Recent Publications from Department of Genetics.
Found 1410 publication(s).

• Yang, Y., Gomez, M., Marsh, T., Poillet-Perez, L., Sawant, A., Chen, L., Park, N. R., Jackson, S. R., Hu, Z., Alon, N., Liu, C., Debnath, J., Guan, J. L., Davidson, S., Verzi, M., & White, E. (2022). Autophagy in PDGFRα+ mesenchymal cells is essential for intestinal stem cell survival. Proceedings of the National Academy of Sciences of the United States of America, 119, e2202016119. PubMed
• McKim, K. S. (2022). Highway to hell-thy meiotic divisions: Chromosome passenger complex functions driven by microtubules: CPC interactions with both the chromosomes and microtubules are important for spindle assembly and function: CPC interactions with both the chromosomes and microtubules are important for spindle assembly and function. BioEssays : news and reviews in molecular, cellular and developmental biology, 44, e2100202. PubMed
• Baxter, S. M., Posey, J. E., Lake, N. J., Sobreira, N., Chong, J. X., Buyske, S., Blue, E. E., Chadwick, L. H., Coban-Akdemir, Z. H., Doheny, K. F., Davis, C. P., Lek, M., Wellington, C., Jhangiani, S. N., Gerstein, M., Gibbs, R. A., Lifton, R. P., MacArthur, D. G., Matise, T. C., Lupski, J. R., Valle, D., Bamshad, M. J., Hamosh, A., Mane, S., Nickerson, D. A., ,, Rehm, H. L., & O'Donnell-Luria, A. (2022). Centers for Mendelian Genomics: A decade of facilitating gene discovery. Genetics in medicine : official journal of the American College of Medical Genetics, 24, 784-797. PubMed
• Pukhrambam, C., Molodtsov, V., Kooshkbaghi, M., Tareen, A., Vu, H., Skalenko, K. S., Su, M., Yin, Z., Winkelman, J. T., Kinney, J. B., Ebright, R. H., & Nickels, B. E. (2022). Structural and mechanistic basis of σ-dependent transcriptional pausing. Proceedings of the National Academy of Sciences of the United States of America, 119, e2201301119. PubMed
• Downie, C. G., Dimos, S. F., Bien, S. A., Hu, Y., Darst, B. F., Polfus, L. M., Wang, Y., Wojcik, G. L., Tao, R., Raffield, L. M., Armstrong, N. D., Polikowsky, H. G., Below, J. E., Correa, A., Irvin, M. R., Rasmussen-Torvik, L. J. F., Carlson, C. S., Phillips, L. S., Liu, S., Pankow, J. S., Rich, S. S., Rotter, J. I., Buyske, S., Matise, T. C., North, K. E., Avery, C. L., Haiman, C. A., Loos, R. J. F., Kooperberg, C., Graff, M., & Highland, H. M. (2022). Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study. Diabetologia, 65, 477-489. PubMed
• Kamitaki, B. K., Janmohamed, M., Kandula, P., Elder, C., Mani, R., Wong, S., Perucca, P., O'Brien, T. J., Lin, H., Heiman, G. A., & Choi, H. (2022). Clinical and EEG factors associated with antiseizure medication resistance in idiopathic generalized epilepsy. Epilepsia, 63, 150-161. PubMed
• Das, S., Feng, Q., Balasubramanian, I., Lin, X., Liu, H., Pellón-Cardenas, O., Yu, S., Zhang, X., Liu, Y., Wei, Z., Bonder, E. M., Verzi, M. P., Hsu, W., Zhang, L., Wang, T. C., & Gao, N. (2022). Colonic healing requires Wnt produced by epithelium as well as Tagln+ and Acta2+ stromal cells. Development (Cambridge, England), 149. PubMed
• Fuentes, I., Morishita, Y., Gonzalez-Salinas, S., Champagne, F. A., Uchida, S., & Shumyatsky, G. P. (2022). Experience-Regulated Neuronal Signaling in Maternal Behavior. Frontiers in molecular neuroscience, 15, 844295. PubMed
