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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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 |