Mosaicism is increasingly recognized as a cause of developmental disorders with the advent of next-generation sequencing (NGS). Mosaic mutations of
Ghayda Mirzaa, Andrew E. Timms, Valerio Conti, Evan August Boyle, Katta M. Girisha, Beth Martin, Martin Kircher, Carissa Olds, Jane Juusola, Sarah Collins, Kaylee Park, Melissa Carter, Ian Glass, Inge Krägeloh-Mann, David Chitayat, Aditi Shah Parikh, Rachael Bradshaw, Erin Torti, Stephen Braddock, Leah Burke, Sondhya Ghedia, Mark Stephan, Fiona Stewart, Chitra Prasad, Melanie Napier, Sulagna Saitta, Rachel Straussberg, Michael Gabbett, Bridget C. O’Connor, Catherine E. Keegan, Lim Jiin Yin, Angeline Hwei Meeng Lai, Nicole Martin, Margaret McKinnon, Marie-Claude Addor, Luigi Boccuto, Charles E. Schwartz, Agustina Lanoel, Robert L. Conway, Koenraad Devriendt, Katrina Tatton-Brown, Mary Ella Pierpont, Michael Painter, Lisa Worgan, James Reggin, Raoul Hennekam, Karen Tsuchiya, Colin C. Pritchard, Mariana Aracena, Karen W. Gripp, Maria Cordisco, Hilde Van Esch, Livia Garavelli, Cynthia Curry, Anne Goriely, Hulya Kayserilli, Jay Shendure, John Graham Jr., Renzo Guerrini, William B. Dobyns
Title and authors | Publication | Year |
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Embryological cellular origins and hypoxia-mediated mechanisms in PIK3CA-Driven refractory vascular malformations
Sota Torii, Keiki Nagaharu, Nanako Nakanishi, Hidehito Usui, Yumiko Hori, Katsutoshi Hirose, Satoru Toyosawa, Eiichi Morii, Mitsunaga Narushima, Yoshiaki Kubota, Osamu Nakagawa, Kyoko Imanaka-Yoshida, Kazuaki Maruyama |
EMBO molecular medicine | 2025 |
Uncovering somatic mosaic variants of PIK3CA-related overgrowth disorders – three cases with different clinical presentations
Tooming M, Mertsina P, Kahre T, Teek R, Vainumäe I, Lilles S, Wojcik MH, Ilves P, Õunap K |
Frontiers in Genetics | 2025 |
Isolated lateralized overgrowth and the need for tumor screening: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)
Erwin AL, Abu El Haija A, Bennett JT, Biesecker LG, Deardorff MA, Hathaway ER, Li MM, Martinez-Agosto J, Walsh M, Kalish JM |
Genetics in medicine : official journal of the American College of Medical Genetics | 2025 |
The mechanism of oncogenic PI3K lipid kinase variants at the membrane and their cryptic pockets
Jang H, Yavuz BR, Zhang M, Liu Y, Nussinov R |
bioRxiv | 2025 |
FDA Approval Summary: Alpelisib for PIK3CA-Related Overgrowth Spectrum.
Singh S, Bradford D, Li X, Mishra-Kalyani PS, Shen YL, Wang L, Zhao H, Xiong Y, Liu J, Charlab R, Kraft J, Khasar S, Miller CP, Rivera DR, Kluetz PG, Pazdur R, Beaver JA, Singh H, Donoghue M |
Clinical cancer research | 2024 |
Assessment of gene–disease associations and recommendations for genetic testing for somatic variants in vascular anomalies by VASCERN-VASCA
Revencu N, Eijkelenboom A, Bracquemart C, Alhopuro P, Armstrong J, Baselga E, Cesario C, Dentici ML, Eyries M, Frisk S, Karstensen HG, Gene-Olaciregui N, Kivirikko S, Lavarino C, Mero IL, Michiels R, Pisaneschi E, Schönewolf-Greulich B, Wieland I, Zenker M, Vikkula M |
Orphanet Journal of Rare Diseases | 2024 |
PIK3CA mutations enhance the adipogenesis of ADSCs in facial infiltrating lipomatosis through TRPV1
Chen H, Sun B, Gao W, Qiu Y, Wei W, Li Y, Ye W, Song H, Hua C, Lin X |
iScience | 2024 |
Delineation of the phenotypes and genotypes of facial infiltrating lipomatosis associated with PIK3CA mutations
Chen H, Sun B, Gao W, Qiu Y, Hua C, Lin X |
Orphanet Journal of Rare Diseases | 2023 |
Case report: Progressive pulmonary artery hypertension in a case of megalencephaly-capillary malformation syndrome
Yoh Y, Shiohama T, Uchida T, Ebata R, Kobayashi H, Okunushi K, Kato M, Watanabe K, Nakashima M, Saitsu H, Hamada H |
Frontiers in Genetics | 2023 |
Somatic mutation spectrum of a Chinese cohort of pediatrics with vascular malformations.