• Gu, W., Wang, H., Huang, X., Kraiczy, J., Singh, P. N. P., Ng, C., Dagdeviren, S., Houghton, S., Pellon-Cardenas, O., Lan, Y., Nie, Y., Zhang, J., Banerjee, K. K., Onufer, E. J., Warner, B. W., Spence, J., Scherl, E., Rafii, S., Lee, R. T., Verzi, M. P., Redmond, D., Longman, R., Helin, K., Shivdasani, R. A., & Zhou, Q. (2022). SATB2 preserves colon stem cell identity and mediates ileum-colon conversion via enhancer remodeling. Cell stem cell, 29, 101-115.e10. PubMed
• Yadavalli, S. S., & Yuan, J. (2022). Bacterial Small Membrane Proteins: the Swiss Army Knife of Regulators at the Lipid Bilayer. Journal of bacteriology, 204, e0034421. PubMed
• Chiou, K. L., Janiak, M. C., Schneider-Crease, I. A., Sen, S., Ayele, F., Chuma, I. S., Knauf, S., Lemma, A., Signore, A. V., D'Ippolito, A. M., Abebe, B., Haile, A. A., Kebede, F., Fashing, P. J., Nguyen, N., McCann, C., Houck, M. L., Wall, J. D., Burrell, A. S., Bergey, C. M., Rogers, J., Phillips-Conroy, J. E., Jolly, C. J., Melin, A. D., Storz, J. F., Lu, A., Beehner, J. C., Bergman, T. J., & Snyder-Mackler, N. (2022). Genomic signatures of high-altitude adaptation and chromosomal polymorphism in geladas. Nature ecology & evolution, 6, 630-643. PubMed
• Connacher, R., Williams, M., Prem, S., Yeung, P. L., Matteson, P., Mehta, M., Markov, A., Peng, C., Zhou, X., McDermott, C. R., Pang, Z. P., Flax, J., Brzustowicz, L., Lu, C. W., Millonig, J. H., & DiCicco-Bloom, E. (2022). Autism NPCs from both idiopathic and CNV 16p11.2 deletion patients exhibit dysregulation of proliferation and mitogenic responses. Stem cell reports, 17, 1380-1394. PubMed
• Hawkins, M. B., Jandzik, D., Tulenko, F. J., Cass, A. N., Nakamura, T., Shubin, N. H., Davis, M. C., & Stock, D. W. (2022). An Fgf-Shh positive feedback loop drives growth in developing unpaired fins. Proceedings of the National Academy of Sciences of the United States of America, 119, e2120150119. PubMed
• Henderson, C., Brustolin, M., Hegde, S., Dayama, G., Lau, N., Hughes, G. L., Bergey, C., & Rasgon, J. L. (2022). Transcriptomic and small RNA response to Mayaro virus infection in Anopheles stephensi mosquitoes. PLoS neglected tropical diseases, 16, e0010507. PubMed
• Lubin, J. H., Zardecki, C., Dolan, E. M., Lu, C., Shen, Z., Dutta, S., Westbrook, J. D., Hudson, B. P., Goodsell, D. S., Williams, J. K., Voigt, M., Sarma, V., Xie, L., Venkatachalam, T., Arnold, S., Alfaro Alvarado, L. H., Catalfano, K., Khan, A., McCarthy, E., Staggers, S., Tinsley, B., Trudeau, A., Singh, J., Whitmore, L., Zheng, H., Benedek, M., Currier, J., Dresel, M., Duvvuru, A., Dyszel, B., Fingar, E., Hennen, E. M., Kirsch, M., Khan, A. A., Labrie-Cleary, C., Laporte, S., Lenkeit, E., Martin, K., Orellana, M., Ortiz-Alvarez de la Campa, M., Paredes, I., Wheeler, B., Rupert, A., Sam, A., See, K., Soto Zapata, S., Craig, P. A., Hall, B. L., Jiang, J., Koeppe, J. R., Mills, S. A., Pikaart, M. J., Roberts, R., Bromberg, Y., Hoyer, J. S., Duffy, S., Tischfield, J., Ruiz, F. X., Arnold, E., Baum, J., Sandberg, J., Brannigan, G., Khare, S. D., & Burley, S. K. (2022). Evolution of the SARS-CoV-2 proteome in three dimensions (3D) during the first 6 months of the COVID-19 pandemic. Proteins, 90, 1054-1080. PubMed
• Cope, A. L., Vellappan, S., Favate, J. S., Skalenko, K. S., Yadavalli, S. S., & Shah, P. (2022). Exploring Ribosome-Positioning on Translating Transcripts with Ribosome Profiling. Methods in molecular biology (Clifton, N.J.), 2404, 83-110. PubMed
