Genomic diagnosis for children with intellectual disability and/or developmental delay
Bowling, Kevin M, Thompson, Michelle L, Amaral, Michelle D, Finnila, Candice R, Hiatt, Susan M, Engel, Krysta L, Cochran, J Nicholas, Brothers, Kyle B, East, Kelly M, Gray, David E, Kelley, Whitley V, Lamb, Neil E, Lose, Edward J, Rich, Carla A, Simmons, Shirley, Whittle, Jana S, Weaver, Benjamin T, Nesmith, Amy S, Myers, Richard M, Barsh, Gregory S, Bebin, E Martina, Cooper, Gregory M
Published in Genome medicine (30.05.2017)
Published in Genome medicine (30.05.2017)
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Identification of Krüppel-like factor 4 as a potential tumor suppressor gene in colorectal cancer
WEIDONG ZHAO, HISAMUDDIN, Irfan M, NANDAN, Mandayam O, BABBIN, Brian A, LAMB, Neil E, YANG, Vincent W
Published in Oncogene (15.01.2004)
Published in Oncogene (15.01.2004)
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Characteristics and experiences of patients from a community-based and consumer-directed hereditary cancer population screening initiative
Greve, Veronica, Odom, Katherine, Pudner, Susanna, Lamb, Neil E., Cooper, Sara J., East, Kelly
Published in HGG advances (13.01.2022)
Published in HGG advances (13.01.2022)
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Association between Maternal Age and Meiotic Recombination for Trisomy 21
Lamb, Neil E., Yu, Kai, Shaffer, John, Feingold, Eleanor, Sherman, Stephanie L.
Published in American journal of human genetics (01.01.2005)
Published in American journal of human genetics (01.01.2005)
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Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II
Lamb, Neil E, Freeman, Sallie B, Savage-Austin, Amanda, Pettay, Dorothy, Taft, Lisa, Hersey, Jane, Gu, Yuanchao, Shen, Joe, Saker, Denise, May, Kristen M, Avramopoulos, Dimitris, Petersen, Michael B, Hallberg, Anni, Mikkelsen, Margareta, Hassold, Terry J, Sherman, Stephanie L
Published in Nature genetics (01.12.1996)
Published in Nature genetics (01.12.1996)
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Recombination rate and reproductive success in humans
Kong, Augustine, Stefansson, Kari, Barnard, John, Gudbjartsson, Daniel F, Thorleifsson, Gudmar, Jonsdottir, Gudrun, Sigurdardottir, Sigrun, Richardsson, Bjorgvin, Jonsdottir, Jonina, Thorgeirsson, Thorgeir, Frigge, Michael L, Lamb, Neil E, Sherman, Stephanie, Gulcher, Jeffrey R
Published in Nature genetics (01.11.2004)
Published in Nature genetics (01.11.2004)
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Biotech 101: An Educational Outreach Program in Genetics and Biotechnology
East, Kelly M., Hott, Adam M., Callanan, Nancy P., Lamb, Neil E.
Published in Journal of genetic counseling (01.10.2012)
Published in Journal of genetic counseling (01.10.2012)
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A new method for identifying informative genetic markers in selectively bred rats
Weinshenker, David, Wilson, Malania M, Williams, Katherine M, Weiss, Jay M, Lamb, Neil E, Twigger, Simon N
Published in Mammalian genome (01.10.2005)
Published in Mammalian genome (01.10.2005)
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Obligate Short-Arm Exchange in De Novo Robertsonian Translocation Formation Influences Placement of Crossovers in Chromosome 21 Nondisjunction
Berend, Sue Ann, Page, Scott L., Atkinson, William, McCaskill, Christopher, Lamb, Neil E., Sherman, Stephanie L., Shaffer, Lisa G.