Zhang B, He R, Xu Z, Sun Y, Wei L, Li L, Liu Y, Guo W, Song L, Wang H, Lin Z, Ma L |
Orphanet Journal of Rare Diseases | 2023 |
Targeted next-generation sequencing for detection of PIK3CA mutations in archival tissues from patients with Klippel-Trenaunay syndrome in an Asian population : List the full names and institutional addresses for all authors.
Sasaki Y, Ishikawa K, Hatanaka KC, Oyamada Y, Sakuhara Y, Shimizu T, Saito T, Murao N, Onodera T, Miura T, Maeda T, Funayama E, Hatanaka Y, Yamamoto Y, Sasaki S |
Orphanet Journal of Rare Diseases | 2023 |
Protein interaction network analysis of mTOR signaling reveals modular organization
Wehle DT, Bass CS, Sulc J, Mirzaa G, Smith SE |
The Journal of biological chemistry | 2023 |
Protein interaction network analysis of mTOR signaling reveals modular organization
Wehle DT, Bass CS, Sulc J, Mirzaa G, Smith SE |
2023 | |
Epidemiology of the disorders of the Pik3ca-related overgrowth spectrum (Pros)
Reynolds G, Cardaropoli S, Carli D, Luca M, Gazzin A, Coppo P, La Selva R, Piglionica M, Bagnulo R, Turchiano A, Ranieri C, Resta N, Mussa A |
European Journal of Human Genetics | 2023 |
Neurodevelopmental disorders and cancer networks share pathways, but differ in mechanisms, signaling strength, and outcome
Yavuz BR, Arici MK, Demirel HC, Tsai CJ, Jang H, Nussinov R, Tuncbag N |
npj Genomic Medicine | 2023 |
An expanded clinical spectrum of hypoinsulinaemic hypoketotic hypoglycaemia.
Welters A, Leiter SM, Bachmann N, Bergmann C, Hoermann H, Korsch E, Meissner T, Payne F, Williams R, Hussain K, Semple RK, Kummer S |
Orphanet Journal of Rare Diseases | 2023 |
Work-Up and Treatment Strategies for Individuals with PIK3CA-Related Disorders: A Consensus of Experts from the Scientific Committee of the Italian Macrodactyly and PROS Association
Gazzin A, Leoni C, Viscogliosi G, Borgini F, Perri L, Iacoviello M, Piglionica M, De Pellegrin M, Ferrero GB, Bartuli A, Zampino G, Buonuomo PS, Resta N, Mussa A |
Genes & development | 2023 |
The molecular genetics of PI3K/PTEN/AKT/mTOR pathway in the malformations of cortical development
Ma Q, Chen G, Li Y, Guo Z, Zhang X |
Genes & Diseases | 2023 |
Profiling PIK3CA variants in disorders of somatic mosaicism
Mojarad BA, Hernandez PV, Evenson MJ, Corliss MM, Stein SL, Theos A, Coughlin CC, Sisk B, Menezes M, Schroeder MC, Heusel JW, Neidich JA, Cao Y |
Genetics in Medicine Open | 2023 |
Co-existence of 2 clinically significant variants causing disorders of somatic mosaicism
Cao Y, Evenson MJ, Corliss MM, Schroeder MC, Heusel JW, Neidich JA |
Genetics in Medicine Open | 2023 |
Diagnostic Approach to Macrocephaly in Children
A Accogli, A Geraldo, G Piccolo, A Riva, M Scala, G Balagura, V Salpietro, F Madia, M Maghnie, F Zara, P Striano, D Tortora, M Severino, V Capra |
Frontiers in Pediatrics | 2022 |
A Review on Cutaneous and Musculoskeletal Manifestations of CLOVES Syndrome
Emel Öztürk Durmaz, Deniz Demircioğlu, Pınar Yalınay Dikmen, Yasemin Alanay, Ahmet Alanay, Cüyan Demirkesen, Fatma Tokat, Ercan Karaarslan |