• Highland, H. M., Wojcik, G. L., Graff, M., Nishimura, K. K., Hodonsky, C. J., Baldassari, A. R., Cote, A. C., Cheng, I., Gignoux, C. R., Tao, R., Li, Y., Boerwinkle, E., Fornage, M., Haessler, J., Hindorff, L. A., Hu, Y., Justice, A. E., Lin, B. M., Lin, D., Stram, D. O., Haiman, C. A., Kooperberg, C., Le Marchand, L., Matise, T. C., Kenny, E. E., Carlson, C. S., Stahl, E. A., Avery, C. L., North, K. E., Ambite, J. L., Buyske, S., Loos, R. J., Peters, U., Young, K. L., Bien, S. A., & Huckins, L. M. (2022). Predicted gene expression in ancestrally diverse populations leads to discovery of susceptibility loci for lifestyle and cardiometabolic traits. American journal of human genetics, 109, 669-679. PubMed
• Axelrod, D. E. (2022). Chronotherapy of Early Colon Cancer: Advantage of Morning Dose Schedules. Cancer informatics, 21, 11769351211067697. PubMed
• Liu, Y., Yu, L., Pukhrambam, C., Winkelman, J. T., Firlar, E., Kaelber, J. T., Zhang, Y., Nickels, B. E., & Ebright, R. H. (2022). Structural and mechanistic basis of reiterative transcription initiation. Proceedings of the National Academy of Sciences of the United States of America, 119. PubMed
• Fleet, J. C., Aldea, D., Chen, L., Christakos, S., & Verzi, M. (2022). Regulatory domains controlling high intestinal vitamin D receptor gene expression are conserved in mouse and human. The Journal of biological chemistry, 298, 101616. PubMed
• Lai, D., Johnson, E. C., Colbert, S., Pandey, G., Chan, G., Bauer, L., Francis, M. W., Hesselbrock, V., Kamarajan, C., Kramer, J., Kuang, W., Kuo, S., Kuperman, S., Liu, Y., McCutcheon, V., Pang, Z., Plawecki, M. H., Schuckit, M., Tischfield, J., Wetherill, L., Zang, Y., Edenberg, H. J., Porjesz, B., Agrawal, A., & Foroud, T. (2022). Evaluating risk for alcohol use disorder: Polygenic risk scores and family history. Alcoholism, clinical and experimental research, 46, 374-383. PubMed
• Nikonorova, I. A., Wang, J., Cope, A. L., Tilton, P. E., Power, K. M., Walsh, J. D., Akella, J. S., Krauchunas, A. R., Shah, P., & Barr, M. M. (2022). Isolation, profiling, and tracking of extracellular vesicle cargo in Caenorhabditis elegans. Current biology : CB, 32, 1924-1936.e6. PubMed
• Marciniak, S., Bergey, C. M., Silva, A. M., Hałuszko, A., Furmanek, M., Veselka, B., Velemínský, P., Vercellotti, G., Wahl, J., Zariņa, G., Longhi, C., Kolář, J., Garrido-Pena, R., Flores-Fernández, R., Herrero-Corral, A. M., Simalcsik, A., Müller, W., Sheridan, A., Miliauskienė,, Jankauskas, R., Moiseyev, V., Köhler, K., Király,, Gamarra, B., Cheronet, O., Szeverényi, V., Kiss, V., Szeniczey, T., Kiss, K., Zoffmann, Z. K., Koós, J., Hellebrandt, M., Maier, R. M., Domboróczki, L., Virag, C., Novak, M., Reich, D., Hajdu, T., Von Cramon-Taubadel, N., Pinhasi, R., & Perry, G. H. (2022). An integrative skeletal and paleogenomic analysis of stature variation suggests relatively reduced health for early European farmers. Proceedings of the National Academy of Sciences of the United States of America, 119, e2106743119. PubMed
• Mori, S., & Nakamura, T. (2022). Redeployment of odontode gene regulatory network underlies dermal denticle formation and evolution in suckermouth armored catfish. Scientific reports, 12, 6172. PubMed
• Cope, A. L., & Shah, P. (2022). Intragenomic variation in non-adaptive nucleotide biases causes underestimation of selection on synonymous codon usage. PLoS genetics, 18, e1010256. PubMed
• Saito, Y., Hawley, B. R., Puno, M. R., Sarathy, S. N., Lima, C. D., Jaffrey, S. R., Darnell, R. B., Keeney, S., & Jain, D. (2022). YTHDC2 control of gametogenesis requires helicase activity but not mA binding. Genes & development, 36, 180-194. PubMed
