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The genome of the model beetle and pest Tribolium castaneum
by Gibbs, Richard A
Nature, 2008-04-24, Vol.452 (7190), p.949-955
2.
Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution
by Hillier, L.W
Nature, 2004, Vol.432 (7018), p.695-716
3.
Insights into social insects from the genome of the honeybee Apis mellifera
by Worley, Kim C
Nature, 2006-10-26, Vol.443 (7114), p.931-949
4.
Genomic Analyses Reveal Mutational Signatures and Frequently Altered Genes in Esophageal Squamous Cell Carcinoma
by Zhang, Ling
American journal of human genetics, 2015-04-02, Vol.96 (4), p.597-611
5.
Germline BAP1 mutation predisposes to uveal melanoma, lung adenocarcinoma, meningioma, and other cancers
by Abdel-Rahman, Mohamed H
Journal of medical genetics, 2011-12, Vol.48 (12), p.856-859
6.
High-resolution mapping of meiotic crossovers and non-crossovers in yeast
by Steinmetz, Lars M
Nature, 2008-07-24, Vol.454 (7203), p.479-485
7.
Deleterious Mutations in LRBA Are Associated with a Syndrome of Immune Deficiency and Autoimmunity
by Lopez-Herrera, Gabriela
American journal of human genetics, 2012-06-08, Vol.90 (6), p.986-1001
8.
Genome-wide Association Study Identifies TNFSF15 and POU2AF1 as Susceptibility Loci for Primary Biliary Cirrhosis in the Japanese Population
by NAKAMURA, Minoru
American journal of human genetics, 2012, Vol.91 (4), p.721-728
9.
Exonic Deletions in AUTS2 Cause a Syndromic Form of Intellectual Disability and Suggest a Critical Role for the C Terminus
by Beunders, Gea
American journal of human genetics, 2013-02-07, Vol.92 (2), p.210-220
10.
Interplay of somatic alterations and immune infiltration modulates response to PD-1 blockade in advanced clear cell renal cell carcinoma
by Braun, David A
Nature medicine, 2020-06, Vol.26 (6), p.909-918
11.
Precise base editing in rice, wheat and maize with a Cas9-cytidine deaminase fusion
by Zong, Yuan
Nature biotechnology, 2017-05, Vol.35 (5), p.438-440
12.
Impaired Presynaptic High-Affinity Choline Transporter Causes a Congenital Myasthenic Syndrome with Episodic Apnea
by Bauché, Stéphanie
American journal of human genetics, 2016-09-01, Vol.99 (3), p.753-761
13.
Biology and evolution of poorly differentiated neuroendocrine tumors
by Rickman, David S
Nature medicine, 2017-06-06, Vol.23 (6), p.1-673
14.
Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families
by Leppa, Virpi M
American journal of human genetics, 2016-09-01, Vol.99 (3), p.540-554
15.
The grapevine genome sequence suggests ancestral hexaploidization in major angiosperm phyla
by Jaillon, Olivier
Nature, 2007-09-27, Vol.449 (7161), p.463-467
16.
Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant
by Li, Jun
American journal of human genetics, 2016-05-05, Vol.98 (5), p.830-842
17.
Copy Number Variants Are Enriched in Individuals With Early-Onset Obesity and Highlight Novel Pathogenic Pathways
by Pettersson, Maria
The journal of clinical endocrinology and metabolism, 2017-08, Vol.102 (8), p.3029-3039
18.
Fibrinogen as a key regulator of inflammation in disease
by Davalos, Dimitrios
Seminars in immunopathology, 2011-10-31, Vol.34 (1), p.43-62
19.
Excess of De Novo Deleterious Mutations in Genes Associated with Glutamatergic Systems in Nonsyndromic Intellectual Disability
by Hamdan, Fadi F
American journal of human genetics, 2011, Vol.88 (3), p.306-316
20.
Clinical application of exome sequencing in undiagnosed genetic conditions
by Need, Anna C
Journal of medical genetics, 2012-06, Vol.49 (6), p.353-361
