Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosis von Goodship, Judith, Ruiz-Perez, Victor L, Ide, Susan E, Strom, Tim M, Lorenz, Bettina, Wilson, David, Woods, Kathryn, King, Lynn, Francomano, Clair, Freisinger, Peter, Spranger, Stephanie, Marino, Bruno, Dallapiccola, Bruno, Wright, Michael, Meitinger, Thomas, Polymeropoulos, Mihael H

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Mapping of a Gene for Parkinson's Disease to Chromosome 4q21-q23 von Polymeropoulos, Mihael H., Higgins, Joseph J., Golbe, Lawrence I., Johnson, William G., Ide, Susan E., Di Iorio, Giuseppe, Sanges, Giuseppe, Stenroos, Edward S., Pho, Lana T., Schaffer, Alejandro A., Lazzarini, Alice M., Nussbaum, Robert L., Duvoisin, Roger C.

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RETURNING GENETIC RESEARCH RESULTS TO INDIVIDUALS: POINTS-TO-CONSIDER von RENEGAR, GAILE, WEBSTER, CHRISTOPHER J., STUERZEBECHER, STEFFEN, HARTY, LEA, IDE, SUSAN E., BALKITE, BETH, ROGALSKI-SALTER, TARYN A., COHEN, NADINE, SPEAR, BRIAN B., BARNES, DIANE M., BRAZELL, CELIA

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Mutation in the α-synuclein gene identified in families with Parkinson's disease von POLYMEROPOULOS, M. H, LAVEDAN, C, STENROOS, E. S, CHANDRASEKHARAPPA, S, ATHANASSIADOU, A, PAPAPETROPOULOS, T, JOHNSON, W. G, LAZZARINI, A. M, DUVOISIN, R. C, DI LORIO, G, GOLBE, L. I, NUSSBAUM, R. L, LEROY, E, IDE, S. E, DEHEJIA, A, DUTRA, A, PIKE, B, ROOT, H, RUBENSTEIN, J, BOYER, R

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Stimulus MDS-US Trial in Progress: Evaluating Sabatolimab in Combination with Hypomethylating Agents (HMAs) in Patients with Intermediate-, High-, or Very High-Risk Myelodysplastic... von Zeidan, Amer M., DeZern, Amy E., Borate, Uma, Kobata, Krissy, Ide, Susan E., Sabo, John, Marques Ramos, Pedro, Sun, Haiying, Lyons, Roger M., Garcia-Manero, Guillermo

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The Gene for the Ellis–van Creveld Syndrome Is Located on Chromosome 4p16 von Polymeropoulos, Mihael H., Ide, Susan E., Wright, Michael, Goodship, Judith, Weissenbach, Jean, Pyeritz, Reed E., Da Silva, Elias O., Ortiz De Luna, Rosa Isela, Francomano, Clair A.

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The gene for pycnodysostosis maps to human chromosome 1cen-q21 von Polymeropoulos, Mihael H, Ortiz De Luna, Rosa Isela, Torres, Rosarelis, Francomano, Clair A, Ide, Susan E, Rubenstein, Jeffrey

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Efficacy, Safety, and Confirmation of the Recommended Phase 2 Dose of Ruxolitinib Plus Panobinostat in Patients with Intermediate or High-Risk Myelofibrosis von Kiladjian, Jean-Jacques, Heidel, Florian H, Vannucchi, Alessandro M., Ribrag, Vincent, Passamonti, Francesco, Hayat, Amjad, Conneally, Eibhlin, Martino, Bruno, Kindler, Thomas, Lipka, Daniel B., Acharyya, Suddhasatta, Gopalakrishna, Prashanth, Ide, Susan E, Loechner, Sabine, Mu, Song, Harrison, Claire N