Clinical, cosmetic and investigational dermatology | 2022 |
The utility of cerebrospinal fluid–derived cell-free DNA in molecular diagnostics for the PIK3CA-related megalencephaly-capillary malformation (MCAP) syndrome: a case report
Chen WL, Pao E, Owens J, Glass I, Pritchard C, Shirts BH, Lockwood C, Mirzaa GM |
Cold Spring Harbor Molecular Case Studies | 2022 |
Pulmonary Vein Stenosis Associated with Germline PIK3CA Mutation
Yung D, Freeman K, Mirzaa G |
Children | 2022 |
Clinical and Molecular Spectrum of Sporadic Vascular Malformations: A Single-Center Study.
Diociaiuti A, Rotunno R, Pisaneschi E, Cesario C, Carnevale C, Condorelli AG, Rollo M, Di Cecca S, Quintarelli C, Novelli A, Zambruno G, El Hachem M |
Biomedicines | 2022 |
Osteopathy in Complex Lymphatic Anomalies
Solorzano E, Alejo AL, Ball HC, Magoline J, Khalil Y, Kelly M, Safadi FF |
International journal of molecular sciences | 2022 |
Brain Abnormalities in PIK3CA-Related Overgrowth Spectrum: Physician, Patient, and Caregiver Experiences.
Dexheimer J, Mirzaa GM |
Advances in Therapy | 2022 |
Revertant Mosaicism in Genodermatoses: Natural Gene Therapy Right before Your Eyes
van den Akker PC, Bolling MC, Pasmooij AM |
Biomedicines | 2022 |
Clinical and genetic analyses of patients with lateralized overgrowth
Kim YM, Lee Y, Choi Y, Choi IH, Heo SH, Choi JM, Do HS, Jang JH, Yum MS, Yoo HW, Lee BH |
BMC Medical Genomics | 2022 |
Clinical Response to PI3K-α Inhibition in a Cohort of Children and Adults With PIK3CA-Related Overgrowth Spectrum Disorders.
Raghavendran P, Albers SE, Phillips JD, Zarnegar-Lumley S, Borst AJ |
2022 | |
The Genetic Architecture of Vascular Anomalies: Current Data and Future Therapeutic Perspectives Correlated with Molecular Mechanisms.
Butnariu LI, Gorduza EV, Florea L, Țarcă E, Moisă ȘM, Trandafir LM, Stoleriu S, Bădescu MC, Luca AC, Popa S, Radu I, Cojocaru E |
International journal of molecular sciences | 2022 |
Profiling PI3K-AKT-MTOR variants in focal brain malformations reveals new insights for diagnostic care.
Pirozzi F, Berkseth M, Shear R, Gonzalez L, Timms AE, Sulc J, Pao E, Oyama N, Forzano F, Conti V, Guerrini R, Doherty ES, Saitta SC, Lockwood CM, Pritchard CC, Dobyns WB, Novotny E, Wright JNN, Saneto RP, Friedman S, Hauptman J, Ojemann J, Kapur RP, Mirzaa GM |
Brain : a journal of neurology | 2022 |
Neuroimaging features of genetic syndromes associated with CNS overgrowth.
Zamary AR, Mamlouk MD |
Pediatric Radiology | 2022 |
The ClinGen Brain Malformation Variant Curation Expert Panel: Rules for somatic variants in AKT3, MTOR, PIK3CA, and PIK3R2
Lai A, Soucy A, El Achkar CM, Barkovich AJ, Cao Y, DiStefano M, Evenson M, Guerrini R, Knight D, Lee YS, Mefford HC, Miller DT, Mirzaa G, Mochida G, Rodan LH, Patel M, Smith L, Spencer S, Walsh CA, Yang E, Yuskaitis CJ, Yu T, Poduri A |
Genetics in Medicine | 2022 |
Single-cell transcriptomics for the assessment of cardiac disease.
