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Works matching AU Laffin, Jennifer J.

Results: 6

1

Validation of a comprehensive long-read sequencing platform for broad clinical genetic diagnosis.

Published in:

Frontiers in Genetics, 2025, p. 1, doi. 10.3389/fgene.2025.1499456

By:

Sen, Siddhartha;
Handler, Hillary P.;
Victorsen, Alec;
Flaten, Zach;
Ellison, Aidan;
Knutson, Todd P.;
Munro, Sarah A.;
Martinez, Ryan J.;
Billington, Charles John;
Laffin, Jennifer J.;
Bray, Sarah;
Mroz, Pawel;
Yohe, Sophia;
Nelson, Andrew C.;
Bower, Matthew;
Thyagarajan, Bharat

Publication type:

Article

2

Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome.

Published in:

European Journal of Human Genetics, 2013, v. 21, n. 4, p. 455, doi. 10.1038/ejhg.2012.165

By:

Raca, Gordana;
Baas, Becky S;
Kirmani, Salman;
Laffin, Jennifer J;
Jackson, Craig A;
Strand, Edythe A;
Jakielski, Kathy J;
Shriberg, Lawrence D

Publication type:

Article

3

Analytical validation of a novel multi-target blood-based test to detect hepatocellular carcinoma.

Published in:

Expert Review of Molecular Diagnostics, 2021, v. 21, n. 11, p. 1245, doi. 10.1080/14737159.2021.1981290

By:

Johnson, Andrea M.;
Dudek, Jeanne M.;
Edwards, David K.;
Myers, Theran A.;
Joseph, Patrick;
Laffin, Jennifer J.;
Bruinsma, Janelle J.

Publication type:

Article

4

Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.

Published in:

Journal of Neurodevelopmental Disorders, 2013, v. 5, n. 1, p. 1, doi. 10.1186/1866-1955-5-29

By:

Worthey, Elizabeth A.;
Raca, Gordana;
Laffin, Jennifer J.;
Wilk, Brandon M.;
Harris, Jeremy M.;
Jakielski, Kathy J.;
Dimmock, David P.;
Strand, Edythe A.;
Shriberg, Lawrence D.

Publication type:

Article

5

Phenotype of FOXP2 haploinsufficiency in a mother and son.

Published in:

American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 1, p. 174, doi. 10.1002/ajmg.a.34354

By:

Rice, Gregory M.;
Raca, Gordana;
Jakielski, Kathy J.;
Laffin, Jennifer J.;
Iyama-Kurtycz, Christina M.;
Hartley, Sigan L.;
Sprague, Rae E.;
Heintzelman, Anne T.;
Shriberg, Lawrence D.

Publication type:

Article

6

Chromosomal instability sensitizes patient breast tumors to multipolar divisions induced by paclitaxel.

Published in:

Science Translational Medicine, 2021, v. 13, n. 610, p. 1, doi. 10.1126/scitranslmed.abd4811

By:

Scribano, Christina M.;
Wan, Jun;
Esbona, Karla;
Tucker, John B.;
Lasek, Amber;
Zhou, Amber S.;
Zasadil, Lauren M.;
Molini, Ryan;
Fitzgerald, Jonathan;
Lager, Angela M.;
Laffin, Jennifer J.;
Correia-Staudt, Kayla;
Wisinski, Kari B.;
Tevaarwerk, Amye J.;
O'Regan, Ruth;
McGregor, Stephanie M.;
Fowler, Amy M.;
Chappell, Richard J.;
Bugni, Tim S.;
Burkard, Mark E.

Publication type:

Article