Evaluation of molecular inversion probe versus TruSeq® custom methods for targeted next-generation sequencing von Almomani, Rowida, Marchi, Margherita, Sopacua, Maurice, Lindsey, Patrick, Salvi, Erika, Koning, Bart de, Santoro, Silvia, Magri, Stefania, Smeets, Hubert J M, Martinelli Boneschi, Filippo, Malik, Rayaz R, Ziegler, Dan, Hoeijmakers, Janneke G J, Bönhof, Gidon, Dib-Hajj, Sulayman, Waxman, Stephen G, Merkies, Ingemar S J, Lauria, Giuseppe, Faber, Catharina G, Gerrits, Monique M

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Gradient descent-based freeform optics design for illumination using algorithmic differentiable non-sequential ray tracing von Koning, Bart de, Heemels, Alexander, Adam, Aurèle, Möller, Matthias

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Optimizing freeform lenses for extended sources with algorithmic differentiable ray tracing and truncated hierarchical B-splines von Heemels, Alexander, de Koning, Bart, Möller, Matthias, Adam, Aurèle

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Diagnostic exome-based preconception carrier testing in consanguineous couples: results from the first 100 couples in clinical practice von Sallevelt, Suzanne C.E.H., Stegmann, Alexander P.A., de Koning, Bart, Velter, Crool, Steyls, Anja, van Esch, Melanie, Lakeman, Phillis, Yntema, Helger, Esteki, Masoud Zamani, de Die-Smulders, Christine E.M., Gilissen, Christian, van den Wijngaard, Arthur, Brunner, Han G., Paulussen, Aimée D.C.

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Correction: Evaluation of molecular inversion probe versus TruSeq® custom methods for targeted next-generation sequencing von Almomani, Rowida, Marchi, Margherita, Sopacua, Maurice, Lindsey, Patrick, Salvi, Erika, de Koning, Bart, Santoro, Silvia, Magri, Stefania, Smeets, Hubert J M, Boneschi, Filippo Martinelli, Malik, Rayaz A, Ziegler, Dan, Hoeijmakers, Janneke G J, Bönhof, Gidon, Dib-Hajj, Sulayman, Waxman, Stephen G, Merkies, Ingemar S J, Lauria, Giuseppe, Faber, Catharina G, Gerrits, Monique M

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Cost-effective sequence analysis of 113 genes in 1,192 probands with retinitis pigmentosa and Leber congenital amaurosis von Panneman, Daan M, Hitti-Malin, Rebekkah J, Holtes, Lara K, de Bruijn, Suzanne E, Reurink, Janine, Boonen, Erica G M, Khan, Muhammad Imran, Ali, Manir, Andréasson, Sten, De Baere, Elfride, Banfi, Sandro, Bauwens, Miriam, Ben-Yosef, Tamar, Bocquet, Béatrice, De Bruyne, Marieke, de la Cerda, Berta, Coppieters, Frauke, Farinelli, Pietro, Guignard, Thomas, Inglehearn, Chris F, Karali, Marianthi, Kjellström, Ulrika, Koenekoop, Robert, de Koning, Bart, Leroy, Bart P, McKibbin, Martin, Meunier, Isabelle, Nikopoulos, Konstantinos, Nishiguchi, Koji M, Poulter, James A, Rivolta, Carlo, Rodríguez de la Rúa, Enrique, Saunders, Patrick, Simonelli, Francesca, Tatour, Yasmin, Testa, Francesco, Thiadens, Alberta A H J, Toomes, Carmel, Tracewska, Anna M, Tran, Hoai Viet, Ushida, Hiroaki, Vaclavik, Veronika, Verhoeven, Virginie J M, van de Vorst, Maartje, Gilissen, Christian, Hoischen, Alexander, Cremers, Frans P M, Roosing, Susanne

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Medication review using a Systematic Tool to Reduce Inappropriate Prescribing (STRIP) in adults with an intellectual disability: A pilot study von Zaal, Rianne J., Ebbers, Susan, Borms, Mirka, Koning, Bart de, Mombarg, Erna, Ooms, Piet, Vollaard, Hans, van den Bemt, Patricia M.L.A., Evenhuis, Heleen M.

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Rapid Resolution of Blended or Composite Multigenic Disease in Infants by Whole-Exome Sequencing von Theunissen, Tom E.J., MSc, Sallevelt, Suzanne C.E.H., MD, Hellebrekers, Debby M.E.I., PhD, de Koning, Bart, PhD, Hendrickx, Alexandra T.M., BASc, van den Bosch, Bianca J.C., PhD, Kamps, Rick, BASc, Schoonderwoerd, Kees, PhD, Szklarczyk, Radek, PhD, Mulder-Den Hartog, Elvira N.M., MSc, de Coo, Irenaeus F.M., MD, PhD, Smeets, Hubert J.M., PhD

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Archaeal MBF1 binds to 30S and 70S ribosomes via its helix-turn-helix domain von Blombach, Fabian, Launay, Helene, Snijders, Ambrosius P L, Zorraquino, Violeta, Wu, Hao, de Koning, Bart, Brouns, Stan J J, Ettema, Thijs J G, Camilloni, Carlo, Cavalli, Andrea, Vendruscolo, Michele, Dickman, Mark J, Cabrita, Lisa D, La Teana, Anna, Benelli, Dario, Londei, Paola, Christodoulou, John, van der Oost, John