Published in American journal of human genetics (01.02.2003)
Published in American journal of human genetics (01.02.2003)
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Systematic reanalysis of genomic data improves quality of variant interpretation
Hiatt, S.M., Amaral, M.D., Bowling, K.M., Finnila, C.R., Thompson, M.L., Gray, D.E., Lawlor, J.M.J., Cochran, J.N., Bebin, E.M., Brothers, K.B., East, K.M., Kelley, W.V., Lamb, N.E., Levy, S.E., Lose, E.J., Neu, M.B., Rich, C.A., Simmons, S., Myers, R.M., Barsh, G.S., Cooper, G.M.
Published in Clinical genetics (01.07.2018)
Published in Clinical genetics (01.07.2018)
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Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine
Goddard, Katrina A.B., Jarvik, Gail P., Amendola, Laura M., Berg, Jonathan S., Blout, Carrie L., Brothers, Kyle B., Caga-anan, Charlisse F., Clayton, Ellen W., East, Kelly, Evans, James P., Fullerton, Stephanie M., Holm, Ingrid A., Kaufman, David, Knoppers, Bartha M., McCullough, Laurence, McGuire, Amy, Myers, Richard M., Nickerson, Deborah A., Robinson, Dan, Salama, Joseph S., Scollon, Sarah, Shirts, Brian, Tabor, Holly K., Tarczy-Hornoch, Peter, Veenstra, David L., Wagle, Nikhil, Wynn, Julia, Amendola, Laura, Aronson, Samuel J., Arora, Shubhangi, Azzariti, Danielle R., Biesecker, Barbara B., Byers, Peter H., Calikoglu, Muge G., Cirino, Allison L., Conlin, Laura K., Cooper, Greg M., Crosslin, David R., Davis, James V., Dugan, Noreen P., Exe, Nicole, Fan, Zheng, Filipski, Kelly, Fishler, Kristen, Ghrundmeier, Bob, Gilmore, Marian J., Gordon, Adam S., Gornick, Michele C., Grady, William M., Gutierrez, Amanda M., Hensman, Naomi, Himes, Patricia, Hisama, Fuki M., Hull, Sara, Joffe, Steve, Karavite, Dean, Kauffman, Tia L., Kaufman, Dave, Kim, Jerry H., Klein, William, Krantz, Ian, Le, Lan Q., Lebo, Matthew S., Leo, Michael C., Lewis, Katie, Lewis, Michelle, Lindeman, Neal I., Lonigro, Bob, Lose, Edward J., Lupo, Philip J., Machini, Kalotina, Marchuk, Daniel S., McMullen, Carmit, Miller, Victoria A., Moore, Elizabeth G., Ng, David, Oliver, Nelly M., Parsons, Will, Patrick, Donald L., Plon, Sharon, Powell, Bradford C., Breitkopf, Carmen Radecki, Raskind, Wendy H., Rini, Christine, Robertson, Peggy D., Salama, Joseph, Shirts, Brian H., Siddiqui, Javed, Silverman, Elian, Simmons, Shirley, Simons, Janae V., Stoffel, Elena, Tilley, Christian R., Tomlinson, Ashley, Trinidad, Susan, Ubel, Peter, Walsh, Rebecca C., Wilfond, Ben, Wilhelmsen, Kirk C., Young, Carol
Published in American journal of human genetics (07.07.2016)
Published in American journal of human genetics (07.07.2016)
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Journal Article
Characterization of Susceptible Chiasma Configurations that Increase the Risk for Maternal Nondisjunction of Chromosome 21
Lamb, Neil E., Feingold, Eleanor, Savage, Amanda, Avramopoulos, Dimitris, Freeman, Sallie, Gu, Yuanchao, Hallberg, Anni, Hersey, Jane, Karadima, Georgia, Pettay, Dorothy, Saker, Denise, Shen, Joe, Taft, Lisa, Mikkelsen, Margareta, Petersen, Michael B., Hassold, Terry, Sherman, Stephanie L.
Published in Human molecular genetics (01.09.1997)
Published in Human molecular genetics (01.09.1997)
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