• Stanek, T. J., Cao, W., Mehra, R. M., & Ellison, C. E. (2022). Sex-specific variation in R-loop formation in Drosophila melanogaster. PLoS genetics, 18, e1010268. PubMed
• Blengini, C. S., & Schindler, K. (2022). Acentriolar spindle assembly in mammalian female meiosis and the consequences of its perturbations on human reproduction†. Biology of reproduction, 106, 253-263. PubMed
• Bergey, C., Marshall, Z., DeDeo, S., & Yurovsky, D. (2022). Learning Communicative Acts in Children's Conversations: A Hidden Topic Markov Model Analysis of the CHILDES Corpora. Topics in cognitive science, 14, 388-399. PubMed
• McGraw, E., Rispoli, J., Horner, M. B., & Heiman, G. A. (2022). Genetic counseling certificate program: A program evaluation of undergraduate exposure to genetic counseling. Journal of genetic counseling, 31, 1003-1007. PubMed
• Connacher, R., Williams, M., Prem, S., Yeung, P. L., Matteson, P., Mehta, M., Markov, A., Peng, C., Zhou, X., McDermott, C. R., Pang, Z. P., Flax, J., Brzustowicz, L., Lu, C. W., Millonig, J. H., & DiCicco-Bloom, E. (2022). Autism NPCs from both idiopathic and CNV 16p11.2 deletion patients exhibit dysregulation of proliferation and mitogenic responses. Stem cell reports, 17, 1786. PubMed
• Lee, S., Abed, D. A., Nguyen, M. U., Verzi, M. P., & Hu, L. (2022). Structure-activity relationships of 1,4-bis(arylsulfonamido)-benzene or naphthalene-N,N'-diacetic acids with varying C2-substituents as inhibitors of Keap1-Nrf2 protein-protein interaction. European journal of medicinal chemistry, 237, 114380. PubMed
• Wong, A., Zhou, A., Cao, X., Mahaganapathy, V., Azaro, M., Gwin, C., Wilson, S., Buyske, S., Bartlett, C. W., Flax, J. F., Brzustowicz, L. M., & Xing, J. (2022). MicroRNA and MicroRNA-Target Variants Associated with Autism Spectrum Disorder and Related Disorders. Genes, 13. PubMed
• Kays, R., Cove, M. V., Diaz, J., Todd, K., Bresnan, C., Snider, M., Lee, T. E., Jasper, J. G., Douglas, B., Crupi, A. P., Weiss, K. C. B., Rowe, H., Sprague, T., Schipper, J., Lepczyk, C. A., Fantle-Lepczyk, J. E., Davenport, J., Zimova, M., Farris, Z., Williamson, J., Fisher-Reid, M. C., Rezendes, D., King, S. M., Chrysafis, P., Jensen, A. J., Jachowski, D. S., King, K. C., Herrera, D. J., Moore, S., Van der Merwe, M., Lombardi, J. V., Sergeyev, M., Tewes, M. E., Horan, R. V., Rentz, M. S., Driver, A., Brandt, R. S. E., Nagy, C., Alexander, P., Maher, S. P., Darracq, A. K., Barr, E. G., Hess, G., Webb, S. L., Proctor, M. D., Vanek, J. P., Lafferty, D. J. R., Hubbard, T., Jiménez, J. E., McCain, C., Favreau, J., Fogarty, J., Hill, J., Hammerich, S., Gray, M., Rega-Brodsky, C. C., Durbin, C., Flaherty, E. A., Brooke, J., Coster, S. S., Lathrop, R. G., Russell, K., Bogan, D. A., Shamon, H., Rooney, B., Rockhill, A., Lonsinger, R. C., O'Mara, M. T., Compton, J. A., Barthelmess, E. L., Andy, K. E., Belant, J. L., Petroelje, T., Wehr, N. H., Beyer, D. E., Scognamillo, D. G., Schalk, C., Day, K., Ellison, C. N., Ruthven, C., Nunley, B., Fritts, S., Whittier, C. A., Neiswenter, S. A., Pelletier, R., DeGregorio, B. A., Kuprewicz, E. K., Davis, M. L., Baruzzi, C., Lashley, M. A., McDonald, B., Mason, D., Risch, D. R., Allen, M. L., Whipple, L. S., Sperry, J. H., Alexander, E., Wolff, P. J., Hagen, R. H., Mortelliti, A., Bolinjcar, A., Wilson, A. M., Van