Miranda AMA, Janbandhu V, Maatz H, Kanemaru K, Cranley J, Teichmann SA, Hübner N, Schneider MD, Harvey RP, Noseda M |
Nature reviews. Cardiology | 2022 |
PIK3CA-related overgrowth with an uncommon phenotype: case report
Rotunno R, Diociaiuti A, Pisaneschi E, Carnevale C, Dentici M, El Hachem M |
Italian Journal of Pediatrics | 2022 |
Alpelisib for the treatment of PIK3CA-related head and neck lymphatic malformations and overgrowth.
Wenger TL, Ganti S, Bull C, Lutsky E, Bennett JT, Zenner K, Jensen DM, Dmyterko V, Mercan E, Shivaram GM, Friedman SD, Bindschadler M, Drusin M, Perkins JN, Kong A, Bly RA, Dahl JP, Bonilla-Velez J, Perkins JA, Wenger TL, Ganti S, Bull C, Lutsky E, Bennett JT, Zenner K, Jensen DM, Dmyterko V, Mercan E, Shivaram GM, Friedman SD, Bindschadler M, Drusin M, Perkins JN, Kong A, Bly RA, Dahl JP, Bonilla-Velez J, Perkins JA |
Genetics in Medicine | 2022 |
Epilepsy in the mTORopathies: opportunities for precision medicine
PB Moloney, GL Cavalleri, N Delanty |
2021 | |
A review of mechanisms of disease across PIK3CA-related disorders with vascular manifestations
G Canaud, AM Hammill, D Adams, M Vikkula, KM Keppler-Noreuil |
Orphanet Journal of Rare Diseases | 2021 |
Functional analysis of a gene-edited mouse model to gain insights into the disease mechanisms of a titin missense variant
H Jiang, C Hooper, M Kelly, V Steeples, JN Simon, J Beglov, AJ Azad, L Leinhos, P Bennett, E Ehler, JI Kalisch-Smith, DB Sparrow, R Fischer, R Heilig, H Isackson, M Ehsan, G Patone, N Huebner, B Davies, H Watkins, K Gehmlich |
Basic Research in Cardiology | 2021 |
The Role of Neuroimaging and Genetic Analysis in the Diagnosis of Children With Cerebral Palsy
V Horber, U Grasshoff, E Sellier, C Arnaud, I Krägeloh-Mann, K Himmelmann |
Frontiers in neurology | 2021 |
Positive correlation between transcriptomic stemness and PI3K/AKT/mTOR signaling scores in breast cancer, and a counterintuitive relationship with PIK3CA genotype
RR Madsen, EC Erickson, OM Rueda, X Robin, C Caldas, A Toker, RK Semple, B Vanhaesebroeck, P McKinnon |
PLoS genetics | 2021 |
A standard of care for individuals with PIK3CA ‐related disorders: An international expert consensus statement
S Douzgou, M Rawson, E Baselga, M Danielpour, L Faivre, A Kashanian, KM KepplerNoreuil, P Kuentz, GM Mancini, MC Maniere, V MartinezGlez, VE Parker, RK Semple, S Srivastava, P Vabres, MC Wit, JM Graham, J ClaytonSmith, GM Mirzaa, LG Biesecker |
Clinical Genetics | 2021 |
Cerebrofacial vascular metameric syndrome is caused by somatic pathogenic variants in PIK3CA
S Sheppard, V Sanders, A Srinivasan, L Finn, D Adams, A Elton, C Amlie-Lefond, Z Nelson, V Dmyterko, D Jensen, K Zenner, J Perkins, J Bennett |
Molecular Case Studies | 2021 |
The blended phenotype of a germline RIT1 and a mosaic PIK3CA variant
Berland S, Jareld J, Hickson N, Schlecht H, Houge G, Douzgou S |
Cold Spring Harbor Molecular Case Studies | 2021 |
Mosaicism in clinical genetics
Mefford HC |
Cold Spring Harbor Molecular Case Studies | 2021 |
Somatic variants in epilepsy – advancing gene discovery and disease mechanisms
EL Heinzen |
