Search details
1.
Practical recommendations for using ctDNA in clinical decision making.
Nature
; 619(7969): 259-268, 2023 Jul.
Article
in English
| MEDLINE | ID: mdl-37438589
2.
A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3.
Am J Hum Genet
; 111(1): 96-118, 2024 Jan 04.
Article
in English
| MEDLINE | ID: mdl-38181735
3.
SWOG S1820: A pilot randomized trial of the Altering Intake, Managing Bowel Symptoms Intervention in Survivors of Rectal Cancer.
Cancer
; 130(13): 2384-2394, 2024 Jul 01.
Article
in English
| MEDLINE | ID: mdl-38386696
4.
Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections.
Genet Med
; 26(2): 101023, 2024 Feb.
Article
in English
| MEDLINE | ID: mdl-37947183
5.
Colorectal cancer pre-diagnostic symptoms are associated with anatomic cancer site.
BMC Gastroenterol
; 24(1): 65, 2024 Feb 06.
Article
in English
| MEDLINE | ID: mdl-38317073
6.
Use of Circulating Tumor DNA to Guide Decision-making in Adjuvant Colon Cancer.
Curr Oncol Rep
; 2024 Jun 06.
Article
in English
| MEDLINE | ID: mdl-38842605
7.
Baseline characteristics and recruitment for SWOG S1820: altering intake, managing bowel symptoms in survivors of rectal cancer (AIMS-RC).
Support Care Cancer
; 32(6): 371, 2024 May 22.
Article
in English
| MEDLINE | ID: mdl-38775966
8.
Functional quality of life among newly diagnosed young adult colorectal cancer survivors compared to older adults: results from the ColoCare Study.
Support Care Cancer
; 32(5): 298, 2024 Apr 19.
Article
in English
| MEDLINE | ID: mdl-38639810
9.
Associations of combined physical activity and body mass index groups with colorectal cancer survival outcomes.
BMC Cancer
; 23(1): 300, 2023 Apr 03.
Article
in English
| MEDLINE | ID: mdl-37013476
10.
SCN1A gain-of-function mutation causing an early onset epileptic encephalopathy.
Epilepsia
; 64(5): 1318-1330, 2023 05.
Article
in English
| MEDLINE | ID: mdl-36287100
11.
Anal Carcinoma, Version 2.2023, NCCN Clinical Practice Guidelines in Oncology.
J Natl Compr Canc Netw
; 21(6): 653-677, 2023 06.
Article
in English
| MEDLINE | ID: mdl-37308125
12.
Lynch Syndrome: From Screening to Diagnosis to Treatment in the Era of Modern Molecular Oncology.
Annu Rev Genomics Hum Genet
; 20: 293-307, 2019 08 31.
Article
in English
| MEDLINE | ID: mdl-30848956
13.
A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3.
Am J Hum Genet
; 111(4): 805, 2024 Apr 04.
Article
in English
| MEDLINE | ID: mdl-38508193
14.
A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3.
Am J Hum Genet
; 111(6): 1239, 2024 Jun 06.
Article
in English
| MEDLINE | ID: mdl-38723631
15.
KRAS Mutation Variants and Co-occurring PI3K Pathway Alterations Impact Survival for Patients with Pancreatic Ductal Adenocarcinomas.
Oncologist
; 27(12): 1025-1033, 2022 12 09.
Article
in English
| MEDLINE | ID: mdl-36124727
16.
Rectal Cancer, Version 2.2022, NCCN Clinical Practice Guidelines in Oncology.
J Natl Compr Canc Netw
; 20(10): 1139-1167, 2022 10.
Article
in English
| MEDLINE | ID: mdl-36240850
17.
Caregiver assessment of quality of life in individuals with genetic developmental and epileptic encephalopathies.
Dev Med Child Neurol
; 64(8): 957-964, 2022 08.
Article
in English
| MEDLINE | ID: mdl-35229292
18.
Assessment of pegylated arginine deiminase and modified FOLFOX6 in patients with advanced hepatocellular carcinoma: Results of an international, single-arm, phase 2 study.
Cancer
; 127(24): 4585-4593, 2021 Dec 15.
Article
in English
| MEDLINE | ID: mdl-34415578
19.
Colon Cancer, Version 2.2021, NCCN Clinical Practice Guidelines in Oncology.
J Natl Compr Canc Netw
; 19(3): 329-359, 2021 03 02.
Article
in English
| MEDLINE | ID: mdl-33724754
20.
NCCN Guidelines Insights: Rectal Cancer, Version 6.2020.
J Natl Compr Canc Netw
; 18(7): 806-815, 2020 07.
Article
in English
| MEDLINE | ID: mdl-32634771