Norman, S., Powell, C., Coletto, H., Schauss, M., Bontrager, H., Beasley, J., Ellis-Felege, S. N., Wehr, S. R., Giery, S. T., Pekins, C. E., LaRose, S. H., Revord, R. S., Hansen, C. P., Hansen, L., Millspaugh, J. J., Zorn, A., Gerber, B. D., Rezendes, K., Adley, J., Sevin, J., Green, A. M., Şekercioğlu, H., Pendergast, M. E., Mullen, K., Bird, T., Edelman, A. J., Romero, A., O'Neill, B. J., Schmitz, N., Vandermus, R. A., Alston, J. M., Kuhn, K. M., Hasstedt, S. C., Lesmeister, D. B., Appel, C. L., Rota, C., Stenglein, J. L., Anhalt-Depies, C., Nelson, C. L., Long, R. A., Remine, K. R., Jordan, M. J., Elbroch, L. M., Bergman, D., Cendejas-Zarelli, S., Sager-Fradkin, K., Conner, M., Morris, G., Parsons, E., Hernández-Yáñez, H., & McShea, W. J. (2022). SNAPSHOT USA 2020: A second coordinated national camera trap survey of the United States during the COVID-19 pandemic. Ecology. PubMed
• Aita, R., Aldea, D., Hassan, S., Hur, J., Pellon-Cardenas, O., Cohen, E., Chen, L., Shroyer, N., Christakos, S., Verzi, M. P., & Fleet, J. C. (2022). Genomic Analysis of 1,25-dihydroxyvitamin D Action in Mouse Intestine Reveals Compartment and Segment-Specific Gene Regulatory Effects. The Journal of biological chemistry. PubMed
• Vora, M., Mondal, A., Jia, D., Gaddipati, P., Akel, M., Gilleran, J., Roberge, J., Rongo, C., & Langenfeld, J. (2022). Bone morphogenetic protein signaling regulation of AMPK and PI3K in lung cancer cells and C. elegans. Cell & bioscience, 12, 76. PubMed
• Smith, S. P., Shahamatdar, S., Cheng, W., Zhang, S., Paik, J., Graff, M., Haiman, C., Matise, T. C., North, K. E., Peters, U., Kenny, E., Gignoux, C., Wojcik, G., Crawford, L., & Ramachandran, S. (2022). Enrichment analyses identify shared associations for 25 quantitative traits in over 600,000 individuals from seven diverse ancestries. American journal of human genetics, 109, 871-884. PubMed
• Fellmeth, J. E., & McKim, K. S. (2022). A Brief History of (Female) Meiosis. Genes, 13. PubMed
• Kratka, C., Drutovic, D., Blengini, C. S., & Schindler, K. (2022). Using ZINC08918027 inhibitor to determine Aurora kinase-chromosomal passenger complex isoforms in mouse oocytes. BMC research notes, 15, 96. PubMed
• Sun, S., Miller, M., Wang, Y., Tyc, K. M., Cao, X., Scott, R. T., Tao, X., Bromberg, Y., Schindler, K., & Xing, J. (2022). Predicting embryonic aneuploidy rate in IVF patients using whole-exome sequencing. Human genetics. PubMed
• Cope, A. L., Anderson, F., Favate, J., Jackson, M., Mok, A., Kurowska, A., Liu, J., MacKenzie, E., Shivakumar, V., Tilton, P., Winterbourne, S. M., Xue, S., Kavoussanakis, K., Lareau, L. F., Shah, P., & Wallace, E. W. J. (2022). riboviz 2: A flexible and robust ribosome profiling data analysis and visualization workflow. Bioinformatics (Oxford, England). PubMed
• Wang, L. I., DeFosse, T., Jang, J. K., Battaglia, R. A., Wagner, V. F., & McKim, K. S. (2021). Borealin directs recruitment of the CPC to oocyte chromosomes and movement to the microtubules. The Journal of cell biology, 220. PubMed
• Blengini, C. S., Nguyen, A. L., Aboelenain, M., & Schindler, K. (2021). Age-dependent integrity of the meiotic spindle assembly checkpoint in females requires Aurora kinase B. Aging cell, 20, e13489. PubMed
• Jang, J. K., Gladstein, A. C., Das, A., Shapiro, J. G., Sisco, Z. L., & McKim, K. S. (2021). Multiple pools of PP2A regulate spindle assembly, kinetochore attachments and cohesion in Drosophila oocytes. Journal of cell science, 134. PubMed