Current Opinion in Genetics & Development | 2020 |
Disorders Caused by Genetic Mosaicism
U Moog, U Felbor, C Has, B Zirn |
Deutsches Ärzteblatt international | 2020 |
International consensus recommendations on the diagnostic work-up for malformations of cortical development
R Oegema, TS Barakat, M Wilke, K Stouffs, D Amrom, E Aronica, N Bahi-Buisson, V Conti, AE Fry, T Geis, DG Andres, E Parrini, I Pogledic, E Said, D Soler, LM Valor, MS Zaki, G Mirzaa, WB Dobyns, O Reiner, R Guerrini, DT Pilz, U Hehr, RJ Leventer, AC Jansen, GM Mancini, ND Donato |
Nature Reviews Neurology | 2020 |
PIK3CA variants selectively initiate brain hyperactivity during gliomagenesis
K Yu, CC Lin, A Hatcher, B Lozzi, K Kong, E Huang-Hobbs, YT Cheng, VB Beechar, W Zhu, Y Zhang, F Chen, GB Mills, CA Mohila, CJ Creighton, JL Noebels, KL Scott, B Deneen |
Nature | 2020 |
Pathogenic postzygotic mosaicism in the tyrosine receptor kinase pathway: potential unidentified human disease hidden away in a few cells
I TiemannBoege, T Mair, A Yasari, M Zurovec |
The FEBS journal | 2020 |
Phenotypic and genetic spectrum of isolated macrodactyly: somatic mosaicism of PIK3CA and AKT1 oncogenic variants
W Tian, Y Huang, L Sun, Y Guo, S Zhao, M Lin, X Dong, W Zhong, Y Yin, Z Chen, N Zhang, Y Zhang, L Wang, J Lin, Z Yan, X Yang, J Zhao, G Qiu, J Zhang, Z Wu, N Wu |
Orphanet Journal of Rare Diseases | 2020 |
Somatic Variant Analysis Identifies Targets for Tailored Therapies in Patients with Vascular Malformations
S Paolacci, RE Mattassi, G Marceddu, E Manara, A Zulian, G Guerri, LD Antoni, C Arduino, D Cavalca, M Bertelli |
Journal of Clinical Medicine | 2020 |
Characterization and Childhood Tumor Risk Assessment of Genetic and Epigenetic Syndromes Associated With Lateralized Overgrowth
JR Griff, KA Duffy, JM Kalish |
Frontiers in Pediatrics | 2020 |
Detailed analysis of phenotypes and genotypes in megalencephaly-capillary malformation-polymicrogyria syndrome caused by somatic mosaicism of PIK3CA mutations
HJ Park, CH Shin, WJ Yoo, TJ Cho, MJ Kim, MW Seong, SS Park, JH Lee, NS Sim, JM Ko |
Orphanet Journal of Rare Diseases | 2020 |
Gingival Biopsy to Detect Mosaicism in Overgrowth Syndromes: Report of Two Cases of Megalencephaly-Capillary Malformation Syndrome with Periodontal Anomalies
M Marty, C Bonnaud, N Jones, M Longy, F Vaysse, E Bieth, I Bailleul-Forestier |
Case Reports in Dentistry | 2020 |
Segmental Ipsilateral Odontognathic Dysplasia (Mandibular Involvement in Segmental Odontomaxillary Dysplasia?) and Identification of PIK3CA Somatic Variant in Lesional Mandibular Gingival Tissue
TM Gibson, K Rafferty, E Ryan, A Ganguly, IG Koutlas |
Head and Neck Pathology | 2020 |
Missed diagnoses: Clinically relevant lessons learned through medical mysteries solved by the Undiagnosed Diseases Network
H Cope, R Spillmann, JA Rosenfeld, E Brokamp, R Signer, K Schoch, EG Kelley, JA Sullivan, E Macnamara, S Lincoln, K GoldenGrant, JP Orengo, G Clark, LC Burrage, JE Posey, J Punetha, A Robertson, J Cogan, JA Phillips, J MartinezAgosto, V Shashi |
Molecular Genetics & Genomic Medicine | 2020 |
