUT+)E. Andres Rivera-Munoz, Xiaonan Zhao, Jill Anne Rosenfeld, Pamela N. Luna, Chad A. Shaw, Jennifer Ellen Posey, Daryl A. Scott · 2025 · European Journal of Human Genetics
- Identification and functional interpretation of miRNAs affected by rare CNVs in CAKUTKristina Mitrovic, Ivan Životić, Ivana Kolić, Ana D. Djordjevic, Jelena J. Žakula, Jelena Filipović Tričković, Maja Živković, Aleksandra Stanković, Ivan B. Jovanović · 2022 · Scientific Reports
- Plasma and Urinary Platelet Factor 4 as Biomarkers for Cardiovascular Risk in Children with Chronic Kidney DiseaseChien‐Ning Hsu, Wei-Ting Liao, Weiling Chen, Guo‐Ping Chang‐Chien, Sufan Lin, You‐Lin Tain · 2023 · Biomedicines
- Prenatal metal levels and congenital anomalies of the kidney and urinary tract: The Japan Environment and Children's StudyYuka Iwaya, Masafumi Sanefuji, Kei Nishiyama, Yuri Sonoda, Norio Hamada, Reiko Suga, Masayuki Ochiai, Masayuki Shimono, Koichi Kusuhara, Shouichi Ohga · 2023 · The Science of The Total Environment
- Congenital Solitary Functioning Kidney: A ReviewEduarda Almeida Wakabayashi, Alexandre Negrão Pantaleão, Renata Araújo Avendanha, Felipe Baptista Brunheroto, Ana Cristina Simões e Silva · 2022 · Current Medicinal Chemistry
- Laparoscopic treatment of bilateral duplex kidney and ectopic ureter: A case reportShubin Wang, Li Wan, Yong Wang, Zheng-Jin Yi, Chuan Xiao, Jing-Zhao Cao, Xiangyu Liu, Rui-Peng Tang, Luo Yun · 2022 · World Journal of Clinical Cases
- Rac1 deficiency impairs postnatal development of the renal papillaNobuhiro Ayuzawa, Mitsuhiro Nishimoto, Wakako Kawarazaki, Shigeyoshi Oba, Takeshi Marumo, Atsu Aiba, Toshiro Fujita · 2022 · Scientific Reports
- Prioritization of Monogenic Congenital Anomalies of the Kidney and Urinary Tract Candidate Genes with Existing Single-Cell Transcriptomics Data of the Human Fetal KidneyLuca M. Schierbaum, Sophia Schneider, Florian Buerger, Abdul A. Halawi, Steve Seltzsam, Chunyan Wang, Bixia Zheng, Chen-Han Wilfried Wu, Rufeng Dai, Dervla M. Connaughton et al. · 2023 · The Nephron journals/Nephron journals
- Wnt/β-Catenin Signaling and Congenital Abnormalities of Kidney and Urinary TractCuicui Yu, Bixia Zheng, Luyan Zhang, Aihua Zhang, Zhanjun Jia, Guixia Ding · 2024 · Kidney Diseases
- The Renal Sequelae of Alagille Syndrome as a Product of Altered Notch Signaling During Kidney DevelopmentRené Romero · 2018 · Springer eBooks
- Impact of maternal health on neonatal and long-term kidney outcomesNivedita Kamath, Saudamini Vijay Nesargi, Divya Bajpai, Pravin Singarayar, Enrico Vidal, Valérie A. Luyckx · 2025 · Pediatric Nephrology
- Congenital Anomalies of Kidney and Urinary Tract in Children – Clinical Spectrum and ComplicationsSharmina KT, Rehna K Rahman, Anand Mr, Abraham Mammen · 2026 · The Indian Journal of Pediatrics
- Maternal periconceptional folic acid supplementation and risk for fetal congenital genitourinary system defectsZixi Pang, Lei Jin, Jie Zhang, Wenying Meng, Di Wang, Lei Jin · 2023 · Pediatric Research
- Case report: A novel compound heterozygous variant in the TNXB gene causes single kidney agenesis and vesicoureteral refluxLei Liang, Haotian Wu, Haixia Meng, Lin Fu, Jianrong Zhao · 2024 · Frontiers in Endocrinology
- Association of the national level of human development with the incidence and mortality of congenital birth defects in 2019: A cross-sectional study from 189 countriesChen Du, Ziquan Zhang, Shuzhe Xiao, Yanwen Li, Ruiwen Jiang, Weihua Jian, Zhuxiao Ren, Yiting Lv, Zhizhang Pan, Jie Yang · 2024 · BioScience Trends