• Criss, Z. K., Bhasin, N., Di Rienzi, S. C., Rajan, A., Deans-Fielder, K., Swaminathan, G., Kamyabi, N., Zeng, X. L., Doddapaneni, H., Menon, V. K., Chakravarti, D., Estrella, C., Yu, X., Patil, K., Petrosino, J. F., Fleet, J. C., Verzi, M. P., Christakos, S., Helmrath, M. A., Arimura, S., DePinho, R. A., Britton, R. A., Maresso, A. W., Grande-Allen, K. J., Blutt, S. E., Crawford, S. E., Estes, M. K., Ramani, S., & Shroyer, N. F. (2021). Drivers of transcriptional variance in human intestinal epithelial organoids. Physiological genomics, 53, 486-508. PubMed
• Halvorsen, M., Szatkiewicz, J., Mudgal, P., Yu, D., ,, Nordsletten, A. E., Mataix-Cols, D., Mathews, C. A., Scharf, J. M., Mattheisen, M., Robertson, M. M., McQuillin, A., & Crowley, J. J. (2021). Elevated common variant genetic risk for tourette syndrome in a densely-affected pedigree. Molecular psychiatry, 26, 7522-7529. PubMed
• Joshi, K. K., Matlack, T. L., Pyonteck, S., Vora, M., Menzel, R., & Rongo, C. (2021). Biogenic amine neurotransmitters promote eicosanoid production and protein homeostasis. EMBO reports, 22, e51063. PubMed
• Biswas, L., Tyc, K., El Yakoubi, W., Morgan, K., Xing, J., & Schindler, K. (2021). Meiosis interrupted: the genetics of female infertility via meiotic failure. Reproduction (Cambridge, England), 161, R13-R35. PubMed
• Enny, A., Shanabag, A., Thompson, A. W., Racicot, B., Braasch, I., & Nakamura, T. (2021). Cellular mechanisms of frontal bone development in spotted gar (Lepisosteus oculatus). Developmental dynamics : an official publication of the American Association of Anatomists, 250, 1668-1682. PubMed
• Bruse, S., Moreau, M., Bromberg, Y., Jang, J. H., Wang, N., Ha, H., Picchi, M., Lin, Y., Langley, R. J., Qualls, C., Klesney-Tait, J., Zabner, J., Leng, S., Mao, J., Belinsky, S. A., Xing, J., & Nyunoya, T. (2021). Correction to: Whole exome sequencing identifies novel candidate genes that modify chronic obstructive pulmonary disease susceptibility. Human genomics, 15, 74. PubMed
• Verzi, M. P. (2021). GATA4 in Regional Affairs. Cellular and molecular gastroenterology and hepatology, 12, 1505-1506. PubMed
• Skalenko, K. S., Li, L., Zhang, Y., Vvedenskaya, I. O., Winkelman, J. T., Cope, A. L., Taylor, D. M., Shah, P., Ebright, R. H., Kinney, J. B., Zhang, Y., & Nickels, B. E. (2021). Promoter-sequence determinants and structural basis of primer-dependent transcription initiation in . Proceedings of the National Academy of Sciences of the United States of America, 118. PubMed
• Tong, K., Kothari, O. A., Haro, K. S., Panda, A., Bandari, M. M., Carrick, J. N., Hur, J. J., Zhang, L., Chan, C. S., Xing, J., Gatza, M. L., Ganesan, S., & Verzi, M. P. (2021). SMAD4 is critical in suppression of BRAF-V600E serrated tumorigenesis. Oncogene, 40, 6034-6048. PubMed
• Lawlor, M. A., Cao, W., & Ellison, C. E. (2021). A transposon expression burst accompanies the activation of Y-chromosome fertility genes during Drosophila spermatogenesis. Nature communications, 12, 6854. PubMed
• Lim, Y., Berry, B., Viteri, S., McCall, M., Park, E. C., Rongo, C., Brookes, P. S., & Nehrke, K. (2021). FNDC-1-mediated mitophagy and ATFS-1 coordinate to protect against hypoxia-reoxygenation. Autophagy, 17, 3389-3401. PubMed
• Pak, C., Danko, T., Mirabella, V. R., Wang, J., Liu, Y., Vangipuram, M., Grieder, S., Zhang, X., Ward, T., Huang, Y. A., Jin, K., Dexheimer, P., Bardes, E., Mitelpunkt, A., Ma, J., McLachlan, M., Moore, J. C., Qu, P., Purmann, C., Dage, J. L., Swanson, B. J., Urban, A. E., Aronow, B. J., Pang, Z. P., Levinson, D. F., Wernig, M., & Südhof, T. C. (2021). Cross-platform validation of neurotransmitter release impairments in schizophrenia patient-derived -mutant neurons. Proceedings of the National Academy of Sciences of the United States of America, 118. PubMed
