Molecular genetic framework underlying pulmonary arterial hypertension von Southgate, Laura, Machado, Rajiv D., Gräf, Stefan, Morrell, Nicholas W.

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ASEAN Resistance to Sovereignty Violation : Interests, Balancing and the Role of the Vanguard State von Southgate, Laura

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Letter regarding “Distal Limb Defects and Aplasia Cutis: Adams–Oliver Syndrome” von Southgate, Laura, PhD

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A systematic review and meta-analysis of set-shifting ability in eating disorders von ROBERTS, MARION E., TCHANTURIA, KATE, STAHL, DANIEL, SOUTHGATE, LAURA, TREASURE, JANET

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Elevated levels of inflammatory cytokines predict survival in idiopathic and familial pulmonary arterial hypertension von Soon, Elaine, Holmes, Alan M, Treacy, Carmen M, Doughty, Natalie J, Southgate, Laura, Machado, Rajiv D, Trembath, Richard C, Jennings, Simon, Barker, Lucy, Nicklin, Paul, Walker, Christoph, Budd, David C, Pepke-Zaba, Joanna, Morrell, Nicholas W

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Pulmonary Arterial Hypertension: A Current Perspective on Established and Emerging Molecular Genetic Defects von Machado, Rajiv D., Southgate, Laura, Eichstaedt, Christina A., Aldred, Micheala A., Austin, Eric D., Best, D. Hunter, Chung, Wendy K., Benjamin, Nicola, Elliott, C. Gregory, Eyries, Mélanie, Fischer, Christine, Gräf, Stefan, Hinderhofer, Katrin, Humbert, Marc, Keiles, Steven B., Loyd, James E., Morrell, Nicholas W., Newman, John H., Soubrier, Florent, Trembath, Richard C., Viales, Rebecca Rodríguez, Grünig, Ekkehard

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Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis von Rhodes, Christopher J, Batai, Ken, Bleda, Marta, Southgate, Laura, Germain, Marine, Pauciulo, Michael W, Aman, Jurjan, Girerd, Barbara, Arora, Amit, Knight, Jo, Hanscombe, Ken B, Karnes, Jason H, Kaakinen, Marika, Harbaum, Lars, Cebola, Inês, Ferrer, Jorge, Lutz, Katie, Swietlik, Emilia M, Ahmad, Ferhaan, Amouyel, Philippe, Archer, Stephen L, Argula, Rahul, Austin, Eric D, Badesch, David, Barnett, Christopher, Benza, Raymond, Bhatt, Nitin, Burger, Charles D, Chakinala, Murali, Church, Colin, Coghlan, John G, Condliffe, Robin, Danesino, Cesare, Debette, Stéphanie, Elliott, C Gregory, Elwing, Jean, Fortin, Terry, Frantz, Robert P, Frost, Adaani, Garcia, Joe G N, Ghio, Stefano, Ghofrani, Hossein-Ardeschir, Gibbs, J Simon R, Harley, John, He, Hua, Hill, Nicholas S, Hirsch, Russel, Houweling, Arjan C, Howard, Luke S, Ivy, Dunbar, Kiely, David G, Klinger, James, Kovacs, Gabor, Lahm, Tim, Machado, Rajiv D, Marsolo, Keith, Martin, Lisa J, Moledina, Shahin, Montani, David, Nathan, Steven D, Olschewski, Andrea, Olschewski, Horst, Oudiz, Ronald J, Pepke-Zaba, Joanna, Rehman, Zia, Robbins, Ivan, Roden, Dan M, Rosenzweig, Erika B, Saydain, Ghulam, Scelsi, Laura, Schilz, Robert, Seeger, Werner, Simms, Robert W, Simon, Marc, Sitbon, Olivier, Suntharalingam, Jay, Tang, Haiyang, Tchourbanov, Alexander Y, Thenappan, Thenappan, Treacy, Carmen M, Vonk Noordegraaf, Anton, Waisfisz, Quinten, Walsworth, Anna K, Walter, Robert E, Wharton, John, White, R James, Wilt, Jeffrey, Wort, Stephen J, Yung, Delphine, Lawrie, Allan, Humbert, Marc, Soubrier, Florent, Trégouët, David-Alexandre, Prokopenko, Inga, Gräf, Stefan, Nichols, William C, Trembath, Richard C, Desai, Ankit A, Morrell, Nicholas W, Wilkins, Martin R