Clinical profile of overgrowth syndromes consistent with PROS (PIK3CA-related overgrowth syndromes)—A case series
L Mathew, R George, S Sudhakar, SN Keshava, NA Fouzia |
Indian Dermatology Online Journal | 2020 |
Orofacial overgrowth with peripheral nerve enlargement and perineuriomatous pseudo-onion bulb proliferations is part of the PIK3CA-related overgrowth spectrum
I Koutlas, A Anbinder, R Alshagroud, A Cavalcante, M Kindi, M Crenshaw, J Sapp, H Kondolf, M Lindhurst, J Dudley, J Johnston, E Ryan, K Rafferty, A Ganguly, L Biesecker |
2020 | |
Genotype correlates with clinical severity in PIK3CA-associated lymphatic malformations
Kaitlyn B Zenner, Chi Vicky Cheng, Dana Jensen, Andre E Timms, Giridhar Shivaram, Randall Bly, Sheila Ganti, Kathryn Whitlock, William Dobyns, Jonathan Perkins, James Bennett |
JCI Insight | 2019 |
Growth hormone deficiency in megalencephaly‐capillary malformation syndrome: An association with activating mutations in PIK3CA
S Davis, MA Ware, J Zeiger, MA Deardorff, K Grand, A Grimberg, S Hsu, M Kelsey, S Majidi, RP Matthew, M Napier, N Nokoff, C Prasad, AC Riggs, ML McKinnon, G Mirzaa |
American journal of medical genetics. Part A | 2019 |
Mouse Models for Exploring the Biological Consequences and Clinical Significance of PIK3CA Mutations
CB Mitchell, WA Phillips |
Biomolecules | 2019 |
Diagnostic Utility of Next-Generation Sequencing for Disorders of Somatic Mosaicism: A Five-Year Cumulative Cohort
SN McNulty, MJ Evenson, MM Corliss, LD Love-Gregory, MC Schroeder, Y Cao, YS Lee, BA Drolet, JA Neidich, CE Cottrell, JW Heusel |
The American Journal of Human Genetics | 2019 |
Revisiting PI3-kinase signalling in angiogenesis
P Kobialka, M Graupera |
2019 | |
Molecular diagnosis of somatic overgrowth conditions: A single-center experience
E Lalonde, J Ebrahimzadeh, K Rafferty, J Richards-Yutz, R Grant, E Toorens, JM Rosado, E Schindewolf, T Ganguly, JM Kalish, MA Deardorff, A Ganguly |
Molecular Genetics & Genomic Medicine | 2019 |
A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencing
Y Cao, MJ Tokita, ES Chen, R Ghosh, T Chen, Y Feng, E Gorman, F Gibellini, PA Ward, A Braxton, X Wang, L Meng, R Xiao, W Bi, F Xia, CM Eng, Y Yang, T Gambin, C Shaw, P Liu, P Stankiewicz |
Genome Medicine | 2019 |
A girl with CLOVES syndrome with a recurrent PIK3CA somatic mutation and pancreatic steatosis
H Hanafusa, N Morisada, T Nomura, D Kobayashi, Y Akasaka, MJ Ye, K Nozu, N Nishimura, K Iijima, H Nakao |
Human Genome Variation | 2019 |
Beyond the Exome: The Non-coding Genome and Enhancers in Neurodevelopmental Disorders and Malformations of Cortical Development
E Perenthaler, S Yousefi, E Niggl, TS Barakat |
Frontiers in cellular neuroscience | 2019 |
PI3K/mTOR Pathway Inhibition: Opportunities in Oncology and Rare Genetic Diseases
P Hillmann, D Fabbro |
International journal of molecular sciences | 2019 |
Mosaic RAS/MAPK variants cause sporadic vascular malformations which respond to targeted therapy
