| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Age dependency of the polygenic risk score for colorectal cancer
|
Li, Shuai
|
|
|
108 |
3 |
p. 525-526
|
artikel
|
| 2 |
2020 ASHG awards and addresses
|
|
|
|
108 |
3 |
p. 373-374
|
artikel
|
| 3 |
ASHG 2020 Curt Stern Award introduction: Fowzan Sami Alkuraya
|
Morton, Cynthia C.
|
|
|
108 |
3 |
p. 392-394
|
artikel
|
| 4 |
2020 ASHG presidential address: the ‘BIG TENT’ of genetics/genomics and our world
|
Wynshaw-Boris, Anthony
|
|
|
108 |
3 |
p. 375-382
|
artikel
|
| 5 |
2020 Curt Stern Award address: a more perfect clinical genome—how consanguineous populations contribute to the medical annotation of the human genome
|
Alkuraya, Fowzan S.
|
|
|
108 |
3 |
p. 395-399
|
artikel
|
| 6 |
Genetic control of the human brain proteome
|
Robins, Chloe
|
|
|
108 |
3 |
p. 400-410
|
artikel
|
| 7 |
Homozygous pathogenic variants in ACTL9 cause fertilization failure and male infertility in humans and mice
|
Dai, Jing
|
|
|
108 |
3 |
p. 469-481
|
artikel
|
| 8 |
How science will help us move forward in 2021
|
|
|
|
108 |
3 |
p. 371-372
|
artikel
|
| 9 |
Human ancient DNA analyses reveal the high burden of tuberculosis in Europeans over the last 2,000 years
|
Kerner, Gaspard
|
|
|
108 |
3 |
p. 517-524
|
artikel
|
| 10 |
Integrative analysis of liver-specific non-coding regulatory SNPs associated with the risk of coronary artery disease
|
Selvarajan, Ilakya
|
|
|
108 |
3 |
p. 411-430
|
artikel
|
| 11 |
Loss of α-actinin-3 during human evolution provides superior cold resilience and muscle heat generation
|
Wyckelsma, Victoria L.
|
|
|
108 |
3 |
p. 446-457
|
artikel
|
| 12 |
Mendelian pathway analysis of laboratory traits reveals distinct roles for ciliary subcompartments in common disease pathogenesis
|
Drivas, Theodore George
|
|
|
108 |
3 |
p. 482-501
|
artikel
|
| 13 |
Rare and de novo coding variants in chromodomain genes in Chiari I malformation
|
Sadler, Brooke
|
|
|
108 |
3 |
p. 530-531
|
artikel
|
| 14 |
Response to Li and Hopper
|
Thomas, Minta
|
|
|
108 |
3 |
p. 527-529
|
artikel
|
| 15 |
SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females
|
Radio, Francesca Clementina
|
|
|
108 |
3 |
p. 502-516
|
artikel
|
| 16 |
Strong functional data for pathogenicity or neutrality classify BRCA2 DNA-binding-domain variants of uncertain significance
|
Richardson, Marcy E.
|
|
|
108 |
3 |
p. 458-468
|
artikel
|
| 17 |
This month in The Journal
|
Ratzel, Sarah
|
|
|
108 |
3 |
p. 369-370
|
artikel
|
| 18 |
Whole-genome sequencing of African Americans implicates differential genetic architecture in inflammatory bowel disease
|
Somineni, Hari K.
|
|
|
108 |
3 |
p. 431-445
|
artikel
|
| 19 |
2020 William Allan Award address: genetics as a way of thinking—cultural inheritance from our teachers
|
King, Mary-Claire
|
|
|
108 |
3 |
p. 386-391
|
artikel
|
| 20 |
2020 William Allan Award introduction: Mary-Claire King
|
Eichler, Evan E.
|
|
|
108 |
3 |
p. 383-385
|
artikel
|
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