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Genome‐Wide Association Study Identifies Risk Loci for Cluster Headache von O'Connor, Emer, Fourier, Carmen, Ran, Caroline, Sivakumar, Prasanth, Liesecke, Franziska, Southgate, Laura, Harder, Aster V. E., Vijfhuizen, Lisanne S., Yip, Janice, Giffin, Nicola, Silver, Nicholas, Ahmed, Fayyaz, Hostettler, Isabel C., Davies, Brendan, Cader, M. Zameel, Simpson, Benjamin S., Sullivan, Roisin, Efthymiou, Stephanie, Adebimpe, Joycee, Quinn, Olivia, Campbell, Ciaran, Cavalleri, Gianpiero L., Vikelis, Michail, Kelderman, Tim, Paemeleire, Koen, Kilbride, Emer, Grangeon, Lou, Lagrata, Susie, Danno, Daisuke, Trembath, Richard, Wood, Nicholas W., Kockum, Ingrid, Winsvold, Bendik S., Steinberg, Anna, Sjöstrand, Christina, Waldenlind, Elisabet, Vandrovcova, Jana, Houlden, Henry, Matharu, Manjit, Belin, Andrea Carmine

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Extraction and high-throughput sequencing of oak heartwood DNA: Assessing the feasibility of genome-wide DNA methylation profiling von Rossi, Federico, Crnjar, Alessandro, Comitani, Federico, Feliciano, Rodrigo, Jahn, Leonie, Malim, George, Southgate, Laura, Kay, Emily, Oakey, Rebecca, Buggs, Richard, Moir, Andy, Kistler, Logan, Mateos, Ana Rodriguez, Molteni, Carla, Schulz, Reiner

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Heterozygous Loss-of-Function Mutations in DLL4 Cause Adams-Oliver Syndrome von Meester, Josephina A.N., Southgate, Laura, Stittrich, Anna-Barbara, Venselaar, Hanka, Beekmans, Sander J.A., den Hollander, Nicolette, Bijlsma, Emilia K., Helderman-van den Enden, Appolonia, Verheij, Joke B.G.M., Glusman, Gustavo, Roach, Jared C., Lehman, Anna, Patel, Millan S., de Vries, Bert B.A., Ruivenkamp, Claudia, Itin, Peter, Prescott, Katrina, Clarke, Sheila, Trembath, Richard, Zenker, Martin, Sukalo, Maja, Van Laer, Lut, Loeys, Bart, Wuyts, Wim

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Molecular genetic characterization of SMAD signaling molecules in pulmonary arterial hypertension von Nasim, Md. Talat, Ogo, Takeshi, Ahmed, Mohammad, Randall, Rebecca, Chowdhury, Hasnin M., Snape, Katie M., Bradshaw, Teisha Y., Southgate, Laura, Lee, Grace J., Jackson, Ian, Lord, Graham M., Gibbs, J. Simon R., Wilkins, Martin R., Ohta-Ogo, Keiko, Nakamura, Kazufumi, Girerd, Barbara, Coulet, Florence, Soubrier, Florent, Humbert, Marc, Morrell, Nicholas W., Trembath, Richard C., Machado, Rajiv D.

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Molecular genetics of pulmonary hypertension in children von Taha, Fatima, Southgate, Laura

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Gain-of-Function Mutations of ARHGAP31, a Cdc42/Rac1 GTPase Regulator, Cause Syndromic Cutis Aplasia and Limb Anomalies von Southgate, Laura, Machado, Rajiv D., Snape, Katie M., Primeau, Martin, Dafou, Dimitra, Ruddy, Deborah M., Branney, Peter A., Fisher, Malcolm, Lee, Grace J., Simpson, Michael A., He, Yi, Bradshaw, Teisha Y., Blaumeiser, Bettina, Winship, William S., Reardon, Willie, Maher, Eamonn R., FitzPatrick, David R., Wuyts, Wim, Zenker, Martin, Lamarche-Vane, Nathalie, Trembath, Richard C.

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Explaining the United States’ Foreign Policy Failure in Southeast Asia since 2008 von Southgate, Laura

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A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct fromKabuki syndrome von Cuvertino Sara, Hartill Verity, Colyer, Alice, Garner, Terence, Nair, Nisha, Al-Gazali Lihadh, Canham, Natalie, Faundes Victor, Flinter Frances, Hertecant Jozef, Holder-Espinasse Muriel, Jackson, Brian, Lynch, Sally Ann, Nadat Fatima, Narasimhan, Vagheesh M, Peckham, Michelle, Sellers, Robert, Seri, Marco, Montanari, Francesca, Southgate, Laura, Squeo, Gabriella Maria, Trembath, Richard, van Heel David, Venuto Santina, Weisberg, Daniel, Stals, Karen, Ellard Sian, Barton, Anne, Kimber, Susan J, Sheridan, Eamonn, Merla Giuseppe, Stevens, Adam, Johnson, Colin A, Banka Siddharth

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Genetics and Genomics of Pulmonary Arterial Hypertension

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ASEAN Resistance to Sovereignty Violation: Interests, Balancing and the Role of the Vanguard State von Southgate, Laura

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China’s sovereignty violations in the East and South China Seas: How should Europe respond? von Southgate, Laura

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The DOCK protein family in vascular development and disease von Benson, Clare E., Southgate, Laura

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Insomnia and paranoia von Freeman, Daniel, Pugh, Katherine, Vorontsova, Natasha, Southgate, Laura

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