Lara Al-Olabi, Satyamaanasa Polubothu, Katherine Dowsett, Katrina Andrews, Paulina Stadnik, Agnel Joseph, Rachel Knox, Alan Pittman, Graeme Clark, William Baird, Neil Bulstrode, Mary Glover, Kristiana Gordon, Darren Hargrave, Sue Huson, Thomas Jacques, Gregory James, Hannah Kondolf, Loshan Kangesu, KimM. Keppler-Noreuil, Amjad Khan, Marjorie Lindhurst, Mark Lipson, Sahar Mansour, Justine O'Hara, Caroline Mahon, Anda Mosica, Celia Moss, Aditi Murthy, Juling Ong, Victoria Parker, Jean-Baptiste Rivière, Julie Sapp, Neil Sebire, Rahul Shah, Branavan Sivakumar, Anna Thomas, Alex Virasami, Regula Waelchli, Zhiqiang Zeng, Leslie G Biesecker, Alex Barnacle, Maya Topf, Robert Semple, E. Elizabeth Patton, Veronica Kinsler |
Journal of Clinical Investigation | 2018 |
Safety and efficacy of low-dose sirolimus in the PIK3CA-related overgrowth spectrum
VE Parker, KM Keppler-Noreuil, L Faivre, M Luu, NL Oden, LD Silva, JC Sapp, K Andrews, M Bardou, KY Chen, TN Darling, E Gautier, BR Goldspiel, S Hadj-Rabia, J Harris, G Kounidas, P Kumar, MJ Lindhurst, R Loffroy, L Martin, A Phan, KI Rother, BC Widemann, PL Wolters, C Coubes, L Pinson, M Willems, C Vincent-Delorme, P Vabres, RK Semple, LG Biesecker |
Genetics in Medicine | 2018 |
Cancer-Associated PIK3CA Mutations in Overgrowth Disorders
RR Madsen, B Vanhaesebroeck, RK Semple |
Trends in Molecular Medicine | 2018 |
Targeted therapy in patients with PIK3CA-related overgrowth syndrome
Q Venot, T Blanc, SH Rabia, L Berteloot, S Ladraa, JP Duong, E Blanc, SC Johnson, C Hoguin, O Boccara, S Sarnacki, N Boddaert, S Pannier, F Martinez, S Magassa, J Yamaguchi, B Knebelmann, P Merville, N Grenier, D Joly, V Cormier-Daire, C Michot, C Bole-Feysot, A Picard, V Soupre, S Lyonnet, J Sadoine, L Slimani, C Chaussain, C Laroche-Raynaud, L Guibaud, C Broissand, J Amiel, C Legendre, F Terzi, G Canaud |
Nature | 2018 |
Upper limb muscle overgrowth with hypoplasia of the index finger: a new over-growth syndrome caused by the somatic PIK3CA mutation c.3140A>G
MM Al-Qattan, A Hadadi, AM Al-Thunayan, AA Eldali, MA AlBalwi |
BMC Medical Genetics | 2018 |
Causal somatic mutations in urine DNA from persons with the CLOVES subgroup of the PIK3CA-related overgrowth spectrum
ME Michel, DJ Konczyk, KS Yeung, R Murillo, MP Vivero, AM Hall, D Zurakowski, D Adams, A Gupta, AY Huang, BH Chung, ML Warman |
Clinical Genetics | 2018 |
Clinical pitfalls in the diagnosis of segmental overgrowth syndromes: a child with the c.2740G > A mutation in PIK3CA gene
A Maguolo, F Antoniazzi, A Spano, E Fiorini, R Gaudino, M Mauro, G Cantalupo, P Biban, S Maitz, P Cavarzere |
Italian Journal of Pediatrics | 2018 |
Characterization of a severe case of PIK3CA -related overgrowth at autopsy by droplet digital polymerase chain reaction and report of PIK3CA sequencing in 22 patients: Characterization of a severe case of PIK3CA -related overgrowth at autopsy by droplet digital PCR and report of PIK3CA sequencing in 22 patients
AM Piacitelli, DM Jensen, H Brandling-Bennett, MM Gray, M Batra, J Gust, A Thaker, C Paschal, K Tsuchiya, CC Pritchard, J Perkins, GM Mirzaa, JT Bennett |
American journal of medical genetics. Part A | 2018 |
Somatic activating mutations in PIK3CA cause generalized lymphatic anomaly