• Vancappel, A., Jansen, E., Ouhmad, N., Desmidt, T., Etain, B., Bergey, C., D'Ussel, M., Krebs, M. O., Paquet, C., Réveillère, C., Hingray, C., & El-Hage, W. (2021). Psychological Impact of Exposure to the COVID-19 Sanitary Crisis on French Healthcare Workers: Risk Factors and Coping Strategies. Frontiers in psychiatry, 12, 701127. PubMed
• Guan, Y., Keeney, S., Jain, D., & Wang, P. J. (2021). yama, a mutant allele of Mov10l1, disrupts retrotransposon silencing and piRNA biogenesis. PLoS genetics, 17, e1009265. PubMed
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• Del Villano, D. C., Miller, S. I., Schacter, L. P., & Tischfield, J. A. (1980). Elevated superoxide dismutase in black alcoholics. Science (New York, N.Y.), 207, 991-3. PubMed
• Del Villano, B. C., & Tischfield, J. A. (1979). A radioimmune assay for human cupro-zinc superoxide dismutase and its application to erythrocytes. Journal of immunological methods, 29, 253-62. PubMed
• Tischfield, J., Schafer, I. A., Dickerman, L. H., Trill, J., Mulivor, R. A., Greene, A. E., & Coriell, L. L. (1979). Lesch-Nyhan syndrome. Repository identification Nos. GM-2290, 2291, 2292, 2338, 3115, 3116, and 3117. Cytogenetics and cell genetics, 24, 199-200. PubMed
• Del Villano, B. C., Tischfield, J. A., Schacter, L. P., Stilwil, D., & Miller, S. I. (1979). Cupro-zinc superoxide dismutase: a possible biologic marker for alcoholism (studies in black patients). Alcoholism, clinical and experimental research, 3, 291-6. PubMed
• Gerner-Smidt, P., Friedrich, U., Petersen, G. B., & Tischfield, J. A. (1978). A balanced translocation t(11;16)(q13;p11), a cytogenetic study and an attempt at gene localization. Human genetics, 42, 61-6. PubMed
• Dickerman, L. H., & Tischfield, J. A. (1978). Comparative effects of adenine analogs upon metabolic cooperation between Chinese hamster cells with different levels of adenine phosphoribosyltransferase activity. Mutation research, 49, 83-94. PubMed
• Di Girolamo, F., & Rongo, C. A. (1977). [Sulpiride treatment of schizophrenics. Endocrine effects and aggressivity]. Quaderni di criminologia clinica, 19, 237-47. PubMed
• Stanbridge, E. J., Tischfield, J. A., & Schneider, E. L. (1975). Appearance of hypoxanthine guanine phosphoribosyltransferase activity as a consequence of mycoplasma contamination. Nature, 256, 329-31. PubMed
• Creagan, R. P., Carritt, B., Chen, S., Kucherlapati, R., McMorris, F. A., Ricciuti, F., Tan, Y. H., Tischfield, J. A., & Ruddle, F. H. (1974). Proceedings: Confirmation of the synteny of the human genes for cytoplasmic isocitrate dehydrogenase and cytoplasmic malate dehydrogenase and assignment to chromosome 2. Cytogenetics and cell genetics, 13, 79-82. PubMed
• Tischfield, J. A., Creagan, R. P., Ricciuti, F., & Ruddle, F. H. (1974). Proceedings: Assignment of the gene in man for mitochondrial superoxide dismutase (indophenol oxidase-B, tetrameric) to chromosome 6. Cytogenetics and cell genetics, 13, 164-6. PubMed
• Tischfield, J. A., Creagan, R. P., & Ruddle, F. H. (1974). Proceedings: Assignment of a selectable gene: adenine phosphoribosyltransferase to chromosme 16. Cytogenetics and cell genetics, 13, 167-72. PubMed