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Specific MRI Abnormalities Reveal Severe Perrault Syndrome due to CLPP Defects von Theunissen, Tom E J, Szklarczyk, Radek, Gerards, Mike, Hellebrekers, Debby M E I, Mulder-Den Hartog, Elvira N M, Vanoevelen, Jo, Kamps, Rick, de Koning, Bart, Rutledge, S Lane, Schmitt-Mechelke, Thomas, van Berkel, Carola G M, van der Knaap, Marjo S, de Coo, Irenaeus F M, Smeets, Hubert J M

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Integrity Scandals of Politicians: A Political Integrity Index von Huberts, Leo, Kaptein, Muel, de Koning, Bart

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DataInterpolations.jl: Fast Interpolations of 1D data von Bhagavan, Sathvik, de Koning, Bart, Maddhashiya, Shubham, Rackauckas, Christopher

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Dutch genome diagnostic laboratories accelerated and improved variant interpretation and increased accuracy by sharing data von Fokkema, Ivo F. A. C., Velde, Kasper J., Slofstra, Mariska K., Ruivenkamp, Claudia A. L., Vogel, Maartje J., Pfundt, Rolph, Blok, Marinus J., Lekanne Deprez, Ronald H., Waisfisz, Quinten, Abbott, Kristin M., Sinke, Richard J., Rahman, Rubayte, Nijman, Isaäc J., Koning, Bart, Thijs, Gert, Wieskamp, Nienke, Moritz, Ruben J. G., Charbon, Bart, Saris, Jasper J., den Dunnen, Johan T., Laros, Jeroen F. J., Swertz, Morris A., Gijn, Marielle E.

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Interlaboratory comparison of sample preparation methods, database expansions, and cutoff values for identification of yeasts by matrix-assisted laser desorption ionization-time of... von Vlek, Anneloes, Kolecka, Anna, Khayhan, Kantarawee, Theelen, Bart, Groenewald, Marizeth, Boel, Edwin, Boekhout, Teun

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Clinical-grade whole genome sequencing-based haplarithmisis enables all forms of preimplantation genetic testing von Janssen, Anouk E. J., Koeck, Rebekka M., Essers, Rick, Cao, Ping, van Dijk, Wanwisa, Drüsedau, Marion, Meekels, Jeroen, Yaldiz, Burcu, van de Vorst, Maartje, de Koning, Bart, Hellebrekers, Debby M. E. I., Stevens, Servi J. C., Sun, Su Ming, Heijligers, Malou, de Munnik, Sonja A., van Uum, Chris M. J., Achten, Jelle, Hamers, Lars, Naghdi, Marjan, Vissers, Lisenka E. L. M., van Golde, Ron J. T., de Wert, Guido, Dreesen, Jos C. F. M., de Die-Smulders, Christine, Coonen, Edith, Brunner, Han G., van den Wijngaard, Arthur, Paulussen, Aimee D. C., Zamani Esteki, Masoud

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Exome sequencing reveals a novel Moroccan founder mutation in SLC19A3 as a new cause of early-childhood fatal Leigh syndrome von GERARDS, Mike, KAMPS, Rick, RATBI, Ilham, COPPIETERS, Wouter, KARIM, Latifa, DE COO, René, VAN DEN BOSCH, Bianca, SMELTS, Hubert, VAN OEVELEN, Jo, BOESTEN, Iris, JONGEN, Eveline, DE KONING, Bart, SCHOLTE, Hans R, DE ANGST, Isabel, SCHOONDERWOERD, Kees, SEFIANI, Abdelaziz

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Fidelity in Archaeal Information Processing von de Koning, Bart, Blombach, Fabian, Brouns, Stan J. J., van der Oost, John

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Whole Exome Sequencing Is the Preferred Strategy to Identify the Genetic Defect in Patients With a Probable or Possible Mitochondrial Cause von Theunissen, Tom E J, Nguyen, Minh, Kamps, Rick, Hendrickx, Alexandra T, Sallevelt, Suzanne C E H, Gottschalk, Ralph W H, Calis, Chantal M, Stassen, Alphons P M, de Koning, Bart, Mulder-Den Hartog, Elvira N M, Schoonderwoerd, Kees, Fuchs, Sabine A, Hilhorst-Hofstee, Yvonne, de Visser, Marianne, Vanoevelen, Jo, Szklarczyk, Radek, Gerards, Mike, de Coo, Irenaeus F M, Hellebrekers, Debby M E I, Smeets, Hubert J M

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A comprehensive strategy for exome-based preconception carrier screening von Sallevelt, Suzanne C.E.H., de Koning, Bart, Szklarczyk, Radek, Paulussen, Aimee D.C., de Die-Smulders, Christine E.M., Smeets, Hubert J.M.

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A comprehensive strategy for exome-based preconception carrier screening von Sallevelt, Suzanne C E H, de Koning, Bart, Szklarczyk, Radek, Paulussen, Aimee D C, de Die-Smulders, Christine E M, Smeets, Hubert J M

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