Is it time to re‐think how we look for teratogenic effects in exposure cohort studies? von Friedman, Jan M.

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Massively Parallel Sequencing: The Next Big Thing in Genetic Medicine von Tucker, Tracy, Marra, Marco, Friedman, Jan M.

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Clinical and genetic aspects of neurofibromatosis 1 von Jett, Kimberly, Friedman, Jan M.

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Safety of Selective Serotonin Reuptake Inhibitors in Pregnancy: A Review of Current Evidence von Alwan, Sura, Friedman, Jan M., Chambers, Christina

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Exome sequencing for gene discovery in lethal fetal disorders - harnessing the value of extreme phenotypes von Filges, Isabel, Friedman, Jan M.

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The composition and capacity of the clinical genetics workforce in high-income countries: a scoping review von Dragojlovic, Nick, Borle, Kennedy, Kopac, Nicola, Ellis, Ursula, Birch, Patricia, Adam, Shelin, Friedman, Jan M., Nisselle, Amy, Elliott, Alison M., Lynd, Larry D.

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Specific SSRIs and birth defects: bayesian analysis to interpret new data in the context of previous reports von Reefhuis, Jennita, Devine, Owen, Friedman, Jan M, Louik, Carol, Honein, Margaret A

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The importance of genetic counselling in genome-wide sequencing von Elliott, Alison M., Friedman, Jan M.

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Straglr: discovering and genotyping tandem repeat expansions using whole genome long-read sequences von Chiu, Readman, Rajan-Babu, Indhu-Shree, Friedman, Jan M., Birol, Inanc

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Low risk of solid tumors in persons with Down syndrome von Hasle, Henrik, Friedman, Jan M., Olsen, Jørgen H., Rasmussen, Sonja A.

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Exome Sequencing and Clinical Diagnosis von Friedman, Jan M, Jones, Kenneth Lyons, Carey, John C

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Maternal treatment with opioid analgesics and risk for birth defects von Broussard, Cheryl S., PhD, Rasmussen, Sonja A., MD, MS, Reefhuis, Jennita, PhD, Friedman, Jan M., MD, PhD, Jann, Michael W., PharmD, Riehle-Colarusso, Tiffany, MD, MSE, Honein, Margaret A., PhD, MPH

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Bob Brent: Medical expert, expert medical witness, and expert on medical expert witnessing von Friedman, Jan M

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The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists von Boycott, Kym, Hartley, Taila, Adam, Shelin, Bernier, Francois, Chong, Karen, Fernandez, Bridget A, Friedman, Jan M, Geraghty, Michael T, Hume, Stacey, Knoppers, Bartha M, Laberge, Anne-Marie, Majewski, Jacek, Mendoza-Londono, Roberto, Meyn, M Stephen, Michaud, Jacques L, Nelson, Tanya N, Richer, Julie, Sadikovic, Bekim, Skidmore, David L, Stockley, Tracy, Taylor, Sherry, van Karnebeek, Clara, Zawati, Ma'n H, Lauzon, Julie, Armour, Christine M

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Genome-wide sequencing as a first-tier screening test for short tandem repeat expansions von Rajan-Babu, Indhu-Shree, Pen, Junran J., Chiu, Readman, Li, Chenkai, Mohajeri, Arezoo, Dolzhenko, Egor, Eberle, Michael A., Birol, Inanc, Friedman, Jan M.

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Sequence composition changes in short tandem repeats: heterogeneity, detection, mechanisms and clinical implications von Rajan-Babu, Indhu-Shree, Dolzhenko, Egor, Eberle, Michael A., Friedman, Jan M.

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Use of Selective Serotonin-Reuptake Inhibitors in Pregnancy and the Risk of Birth Defects von Alwan, Sura, Reefhuis, Jennita, Rasmussen, Sonja A, Olney, Richard S, Friedman, Jan M

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A novel recurrent mutation in ATP1A3 causes CAPOS syndrome von Demos, Michelle K, van Karnebeek, Clara Dm, Ross, Colin Jd, Adam, Shelin, Shen, Yaoqing, Zhan, Shing Hei, Shyr, Casper, Horvath, Gabriella, Suri, Mohnish, Fryer, Alan, Jones, Steven Jm, Friedman, Jan M

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Patterns of Antidepressant Medication Use Among Pregnant Women in a United States Population von Alwan, Sura, Reefhuis, Jennita, Rasmussen, Sonja A., Friedman, Jan M.

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Exome Sequencing as Part of a Multidisciplinary Approach to Diagnosis—Reply von Friedman, Jan M, Jones, Kenneth Lyons, Carey, John C

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