• Tischfield, J. A., Creagan, R. P., Nichols, E., & Ruddle, F. H. (1974). Proceedings: Assignment of adenosine deaminase to chromosome 20. Cytogenetics and cell genetics, 13, 160-3. PubMed
• Tischfield, J. A., Creagan, R. P., Nichols, E. A., & Ruddle, F. H. (1974). Assignment of a gene for adenosine deaminase to human chromosome 20. Human heredity, 24, 1-11. PubMed
• Tan, Y. H., Tischfield, J. A., & Ruddle, F. H. (1974). Proceedings: The genetics of the antiviral state in human cells. Cytogenetics and cell genetics, 13, 158-9. PubMed
• Creagan, R. P., Tan, Y. H., Chen, S., Tischfield, J. A., & Ruddle, F. H. (1974). Proceedings: Mouse-human somatic cell hybrids utilizing human parental cells containing a (14;22) translocation: assignment of the gene for nucleoside phosphorylase to chromosome 14. Cytogenetics and cell genetics, 13, 83-5. PubMed
• Tan, Y. H., Schneider, E. L., Tischfield, J., Epstein, C. J., & Ruddle, F. H. (1974). Human chromosome 21 dosage: effect on the expression of the interferon induced antiviral state. Science (New York, N.Y.), 186, 61-3. PubMed
• Creagan, R. P., Carritt, B., Chen, S., Kucherlapati, R., McMorris, F. A., Ricciuti, F., Tan, Y. H., Tischfield, J. A., & Ruddle, F. H. (1974). Chromosome assignments of genes in man using mouse-human somatic cell hybrids: Cytoplasmic isocitrate dehydrogenase (IDH 1) and malate dehydrogenase (MDH 1) to chromosomes 2. American journal of human genetics, 26, 604-13. PubMed
• Tischfield, J. A., & Ruddle, F. H. (1974). Assignment of the gene for adenine phosphoribosyltransferase to human chromosome 16 by mouse-human somatic cell hybridization. Proceedings of the National Academy of Sciences of the United States of America, 71, 45-9. PubMed
• Creagan, R. P., Tischfield, J. A., Nichols, E. A., & Ruddle, F. H. (1973). Letter: Autosomal assignment of the gene for the form of adenosine deaminase which is deficient in patients with combined immunodeficiency syndrome. Lancet (London, England), 2, 1449. PubMed
• Creagan, R., Tischfield, J., Ricciuti, F., & Ruddle, F. H. (1973). Chromosome assignments of genes in man using mouse-human somatic cell hybrids: mitochondrial superoxide dismutase (indophenol oxidase-B, tetrameric) to chromosome 6. Humangenetik, 20, 203-9. PubMed
• Creagan, R., Tischfield, J., McMorris, F. A., Chen, S., Hirschi, M., Chen, T. R., Ricciuti, F., & Ruddle, F. H. (1973). Assignment of the genes for human peptidase A to chromosome 18 and cytoplasmic glutamic oxaloacetate transaminase to chromosome 10 using somatic-cell hybrids. Cytogenetics and cell genetics, 12, 187-98. PubMed
• Tischfield, J. A., Bernhard, H. P., & Ruddle, F. H. (1973). A new electrophoretic-autoradiographic method for the visual detection of phosphotransferases. Analytical biochemistry, 53, 545-54. PubMed
• Chen, T. R., McMorris, F. A., Creagan, R., Ricciuti, F., Tischfield, J., & Ruddle, F. (1973). Assignment of the genes for malate oxidoreductase decarboxylating to chromosome 6 and peptidase B and lactate dehydrogenase B to chromosome 12 in man. American journal of human genetics, 25, 200-7. PubMed
• McMorris, F. A., Chen, T. R., Ricciuti, F., Tischfield, J., Creagan, R., & Ruddle, F. (1973). Chromosome assignments in man of the genes for two hexosephosphate isomerases. Science (New York, N.Y.), 179, 1129-31. PubMed
• Tan, Y. H., Tischfield, J., & Ruddle, F. H. (1973). The linkage of genes for the human interferon-induced antiviral protein and indophenol oxidase-B traits to chromosome G-21. The Journal of experimental medicine, 137, 317-30. PubMed