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Addiction and autonomy returning genetic research results o neuroethics von Levy, Neil, Foddy, Bennett, Savulescu, Julian, Renegar, Gaile, Webster, Christopher J, Stuerzebecher, Steffen, Harty, Lea, Ide, Susan E, Balkite, Beth, Rogalski-Salter, Taryn A, Cohen, Nadine, Spear, Brian B, Barnes, Diane M, Brazell, Celia, Glannon, Walter

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Mutation in the (alpha)-synuclein gene identified in families with Parkinson's disease von Polymeropoulos, Mihael H, Lavedan, Christian, Leroy, Elisabeth, Ide, Susan E

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Brachydactyly Type C Gene Maps to Human Chromosome 12q24 von Polymeropoulos, Mihael H., Ide, Susan E., Magyari, Trish, Francomano, Clair A.

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The G209A mutation in the alpha-synuclein gene in Brazilian families with Parkinson's disease von Teive, H A, Raskin, S, Iwamoto, F M, Germiniani, F M, Baran, M H, Werneck, L C, Allan, N, Quagliato, E, Leroy, E, Ide, S E, Polymeropoulos, M H

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Exclusion of the MSX1 homeobox gene as the gene for the Ellis van Creveld syndrome in the Amish von IDE, S. E, ORTIZ DE LUNA, R. I, FRANCOMANO, C. A, POLYMEROPOULOS, M. H

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Lack of mutations in the biotin-binding region of the pyruvate carboxylase (PC) gene in a family with partial PC deficiency von Higgins, Joseph J., Ide, Susan E., Oghalai, John S., Polymeropoulos, Mihael H.

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Contig map of the Parkinson's disease region on 4q21-q23 von Lavedan, C, Dehejia, A, Pike, B, Dutra, A, Leroy, E, Ide, S E, Root, H, Rubenstein, J, Boyer, R L, Chandrasekharappa, S, Makalowska, I, Nussbaum, R L, Polymeropoulos, M H

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The G209A mutation in the alpha-synuclein gene in Brazilian families with Parkinson's disease Mutação G209A no gene da alfa-sinucleína em famílias brasileiras com doença de Parkins... von Hélio A.G. Teive, Salmo Raskin, Fábio M. Iwamoto, Francisco M.B. Germiniani, Maria H.H. Baran, Lineu C. Werneck, Nasser Allan, Elizabeth Quagliato, Elisabeth Leroy, Susan E. Ide, Mihael H. Polymeropoulos

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Dinucleotide repeat polymorphism at the D14S99E locus von Polymeropoulos, Mihael H., Xiao, Hong, Ide, Susan E., Merril, Carl R.

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Mutation in the α-Synuclein Gene Indentified in Families with Parkinson's Disease von Polymeropoulos, Mihael H., Lavedan, Christian, Leroy, Elisabeth, Ide, Susan E., Dehejia, Anindya, Dutra, Amalia, Pike, Brian, Root, Holly, Rubenstein, Jeffrey, Boyer, Rebecca, Stenroos, Edward S., Chandrasekharappa, Settara, Athanassiadou, Aglaia, Papapetropoulos, Theodore, Johnson, William G., Lazzarini, Alice M., Duvoisin, Roger C., Di Iorio, Giuseppe, Golbe, Lawrence I., Nussbaum, Robert L.

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Linkage and cytogenetic mapping of a CAG repeat containing human cDNA to 3p24.2-p22 von Polymeropoulos, Mihael H., Ide, Susan E., Becker, Kevin, Naylor, Susan L.

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Transcription Factor 21 Is Required for Branching Morphogenesis and Regulates the Gdnf-Axis in Kidney Development von Ide, Shintaro, Finer, Gal, Maezawa, Yoshiro, Onay, Tuncer, Souma, Tomokazu, Scott, Rizaldy, Ide, Kana, Akimoto, Yoshihiro, Li, Chengjin, Ye, Minghao, Zhao, Xiangmin, Baba, Yusuke, Minamizuka, Takuya, Jin, Jing, Takemoto, Minoru, Yokote, Koutaro, Quaggin, Susan E

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