L Rodriguez-Laguna, N Agra, K Ibañez, G Oliva-Molina, G Gordo, N Khurana, D Hominick, M Beato, I Colmenero, G Herranz, JM Canizalez, RR Pena, E Vallespín, R Martín-Arenas, Á del Pozo, C Villaverde, A Bustamante, C Ayuso, P Lapunzina, JC Lopez-Gutierrez, MT Dellinger, V Martinez-Glez |
Journal of Experimental Medicine | 2018 |
Identification of mutations in the PI3K-AKT-mTOR signalling pathway in patients with macrocephaly and developmental delay and/or autism
KS Yeung, WW Tso, JJ Ip, CC Mak, GK Leung, MH Tsang, D Ying, SL Pei, SL Lee, W Yang, BH Chung |
Molecular autism | 2017 |
Mutations in Epigenetic Regulation Genes Are a Major Cause of Overgrowth with Intellectual Disability
K Tatton-Brown, C Loveday, S Yost, M Clarke, E Ramsay, A Zachariou, A Elliott, H Wylie, A Ardissone, O Rittinger, F Stewart, IK Temple, T Cole, S Mahamdallie, S Seal, E Ruark, N Rahman |
The American Journal of Human Genetics | 2017 |
Hypoinsulinaemic, hypoketotic hypoglycaemia due to mosaic genetic activation of PI3-kinase
SM Leiter, VE Parker, A Welters, R Knox, N Rocha, G Clark, F Payne, L Lotta, J Harris, J Guerrero-Fernández, I González-Casado, S García-Miñaur, G Gordo, N Wareham, V Martínez-Glez, M Allison, S ORahilly, I Barroso, T Meissner, S Davies, K Hussain, K Temple, AC Barreda-Bonis, S Kummer, RK Semple |
European Journal of Endocrinology | 2017 |
Mutations of AKT3 are associated with a wide spectrum of developmental disorders including extreme megalencephaly
D Alcantara, AE Timms, K Gripp, L Baker, K Park, S Collins, C Cheng, F Stewart, SG Mehta, A Saggar, L Sztriha, M Zombor, O Caluseriu, R Mesterman, MI van Allen, A Jacquinet, S Ygberg, JA Bernstein, AM Wenger, H Guturu, G Bejerano, N Gomez-Ospina, A Lehman, E Alfei, C Pantaleoni, V Conti, R Guerrini, U Moog, JM Graham, R Hevner, WB Dobyns, M ODriscoll, GM Mirzaa |
Brain | 2017 |
Molecular diagnosis of PIK3CA-related overgrowth spectrum (PROS) in 162 patients and recommendations for genetic testing
P Kuentz, J St-Onge, Y Duffourd, JB Courcet, V Carmignac, T Jouan, A Sorlin, C Abasq-Thomas, J Albuisson, J Amiel, D Amram, S Arpin, T Attie-Bitach, N Bahi-Buisson, S Barbarot, G Baujat, D Bessis, O Boccara, M Bonnière, O Boute, AC Bursztejn, C Chiaverini, V Cormier-Daire, C Coubes, B Delobel, P Edery, SE Chehadeh, C Francannet, D Geneviève, A Goldenberg, D Haye, B Isidor, ML Jacquemont, PK Kien, D Lacombe, L Martin, J Martinovic, A Maruani, M Mathieu-Dramard, J Mazereeuw-Hautier, C Michot, C Mignot, J Miquel, F Morice-Picard, F Petit, A Phan, M Rossi, R Touraine, A Verloes, M Vincent, C Vincent-Delorme, S Whalen, M Willems, N Marle, D Lehalle, J Thevenon, C Thauvin-Robinet, S Hadj-Rabia, L Faivre, P Vabres, JB Rivière |
Genetics in Medicine | 2017 |
Somatic overgrowth disorders of the PI3K/AKT/mTOR pathway & therapeutic strategies
KM Keppler-Noreuil, VE Parker, TN Darling, JA Martinez-Agosto |
American Journal of Medical Genetics Part C Seminars in Medical Genetics | 2016 |
New insights into the generation and role of de novo mutations in health and disease
R Acuna-Hidalgo, JA Veltman, A Hoischen |
Genome biology | 2016 |